Skip to main content
Top
Published in: CNS Drugs 10/2005

01-10-2005 | Review Article

Recent Advances in the Development of Treatments for Alcohol and Cocaine Dependence

Focus on Topiramate and Other Modulators of GABA or Glutamate Function

Author: Prof. Bankole A. Johnson

Published in: CNS Drugs | Issue 10/2005

Login to get access

Abstract

Neuroscientific developments have promulgated interest in developing efficacious medications for the treatment of substance dependence. Previous pharmacological strategies that involve the use of relatively specific medications to alter corticomesolimbic dopaminergic neuronal activity —the critical pathway for expression of the reinforcing effects of abused drugs —have yielded modest efficacy in the treatment of alcohol dependence, and no medication has been established as a treatment for cocaine dependence. Since corticomesolimbic dopaminergic neurons interact with other neurotransmitters that modulate the effects of dopamine in the nucleus accumbens, would it not be possible to control these dopaminergic effects more reliably with a medication that acts contempora-neously on more than one neuromodulator of dopaminergic function? Further, since the long-term use of either alcohol or cocaine results in neuronal adaptations as a result of sensitisation, would the chances of effective therapy not be bolstered by administering a medication that was also able to mitigate these chronic effects? Thus, a new conceptual approach is needed.
My proposal is that a medication —in this case topiramate —that principally potentiates inhibitory GABAa receptor-mediated input and antagonises excitatory glutamatergic afferents to the corticomesolimbic dopaminergic system should have therapeutic potential in treating either alcohol or cocaine dependence or perhaps both. This is because the principal neurochemical effects of topiramate would not only serve to decrease the acute reinforcing effects of alcohol or cocaine, but might also facilitate cessation of their use following a period of long-term use by decreasing neuronal sensitisation.
This overview highlights the scientific concepts and clinical evidence for the development of topiramate in the treatment of alcohol dependence and introduces preliminary evidence to indicate that it might also have utility in treating cocaine dependence. Finally, to place the material on topiramate in context, information has been included on the utility and development of other medications that modulate GABA-or glutamate-mediated neuronal systems for the treatment of alcohol or cocaine dependence.
Literature
1.
2.
go back to reference Hyman SE, Malenka RC. Addiction and the brain: the neurobiology of compulsion and its persistence. Nat Rev Neurosci 2001; 2: 695–703PubMedCrossRef Hyman SE, Malenka RC. Addiction and the brain: the neurobiology of compulsion and its persistence. Nat Rev Neurosci 2001; 2: 695–703PubMedCrossRef
4.
go back to reference Weiss F, Porrino LJ. Behavioral neurobiology of alcohol addiction: recent advances and challenges. J Neurosci 2002; 22: 3332–7PubMed Weiss F, Porrino LJ. Behavioral neurobiology of alcohol addiction: recent advances and challenges. J Neurosci 2002; 22: 3332–7PubMed
5.
go back to reference Johnson BA, Ait-Daoud N. Neuropharmacological treatments for alcoholism: scientific basis and clinical findings. Psychopharmacology 2000; 149: 327–44PubMedCrossRef Johnson BA, Ait-Daoud N. Neuropharmacological treatments for alcoholism: scientific basis and clinical findings. Psychopharmacology 2000; 149: 327–44PubMedCrossRef
6.
go back to reference Kreek MJ, LaForge KS, Butelman E. Pharmacotherapy of addictions. Nat Rev Drug Discov 2002; 1: 710–26PubMedCrossRef Kreek MJ, LaForge KS, Butelman E. Pharmacotherapy of addictions. Nat Rev Drug Discov 2002; 1: 710–26PubMedCrossRef
7.
go back to reference Di Chiara G, Imperato A. Drugs abused by humans preferentially increase synaptic dopamine concentrations in the mesolimbic system of freely moving rats. Proc Natl Acad Sci U S A 1988; 85: 5274–8PubMedCrossRef Di Chiara G, Imperato A. Drugs abused by humans preferentially increase synaptic dopamine concentrations in the mesolimbic system of freely moving rats. Proc Natl Acad Sci U S A 1988; 85: 5274–8PubMedCrossRef
8.
go back to reference Rodd-Henricks ZA, McKinzie DL, Crile RS, et al. Regional heterogeneity for the intracranial self-administration of ethanol within the ventral tegmental area of female Wistar rats. Psychopharmacology 2000; 149: 217–24PubMedCrossRef Rodd-Henricks ZA, McKinzie DL, Crile RS, et al. Regional heterogeneity for the intracranial self-administration of ethanol within the ventral tegmental area of female Wistar rats. Psychopharmacology 2000; 149: 217–24PubMedCrossRef
9.
go back to reference Li TK, McBride WJ. Pharmacogenetic models of alcoholism. Clin Neurosci 1995; 3: 182–8PubMed Li TK, McBride WJ. Pharmacogenetic models of alcoholism. Clin Neurosci 1995; 3: 182–8PubMed
10.
go back to reference McBride WJ, Murphy JM, Gatto GJ, et al. CNS mechanisms of alcohol self-administration. Alcohol Alcohol Suppl 1993; 2: 463–7PubMed McBride WJ, Murphy JM, Gatto GJ, et al. CNS mechanisms of alcohol self-administration. Alcohol Alcohol Suppl 1993; 2: 463–7PubMed
11.
go back to reference Melendez RI, Rodd-Henricks ZA, Engleman EA, et al. Microdialysis of dopamine in the nucleus accumbens of alcoholpreferring (P) rats during anticipation and operant self-administration of ethanol. Alcohol Clin Exp Res 2002; 26: 318–25PubMedCrossRef Melendez RI, Rodd-Henricks ZA, Engleman EA, et al. Microdialysis of dopamine in the nucleus accumbens of alcoholpreferring (P) rats during anticipation and operant self-administration of ethanol. Alcohol Clin Exp Res 2002; 26: 318–25PubMedCrossRef
12.
go back to reference Yan QS. Extracellular dopamine and serotonin after ethanol monitored with 5-minute microdialysis. Alcohol 1999; 19: 1–7PubMedCrossRef Yan QS. Extracellular dopamine and serotonin after ethanol monitored with 5-minute microdialysis. Alcohol 1999; 19: 1–7PubMedCrossRef
13.
go back to reference Nurmi M, Ashizawa T, Sinclair JD, et al. Effect of prior ethanol experience on dopamine overflow in accumbens of AA and ANA rats. Eur J Pharmacol 1996; 315: 277–83PubMedCrossRef Nurmi M, Ashizawa T, Sinclair JD, et al. Effect of prior ethanol experience on dopamine overflow in accumbens of AA and ANA rats. Eur J Pharmacol 1996; 315: 277–83PubMedCrossRef
14.
go back to reference Hemby SE. Neurobiology of alcoholism. In: Johnson BA, Ruiz P, Galanter M, editors. Handbook of clinical alcoholism treatment. Baltimore (MD): Lippincott Williams & Wilkins, 2003: 10–8 Hemby SE. Neurobiology of alcoholism. In: Johnson BA, Ruiz P, Galanter M, editors. Handbook of clinical alcoholism treatment. Baltimore (MD): Lippincott Williams & Wilkins, 2003: 10–8
15.
go back to reference Ritz MC, Lamb RJ, Goldberg SR, et al. Cocaine receptors on dopamine transporters are related to self-administration of cocaine. Science 1987; 237: 1219–23PubMedCrossRef Ritz MC, Lamb RJ, Goldberg SR, et al. Cocaine receptors on dopamine transporters are related to self-administration of cocaine. Science 1987; 237: 1219–23PubMedCrossRef
16.
go back to reference Bozarth MA. Neural basis of psychomotor stimulant and opiate reward: evidence suggesting the involvement of a common dopaminergic system. Behav Brain Res 1986; 22: 107–16PubMedCrossRef Bozarth MA. Neural basis of psychomotor stimulant and opiate reward: evidence suggesting the involvement of a common dopaminergic system. Behav Brain Res 1986; 22: 107–16PubMedCrossRef
17.
go back to reference Hemby SE, Johnson BA, Dworkin SI. Neurobiological basis of drug reinforcement. In: Johnson BA, Roache JD, editors. Drug addiction and its treatment: nexus of neuroscience and behavior. Philadelphia (PA): Lippincott-Raven, 1997: 137–69 Hemby SE, Johnson BA, Dworkin SI. Neurobiological basis of drug reinforcement. In: Johnson BA, Roache JD, editors. Drug addiction and its treatment: nexus of neuroscience and behavior. Philadelphia (PA): Lippincott-Raven, 1997: 137–69
18.
go back to reference Carboni E, Imperato A, Perezanni L, et al. Amphetamine, cocaine, phencyclidine, and nomifensine increase extracellular dopamine concentrations preferentially in the nucleus accum-bens of freely moving rats. Neuroscience 1989; 28: 653–61PubMedCrossRef Carboni E, Imperato A, Perezanni L, et al. Amphetamine, cocaine, phencyclidine, and nomifensine increase extracellular dopamine concentrations preferentially in the nucleus accum-bens of freely moving rats. Neuroscience 1989; 28: 653–61PubMedCrossRef
19.
go back to reference Roberts DCS, Corcoran ME, Fibiger HC. On the role of ascending catecholaminergic systems in intravenous self-administration of cocaine. Pharmacol Biochem Behav 1977; 6: 615–20PubMedCrossRef Roberts DCS, Corcoran ME, Fibiger HC. On the role of ascending catecholaminergic systems in intravenous self-administration of cocaine. Pharmacol Biochem Behav 1977; 6: 615–20PubMedCrossRef
20.
go back to reference Roberts DCS, Koob GF, Klonoff P, et al. Extinction and recovery of cocaine self-administration following 6-hydroxy-dopamine lesions of the nucleus accumbens. Pharmacol Biochem Behav 1980; 12: 781–7PubMedCrossRef Roberts DCS, Koob GF, Klonoff P, et al. Extinction and recovery of cocaine self-administration following 6-hydroxy-dopamine lesions of the nucleus accumbens. Pharmacol Biochem Behav 1980; 12: 781–7PubMedCrossRef
21.
go back to reference Roberts DC, Koob GF. Disruption of cocaine self-administration following 6-hydroxydopamine lesions of the ventral tegmental area in rats. Pharmacol Biochem Behav 1982; 17: 901–4PubMedCrossRef Roberts DC, Koob GF. Disruption of cocaine self-administration following 6-hydroxydopamine lesions of the ventral tegmental area in rats. Pharmacol Biochem Behav 1982; 17: 901–4PubMedCrossRef
22.
go back to reference Weiss F, Lorang MT, Bloom FE, et al. Oral alcohol self-administration stimulates dopamine release in the rat nucleus accumbens: genetic and motivational determinants. J Pharmacol Exp Ther 1993; 267: 250–8PubMed Weiss F, Lorang MT, Bloom FE, et al. Oral alcohol self-administration stimulates dopamine release in the rat nucleus accumbens: genetic and motivational determinants. J Pharmacol Exp Ther 1993; 267: 250–8PubMed
23.
go back to reference Bradberry CW. Dose-dependent effect of ethanol on extracellular dopamine in mesolimbic striatum of awake rhesus monkeys: comparison with cocaine across individuals. Psychopharmacology 2002; 165: 67–76PubMedCrossRef Bradberry CW. Dose-dependent effect of ethanol on extracellular dopamine in mesolimbic striatum of awake rhesus monkeys: comparison with cocaine across individuals. Psychopharmacology 2002; 165: 67–76PubMedCrossRef
24.
go back to reference Johnson LR, Aylward RL, Hussain Z, et al. Input from the amygdala to the rat nucleus accumbens: its relationship with tyrosine hydroxylase immunoreactivity and identified neurons. Neuroscience 1994; 61: 851–65PubMedCrossRef Johnson LR, Aylward RL, Hussain Z, et al. Input from the amygdala to the rat nucleus accumbens: its relationship with tyrosine hydroxylase immunoreactivity and identified neurons. Neuroscience 1994; 61: 851–65PubMedCrossRef
25.
go back to reference Sesack SR, Pickel VM. In the rat medial nucleus accumbens, hippocampal and catecholaminergic terminals converge on spiny neurons and are in apposition to each other. Brain Res 1990; 527: 266–79PubMedCrossRef Sesack SR, Pickel VM. In the rat medial nucleus accumbens, hippocampal and catecholaminergic terminals converge on spiny neurons and are in apposition to each other. Brain Res 1990; 527: 266–79PubMedCrossRef
26.
go back to reference Sesack SR, Pickel VM. Prefrontal cortical efferents in the rat synapse on unlabeled neuronal targets of catecholamine terminals in the nucleus accumbens septi and on dopamine neurons in the ventral tegmental area. J Comp Neurol 1992; 320: 145–60PubMedCrossRef Sesack SR, Pickel VM. Prefrontal cortical efferents in the rat synapse on unlabeled neuronal targets of catecholamine terminals in the nucleus accumbens septi and on dopamine neurons in the ventral tegmental area. J Comp Neurol 1992; 320: 145–60PubMedCrossRef
27.
go back to reference Hope BT, Nye HE, Kelz MB, et al. Induction of a long-lasting AP-1 complex composed of altered Fos-like proteins in brain by chronic cocaine and other chronic treatments. Neuron 1994; 13: 1235–44PubMedCrossRef Hope BT, Nye HE, Kelz MB, et al. Induction of a long-lasting AP-1 complex composed of altered Fos-like proteins in brain by chronic cocaine and other chronic treatments. Neuron 1994; 13: 1235–44PubMedCrossRef
28.
go back to reference Carlezon Jr WA, Nestler EJ. Elevated levels of GluRl in the midbrain: a trigger for sensitization to drugs of abuse? Trends Neurosci 2002; 25: 610–5PubMedCrossRef Carlezon Jr WA, Nestler EJ. Elevated levels of GluRl in the midbrain: a trigger for sensitization to drugs of abuse? Trends Neurosci 2002; 25: 610–5PubMedCrossRef
29.
go back to reference Breese CR, Freedman R, Leonard SS. Glutamate receptor subtype expression in human postmortem brain tissue from schizophrenics and alcohol abusers. Brain Res 1995; 674: 82-90PubMedCrossRef Breese CR, Freedman R, Leonard SS. Glutamate receptor subtype expression in human postmortem brain tissue from schizophrenics and alcohol abusers. Brain Res 1995; 674: 82-90PubMedCrossRef
30.
go back to reference Kelz MB, Chen J, Carlezon Jr WA, et al. Expression of the transcription factor deltaFosB in the brain controls sensitivity to cocaine. Nature 1999; 401: 272–6PubMedCrossRef Kelz MB, Chen J, Carlezon Jr WA, et al. Expression of the transcription factor deltaFosB in the brain controls sensitivity to cocaine. Nature 1999; 401: 272–6PubMedCrossRef
31.
go back to reference Shaywitz AJ, Greenberg ME. CREB: a stimulus-induced tran-scription factor activated by a diverse array of extracellular signals. Annu Rev Biochem 1999; 68: 821–61PubMedCrossRef Shaywitz AJ, Greenberg ME. CREB: a stimulus-induced tran-scription factor activated by a diverse array of extracellular signals. Annu Rev Biochem 1999; 68: 821–61PubMedCrossRef
32.
go back to reference Nestler EJ. Molecular basis of long-term plasticity underlying addiction. Nat Rev Neurosci 2001; 2: 119–28PubMedCrossRef Nestler EJ. Molecular basis of long-term plasticity underlying addiction. Nat Rev Neurosci 2001; 2: 119–28PubMedCrossRef
33.
go back to reference Shank RP, Gardocki JF, Streeter AJ, et al. An overview of the preclinical aspects of topiramate: pharmacology, pharmacokinetics, and mechanism of action. Epilepsia 2000; 41Suppl. 1: S3–9PubMedCrossRef Shank RP, Gardocki JF, Streeter AJ, et al. An overview of the preclinical aspects of topiramate: pharmacology, pharmacokinetics, and mechanism of action. Epilepsia 2000; 41Suppl. 1: S3–9PubMedCrossRef
34.
go back to reference Johnson & Johnson Pharmaceutical Research & Development. Investigator’s Brochure: RWJ-17021-000 (Topiramate). 8th ed.; 2003 Jul Johnson & Johnson Pharmaceutical Research & Development. Investigator’s Brochure: RWJ-17021-000 (Topiramate). 8th ed.; 2003 Jul
35.
go back to reference ResorJr SR, Resor LD, Woodbury DM, et al. Acetazolamide. In: Levy RH, Mattson RH, Meldrum BS, editors. Antiepileptic drugs. New York (NY): Raven Press, 1995: 969–85 ResorJr SR, Resor LD, Woodbury DM, et al. Acetazolamide. In: Levy RH, Mattson RH, Meldrum BS, editors. Antiepileptic drugs. New York (NY): Raven Press, 1995: 969–85
36.
go back to reference Bialer M, Johannessen SI, Kupferberg HJ, et al. Progress report on new antiepileptic drugs: a summary of the fourth Eilat conference (EILAT IV). Epilepsy Res 1999; 34: 1–41PubMedCrossRef Bialer M, Johannessen SI, Kupferberg HJ, et al. Progress report on new antiepileptic drugs: a summary of the fourth Eilat conference (EILAT IV). Epilepsy Res 1999; 34: 1–41PubMedCrossRef
37.
go back to reference Abou-Khalil B. Topiramate in the long-term management of refractory epilepsy. Topiramate YOL Study Group. Epilepsia 2000; 41Suppl. 1: S72–6PubMedCrossRef Abou-Khalil B. Topiramate in the long-term management of refractory epilepsy. Topiramate YOL Study Group. Epilepsia 2000; 41Suppl. 1: S72–6PubMedCrossRef
38.
go back to reference Montouris GD, Biton V, Rosenfeld WE. Nonfocal generalized tonic-clonic seizures: response during long-term topiramate treatment. Topiramate YTC/YTCE Study Group. Epilepsia 2000; 41Suppl. 1: S77–81PubMedCrossRef Montouris GD, Biton V, Rosenfeld WE. Nonfocal generalized tonic-clonic seizures: response during long-term topiramate treatment. Topiramate YTC/YTCE Study Group. Epilepsia 2000; 41Suppl. 1: S77–81PubMedCrossRef
39.
go back to reference Reddy DS. Newer GABAergic agents for pharmacotherapy of infantile spasms. Drugs Today 2002; 38: 657–75PubMedCrossRef Reddy DS. Newer GABAergic agents for pharmacotherapy of infantile spasms. Drugs Today 2002; 38: 657–75PubMedCrossRef
40.
go back to reference Czuczwar SJ, Patsalos PN. The new generation of GABA enhancers: potential in the treatment of epilepsy. CNS Drugs 2001; 15(5): 339–50PubMedCrossRef Czuczwar SJ, Patsalos PN. The new generation of GABA enhancers: potential in the treatment of epilepsy. CNS Drugs 2001; 15(5): 339–50PubMedCrossRef
41.
go back to reference White HS. Mechanism of action of newer anticonvulsants. J Clin Psychiatry 2003; 64Suppl. 8: 5–8PubMed White HS. Mechanism of action of newer anticonvulsants. J Clin Psychiatry 2003; 64Suppl. 8: 5–8PubMed
43.
go back to reference Niebauer M, Gruenthal M. Topiramate reduces neuronal injury after experimental status epilepticus. Brain Res 1999; 837: 263–9PubMedCrossRef Niebauer M, Gruenthal M. Topiramate reduces neuronal injury after experimental status epilepticus. Brain Res 1999; 837: 263–9PubMedCrossRef
44.
go back to reference Koh S, Jensen FE. Topiramate blocks perinatal hypoxia-induced seizures in rat pups. Ann Neurol 2001; 50: 366–72PubMedCrossRef Koh S, Jensen FE. Topiramate blocks perinatal hypoxia-induced seizures in rat pups. Ann Neurol 2001; 50: 366–72PubMedCrossRef
45.
go back to reference Edmonds Jr HL, Jiang YD, Zhang PY, et al. Topiramate as a neuroprotectant in a rat model of global ischemia-induced neurodegeneration. Life Sci 2001; 69: 2265–77PubMedCrossRef Edmonds Jr HL, Jiang YD, Zhang PY, et al. Topiramate as a neuroprotectant in a rat model of global ischemia-induced neurodegeneration. Life Sci 2001; 69: 2265–77PubMedCrossRef
46.
go back to reference Angehagen M, Ben-Menachem E, Ronnback L, et al. Topiramate protects against glutamate- and kainate-induced neurotoxicity in primary neuronal-astroglial cultures. Epilepsy Res 2003; 54: 63–71PubMedCrossRef Angehagen M, Ben-Menachem E, Ronnback L, et al. Topiramate protects against glutamate- and kainate-induced neurotoxicity in primary neuronal-astroglial cultures. Epilepsy Res 2003; 54: 63–71PubMedCrossRef
47.
go back to reference Khan SH, Wright SL, Banigesh A, et al. Antiischemic effects of topiramate in a transient global forebrain ischemia model: a neurochemical, histological, and behavioral evaluation. Neurochem Res 2003; 28: 1235–9PubMedCrossRef Khan SH, Wright SL, Banigesh A, et al. Antiischemic effects of topiramate in a transient global forebrain ischemia model: a neurochemical, histological, and behavioral evaluation. Neurochem Res 2003; 28: 1235–9PubMedCrossRef
48.
go back to reference Qian J, Noebels JL. Topiramate alters excitatory synaptic transmission in mouse hippocampus. Epilepsy Res 2003; 55: 225–33PubMedCrossRef Qian J, Noebels JL. Topiramate alters excitatory synaptic transmission in mouse hippocampus. Epilepsy Res 2003; 55: 225–33PubMedCrossRef
49.
go back to reference White HS, Brown SD, Woodhead JH, et al. Topiramate enhances GABA-mediated chloride flux and GABA-evoked chloride currents in murine brain neurons and increases seizure threshold. Epilepsy Res 1997; 28: 167–79PubMedCrossRef White HS, Brown SD, Woodhead JH, et al. Topiramate enhances GABA-mediated chloride flux and GABA-evoked chloride currents in murine brain neurons and increases seizure threshold. Epilepsy Res 1997; 28: 167–79PubMedCrossRef
50.
go back to reference White HS, Brown SD, Woodhead JH, et al. Topiramate modu-lates GABA-evoked currents in murine cortical neurons by a nonbenzodiazepine mechanism. Epilepsia 2000; 41Suppl. 1: S17–20PubMedCrossRef White HS, Brown SD, Woodhead JH, et al. Topiramate modu-lates GABA-evoked currents in murine cortical neurons by a nonbenzodiazepine mechanism. Epilepsia 2000; 41Suppl. 1: S17–20PubMedCrossRef
51.
go back to reference Gibbs JW, Sombati S, DeLorenzo RJ, et al. Cellular actions of topiramate: blockade of kainate-evoked inward currents in cultured hippocampal neurons. Epilepsia 2000; 41Suppl. 1: S10–6PubMedCrossRef Gibbs JW, Sombati S, DeLorenzo RJ, et al. Cellular actions of topiramate: blockade of kainate-evoked inward currents in cultured hippocampal neurons. Epilepsia 2000; 41Suppl. 1: S10–6PubMedCrossRef
52.
go back to reference Skradski S, White HS. Topiramate blocks kainate-evoked cobalt influx into cultured neurons. Epilepsia 2000; 41Suppl. 1: S45–7PubMedCrossRef Skradski S, White HS. Topiramate blocks kainate-evoked cobalt influx into cultured neurons. Epilepsia 2000; 41Suppl. 1: S45–7PubMedCrossRef
53.
go back to reference Gryder DS, Rogawski MA. Selective antagonism of GluR5 kainate-receptor-mediated synaptic currents by topiramate in rat basolateral amygdala neurons. J Neurosci 2003; 23: 7069–74PubMed Gryder DS, Rogawski MA. Selective antagonism of GluR5 kainate-receptor-mediated synaptic currents by topiramate in rat basolateral amygdala neurons. J Neurosci 2003; 23: 7069–74PubMed
54.
go back to reference Zhang X, Velumian AA, Jones OT, et al. Modulation of high-voltage-activated calcium channels in dentate granule cells by topiramate. Epilepsia 2000; 41Suppl. 1: S52–60PubMedCrossRef Zhang X, Velumian AA, Jones OT, et al. Modulation of high-voltage-activated calcium channels in dentate granule cells by topiramate. Epilepsia 2000; 41Suppl. 1: S52–60PubMedCrossRef
55.
go back to reference Taverna S, Sancini G, Mantegazza M, et al. Inhibition of transient and persistent Na+ current fractions by the new anticonvulsant topiramate. J Pharmacol Exp Ther 1999; 288: 960–8PubMed Taverna S, Sancini G, Mantegazza M, et al. Inhibition of transient and persistent Na+ current fractions by the new anticonvulsant topiramate. J Pharmacol Exp Ther 1999; 288: 960–8PubMed
56.
go back to reference Herrero AI, Del Olmo N, Gonzalez-Escalada JR, et al. Two new actions of topiramate: inhibition of depolarizing GABA(A)-mediated responses and activation of a potassium conductance. Neuropharmacology 2002; 42: 210–20PubMedCrossRef Herrero AI, Del Olmo N, Gonzalez-Escalada JR, et al. Two new actions of topiramate: inhibition of depolarizing GABA(A)-mediated responses and activation of a potassium conductance. Neuropharmacology 2002; 42: 210–20PubMedCrossRef
57.
go back to reference Dodgson SJ, Shank RP, Maryanoff BE. Topiramate as an inhibitor of carbonic anhydrase isoenzymes. Epilepsia 2000; 41Suppl. 1: S35–9PubMedCrossRef Dodgson SJ, Shank RP, Maryanoff BE. Topiramate as an inhibitor of carbonic anhydrase isoenzymes. Epilepsia 2000; 41Suppl. 1: S35–9PubMedCrossRef
58.
go back to reference Perucca E, Bialer M. The clinical pharmacokinetics of the newer antiepileptic drugs: focus on topiramate, zonisamide and tiagabine. Clin Pharmacokinet 1996; 31: 29–46PubMedCrossRef Perucca E, Bialer M. The clinical pharmacokinetics of the newer antiepileptic drugs: focus on topiramate, zonisamide and tiagabine. Clin Pharmacokinet 1996; 31: 29–46PubMedCrossRef
59.
60.
go back to reference Rosenfeld WE, Liao S, Kramer LD, et al. Comparison of the steady-state pharmacokinetics of topiramate and valproate in patients with epilepsy during monotherapy and concomitant therapy. Epilepsia 1997; 38: 324–33PubMedCrossRef Rosenfeld WE, Liao S, Kramer LD, et al. Comparison of the steady-state pharmacokinetics of topiramate and valproate in patients with epilepsy during monotherapy and concomitant therapy. Epilepsia 1997; 38: 324–33PubMedCrossRef
61.
go back to reference Sachdeo RC, Sachdeo SK, Levy RH, et al. Topiramate and phenytoin pharmacokinetics during repetitive monotherapy and combination therapy to epileptic patients. Epilepsia 2002; 43: 691–6PubMedCrossRef Sachdeo RC, Sachdeo SK, Levy RH, et al. Topiramate and phenytoin pharmacokinetics during repetitive monotherapy and combination therapy to epileptic patients. Epilepsia 2002; 43: 691–6PubMedCrossRef
62.
go back to reference Sachdeo RC, Sachdeo SK, Walker SA, et al. Steady-state pharmacokinetics of topiramate and carbamazepine in patients with epilepsy during monotherapy and concomitant therapy. Epilepsia 1996; 37: 774–80PubMedCrossRef Sachdeo RC, Sachdeo SK, Walker SA, et al. Steady-state pharmacokinetics of topiramate and carbamazepine in patients with epilepsy during monotherapy and concomitant therapy. Epilepsia 1996; 37: 774–80PubMedCrossRef
63.
go back to reference Doose DR, Brodie MJ, Wilson EA, et al. Topiramate and lamotrigine pharmacokinetics during repetitive monotherapy and combination therapy in epilepsy patients. Epilepsia 2003; 44: 917–22PubMedCrossRef Doose DR, Brodie MJ, Wilson EA, et al. Topiramate and lamotrigine pharmacokinetics during repetitive monotherapy and combination therapy in epilepsy patients. Epilepsia 2003; 44: 917–22PubMedCrossRef
64.
go back to reference Doose DR, Wang SS, Padmanabhan M, et al. Effect of topira-mate or carbamazepine on the pharmacokinetics of an oral contraceptive containing norethindrone and ethinyl estradiol in healthy obese and nonobese female subjects. Epilepsia 2003; 44: 540–9PubMedCrossRef Doose DR, Wang SS, Padmanabhan M, et al. Effect of topira-mate or carbamazepine on the pharmacokinetics of an oral contraceptive containing norethindrone and ethinyl estradiol in healthy obese and nonobese female subjects. Epilepsia 2003; 44: 540–9PubMedCrossRef
65.
go back to reference Rosenfeld WE, Doose DR, Walker SA, et al. Effect of topiramate on the pharmacokinetics of an oral contraceptive containing norethindrone and ethinyl estradiol in patients with epilepsy. Epilepsia 1997; 38: 317–23PubMedCrossRef Rosenfeld WE, Doose DR, Walker SA, et al. Effect of topiramate on the pharmacokinetics of an oral contraceptive containing norethindrone and ethinyl estradiol in patients with epilepsy. Epilepsia 1997; 38: 317–23PubMedCrossRef
66.
go back to reference Doose DR, Kohl KA, Desai-Krieger D, et al. No clinically significant effect of topiramate on haloperidol plasma concentration [poster]. Presented at the European College of Neuropsychopharmacology (ECNP) congress; 1999 Sep 21–25; London Doose DR, Kohl KA, Desai-Krieger D, et al. No clinically significant effect of topiramate on haloperidol plasma concentration [poster]. Presented at the European College of Neuropsychopharmacology (ECNP) congress; 1999 Sep 21–25; London
67.
go back to reference Doose DR, Kohl KA, Desai-Krieger D, et al. No significant effect of topiramate on lithium serum concentration. Poster presented at the World Congress of Psychiatry (WPA); 1999 Aug 6–12; Hamburg, Germany Doose DR, Kohl KA, Desai-Krieger D, et al. No significant effect of topiramate on lithium serum concentration. Poster presented at the World Congress of Psychiatry (WPA); 1999 Aug 6–12; Hamburg, Germany
68.
go back to reference Storey JR, Calder CS, Hart DE, et al. Topiramate in migraine prevention: a double-blind, placebo-controlled study. Headache 2001; 41: 968–75PubMedCrossRef Storey JR, Calder CS, Hart DE, et al. Topiramate in migraine prevention: a double-blind, placebo-controlled study. Headache 2001; 41: 968–75PubMedCrossRef
69.
go back to reference Chong MS, Libretto SE. The rationale and use of topiramate for treating neuropathic pain. Clin J Pain 2003; 19: 59–68PubMedCrossRef Chong MS, Libretto SE. The rationale and use of topiramate for treating neuropathic pain. Clin J Pain 2003; 19: 59–68PubMedCrossRef
70.
go back to reference Johnson BA, Ait-Daoud N, Bowden CL, et al. Oral topiramate for treatment of alcohol dependence: a randomised controlled trial. Lancet 2003; 361: 1677–85PubMedCrossRef Johnson BA, Ait-Daoud N, Bowden CL, et al. Oral topiramate for treatment of alcohol dependence: a randomised controlled trial. Lancet 2003; 361: 1677–85PubMedCrossRef
71.
go back to reference Rubio G, Ponce G, Jimenez-Arriero MA, et al. Effects of topiramate in the treatment of alcohol dependence. Pharmacopsychiatry 2004; 37: 37–40PubMedCrossRef Rubio G, Ponce G, Jimenez-Arriero MA, et al. Effects of topiramate in the treatment of alcohol dependence. Pharmacopsychiatry 2004; 37: 37–40PubMedCrossRef
72.
go back to reference Roy Chengappa KN, Levine J, Rathore D, et al. Long-term effects of topiramate on bipolar mood instability, weight change and glycemic control: a case-series. Eur Psychiatry 2001; 16: 186–90PubMedCrossRef Roy Chengappa KN, Levine J, Rathore D, et al. Long-term effects of topiramate on bipolar mood instability, weight change and glycemic control: a case-series. Eur Psychiatry 2001; 16: 186–90PubMedCrossRef
73.
go back to reference Bray GA, Hollander P, Klein S, et al. A 6-month randomized, placebo-controlled, dose-ranging trial of topiramate for weight loss in obesity. Obes Res 2003; 11: 722–33PubMedCrossRef Bray GA, Hollander P, Klein S, et al. A 6-month randomized, placebo-controlled, dose-ranging trial of topiramate for weight loss in obesity. Obes Res 2003; 11: 722–33PubMedCrossRef
74.
go back to reference McElroy SL, Arnold LM, Shapira NA, et al. Topiramate in the treatment of binge eating disorder associated with obesity: a randomized, placebo-controlled trial. Am J Psychiatry 2003; 160: 255–61PubMedCrossRef McElroy SL, Arnold LM, Shapira NA, et al. Topiramate in the treatment of binge eating disorder associated with obesity: a randomized, placebo-controlled trial. Am J Psychiatry 2003; 160: 255–61PubMedCrossRef
75.
go back to reference Biton V, Edwards KR, Montouris GD, et al. Topiramate titration and tolerability. Ann Pharmacother 2001; 35: 173–9PubMedCrossRef Biton V, Edwards KR, Montouris GD, et al. Topiramate titration and tolerability. Ann Pharmacother 2001; 35: 173–9PubMedCrossRef
76.
go back to reference Fraunfelder FW, Fraunfelder FT, Keates EU. Topiramate-asso-ciated acute, bilateral, secondary angle-closure glaucoma. Ophthalmology 2004; 111: 109–11PubMedCrossRef Fraunfelder FW, Fraunfelder FT, Keates EU. Topiramate-asso-ciated acute, bilateral, secondary angle-closure glaucoma. Ophthalmology 2004; 111: 109–11PubMedCrossRef
77.
78.
go back to reference Ben-Zeev B, Watemberg N, Augarten A, et al. Oligohydrosis and hyperthermia: pilot study of a novel topiramate adverse effect. J Child Neurol 2003; 18: 254–7PubMedCrossRef Ben-Zeev B, Watemberg N, Augarten A, et al. Oligohydrosis and hyperthermia: pilot study of a novel topiramate adverse effect. J Child Neurol 2003; 18: 254–7PubMedCrossRef
79.
go back to reference Dodson WE, Kamin M, Kraut L, et al. Topiramate Titration to Response: Analysis of Individualized Therapy Study (TRAITS). Ann Pharmacother 2003; 37: 615–20PubMedCrossRef Dodson WE, Kamin M, Kraut L, et al. Topiramate Titration to Response: Analysis of Individualized Therapy Study (TRAITS). Ann Pharmacother 2003; 37: 615–20PubMedCrossRef
80.
go back to reference Johnson BA. Progress in the development of topiramate for treating alcohol dependence: from a hypothesis to a proof-of-concept study. Alcohol Clin Exp Res 2004; 28: 1137–44PubMedCrossRef Johnson BA. Progress in the development of topiramate for treating alcohol dependence: from a hypothesis to a proof-of-concept study. Alcohol Clin Exp Res 2004; 28: 1137–44PubMedCrossRef
81.
go back to reference Schiffer WK, Gerasimov MR, Marsteller DA, et al. Topiramate selectively attenuates nicotine-induced increases in monoamine release. Synapse 2001; 42: 196–8PubMedCrossRef Schiffer WK, Gerasimov MR, Marsteller DA, et al. Topiramate selectively attenuates nicotine-induced increases in monoamine release. Synapse 2001; 42: 196–8PubMedCrossRef
82.
go back to reference Gasior M, Ungard JT, Witkin JM. Preclinical evaluation of newly approved and potential antiepileptic drugs against cocaine-induced seizures. J Pharmacol Exp Ther 1999; 290: 1148–56PubMed Gasior M, Ungard JT, Witkin JM. Preclinical evaluation of newly approved and potential antiepileptic drugs against cocaine-induced seizures. J Pharmacol Exp Ther 1999; 290: 1148–56PubMed
83.
go back to reference Laviolette SR, Gallegos RA, Henriksen SJ, et al. Opiate state controls bi-directional reward signaling via GABAA receptors in the ventral tegmental area. Nat Neurosci 2004; 7: 160–9PubMedCrossRef Laviolette SR, Gallegos RA, Henriksen SJ, et al. Opiate state controls bi-directional reward signaling via GABAA receptors in the ventral tegmental area. Nat Neurosci 2004; 7: 160–9PubMedCrossRef
84.
go back to reference Murray TD, Berger A. Alcohol withdrawal. Va Med Q 1997; 124: 184–9PubMed Murray TD, Berger A. Alcohol withdrawal. Va Med Q 1997; 124: 184–9PubMed
85.
go back to reference Engberg G, Hajos M. Alcohol withdrawal reaction as a result of adaptive changes of excitatory amino acid receptors. Naunyn Schmiedebergs Arch Pharmacol 1992; 346: 437–41PubMedCrossRef Engberg G, Hajos M. Alcohol withdrawal reaction as a result of adaptive changes of excitatory amino acid receptors. Naunyn Schmiedebergs Arch Pharmacol 1992; 346: 437–41PubMedCrossRef
86.
go back to reference Tsai G, Coyle JT. The role of glutamatergic neurotransmission in the pathophysiology of alcoholism. Annu Rev Med 1998; 49: 173–84PubMedCrossRef Tsai G, Coyle JT. The role of glutamatergic neurotransmission in the pathophysiology of alcoholism. Annu Rev Med 1998; 49: 173–84PubMedCrossRef
87.
go back to reference Ennis M, Aston-Jones G. A potent excitatory input to the nucleus locus coeruleus from the ventrolateral medulla. Neurosci Lett 1986; 71: 299–305PubMedCrossRef Ennis M, Aston-Jones G. A potent excitatory input to the nucleus locus coeruleus from the ventrolateral medulla. Neurosci Lett 1986; 71: 299–305PubMedCrossRef
88.
go back to reference Ennis M, Aston-Jones G. Activation of locus coeruleus from nucleus paragigantocellularis: a new excitatory amino acid pathway in brain. J Neurosci 1988; 8: 3644–57PubMed Ennis M, Aston-Jones G. Activation of locus coeruleus from nucleus paragigantocellularis: a new excitatory amino acid pathway in brain. J Neurosci 1988; 8: 3644–57PubMed
89.
go back to reference Kawahara Y, Kawahara H, Westerink BH. Tonic regulation of the activity of noradrenergic neurons in the locus coeruleus of the conscious rat studied by dual-probe microdialysis. Brain Res 1999; 823: 42–8PubMedCrossRef Kawahara Y, Kawahara H, Westerink BH. Tonic regulation of the activity of noradrenergic neurons in the locus coeruleus of the conscious rat studied by dual-probe microdialysis. Brain Res 1999; 823: 42–8PubMedCrossRef
90.
go back to reference Erhardt S, Hajos M, Lindberg A, et al. Nicotine-induced excita-tion of locus coeruleus neurons is blocked by elevated levels of endogenous kynurenic acid. Synapse 2000; 37: 104–8PubMedCrossRef Erhardt S, Hajos M, Lindberg A, et al. Nicotine-induced excita-tion of locus coeruleus neurons is blocked by elevated levels of endogenous kynurenic acid. Synapse 2000; 37: 104–8PubMedCrossRef
91.
go back to reference Rasmussen K, Vandergriff J. The selective iGluR1-4 (AMPA) antagonist LY300168 attenuates morphine-withdrawal-induced activation of locus coeruleus neurons and behavioural signs of morphine withdrawal. Neuropharmacology 2003; 44: 88–92PubMedCrossRef Rasmussen K, Vandergriff J. The selective iGluR1-4 (AMPA) antagonist LY300168 attenuates morphine-withdrawal-induced activation of locus coeruleus neurons and behavioural signs of morphine withdrawal. Neuropharmacology 2003; 44: 88–92PubMedCrossRef
92.
go back to reference Cagetti E, Baicy KJ, Olsen RW. Topiramate attenuates withdrawal signs after chronic intermittent ethanol in rats. Neuroreport 2004; 15: 207–10PubMedCrossRef Cagetti E, Baicy KJ, Olsen RW. Topiramate attenuates withdrawal signs after chronic intermittent ethanol in rats. Neuroreport 2004; 15: 207–10PubMedCrossRef
93.
go back to reference Smith L, Price-Jones M, Hughes K, et al. Effects of topiramate on kainate- and domoate-activated [14C]guanidinium ion flux through GluR6 channels in transfected BHK cells using Cytostar-T scintillating microplates. Epilepsia 2000; 41Suppl. 1: S48–51PubMedCrossRef Smith L, Price-Jones M, Hughes K, et al. Effects of topiramate on kainate- and domoate-activated [14C]guanidinium ion flux through GluR6 channels in transfected BHK cells using Cytostar-T scintillating microplates. Epilepsia 2000; 41Suppl. 1: S48–51PubMedCrossRef
94.
go back to reference Rustembegovic A, Sofic E, Kroyer G. A pilot study of topiramate (Topamax) in the treatment of tonic-clonic seizures of alcohol withdrawal syndromes. Med Arh 2002; 56: 211–2PubMed Rustembegovic A, Sofic E, Kroyer G. A pilot study of topiramate (Topamax) in the treatment of tonic-clonic seizures of alcohol withdrawal syndromes. Med Arh 2002; 56: 211–2PubMed
95.
go back to reference Krupitsky EM, Rudenko A, Zvartau E, et al. The pilot study of topiramate for alcohol withdrawal syndrome [abstract]. Alcohol Alcohol 2003; 38: 508–9 Krupitsky EM, Rudenko A, Zvartau E, et al. The pilot study of topiramate for alcohol withdrawal syndrome [abstract]. Alcohol Alcohol 2003; 38: 508–9
96.
go back to reference Husum H, Van Kammen D, Termeer E, et al. Topiramate normalizes hippocampal NPY-LI in flinders sensitive line ‘depressed’ rats and upregulates NPY, galanin, and CRH-LI in the hypothalamus: implications for mood-stabilizing and weight loss-inducing effects. Neuropsychopharmacology 2003; 28: 1292–9PubMedCrossRef Husum H, Van Kammen D, Termeer E, et al. Topiramate normalizes hippocampal NPY-LI in flinders sensitive line ‘depressed’ rats and upregulates NPY, galanin, and CRH-LI in the hypothalamus: implications for mood-stabilizing and weight loss-inducing effects. Neuropsychopharmacology 2003; 28: 1292–9PubMedCrossRef
97.
go back to reference Mathé AA, Rudorfer MV, Stenfors C, et al. Effects of electroconvulsive treatment on somatostatin, neuropeptide Y, endothelin, and neurokinin A concentrations in cerebrospinal fluid of depressed patients: a pilot study. Depression 1996; 3: 250–6CrossRef Mathé AA, Rudorfer MV, Stenfors C, et al. Effects of electroconvulsive treatment on somatostatin, neuropeptide Y, endothelin, and neurokinin A concentrations in cerebrospinal fluid of depressed patients: a pilot study. Depression 1996; 3: 250–6CrossRef
98.
go back to reference McIntyre RS, Mancini DA, McCann S, et al. Topiramate versus bupropion SR when added to mood stabilizer therapy for the depressive phase of bipolar disorder: a preliminary single-blind study. Bipolar Disord 2002; 4: 207–13PubMedCrossRef McIntyre RS, Mancini DA, McCann S, et al. Topiramate versus bupropion SR when added to mood stabilizer therapy for the depressive phase of bipolar disorder: a preliminary single-blind study. Bipolar Disord 2002; 4: 207–13PubMedCrossRef
99.
go back to reference Fawcett J, Epstein P, Fiester SJ, et al. Clinical management —imipramine/placebo administration manual: NIMH Treatment of Depression Collaborative Research Program. Psychopharmacol Bull 1987; 23: 309–24PubMed Fawcett J, Epstein P, Fiester SJ, et al. Clinical management —imipramine/placebo administration manual: NIMH Treatment of Depression Collaborative Research Program. Psychopharmacol Bull 1987; 23: 309–24PubMed
100.
go back to reference Edwards G, Orford J, Egert S, et al. Alcoholism: a controlled trial of ‘treatment’ and ‘advice’. J Stud Alcohol 1977; 38: 1004–31PubMed Edwards G, Orford J, Egert S, et al. Alcoholism: a controlled trial of ‘treatment’ and ‘advice’. J Stud Alcohol 1977; 38: 1004–31PubMed
101.
go back to reference Bohn MJ, Barton BA, Barron KE. Psychometric properties and validity of the obsessive-compulsive drinking scale. Alcohol Clin Exp Res 1996; 20: 817–23PubMedCrossRef Bohn MJ, Barton BA, Barron KE. Psychometric properties and validity of the obsessive-compulsive drinking scale. Alcohol Clin Exp Res 1996; 20: 817–23PubMedCrossRef
102.
go back to reference Ait-Daoud N, Johnson BA. Open-label trial of topiramate for treating cocaine dependence. Presented at the College on Problems of Drug Dependence annual meeting; 2004 Jun 13; San Juan Ait-Daoud N, Johnson BA. Open-label trial of topiramate for treating cocaine dependence. Presented at the College on Problems of Drug Dependence annual meeting; 2004 Jun 13; San Juan
103.
go back to reference Kampman KM, Pettinati H, Lynch KG, et al. A pilot trial of topiramate for the treatment of cocaine dependence. Drug Alcohol Depend 2004; 75: 233–40PubMedCrossRef Kampman KM, Pettinati H, Lynch KG, et al. A pilot trial of topiramate for the treatment of cocaine dependence. Drug Alcohol Depend 2004; 75: 233–40PubMedCrossRef
104.
105.
go back to reference Kiefer F, Jahn H, Tarnaske T, et al. Comparing and combining naltrexone and acamprosate in relapse prevention of alcoholism: a double-blind, placebo-controlled study. Arch Gen Psychiatry 2003; 60: 92–9PubMedCrossRef Kiefer F, Jahn H, Tarnaske T, et al. Comparing and combining naltrexone and acamprosate in relapse prevention of alcoholism: a double-blind, placebo-controlled study. Arch Gen Psychiatry 2003; 60: 92–9PubMedCrossRef
106.
go back to reference Yun IA, Wakabayashi KT, Fields HL, et al. The ventral tegmental area is required for the behavioral and nucleus accumbens neuronal firing responses to incentive cues. J Neurosci 2004; 24: 2923–33PubMedCrossRef Yun IA, Wakabayashi KT, Fields HL, et al. The ventral tegmental area is required for the behavioral and nucleus accumbens neuronal firing responses to incentive cues. J Neurosci 2004; 24: 2923–33PubMedCrossRef
107.
go back to reference Colombo G, Agabio R, Carai MA, et al. Ability of baclofen in reducing alcohol intake and withdrawal severity: I. Preclinical evidence. Alcohol Clin Exp Res 2000; 24: 58–66 Colombo G, Agabio R, Carai MA, et al. Ability of baclofen in reducing alcohol intake and withdrawal severity: I. Preclinical evidence. Alcohol Clin Exp Res 2000; 24: 58–66
108.
go back to reference Colombo G, Serra S, Brunetti G, et al. Suppression by baclofen of alcohol deprivation effect in Sardinian alcohol-preferring (sP) rats. Drug Alcohol Depend 2003; 70: 105–8PubMedCrossRef Colombo G, Serra S, Brunetti G, et al. Suppression by baclofen of alcohol deprivation effect in Sardinian alcohol-preferring (sP) rats. Drug Alcohol Depend 2003; 70: 105–8PubMedCrossRef
109.
go back to reference Colombo G, Serra S, Vacca G, et al. Suppression by baclofen of the stimulation of alcohol intake induced by morphine and WIN 55,212-2 in alcohol-preferring rats. Eur J Pharmacol 2004; 492: 189–93PubMedCrossRef Colombo G, Serra S, Vacca G, et al. Suppression by baclofen of the stimulation of alcohol intake induced by morphine and WIN 55,212-2 in alcohol-preferring rats. Eur J Pharmacol 2004; 492: 189–93PubMedCrossRef
110.
go back to reference Addolorato G, Caputo F, Capristo E, et al. Baclofen efficacy in reducing alcohol craving and intake: a preliminary double-blind randomized controlled study. Alcohol Alcohol 2002; 37: 504–8PubMed Addolorato G, Caputo F, Capristo E, et al. Baclofen efficacy in reducing alcohol craving and intake: a preliminary double-blind randomized controlled study. Alcohol Alcohol 2002; 37: 504–8PubMed
111.
go back to reference Ragsdale DS, Avoli M. Sodium channels as molecular targets for antiepileptic drugs. Brain Res Brain Res Rev 1998; 26: 16–28PubMedCrossRef Ragsdale DS, Avoli M. Sodium channels as molecular targets for antiepileptic drugs. Brain Res Brain Res Rev 1998; 26: 16–28PubMedCrossRef
112.
go back to reference Remy S, Gabriel S, Urban BW, et al. A novel mechanism underlying drug resistance in chronic epilepsy. Ann Neurol 2003; 53: 469–79PubMedCrossRef Remy S, Gabriel S, Urban BW, et al. A novel mechanism underlying drug resistance in chronic epilepsy. Ann Neurol 2003; 53: 469–79PubMedCrossRef
113.
go back to reference Malcolm R, Myrick H, Brady KT, et al. Update on anticonvulsants for the treatment of alcohol withdrawal. Am J Addict 2001; 10Suppl. 1: 16–23PubMed Malcolm R, Myrick H, Brady KT, et al. Update on anticonvulsants for the treatment of alcohol withdrawal. Am J Addict 2001; 10Suppl. 1: 16–23PubMed
114.
go back to reference Malcolm R, Myrick H, Roberts J, et al. The effects of carbamazepine and lorazepam on single versus multiple previous alcohol withdrawals in an outpatient randomized trial. J Gen Intern Med 2002; 17: 349–55PubMed Malcolm R, Myrick H, Roberts J, et al. The effects of carbamazepine and lorazepam on single versus multiple previous alcohol withdrawals in an outpatient randomized trial. J Gen Intern Med 2002; 17: 349–55PubMed
115.
go back to reference Sullivan JT, Sykora K, Schneiderman J, et al. Assessment of alcohol withdrawal: the Revised Clinical Institute Withdrawal Assessment for Alcohol scale (CIWA-Ar). Br J Addict 1989; 84: 1353–7PubMedCrossRef Sullivan JT, Sykora K, Schneiderman J, et al. Assessment of alcohol withdrawal: the Revised Clinical Institute Withdrawal Assessment for Alcohol scale (CIWA-Ar). Br J Addict 1989; 84: 1353–7PubMedCrossRef
116.
go back to reference Zung WW. A rating instrument for anxiety disorders. Psychosomatics 1971; 12: 371–9PubMed Zung WW. A rating instrument for anxiety disorders. Psychosomatics 1971; 12: 371–9PubMed
117.
go back to reference Malcolm R, Myrick H, Roberts J, et al. The differential effects of medication on mood, sleep disturbance, and work ability in outpatient alcohol detoxification. Am J Addict 2002; 11: 141–50PubMedCrossRef Malcolm R, Myrick H, Roberts J, et al. The differential effects of medication on mood, sleep disturbance, and work ability in outpatient alcohol detoxification. Am J Addict 2002; 11: 141–50PubMedCrossRef
119.
go back to reference Goa KL, Sorkin EM. Gabapentin: a review of its pharmacological properties and clinical potential in epilepsy. Drugs 1993; 46: 409–27PubMedCrossRef Goa KL, Sorkin EM. Gabapentin: a review of its pharmacological properties and clinical potential in epilepsy. Drugs 1993; 46: 409–27PubMedCrossRef
120.
go back to reference Suman-Chauhan N, Webdale L, Hill DR, et al. Characterisation of [3H]gabapentin binding to a novel site in rat brain: homogenate binding studies. Eur J Pharmacol 1993; 244: 293–301PubMedCrossRef Suman-Chauhan N, Webdale L, Hill DR, et al. Characterisation of [3H]gabapentin binding to a novel site in rat brain: homogenate binding studies. Eur J Pharmacol 1993; 244: 293–301PubMedCrossRef
121.
go back to reference Taylor CP, Gee NS, Su TZ, et al. A summary of mechanistic hypotheses of gabapentin pharmacology. Epilepsy Res 1998; 29: 233–49PubMedCrossRef Taylor CP, Gee NS, Su TZ, et al. A summary of mechanistic hypotheses of gabapentin pharmacology. Epilepsy Res 1998; 29: 233–49PubMedCrossRef
122.
go back to reference Leach JP, Sills GJ, Butler E, et al. Neurochemical actions of gabapentin in mouse brain. Epilepsy Res 1997; 27: 175–80PubMedCrossRef Leach JP, Sills GJ, Butler E, et al. Neurochemical actions of gabapentin in mouse brain. Epilepsy Res 1997; 27: 175–80PubMedCrossRef
123.
go back to reference Löscher W, Honack D, Taylor CP. Gabapentin increases aminooxyacetic acid-induced GABA accumulation in several regions of rat brain. Neurosci Lett 1991; 128: 150–4PubMedCrossRef Löscher W, Honack D, Taylor CP. Gabapentin increases aminooxyacetic acid-induced GABA accumulation in several regions of rat brain. Neurosci Lett 1991; 128: 150–4PubMedCrossRef
124.
go back to reference Bloms-Funke P, Löscher W. The anticonvulsant gabapentin decreases firing rates of substantia nigra pars reticulata neurons. Eur J Pharmacol 1996; 316: 211–8PubMedCrossRef Bloms-Funke P, Löscher W. The anticonvulsant gabapentin decreases firing rates of substantia nigra pars reticulata neurons. Eur J Pharmacol 1996; 316: 211–8PubMedCrossRef
125.
go back to reference Taylor CP, Vartanian MG, Andruszkiewicz R, et al. 3-alkyl GABA and 3-alkylglutamic acid analogues: two new classes of anticonvulsant agents. Epilepsy Res 1992; 11: 103–10PubMedCrossRef Taylor CP, Vartanian MG, Andruszkiewicz R, et al. 3-alkyl GABA and 3-alkylglutamic acid analogues: two new classes of anticonvulsant agents. Epilepsy Res 1992; 11: 103–10PubMedCrossRef
126.
go back to reference Taylor CP. Gabapentin —mechanisms of action. In: Levy RH, Mattson RH, Meldrum BS, editors. Antiepileptic drugs. 4th ed. New York (NY): Raven Press, 1995: 829–41 Taylor CP. Gabapentin —mechanisms of action. In: Levy RH, Mattson RH, Meldrum BS, editors. Antiepileptic drugs. 4th ed. New York (NY): Raven Press, 1995: 829–41
127.
go back to reference Meldrum BS. Update on the mechanism of action of antiepileptic drugs. Epilepsia 1996; 37Suppl. 6: S4–11PubMedCrossRef Meldrum BS. Update on the mechanism of action of antiepileptic drugs. Epilepsia 1996; 37Suppl. 6: S4–11PubMedCrossRef
128.
go back to reference Stewart BH, Kugler AR, Thompson PR, et al. A saturable transport mechanism in the intestinal absorption of gabapentin is the underlying cause of the lack of proportionality between increasing dose and drug levels in plasma. Pharm Res 1993; 10: 276–81PubMedCrossRef Stewart BH, Kugler AR, Thompson PR, et al. A saturable transport mechanism in the intestinal absorption of gabapentin is the underlying cause of the lack of proportionality between increasing dose and drug levels in plasma. Pharm Res 1993; 10: 276–81PubMedCrossRef
129.
go back to reference Gee NS, Brown JP, Dissanayake VU, et al. The novel anticonvulsant drug, gabapentin (Neurontin), binds to the alpha2delta subunit of a calcium channel. J Biol Chem 1996; 271: 5768–76PubMedCrossRef Gee NS, Brown JP, Dissanayake VU, et al. The novel anticonvulsant drug, gabapentin (Neurontin), binds to the alpha2delta subunit of a calcium channel. J Biol Chem 1996; 271: 5768–76PubMedCrossRef
130.
go back to reference Bonnet U, Banger M, Leweke FM, et al. Treatment of alcohol withdrawal syndrome with gabapentin. Pharmacopsychiatry 1999; 32: 107–9PubMedCrossRef Bonnet U, Banger M, Leweke FM, et al. Treatment of alcohol withdrawal syndrome with gabapentin. Pharmacopsychiatry 1999; 32: 107–9PubMedCrossRef
131.
go back to reference Chatterjee CR, Ringold AL. A case report of reduction in alcohol craving and protection against alcohol withdrawal by gabapentin. J Clin Psychiatry 1999; 60: 617PubMedCrossRef Chatterjee CR, Ringold AL. A case report of reduction in alcohol craving and protection against alcohol withdrawal by gabapentin. J Clin Psychiatry 1999; 60: 617PubMedCrossRef
132.
go back to reference Bozikas V, Petrikis P, Gamvrula K, et al. Treatment of alcohol withdrawal with gabapentin. Prog Neuropsychopharmacol Biol Psychiatry 2002; 26: 197–9PubMedCrossRef Bozikas V, Petrikis P, Gamvrula K, et al. Treatment of alcohol withdrawal with gabapentin. Prog Neuropsychopharmacol Biol Psychiatry 2002; 26: 197–9PubMedCrossRef
133.
go back to reference Rustembegovic A, Sofic E, Tahirovic I, et al. A study of gabapentin in the treatment of tonic-clonic seizures of alcohol withdrawal syndrome. Med Arh 2004; 58: 5–6PubMed Rustembegovic A, Sofic E, Tahirovic I, et al. A study of gabapentin in the treatment of tonic-clonic seizures of alcohol withdrawal syndrome. Med Arh 2004; 58: 5–6PubMed
134.
go back to reference Voronin KE, Drobes D, Myrick H, et al. Gabapentin is well tolerated but does not alter drinking in non-treatment seeking alcoholics during natural observation and in a clinical bar lab [abstract]. Alcohol Clin Exp Res 2004; 28(5 Suppl.): 113A Voronin KE, Drobes D, Myrick H, et al. Gabapentin is well tolerated but does not alter drinking in non-treatment seeking alcoholics during natural observation and in a clinical bar lab [abstract]. Alcohol Clin Exp Res 2004; 28(5 Suppl.): 113A
135.
go back to reference Myrick H, Voronin K, Drobes D, et al. Safety of gabapentin in treating alcoholism [abstract]. Alcohol Clin Exp Res 2004; 28(5 Suppl.): 193A Myrick H, Voronin K, Drobes D, et al. Safety of gabapentin in treating alcoholism [abstract]. Alcohol Clin Exp Res 2004; 28(5 Suppl.): 193A
136.
go back to reference Bessman SP, Fishbein WN. Gamma-hydroxybutyrate, a normal brain metabolite. Nature 1963; 200: 1207–8PubMedCrossRef Bessman SP, Fishbein WN. Gamma-hydroxybutyrate, a normal brain metabolite. Nature 1963; 200: 1207–8PubMedCrossRef
137.
go back to reference Colombo G, Agabio R, Diaz G, et al. Gamma-hydroxybutyric acid intake in ethanol-preferring sP and -nonpreferring sNP rats. Physiol Behav 1998; 64: 197–202PubMedCrossRef Colombo G, Agabio R, Diaz G, et al. Gamma-hydroxybutyric acid intake in ethanol-preferring sP and -nonpreferring sNP rats. Physiol Behav 1998; 64: 197–202PubMedCrossRef
138.
go back to reference Poldrugo F, Addolorato G. The role of gamma-hydroxybutyric acid in the treatment of alcoholism: from animal to clinical studies. Alcohol Alcohol 1999; 34: 15–24PubMed Poldrugo F, Addolorato G. The role of gamma-hydroxybutyric acid in the treatment of alcoholism: from animal to clinical studies. Alcohol Alcohol 1999; 34: 15–24PubMed
139.
go back to reference Brancucci A, Berretta N, Mercuri NB, et al. Gamma-hydroxybutyrate and ethanol depress spontaneous excitatory post-synaptic currents in dopaminergic neurons of the substantia nigra. Brain Res 2004; 997: 62–6PubMedCrossRef Brancucci A, Berretta N, Mercuri NB, et al. Gamma-hydroxybutyrate and ethanol depress spontaneous excitatory post-synaptic currents in dopaminergic neurons of the substantia nigra. Brain Res 2004; 997: 62–6PubMedCrossRef
140.
go back to reference Fadda F, Argiolas A, Melis MR, et al. Suppression of voluntary ethanol consumption in rats by gamma-butyrolactone. Life Sci 1983; 32: 1471–7PubMedCrossRef Fadda F, Argiolas A, Melis MR, et al. Suppression of voluntary ethanol consumption in rats by gamma-butyrolactone. Life Sci 1983; 32: 1471–7PubMedCrossRef
141.
go back to reference Fadda F, Colombo G, Mosca E, et al. Suppression by gamma-hydroxybutyric acid of ethanol withdrawal syndrome in rats. Alcohol Alcohol 1989; 24: 447–51PubMed Fadda F, Colombo G, Mosca E, et al. Suppression by gamma-hydroxybutyric acid of ethanol withdrawal syndrome in rats. Alcohol Alcohol 1989; 24: 447–51PubMed
142.
go back to reference Gessa GL, Agabio R, Carai MA, et al. Mechanism of the antialcohol effect of gamma-hydroxybutyric acid. Alcohol 2000; 20: 271–6PubMedCrossRef Gessa GL, Agabio R, Carai MA, et al. Mechanism of the antialcohol effect of gamma-hydroxybutyric acid. Alcohol 2000; 20: 271–6PubMedCrossRef
143.
go back to reference Gallimberti L, Ferri M, Ferrara SD, et al. Gamma-hydroxybutyric acid in the treatment of alcohol dependence: a double-blind study. Alcohol Clin Exp Res 1992; 16: 673–6PubMedCrossRef Gallimberti L, Ferri M, Ferrara SD, et al. Gamma-hydroxybutyric acid in the treatment of alcohol dependence: a double-blind study. Alcohol Clin Exp Res 1992; 16: 673–6PubMedCrossRef
144.
go back to reference Gallimberti L, Canton G, Gentile N, et al. Gamma-hydroxybutyric acid for treatment of alcohol withdrawal syndrome. Lancet 1989; II: 787–9CrossRef Gallimberti L, Canton G, Gentile N, et al. Gamma-hydroxybutyric acid for treatment of alcohol withdrawal syndrome. Lancet 1989; II: 787–9CrossRef
145.
go back to reference Addolorato G, Balducci G, Capristo E, et al. Gamma-hydroxybutyric acid (GHB) in the treatment of alcohol withdrawal syndrome: a randomized comparative study versus benzodiazepine. Alcohol Clin Exp Res 1999; 23: 1596–604PubMed Addolorato G, Balducci G, Capristo E, et al. Gamma-hydroxybutyric acid (GHB) in the treatment of alcohol withdrawal syndrome: a randomized comparative study versus benzodiazepine. Alcohol Clin Exp Res 1999; 23: 1596–604PubMed
146.
go back to reference Nimmerrichter AA, Walter H, Gutierrez-Lobos KE, et al. Double-blind controlled trial of gamma-hydroxybutyrate and clomethiazole in the treatment of alcohol withdrawal. Alcohol Alcohol 2002; 37: 67–73PubMed Nimmerrichter AA, Walter H, Gutierrez-Lobos KE, et al. Double-blind controlled trial of gamma-hydroxybutyrate and clomethiazole in the treatment of alcohol withdrawal. Alcohol Alcohol 2002; 37: 67–73PubMed
147.
go back to reference Caputo F, Addolorato G, Lorenzini F, et al. Gamma-hydroxybutyric acid versus naltrexone in maintaining alcohol abstinence: an open randomized comparative study. Drug Alcohol Depend 2003; 70: 85–91PubMedCrossRef Caputo F, Addolorato G, Lorenzini F, et al. Gamma-hydroxybutyric acid versus naltrexone in maintaining alcohol abstinence: an open randomized comparative study. Drug Alcohol Depend 2003; 70: 85–91PubMedCrossRef
148.
go back to reference Addolorato G, Cibin M, Caputo F, et al. Gamma-hydroxybutyric acid in the treatment of alcoholism: dosage fractioning utility in non-responder alcoholic patients. Drug Alcohol Depend 1998; 53: 7–10PubMedCrossRef Addolorato G, Cibin M, Caputo F, et al. Gamma-hydroxybutyric acid in the treatment of alcoholism: dosage fractioning utility in non-responder alcoholic patients. Drug Alcohol Depend 1998; 53: 7–10PubMedCrossRef
149.
150.
go back to reference O’Connell T, Kaye L, PlosayIII JJ,. Gamma-hydroxybutyrate (GHB): a newer drug of abuse. Am Fam Physician 2000; 62: 2478–83PubMed O’Connell T, Kaye L, PlosayIII JJ,. Gamma-hydroxybutyrate (GHB): a newer drug of abuse. Am Fam Physician 2000; 62: 2478–83PubMed
151.
go back to reference Addolorato G, Caputo F, Leggio L, et al. Safety, tolerability, and efficacy of gamma-hydroxybutyric acid and baclofen in the treatment of alcohol addiction [abstract]. Alcohol Clin Exp Res 2004; 28(5 Suppl.): 193A Addolorato G, Caputo F, Leggio L, et al. Safety, tolerability, and efficacy of gamma-hydroxybutyric acid and baclofen in the treatment of alcohol addiction [abstract]. Alcohol Clin Exp Res 2004; 28(5 Suppl.): 193A
152.
go back to reference Göttlicher M, Minucci S, Zhu P, et al. Valproic acid defines a novel class of HDAC inhibitors inducing differentiation of transformed cells. EMBO J 2001; 20: 6969–78PubMedCrossRef Göttlicher M, Minucci S, Zhu P, et al. Valproic acid defines a novel class of HDAC inhibitors inducing differentiation of transformed cells. EMBO J 2001; 20: 6969–78PubMedCrossRef
153.
go back to reference Phiel CJ, Zhang F, Huang EY, et al. Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen. J Biol Chem 2001; 276: 36734–41PubMedCrossRef Phiel CJ, Zhang F, Huang EY, et al. Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen. J Biol Chem 2001; 276: 36734–41PubMedCrossRef
155.
go back to reference Cunningham MO, Woodhall GL, Jones RS. Valproate modifies spontaneous excitation and inhibition at cortical synapses in vitro. Neuropharmacology 2003; 45: 907–17PubMedCrossRef Cunningham MO, Woodhall GL, Jones RS. Valproate modifies spontaneous excitation and inhibition at cortical synapses in vitro. Neuropharmacology 2003; 45: 907–17PubMedCrossRef
156.
go back to reference Johannessen CU. Mechanisms of action of valproate: a commentatory. Neurochem Int 2000; 37: 103–10PubMedCrossRef Johannessen CU. Mechanisms of action of valproate: a commentatory. Neurochem Int 2000; 37: 103–10PubMedCrossRef
157.
go back to reference Löscher W. Valproate: a reappraisal of its pharmacodynamic properties and mechanisms of action. Prog Neurobiol 1999; 58: 31–59PubMedCrossRef Löscher W. Valproate: a reappraisal of its pharmacodynamic properties and mechanisms of action. Prog Neurobiol 1999; 58: 31–59PubMedCrossRef
158.
go back to reference Rogawski MA, Löscher W. The neurobiology of antiepileptic drugs for the treatment of nonepileptic conditions. Nat Med 2004; 10: 685–92PubMedCrossRef Rogawski MA, Löscher W. The neurobiology of antiepileptic drugs for the treatment of nonepileptic conditions. Nat Med 2004; 10: 685–92PubMedCrossRef
159.
go back to reference McLean MJ, Macdonald RL. Sodium valproate, but not ethosuximide, produces use- and voltage-dependent limitation of high frequency repetitive firing of action potentials of mouse central neurons in cell culture. J Pharmacol Exp Ther 1986; 237: 1001–11PubMed McLean MJ, Macdonald RL. Sodium valproate, but not ethosuximide, produces use- and voltage-dependent limitation of high frequency repetitive firing of action potentials of mouse central neurons in cell culture. J Pharmacol Exp Ther 1986; 237: 1001–11PubMed
160.
go back to reference Taverna S, Mantegazza M, Franceschetti S, et al. Valproate selectively reduces the persistent fraction of Na+ current in neocortical neurons. Epilepsy Res 1998; 32: 304–8PubMedCrossRef Taverna S, Mantegazza M, Franceschetti S, et al. Valproate selectively reduces the persistent fraction of Na+ current in neocortical neurons. Epilepsy Res 1998; 32: 304–8PubMedCrossRef
161.
go back to reference Longo LP, Campbell T, Hubatch S. Divalproex sodium (Depakote) for alcohol withdrawal and relapse prevention. J Addict Dis 2002; 21: 55–64PubMedCrossRef Longo LP, Campbell T, Hubatch S. Divalproex sodium (Depakote) for alcohol withdrawal and relapse prevention. J Addict Dis 2002; 21: 55–64PubMedCrossRef
162.
go back to reference Reoux JP, Saxon AJ, Malte CA, et al. Divalproex sodium in alcohol withdrawal: a randomized double-blind placebo-controlled clinical trial. Alcohol Clin Exp Res 2001; 25: 1324–9PubMedCrossRef Reoux JP, Saxon AJ, Malte CA, et al. Divalproex sodium in alcohol withdrawal: a randomized double-blind placebo-controlled clinical trial. Alcohol Clin Exp Res 2001; 25: 1324–9PubMedCrossRef
163.
go back to reference Anton RF, Moak DH, Latham P. The Obsessive Compulsive Drinking Scale: a self-rated instrument for the quantification of thoughts about alcohol and drinking behavior. Alcohol Clin Exp Res 1995; 19: 92–9PubMedCrossRef Anton RF, Moak DH, Latham P. The Obsessive Compulsive Drinking Scale: a self-rated instrument for the quantification of thoughts about alcohol and drinking behavior. Alcohol Clin Exp Res 1995; 19: 92–9PubMedCrossRef
164.
go back to reference Brady KT, Myrick H, Henderson S, et al. The use of divalproex in alcohol relapse prevention: a pilot study. Drug Alcohol Depend 2002; 67: 323–30PubMedCrossRef Brady KT, Myrick H, Henderson S, et al. The use of divalproex in alcohol relapse prevention: a pilot study. Drug Alcohol Depend 2002; 67: 323–30PubMedCrossRef
165.
go back to reference Coccaro EF, Harvey PD, Kupsaw-Lawrence E, et al. Development of neuropharmacologically based behavioral assessments of impulsive aggressive behavior. J Neuropsychiatry Clin Neurosci 1991; 3: S44–51PubMed Coccaro EF, Harvey PD, Kupsaw-Lawrence E, et al. Development of neuropharmacologically based behavioral assessments of impulsive aggressive behavior. J Neuropsychiatry Clin Neurosci 1991; 3: S44–51PubMed
166.
go back to reference Stromberg MF, Mackler SA, Volpicelli JR, et al. The effect of gamma-vinyl-GABA on the consumption of concurrently available oral cocaine and ethanol in the rat. Pharmacol Biochem Behav 2001; 68: 291–9PubMedCrossRef Stromberg MF, Mackler SA, Volpicelli JR, et al. The effect of gamma-vinyl-GABA on the consumption of concurrently available oral cocaine and ethanol in the rat. Pharmacol Biochem Behav 2001; 68: 291–9PubMedCrossRef
167.
go back to reference Gerasimov MR, Schiffer WK, Brodie JD, et al. Gamma-ami-nobutyric acid mimetic drugs differentially inhibit the dopaminergic response to cocaine. Eur J Pharmacol 2000; 395: 129–35PubMedCrossRef Gerasimov MR, Schiffer WK, Brodie JD, et al. Gamma-ami-nobutyric acid mimetic drugs differentially inhibit the dopaminergic response to cocaine. Eur J Pharmacol 2000; 395: 129–35PubMedCrossRef
168.
go back to reference Wegelius K, Halonen T, Korpi ER. Gamma-vinyl GABA decreases voluntary alcohol consumption in alcohol-preferring AA rats. Pharmacol Toxicol 1993; 73: 150–2PubMedCrossRef Wegelius K, Halonen T, Korpi ER. Gamma-vinyl GABA decreases voluntary alcohol consumption in alcohol-preferring AA rats. Pharmacol Toxicol 1993; 73: 150–2PubMedCrossRef
169.
go back to reference McGeehan AJ, Olive MF. The anti-relapse compound acamprosate inhibits the development of a conditioned place preference to ethanol and cocaine but not morphine. Br J Pharmacol 2003; 138: 9–12PubMedCrossRef McGeehan AJ, Olive MF. The anti-relapse compound acamprosate inhibits the development of a conditioned place preference to ethanol and cocaine but not morphine. Br J Pharmacol 2003; 138: 9–12PubMedCrossRef
170.
go back to reference Cousins MS, Roberts DC, de Wit H. GABA(B) receptor agonists for the treatment of drug addiction: a review of recent findings. Drug Alcohol Depend 2002; 65: 209–20PubMedCrossRef Cousins MS, Roberts DC, de Wit H. GABA(B) receptor agonists for the treatment of drug addiction: a review of recent findings. Drug Alcohol Depend 2002; 65: 209–20PubMedCrossRef
171.
go back to reference Hotsenpiller G, Wolf ME. Baclofen attenuates conditioned locomotion to cues associated with cocaine administration and stabilizes extracellular glutamate levels in rat nucleus accumbens. Neuroscience 2003; 118: 123–34PubMedCrossRef Hotsenpiller G, Wolf ME. Baclofen attenuates conditioned locomotion to cues associated with cocaine administration and stabilizes extracellular glutamate levels in rat nucleus accumbens. Neuroscience 2003; 118: 123–34PubMedCrossRef
172.
go back to reference Di Ciano P, Everitt BJ. The GABA(B) receptor agonist baclofen attenuates cocaine- and heroin-seeking behavior by rats. Neuropsychopharmacology 2003; 28: 510–8PubMedCrossRef Di Ciano P, Everitt BJ. The GABA(B) receptor agonist baclofen attenuates cocaine- and heroin-seeking behavior by rats. Neuropsychopharmacology 2003; 28: 510–8PubMedCrossRef
173.
go back to reference Brebner K, Phelan R, Roberts DC. Effect of baclofen on cocaine self-administration in rats reinforced under fixed-ratio 1 and progressive-ratio schedules. Psychopharmacology 2000; 148: 314–21PubMedCrossRef Brebner K, Phelan R, Roberts DC. Effect of baclofen on cocaine self-administration in rats reinforced under fixed-ratio 1 and progressive-ratio schedules. Psychopharmacology 2000; 148: 314–21PubMedCrossRef
174.
go back to reference Brebner K, Phelan R, Roberts DC. Intra-VTA baclofen attenuates cocaine self-administration on a progressive ratio schedule of reinforcement. Pharmacol Biochem Behav 2000; 66: 857–62PubMedCrossRef Brebner K, Phelan R, Roberts DC. Intra-VTA baclofen attenuates cocaine self-administration on a progressive ratio schedule of reinforcement. Pharmacol Biochem Behav 2000; 66: 857–62PubMedCrossRef
175.
go back to reference Munzar P, Kutkat SW, Miller CR, et al. Failure of baclofen to modulate discriminative-stimulus effects of cocaine or methamphetamine in rats. Eur J Pharmacol 2000; 408: 169–74PubMedCrossRef Munzar P, Kutkat SW, Miller CR, et al. Failure of baclofen to modulate discriminative-stimulus effects of cocaine or methamphetamine in rats. Eur J Pharmacol 2000; 408: 169–74PubMedCrossRef
176.
go back to reference Lile JA, Stoops WW, Allen TS, et al. Baclofen does not alter the reinforcing, subject-rated or cardiovascular effects of intranasal cocaine in humans. Psychopharmacology 2004; 171: 441–9PubMedCrossRef Lile JA, Stoops WW, Allen TS, et al. Baclofen does not alter the reinforcing, subject-rated or cardiovascular effects of intranasal cocaine in humans. Psychopharmacology 2004; 171: 441–9PubMedCrossRef
177.
go back to reference Shoptaw S, Yang X, Rotheram-Fuller EJ, et al. Randomized placebo-controlled trial of baclofen for cocaine dependence: preliminary effects for individuals with chronic patterns of cocaine use. J Clin Psychiatry 2003; 64: 1440–8PubMedCrossRef Shoptaw S, Yang X, Rotheram-Fuller EJ, et al. Randomized placebo-controlled trial of baclofen for cocaine dependence: preliminary effects for individuals with chronic patterns of cocaine use. J Clin Psychiatry 2003; 64: 1440–8PubMedCrossRef
178.
go back to reference Hatsukami D, Keenan R, Halikas J, et al. Effects of carbamazepine on acute responses to smoked cocaine-base in human cocaine users. Psychopharmacology 1991; 104: 120–4PubMedCrossRef Hatsukami D, Keenan R, Halikas J, et al. Effects of carbamazepine on acute responses to smoked cocaine-base in human cocaine users. Psychopharmacology 1991; 104: 120–4PubMedCrossRef
179.
go back to reference Hersh D, Bauer LO, Kranzler HR. Carbamazepine and cocaine-cue reactivity. Drug Alcohol Depend 1995; 39: 213–21PubMedCrossRef Hersh D, Bauer LO, Kranzler HR. Carbamazepine and cocaine-cue reactivity. Drug Alcohol Depend 1995; 39: 213–21PubMedCrossRef
180.
go back to reference Lima AR, Lima MS, Soares BG, et al. Carbamazepine for cocaine dependence. Cochrane Database Syst Rev 2000; (2): CD002023 Lima AR, Lima MS, Soares BG, et al. Carbamazepine for cocaine dependence. Cochrane Database Syst Rev 2000; (2): CD002023
181.
go back to reference Lima AR, Lima MS, Soares BG, et al. Carbamazepine for cocaine dependence. Cochrane Database Syst Rev 2002; (2): CD002023 Lima AR, Lima MS, Soares BG, et al. Carbamazepine for cocaine dependence. Cochrane Database Syst Rev 2002; (2): CD002023
182.
go back to reference Raby WN, Coomaraswamy S. Gabapentin reduces cocaine use among addicts from a community clinic sample. J Clin Psychiatry 2004; 65: 84–6PubMedCrossRef Raby WN, Coomaraswamy S. Gabapentin reduces cocaine use among addicts from a community clinic sample. J Clin Psychiatry 2004; 65: 84–6PubMedCrossRef
183.
go back to reference Myrick H, Henderson S, Brady KT, et al. Gabapentin in the treatment of cocaine dependence: a case series. J Clin Psychiatry 2001; 62: 19–23PubMedCrossRef Myrick H, Henderson S, Brady KT, et al. Gabapentin in the treatment of cocaine dependence: a case series. J Clin Psychiatry 2001; 62: 19–23PubMedCrossRef
184.
go back to reference Schiffer WK, Marsteller D, Dewey SL. Sub-chronic low dose gamma-vinyl GABA (vigabatrin) inhibits cocaine-induced increases in nucleus accumbens dopamine. Psychopharmacology 2003; 168: 339–43PubMedCrossRef Schiffer WK, Marsteller D, Dewey SL. Sub-chronic low dose gamma-vinyl GABA (vigabatrin) inhibits cocaine-induced increases in nucleus accumbens dopamine. Psychopharmacology 2003; 168: 339–43PubMedCrossRef
185.
go back to reference Brodie JD, Figueroa E, Dewey SL. Treating cocaine addiction: from preclinical to clinical trial experience with gamma-vinyl GABA. Synapse 2003; 50: 261–5PubMedCrossRef Brodie JD, Figueroa E, Dewey SL. Treating cocaine addiction: from preclinical to clinical trial experience with gamma-vinyl GABA. Synapse 2003; 50: 261–5PubMedCrossRef
186.
go back to reference Myrick H, Henderson S, Brady KT, et al. Divalproex loading in the treatment of cocaine dependence. J Psychoactive Drugs 2001; 33: 283–7PubMedCrossRef Myrick H, Henderson S, Brady KT, et al. Divalproex loading in the treatment of cocaine dependence. J Psychoactive Drugs 2001; 33: 283–7PubMedCrossRef
187.
go back to reference Gonzalez G, Sevarino K, Sofuoglu M, et al. Tiagabine increases cocaine-free urines in cocaine-dependent methadone-treated patients: results of a randomized pilot study. Addiction 2003; 98: 1625–32PubMedCrossRef Gonzalez G, Sevarino K, Sofuoglu M, et al. Tiagabine increases cocaine-free urines in cocaine-dependent methadone-treated patients: results of a randomized pilot study. Addiction 2003; 98: 1625–32PubMedCrossRef
188.
go back to reference Anton RF, Swift RM. Current pharmacotherapies of alcoholism: a US perspective. Am J Addict 2003; 12Suppl. 1: S53–68PubMedCrossRef Anton RF, Swift RM. Current pharmacotherapies of alcoholism: a US perspective. Am J Addict 2003; 12Suppl. 1: S53–68PubMedCrossRef
Metadata
Title
Recent Advances in the Development of Treatments for Alcohol and Cocaine Dependence
Focus on Topiramate and Other Modulators of GABA or Glutamate Function
Author
Prof. Bankole A. Johnson
Publication date
01-10-2005
Publisher
Springer International Publishing
Published in
CNS Drugs / Issue 10/2005
Print ISSN: 1172-7047
Electronic ISSN: 1179-1934
DOI
https://doi.org/10.2165/00023210-200519100-00005

Other articles of this Issue 10/2005

CNS Drugs 10/2005 Go to the issue