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Published in: Current Sexual Health Reports 4/2017

01-12-2017 | Preclinical and Psychophysiology (F Guarraci and L Marson, Section Editors)

The Role of Ovarian Hormones and the Medial Amygdala in Sexual Motivation

Authors: Mary K. Holder, Jessica A. Mong

Published in: Current Sexual Health Reports | Issue 4/2017

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Abstract

Purpose

Although research into the neurobiology of sexual desire in women is active, relatively little is understood about the origins of sexual motivation in women. The purpose of our review is to discuss factors that influence a central sexual motivational state and generalized arousal as potential drivers of sexual motivation in women and female rats.

Recent Findings

Sexual motivation is the product of interactions of the central motive state and salient sexually relevant cues. Ovarian hormones and generalized arousal influence the central motive state, and endogenous levels of estradiol and progesterone correlate with sexual motivation and behavior in women. The amygdala is a key integratory site for generalized arousal and sexual sensory stimulation, which could then increase sexual motivation through its downstream projections.

Summary

Our model of enhanced female sexual motivation suggests that the combined effects of dopamine and progesterone receptor activation in the medial amygdala increase the incentive properties of a sexual stimulus. Further study into the interactions of ovarian hormones and mediators of generalized arousal on the processing of sexually relevant cues informs our understanding of the neurobiology of female sexual motivation and could lead to the development of therapeutics to treat the dysfunctions of sexual desire in women.
Literature
1.
go back to reference McCabe MP, Sharlip ID, Lewis R, Atalla E, Balon R, Fisher AD, et al. Incidence and prevalence of sexual dysfunction in women and men: a consensus statement from the fourth international consultation on sexual medicine 2015. Journal of Sexual Medicine. 2016;13(2):144–52.PubMedCrossRef McCabe MP, Sharlip ID, Lewis R, Atalla E, Balon R, Fisher AD, et al. Incidence and prevalence of sexual dysfunction in women and men: a consensus statement from the fourth international consultation on sexual medicine 2015. Journal of Sexual Medicine. 2016;13(2):144–52.PubMedCrossRef
2.
go back to reference Studd J, Schwenkhagen A. The historical response to female sexuality. Maturitas. 2009;63(2):107–11.PubMedCrossRef Studd J, Schwenkhagen A. The historical response to female sexuality. Maturitas. 2009;63(2):107–11.PubMedCrossRef
3.
go back to reference Jutel A. Framing disease: the example of female hypoactive sexual desire disorder. Soc Sci Med. 2010;70(7):1084–90.PubMedCrossRef Jutel A. Framing disease: the example of female hypoactive sexual desire disorder. Soc Sci Med. 2010;70(7):1084–90.PubMedCrossRef
5.
go back to reference Kinsey AC, Pomeroy WB, Martin CE, Gerhard PH. Sexual behaviour in the human female. Philadelphia: WB Sanders; 1953. Kinsey AC, Pomeroy WB, Martin CE, Gerhard PH. Sexual behaviour in the human female. Philadelphia: WB Sanders; 1953.
6.
go back to reference Masters WH, Johnson VE. Human sexual response. Boston: Little, Brown; 1966. Masters WH, Johnson VE. Human sexual response. Boston: Little, Brown; 1966.
7.
go back to reference Lewis RW, Fugl-Meyer KS, Bosch R, Fugl-Meyer AR, Laumann EO, Lizza E, et al. Epidemiology/risk factors of sexual dysfunction. J Sex Med. 2004;1(1):35–9.PubMedCrossRef Lewis RW, Fugl-Meyer KS, Bosch R, Fugl-Meyer AR, Laumann EO, Lizza E, et al. Epidemiology/risk factors of sexual dysfunction. J Sex Med. 2004;1(1):35–9.PubMedCrossRef
8.
go back to reference Basson R, Althof S, Davis S, Fugl-Meyer K, Goldstein I, Leiblum S, et al. Summary of the recommendations on sexual dysfunctions in women. J Sex Med. 2004;1(1):24–34.PubMedCrossRef Basson R, Althof S, Davis S, Fugl-Meyer K, Goldstein I, Leiblum S, et al. Summary of the recommendations on sexual dysfunctions in women. J Sex Med. 2004;1(1):24–34.PubMedCrossRef
9.
go back to reference Nappi RE, Martini E, Terreno E, Albani F, Santamaria V, Tonani S, et al. Management of hypoactive sexual desire disorder in women: current and emerging therapies. Int J Womens Health. 2010;2:167–75.PubMedPubMedCentralCrossRef Nappi RE, Martini E, Terreno E, Albani F, Santamaria V, Tonani S, et al. Management of hypoactive sexual desire disorder in women: current and emerging therapies. Int J Womens Health. 2010;2:167–75.PubMedPubMedCentralCrossRef
10.
go back to reference Palacios S. Hypoactive Sexual Desire Disorder and current pharmacotherapeutic options in women. Women's Health. 2011;7(1):95–107.PubMedCrossRef Palacios S. Hypoactive Sexual Desire Disorder and current pharmacotherapeutic options in women. Women's Health. 2011;7(1):95–107.PubMedCrossRef
11.
go back to reference Leiblum SR, Koochaki PE, Rodenberg CA, Barton IP, Rosen RC. Hypoactive sexual desire disorder in postmenopausal women: US results from the Women’s International Study of Health and Sexuality (WISHeS). Menopause. 2006;13(1):46–56.PubMedCrossRef Leiblum SR, Koochaki PE, Rodenberg CA, Barton IP, Rosen RC. Hypoactive sexual desire disorder in postmenopausal women: US results from the Women’s International Study of Health and Sexuality (WISHeS). Menopause. 2006;13(1):46–56.PubMedCrossRef
12.
go back to reference Laumann EO, Paik A, Rosen RC. Sexual dysfunction in the United States: prevalence and predictors. JAMA. 1999;281(6):537–44.PubMedCrossRef Laumann EO, Paik A, Rosen RC. Sexual dysfunction in the United States: prevalence and predictors. JAMA. 1999;281(6):537–44.PubMedCrossRef
13.
go back to reference Levine SB. The nature of sexual desire: a clinician’s perspective. Arch Sex Behav. 2003;32(3):279–85.PubMedCrossRef Levine SB. The nature of sexual desire: a clinician’s perspective. Arch Sex Behav. 2003;32(3):279–85.PubMedCrossRef
14.
go back to reference •• Agmo A. On the intricate relationship between sexual motivation and arousal. Horm Behav. 2011;59(5):681–8. This review summarizes the hypothesis that general arousal is an important factor in sexual motivation PubMedCrossRef •• Agmo A. On the intricate relationship between sexual motivation and arousal. Horm Behav. 2011;59(5):681–8. This review summarizes the hypothesis that general arousal is an important factor in sexual motivation PubMedCrossRef
15.
go back to reference Graham CA, Sanders SA, Milhausen RR, McBride KR. Turning on and turning off: a focus group study of the factors that affect women’s sexual arousal. Arch Sex Behav. 2004;33(6):527–38.PubMedCrossRef Graham CA, Sanders SA, Milhausen RR, McBride KR. Turning on and turning off: a focus group study of the factors that affect women’s sexual arousal. Arch Sex Behav. 2004;33(6):527–38.PubMedCrossRef
16.
go back to reference Wood JM, Mansfield PK, Koch PB. Negotiating sexual agency: postmenopausal women’s meaning and experience of sexual desire. Qual Health Res. 2007;17(2):189–200.PubMedCrossRef Wood JM, Mansfield PK, Koch PB. Negotiating sexual agency: postmenopausal women’s meaning and experience of sexual desire. Qual Health Res. 2007;17(2):189–200.PubMedCrossRef
17.
go back to reference Kaplan HS. Disorders of sexual desire and other new concepts and techniques in sex therapy. New York: Simon & Schuster; 1979. Kaplan HS. Disorders of sexual desire and other new concepts and techniques in sex therapy. New York: Simon & Schuster; 1979.
18.
21.
go back to reference Association AP. Diagnostic and statistical manual of mental disorders (DSM-5). Washington, D.C.: American Psychiatric Association; 2013.CrossRef Association AP. Diagnostic and statistical manual of mental disorders (DSM-5). Washington, D.C.: American Psychiatric Association; 2013.CrossRef
22.
go back to reference Derogatis LR, Sand M, Balon R, Rosen R, Parish SJ. Toward a more evidence-based nosology and nomenclature for female sexual dysfunctions-part I. J Sex Med. 2016;13(12):1881–7.PubMedCrossRef Derogatis LR, Sand M, Balon R, Rosen R, Parish SJ. Toward a more evidence-based nosology and nomenclature for female sexual dysfunctions-part I. J Sex Med. 2016;13(12):1881–7.PubMedCrossRef
23.
go back to reference Parish SJ, Goldstein AT, Goldstein SW, Goldstein I, Pfaus J, Clayton AH, et al. Toward a more evidence-based nosology and nomenclature for female sexual dysfunctions-part II. J Sex Med. 2016;13(12):1888–906.PubMedCrossRef Parish SJ, Goldstein AT, Goldstein SW, Goldstein I, Pfaus J, Clayton AH, et al. Toward a more evidence-based nosology and nomenclature for female sexual dysfunctions-part II. J Sex Med. 2016;13(12):1888–906.PubMedCrossRef
24.
go back to reference • Goldstein I, Kim NN, Clayton AH, DeRogatis LR, Giraldi A, Parish SJ, et al. Hypoactive Sexual Desire Disorder: International Society for the Study of Women’s Sexual Health (ISSWSH) expert consensus panel review. Mayo Clin Proc. 2017;92(1):114–28. This panel review indicates the need to maintain separate diagnosis for sexual desire disorder and sexual arousal disorders in women PubMedCrossRef • Goldstein I, Kim NN, Clayton AH, DeRogatis LR, Giraldi A, Parish SJ, et al. Hypoactive Sexual Desire Disorder: International Society for the Study of Women’s Sexual Health (ISSWSH) expert consensus panel review. Mayo Clin Proc. 2017;92(1):114–28. This panel review indicates the need to maintain separate diagnosis for sexual desire disorder and sexual arousal disorders in women PubMedCrossRef
25.
go back to reference • Sarin S, Amsel RM, Binik YM. Disentangling desire and arousal: a classificatory conundrum. Arch Sex Behav. 2013;42(6):1079–100. This study indicates that there is a distinction between desire and genital arousal disorders PubMedCrossRef • Sarin S, Amsel RM, Binik YM. Disentangling desire and arousal: a classificatory conundrum. Arch Sex Behav. 2013;42(6):1079–100. This study indicates that there is a distinction between desire and genital arousal disorders PubMedCrossRef
26.
go back to reference • Sarin S, Amsel R, Binik YM. A streetcar named “Derousal”? A psychophysiological examination of the desire-arousal distinction in sexually functional and dysfunctional women. J Sex Res. 2016;53(6):711–29. This study empirically identifies three profiles of sexual disorder: a low desire disorder, a genital arousal disorder, and a combination of low desire and genital arousal PubMedCrossRef • Sarin S, Amsel R, Binik YM. A streetcar named “Derousal”? A psychophysiological examination of the desire-arousal distinction in sexually functional and dysfunctional women. J Sex Res. 2016;53(6):711–29. This study empirically identifies three profiles of sexual disorder: a low desire disorder, a genital arousal disorder, and a combination of low desire and genital arousal PubMedCrossRef
27.
go back to reference Bancroft J, Loftus J, Long JS. Distress about sex: a national survey of women in heterosexual relationships. Arch Sex Behav. 2003;32(3):193–208.PubMedCrossRef Bancroft J, Loftus J, Long JS. Distress about sex: a national survey of women in heterosexual relationships. Arch Sex Behav. 2003;32(3):193–208.PubMedCrossRef
28.
go back to reference Laumann EO, Nicolosi A, Glasser DB, Paik A, Gingell C, Moreira E, et al. Sexual problems among women and men aged 40–80 y: prevalence and correlates identified in the Global Study of Sexual Attitudes and Behaviors. Int J Impot Res. 2005;17(1):39–57.PubMedCrossRef Laumann EO, Nicolosi A, Glasser DB, Paik A, Gingell C, Moreira E, et al. Sexual problems among women and men aged 40–80 y: prevalence and correlates identified in the Global Study of Sexual Attitudes and Behaviors. Int J Impot Res. 2005;17(1):39–57.PubMedCrossRef
29.
go back to reference Dennerstein L, Lehert P. Modeling mid-aged women’s sexual functioning: a prospective, population-based study. J Sex Marital Ther. 2004;30(3):173–83.PubMedCrossRef Dennerstein L, Lehert P. Modeling mid-aged women’s sexual functioning: a prospective, population-based study. J Sex Marital Ther. 2004;30(3):173–83.PubMedCrossRef
31.
go back to reference •• Chu X, Gagnidze K, Pfaff D, Agmo A. Estrogens, androgens and generalized behavioral arousal in gonadectomized female and male C57BL/6 mice. Physiol Behav. 2015;147:255–63. This study indicates that while hormones do contribute to generalized arousal, they have stronger arousal effects in the context of sexually relevent stimuli PubMedPubMedCentralCrossRef •• Chu X, Gagnidze K, Pfaff D, Agmo A. Estrogens, androgens and generalized behavioral arousal in gonadectomized female and male C57BL/6 mice. Physiol Behav. 2015;147:255–63. This study indicates that while hormones do contribute to generalized arousal, they have stronger arousal effects in the context of sexually relevent stimuli PubMedPubMedCentralCrossRef
32.
go back to reference Harvey SM. Female sexual behavior: fluctuations during the menstrual cycle. J Psychosom Res. 1987;31(1):101–10.PubMedCrossRef Harvey SM. Female sexual behavior: fluctuations during the menstrual cycle. J Psychosom Res. 1987;31(1):101–10.PubMedCrossRef
33.
go back to reference Bullivant SB, Sellergren SA, Stern K, Spencer NA, Jacob S, Mennella JA, et al. Women’s sexual experience during the menstrual cycle: identification of the sexual phase by noninvasive measurement of luteinizing hormone. J Sex Res. 2004;41(1):82–93.PubMedCrossRef Bullivant SB, Sellergren SA, Stern K, Spencer NA, Jacob S, Mennella JA, et al. Women’s sexual experience during the menstrual cycle: identification of the sexual phase by noninvasive measurement of luteinizing hormone. J Sex Res. 2004;41(1):82–93.PubMedCrossRef
34.
go back to reference Pillsworth EG, Haselton MG, Buss DM. Ovulatory shifts in female sexual desire. J Sex Res. 2004;41(1):55–65.PubMedCrossRef Pillsworth EG, Haselton MG, Buss DM. Ovulatory shifts in female sexual desire. J Sex Res. 2004;41(1):55–65.PubMedCrossRef
35.
go back to reference Haselton MG, Mortezaie M, Pillsworth EG, Bleske-Rechek A, Frederick DA. Ovulatory shifts in human female ornamentation: near ovulation, women dress to impress. Horm Behav. 2007;51(1):40–5.PubMedCrossRef Haselton MG, Mortezaie M, Pillsworth EG, Bleske-Rechek A, Frederick DA. Ovulatory shifts in human female ornamentation: near ovulation, women dress to impress. Horm Behav. 2007;51(1):40–5.PubMedCrossRef
36.
go back to reference Haselton MG, Gangestad SW. Conditional expression of women’s desires and men’s mate guarding across the ovulatory cycle. Horm Behav. 2006;49(4):509–18.PubMedCrossRef Haselton MG, Gangestad SW. Conditional expression of women’s desires and men’s mate guarding across the ovulatory cycle. Horm Behav. 2006;49(4):509–18.PubMedCrossRef
37.
go back to reference Diamond LM, Wallen K. Sexual minority women’s sexual motivation around the time of ovulation. Arch Sex Behav. 2011;40(2):237–46.PubMedCrossRef Diamond LM, Wallen K. Sexual minority women’s sexual motivation around the time of ovulation. Arch Sex Behav. 2011;40(2):237–46.PubMedCrossRef
38.
go back to reference Matteo S, Rissman EF. Increased sexual activity during the midcycle portion of the human menstrual cycle. Horm Behav. 1984;18(3):249–55.PubMedCrossRef Matteo S, Rissman EF. Increased sexual activity during the midcycle portion of the human menstrual cycle. Horm Behav. 1984;18(3):249–55.PubMedCrossRef
39.
go back to reference Prasad A, Mumford SL, Buck Louis GM, Ahrens KA, Sjaarda LA, Schliep KC, et al. Sexual activity, endogenous reproductive hormones and ovulation in premenopausal women. Horm Behav. 2014;66(2):330–8.PubMedPubMedCentralCrossRef Prasad A, Mumford SL, Buck Louis GM, Ahrens KA, Sjaarda LA, Schliep KC, et al. Sexual activity, endogenous reproductive hormones and ovulation in premenopausal women. Horm Behav. 2014;66(2):330–8.PubMedPubMedCentralCrossRef
40.
go back to reference •• Roney JR, Simmons ZL. Hormonal predictors of sexual motivation in natural menstrual cycles. Horm Behav. 2013;63(4):636–45. This study investigates the role of endogenous hormones in driving sexual motivation PubMedCrossRef •• Roney JR, Simmons ZL. Hormonal predictors of sexual motivation in natural menstrual cycles. Horm Behav. 2013;63(4):636–45. This study investigates the role of endogenous hormones in driving sexual motivation PubMedCrossRef
41.
go back to reference Cappelletti M, Wallen K. Increasing women’s sexual desire: the comparative effectiveness of estrogens and androgens. Horm Behav. 2016;78:178–93.PubMedCrossRef Cappelletti M, Wallen K. Increasing women’s sexual desire: the comparative effectiveness of estrogens and androgens. Horm Behav. 2016;78:178–93.PubMedCrossRef
42.
go back to reference Wallen K. Sex and context: hormones and primate sexual motivation. Horm Behav. 2001;40(2):339–57.PubMedCrossRef Wallen K. Sex and context: hormones and primate sexual motivation. Horm Behav. 2001;40(2):339–57.PubMedCrossRef
43.
go back to reference Grebe NM, Gangestad SW, Garver-Apgar CE, Thornhill R. Women’s luteal-phase sexual proceptivity and the functions of extended sexuality. Psychol Sci. 2013;24(10):2106–10.PubMedCrossRef Grebe NM, Gangestad SW, Garver-Apgar CE, Thornhill R. Women’s luteal-phase sexual proceptivity and the functions of extended sexuality. Psychol Sci. 2013;24(10):2106–10.PubMedCrossRef
44.
go back to reference • Grebe NM, Emery Thompson M, Gangestad SW. Hormonal predictors of women’s extra-pair vs. in-pair sexual attraction in natural cycles: implications for extended sexuality. Horm Behav. 2016;78:211–9. This study identifies distinct roles for estradiol and progesterone in sexual desires in naturally cycling women PubMedCrossRef • Grebe NM, Emery Thompson M, Gangestad SW. Hormonal predictors of women’s extra-pair vs. in-pair sexual attraction in natural cycles: implications for extended sexuality. Horm Behav. 2016;78:211–9. This study identifies distinct roles for estradiol and progesterone in sexual desires in naturally cycling women PubMedCrossRef
45.
go back to reference Larson CM, Haselton MG, Gildersleeve KA, Pillsworth EG. Changes in women’s feelings about their romantic relationships across the ovulatory cycle. Horm Behav. 2013;63(1):128–35.PubMedCrossRef Larson CM, Haselton MG, Gildersleeve KA, Pillsworth EG. Changes in women’s feelings about their romantic relationships across the ovulatory cycle. Horm Behav. 2013;63(1):128–35.PubMedCrossRef
46.
go back to reference Larson CM, Pillsworth EG, Haselton MG. Ovulatory shifts in women’s attractions to primary partners and other men: further evidence of the importance of primary partner sexual attractiveness. PLoS One. 2012;7(9):e44456.PubMedPubMedCentralCrossRef Larson CM, Pillsworth EG, Haselton MG. Ovulatory shifts in women’s attractions to primary partners and other men: further evidence of the importance of primary partner sexual attractiveness. PLoS One. 2012;7(9):e44456.PubMedPubMedCentralCrossRef
47.
go back to reference • Roney JR, Simmons ZL. Within-cycle fluctuations in progesterone negatively predict changes in both in-pair and extra-pair desire among partnered women. Horm Behav. 2016;81:45–52. This study highlights the role of estradiol, but not progesterone, in sexual motivation in women PubMedCrossRef • Roney JR, Simmons ZL. Within-cycle fluctuations in progesterone negatively predict changes in both in-pair and extra-pair desire among partnered women. Horm Behav. 2016;81:45–52. This study highlights the role of estradiol, but not progesterone, in sexual motivation in women PubMedCrossRef
48.
go back to reference Maravilla KR, Yang CC. Magnetic resonance imaging and the female sexual response: overview of techniques, results, and future directions. J Sex Med. 2008;5(7):1559–71.PubMedCrossRef Maravilla KR, Yang CC. Magnetic resonance imaging and the female sexual response: overview of techniques, results, and future directions. J Sex Med. 2008;5(7):1559–71.PubMedCrossRef
49.
go back to reference Park K, Kang HK, Seo JJ, Kim HJ, Ryu SB, Jeong GW. Blood-oxygenation-level-dependent functional magnetic resonance imaging for evaluating cerebral regions of female sexual arousal response. Urology. 2001;57(6):1189–94.PubMedCrossRef Park K, Kang HK, Seo JJ, Kim HJ, Ryu SB, Jeong GW. Blood-oxygenation-level-dependent functional magnetic resonance imaging for evaluating cerebral regions of female sexual arousal response. Urology. 2001;57(6):1189–94.PubMedCrossRef
50.
go back to reference Morris JS, Ohman A, Dolan RJ. Conscious and unconscious emotional learning in the human amygdala. Nature. 1998;393(6684):467–70.PubMedCrossRef Morris JS, Ohman A, Dolan RJ. Conscious and unconscious emotional learning in the human amygdala. Nature. 1998;393(6684):467–70.PubMedCrossRef
51.
go back to reference Morris JS, Friston KJ, Buchel C, Frith CD, Young AW, Calder AJ, et al. A neuromodulatory role for the human amygdala in processing emotional facial expressions. Brain. 1998;121(Pt 1):47–57.PubMedCrossRef Morris JS, Friston KJ, Buchel C, Frith CD, Young AW, Calder AJ, et al. A neuromodulatory role for the human amygdala in processing emotional facial expressions. Brain. 1998;121(Pt 1):47–57.PubMedCrossRef
52.
go back to reference Breiter HC, Etcoff NL, Whalen PJ, Kennedy WA, Rauch SL, Buckner RL, et al. Response and habituation of the human amygdala during visual processing of facial expression. Neuron. 1996;17(5):875–87.PubMedCrossRef Breiter HC, Etcoff NL, Whalen PJ, Kennedy WA, Rauch SL, Buckner RL, et al. Response and habituation of the human amygdala during visual processing of facial expression. Neuron. 1996;17(5):875–87.PubMedCrossRef
53.
go back to reference Amaral DG, Price JL, Pitkanen A, Carmichael ST. Anatomical organization of the primate amgydaloid complex. In: Aggleton JP, editor. The amygdala: neurobiological aspects of emotion, memory, and mental dysfunction. New York: Wiley-Liss; 1992. p. 1–66. Amaral DG, Price JL, Pitkanen A, Carmichael ST. Anatomical organization of the primate amgydaloid complex. In: Aggleton JP, editor. The amygdala: neurobiological aspects of emotion, memory, and mental dysfunction. New York: Wiley-Liss; 1992. p. 1–66.
54.
go back to reference Gray TS. Functional and anatomical relationships among the amygdala, basal forebrain, ventral striatum, and cortex. An integrative discussion. Ann N Y Acad Sci. 1999;877:439–44.PubMedCrossRef Gray TS. Functional and anatomical relationships among the amygdala, basal forebrain, ventral striatum, and cortex. An integrative discussion. Ann N Y Acad Sci. 1999;877:439–44.PubMedCrossRef
55.
go back to reference Pitkänen A. Connectivity of the rat amygdaloid complex. In: Aggleton JP, editor. The amygdala. 2nd ed. New York: Oxford University Press; 2000. p. 31–115. Pitkänen A. Connectivity of the rat amygdaloid complex. In: Aggleton JP, editor. The amygdala. 2nd ed. New York: Oxford University Press; 2000. p. 31–115.
56.
go back to reference De Olmos J, Alheid GF, Beltramino CA. Amydala. In: Paxinos G, editor. The rat nervous system volume 1 forebrain and midbrain. Orlando: Academic Press Inc; 1985. p. 223–334. De Olmos J, Alheid GF, Beltramino CA. Amydala. In: Paxinos G, editor. The rat nervous system volume 1 forebrain and midbrain. Orlando: Academic Press Inc; 1985. p. 223–334.
57.
go back to reference Lynd-Balta E, Haber SN. The organization of midbrain projections to the ventral striatum in the primate. Neuroscience. 1994;59(3):609–23.PubMedCrossRef Lynd-Balta E, Haber SN. The organization of midbrain projections to the ventral striatum in the primate. Neuroscience. 1994;59(3):609–23.PubMedCrossRef
58.
go back to reference Schultz W, Dayan P, Montague PR. A neural substrate of prediction and reward. Science. 1997;275(5306):1593–9.PubMedCrossRef Schultz W, Dayan P, Montague PR. A neural substrate of prediction and reward. Science. 1997;275(5306):1593–9.PubMedCrossRef
59.
go back to reference Keller M, Baum MJ, Brock O, Brennan PA, Bakker J. The main and the accessory olfactory systems interact in the control of mate recognition and sexual behavior. Behav Brain Res. 2009;200(2):268–76.PubMedCrossRef Keller M, Baum MJ, Brock O, Brennan PA, Bakker J. The main and the accessory olfactory systems interact in the control of mate recognition and sexual behavior. Behav Brain Res. 2009;200(2):268–76.PubMedCrossRef
60.
go back to reference Kevetter GA, Winans SS. Connections of the corticomedial amygdala in the golden hamster. I. Efferents of the “vomeronasal amygdala”. J Comp Neurol. 1981;197(1):81–98.PubMedCrossRef Kevetter GA, Winans SS. Connections of the corticomedial amygdala in the golden hamster. I. Efferents of the “vomeronasal amygdala”. J Comp Neurol. 1981;197(1):81–98.PubMedCrossRef
61.
go back to reference Simerly RB. Wired for reproduction: organization and development of sexually dimorphic circuits in the mammalian forebrain. Annu Rev Neurosci. 2002;25:507–36.PubMedCrossRef Simerly RB. Wired for reproduction: organization and development of sexually dimorphic circuits in the mammalian forebrain. Annu Rev Neurosci. 2002;25:507–36.PubMedCrossRef
62.
go back to reference Baum MJ. Sexual differentiation of pheromone processing: links to male-typical mating behavior and partner preference. Horm Behav. 2009;55(5):579–88.PubMedPubMedCentralCrossRef Baum MJ. Sexual differentiation of pheromone processing: links to male-typical mating behavior and partner preference. Horm Behav. 2009;55(5):579–88.PubMedPubMedCentralCrossRef
63.
go back to reference Canteras NS, Simerly RB, Swanson LW. Organization of projections from the medial nucleus of the amygdala: a PHAL study in the rat. J Comp Neurol. 1995;360(2):213–45.PubMedCrossRef Canteras NS, Simerly RB, Swanson LW. Organization of projections from the medial nucleus of the amygdala: a PHAL study in the rat. J Comp Neurol. 1995;360(2):213–45.PubMedCrossRef
64.
go back to reference Russchen FT, Amaral DG, Price JL. The afferent input to the magnocellular division of the mediodorsal thalamic nucleus in the monkey, Macaca fascicularis. J Comp Neurol. 1987;256(2):175–210.PubMedCrossRef Russchen FT, Amaral DG, Price JL. The afferent input to the magnocellular division of the mediodorsal thalamic nucleus in the monkey, Macaca fascicularis. J Comp Neurol. 1987;256(2):175–210.PubMedCrossRef
65.
go back to reference Wehrum S, Klucken T, Kagerer S, Walter B, Hermann A, Vaitl D, et al. Gender commonalities and differences in the neural processing of visual sexual stimuli. J Sex Med. 2013;10(5):1328–42.PubMedCrossRef Wehrum S, Klucken T, Kagerer S, Walter B, Hermann A, Vaitl D, et al. Gender commonalities and differences in the neural processing of visual sexual stimuli. J Sex Med. 2013;10(5):1328–42.PubMedCrossRef
66.
go back to reference Kim TH, Kang HK, Jeong GW. Assessment of brain metabolites change during visual sexual stimulation in healthy women using functional MR spectroscopy. J Sex Med. 2013;10(4):1001–11.PubMedCrossRef Kim TH, Kang HK, Jeong GW. Assessment of brain metabolites change during visual sexual stimulation in healthy women using functional MR spectroscopy. J Sex Med. 2013;10(4):1001–11.PubMedCrossRef
67.
go back to reference • Sylva D, Safron A, Rosenthal AM, Reber PJ, Parrish TB, Bailey JM. Neural correlates of sexual arousal in heterosexual and homosexual women and men. Horm Behav. 2013;64(4):673–84. This study highlights the role of the amygdala and its downstream projections in sexual arousal PubMedCrossRef • Sylva D, Safron A, Rosenthal AM, Reber PJ, Parrish TB, Bailey JM. Neural correlates of sexual arousal in heterosexual and homosexual women and men. Horm Behav. 2013;64(4):673–84. This study highlights the role of the amygdala and its downstream projections in sexual arousal PubMedCrossRef
68.
go back to reference Arnow BA, Millheiser L, Garrett A, Lake Polan M, Glover GH, Hill KR, et al. Women with hypoactive sexual desire disorder compared to normal females: a functional magnetic resonance imaging study. Neuroscience. 2009;158(2):484–502.PubMedCrossRef Arnow BA, Millheiser L, Garrett A, Lake Polan M, Glover GH, Hill KR, et al. Women with hypoactive sexual desire disorder compared to normal females: a functional magnetic resonance imaging study. Neuroscience. 2009;158(2):484–502.PubMedCrossRef
69.
go back to reference Hamann S, Mao H. Positive and negative emotional verbal stimuli elicit activity in the left amygdala. Neuroreport. 2002;13(1):15–9.PubMedCrossRef Hamann S, Mao H. Positive and negative emotional verbal stimuli elicit activity in the left amygdala. Neuroreport. 2002;13(1):15–9.PubMedCrossRef
70.
go back to reference Hamann SB, Ely TD, Hoffman JM, Kilts CD. Ecstasy and agony: activation of the human amygdala in positive and negative emotion. Psychol Sci. 2002;13(2):135–41.PubMedCrossRef Hamann SB, Ely TD, Hoffman JM, Kilts CD. Ecstasy and agony: activation of the human amygdala in positive and negative emotion. Psychol Sci. 2002;13(2):135–41.PubMedCrossRef
71.
go back to reference Zald DH, Pardo JV. Emotion, olfaction, and the human amygdala: amygdala activation during aversive olfactory stimulation. Proc Natl Acad Sci U S A. 1997;94(8):4119–24.PubMedPubMedCentralCrossRef Zald DH, Pardo JV. Emotion, olfaction, and the human amygdala: amygdala activation during aversive olfactory stimulation. Proc Natl Acad Sci U S A. 1997;94(8):4119–24.PubMedPubMedCentralCrossRef
72.
go back to reference Walter M, Bermpohl F, Mouras H, Schiltz K, Tempelmann C, Rotte M, et al. Distinguishing specific sexual and general emotional effects in fMRI-subcortical and cortical arousal during erotic picture viewing. NeuroImage. 2008;40(4):1482–94.PubMedCrossRef Walter M, Bermpohl F, Mouras H, Schiltz K, Tempelmann C, Rotte M, et al. Distinguishing specific sexual and general emotional effects in fMRI-subcortical and cortical arousal during erotic picture viewing. NeuroImage. 2008;40(4):1482–94.PubMedCrossRef
73.
go back to reference • Wise NJ, Frangos E, Komisaruk BR. Activation of sensory cortex by imagined genital stimulation: an fMRI analysis. Socioaffect Neurosci Psychol. 2016;6:31481. This imaging study suggests that imagined genital stimulation activates similar brain regions as sexual arousal, indicating that fantasy, a measure of desire, may lead to arousal PubMedCrossRef • Wise NJ, Frangos E, Komisaruk BR. Activation of sensory cortex by imagined genital stimulation: an fMRI analysis. Socioaffect Neurosci Psychol. 2016;6:31481. This imaging study suggests that imagined genital stimulation activates similar brain regions as sexual arousal, indicating that fantasy, a measure of desire, may lead to arousal PubMedCrossRef
74.
go back to reference Gizewski ER, Krause E, Karama S, Baars A, Senf W, Forsting M. There are differences in cerebral activation between females in distinct menstrual phases during viewing of erotic stimuli: a fMRI study. Exp Brain Res. 2006;174(1):101–8.PubMedCrossRef Gizewski ER, Krause E, Karama S, Baars A, Senf W, Forsting M. There are differences in cerebral activation between females in distinct menstrual phases during viewing of erotic stimuli: a fMRI study. Exp Brain Res. 2006;174(1):101–8.PubMedCrossRef
75.
go back to reference Zhu X, Wang X, Parkinson C, Cai C, Gao S, Hu P. Brain activation evoked by erotic films varies with different menstrual phases: an fMRI study. Behav Brain Res. 2010;206(2):279–85.PubMedCrossRef Zhu X, Wang X, Parkinson C, Cai C, Gao S, Hu P. Brain activation evoked by erotic films varies with different menstrual phases: an fMRI study. Behav Brain Res. 2010;206(2):279–85.PubMedCrossRef
76.
go back to reference Wallen K, Rupp HA. Women’s interest in visual sexual stimuli varies with menstrual cycle phase at first exposure and predicts later interest. Horm Behav. 2010;57(2):263–8.PubMedCrossRef Wallen K, Rupp HA. Women’s interest in visual sexual stimuli varies with menstrual cycle phase at first exposure and predicts later interest. Horm Behav. 2010;57(2):263–8.PubMedCrossRef
77.
go back to reference Pfaus JG, Kippin TE, Coria-Avila G. What can animal models tell us about human sexual response? Annu Rev Sex Res. 2003;14:1–63.PubMed Pfaus JG, Kippin TE, Coria-Avila G. What can animal models tell us about human sexual response? Annu Rev Sex Res. 2003;14:1–63.PubMed
78.
go back to reference Blaustein JD. Neuroendocrine regulation of feminine sexual behavior: lessons from rodent models and thoughts about humans. Ann Rev Psych. 2008;59:93–118.CrossRef Blaustein JD. Neuroendocrine regulation of feminine sexual behavior: lessons from rodent models and thoughts about humans. Ann Rev Psych. 2008;59:93–118.CrossRef
79.
go back to reference Erskine MS. Solicitation behavior in the estrous female rat: a review. Horm Behav. 1989;23:473–502.PubMedCrossRef Erskine MS. Solicitation behavior in the estrous female rat: a review. Horm Behav. 1989;23:473–502.PubMedCrossRef
80.
go back to reference McClintock MK, Adler NT. The role of the female during copulation in wild and domestic Norway rats (Rattus norvegicus). Behaviour. 1978;67(1/2):67–96.CrossRef McClintock MK, Adler NT. The role of the female during copulation in wild and domestic Norway rats (Rattus norvegicus). Behaviour. 1978;67(1/2):67–96.CrossRef
81.
go back to reference Madlafousek J, Hliňák Z. Importance of female’s precopulatory behavior in the primary initiation of male’s copulatory behaviour in the laboratory rat. Behaviour. 1983;86(3/4):237–49.CrossRef Madlafousek J, Hliňák Z. Importance of female’s precopulatory behavior in the primary initiation of male’s copulatory behaviour in the laboratory rat. Behaviour. 1983;86(3/4):237–49.CrossRef
82.
go back to reference Chu X, Agmo A. Sociosexual behaviours in cycling, intact female rats (Rattus norvegicus) housed in a seminatural environment. Behaviour. 2014;151(8):1143–84.CrossRef Chu X, Agmo A. Sociosexual behaviours in cycling, intact female rats (Rattus norvegicus) housed in a seminatural environment. Behaviour. 2014;151(8):1143–84.CrossRef
83.
go back to reference Chu X, Agmo A. Sociosexual behaviors during the transition from non-receptivity to receptivity in rats housed in a seminatural environment. Behav Process. 2015;113:24–34.CrossRef Chu X, Agmo A. Sociosexual behaviors during the transition from non-receptivity to receptivity in rats housed in a seminatural environment. Behav Process. 2015;113:24–34.CrossRef
84.
go back to reference Bergheim D, Chu X, Agmo A. The function and meaning of female rat paracopulatory (proceptive) behaviors. Behav Process. 2015;118:34–41.CrossRef Bergheim D, Chu X, Agmo A. The function and meaning of female rat paracopulatory (proceptive) behaviors. Behav Process. 2015;118:34–41.CrossRef
85.
go back to reference Freeman M. The neuroendocrine control of the ovarian cycle of the rat. In: Knobil E, Neill J, editors. The physiology of reproduction. 2nd ed. New York: Raven; 1994. p. 613. Freeman M. The neuroendocrine control of the ovarian cycle of the rat. In: Knobil E, Neill J, editors. The physiology of reproduction. 2nd ed. New York: Raven; 1994. p. 613.
86.
go back to reference Nequin LG, Alvarez J, Schwartz NB. Measurement of serum steroid and gonadotropin levels and uterine and ovarian variables throughout 4 day and 5 day estrous cycles in the rat. Biol Reprod. 1979;20(3):659–70.PubMedCrossRef Nequin LG, Alvarez J, Schwartz NB. Measurement of serum steroid and gonadotropin levels and uterine and ovarian variables throughout 4 day and 5 day estrous cycles in the rat. Biol Reprod. 1979;20(3):659–70.PubMedCrossRef
87.
go back to reference Beach FA. Sexual attractivity, proceptivity and receptivity in female mammals. Horm Behav. 1976;7:105–38.PubMedCrossRef Beach FA. Sexual attractivity, proceptivity and receptivity in female mammals. Horm Behav. 1976;7:105–38.PubMedCrossRef
88.
go back to reference Pfaff DW, Sakuma Y. Deficit in the lordosis reflex of female rats caused by lesions in the ventromedial nucleus of the hypothalamus. J Physiol. 1979;288:203–10.PubMedPubMedCentral Pfaff DW, Sakuma Y. Deficit in the lordosis reflex of female rats caused by lesions in the ventromedial nucleus of the hypothalamus. J Physiol. 1979;288:203–10.PubMedPubMedCentral
89.
go back to reference Pfaff DW, Sakuma Y. Facilitation of the lordosis reflex of female rats from the ventromedial nucleus of the hypothalamus. J Physiol. 1979;288:189–202.PubMedPubMedCentral Pfaff DW, Sakuma Y. Facilitation of the lordosis reflex of female rats from the ventromedial nucleus of the hypothalamus. J Physiol. 1979;288:189–202.PubMedPubMedCentral
90.
go back to reference Rawson RA, Washton A, Domier CP, Reiber C. Drugs and sexual effects: role of drug type and gender. J Subst Abus Treat. 2002;22:103–8.CrossRef Rawson RA, Washton A, Domier CP, Reiber C. Drugs and sexual effects: role of drug type and gender. J Subst Abus Treat. 2002;22:103–8.CrossRef
91.
go back to reference Semple SJ, Grant I, Patterson TL. Female methamphetamine users: social characteristics and sexual risk behavior. Women Health. 2004;40(3):35–50.PubMedCrossRef Semple SJ, Grant I, Patterson TL. Female methamphetamine users: social characteristics and sexual risk behavior. Women Health. 2004;40(3):35–50.PubMedCrossRef
92.
go back to reference •• Holder MK, Hadjimarkou MM, Zup SL, Blutstein T, Benham RS, McCarthy MM, et al. Methamphetamine facilitates female sexual behavior and enhances neuronal activation in the medial amygdala and ventromedial nucleus of the hypothalamus. Psychoneuroendocrinology. 2010;35(2):197–208. This study establishes a rodent model of enhanced proceptive behaviors by methamphetamine PubMedCrossRef •• Holder MK, Hadjimarkou MM, Zup SL, Blutstein T, Benham RS, McCarthy MM, et al. Methamphetamine facilitates female sexual behavior and enhances neuronal activation in the medial amygdala and ventromedial nucleus of the hypothalamus. Psychoneuroendocrinology. 2010;35(2):197–208. This study establishes a rodent model of enhanced proceptive behaviors by methamphetamine PubMedCrossRef
93.
go back to reference •• Holder MK, Mong JA. Methamphetamine enhances paced mating behaviors and neuroplasticity in the medial amygdala of female rats. Horm Behav. 2010;58:519–25. This study highlights the effects of methamphetamine on measures of female sexual motivation PubMedPubMedCentralCrossRef •• Holder MK, Mong JA. Methamphetamine enhances paced mating behaviors and neuroplasticity in the medial amygdala of female rats. Horm Behav. 2010;58:519–25. This study highlights the effects of methamphetamine on measures of female sexual motivation PubMedPubMedCentralCrossRef
94.
go back to reference • Winland C, Haycox C, Bolton JL, Jampana S, Oakley BJ, Ford B, et al. Methamphetamine enhances sexual behavior in female rats. Pharmacol Biochem Behav. 2011;98(4):575–82. This study indicates methamphetamine increases sexual approach behaviors to a male rat PubMedCrossRef • Winland C, Haycox C, Bolton JL, Jampana S, Oakley BJ, Ford B, et al. Methamphetamine enhances sexual behavior in female rats. Pharmacol Biochem Behav. 2011;98(4):575–82. This study indicates methamphetamine increases sexual approach behaviors to a male rat PubMedCrossRef
95.
go back to reference •• Rudzinskas SA, Mong JA. Androgen-primed castrate males are sufficient for methamphetamine-facilitated increases in proceptive behavior in female rats. Horm Behav. 2016;78:52–9. This study indicates that methamphetamine increases sexual motivation by enhancing sexually relevant sensory cues PubMedCrossRef •• Rudzinskas SA, Mong JA. Androgen-primed castrate males are sufficient for methamphetamine-facilitated increases in proceptive behavior in female rats. Horm Behav. 2016;78:52–9. This study indicates that methamphetamine increases sexual motivation by enhancing sexually relevant sensory cues PubMedCrossRef
96.
go back to reference •• Holder MK, Veichweg SS, Mong JA. Methamphetamine-enhanced female sexual motivation is dependent on dopamine and progesterone signaling in the medial amygdala. Horm Behav. 2015;67:1–11. This study highlights the importance of dopamine and progesterone receptors in the medial amygdala for enhancements of sexually motivated behaviors by methamphetamine PubMedCrossRef •• Holder MK, Veichweg SS, Mong JA. Methamphetamine-enhanced female sexual motivation is dependent on dopamine and progesterone signaling in the medial amygdala. Horm Behav. 2015;67:1–11. This study highlights the importance of dopamine and progesterone receptors in the medial amygdala for enhancements of sexually motivated behaviors by methamphetamine PubMedCrossRef
97.
go back to reference Afonso VM, Lehmann H, Tse M, Woehrling A, Pfaus JG. Estrogen and the neural mediation of female-male mounting in the rat. Behav Neurosci. 2009;123(2):369–81.PubMedCrossRef Afonso VM, Lehmann H, Tse M, Woehrling A, Pfaus JG. Estrogen and the neural mediation of female-male mounting in the rat. Behav Neurosci. 2009;123(2):369–81.PubMedCrossRef
98.
go back to reference •• Williams KM, Mong JA. Methamphetamine and ovarian steroid responsive cells in the posteriodorsal medial amygdala are required for methamphetamine-enhanced proceptive behaviors. Sci Rep. 2017;7:39817. This study highlights the role for cells responsive to both ovarian hormones and methamphetamine in the medial amygdala for proceptive behaviors enhanced by methamphetamine PubMedPubMedCentralCrossRef •• Williams KM, Mong JA. Methamphetamine and ovarian steroid responsive cells in the posteriodorsal medial amygdala are required for methamphetamine-enhanced proceptive behaviors. Sci Rep. 2017;7:39817. This study highlights the role for cells responsive to both ovarian hormones and methamphetamine in the medial amygdala for proceptive behaviors enhanced by methamphetamine PubMedPubMedCentralCrossRef
99.
go back to reference Erskine MS. Mating-induced increases in FOS protein in preoptic area and medial amygdala of cycling female rats. Brain Res Bull. 1993;32(5):447–51.PubMedCrossRef Erskine MS. Mating-induced increases in FOS protein in preoptic area and medial amygdala of cycling female rats. Brain Res Bull. 1993;32(5):447–51.PubMedCrossRef
100.
go back to reference Polston EK, Erskine MS. Patterns of induction of the immediate-early genes c-fos and egr-1 in the female rat brain following differential amounts of mating stimulation. Neuroendocrinology. 1995;62(4):371–84.CrossRef Polston EK, Erskine MS. Patterns of induction of the immediate-early genes c-fos and egr-1 in the female rat brain following differential amounts of mating stimulation. Neuroendocrinology. 1995;62(4):371–84.CrossRef
101.
go back to reference Guarraci FA, Megroz AB, Clark AS. Paced mating behavior in the female rat following lesions of three regions responsive to vaginocervical stimulation. Brain Res. 2004;999(1):40–52.PubMedCrossRef Guarraci FA, Megroz AB, Clark AS. Paced mating behavior in the female rat following lesions of three regions responsive to vaginocervical stimulation. Brain Res. 2004;999(1):40–52.PubMedCrossRef
102.
go back to reference Huang Q, Zhou D, Chase K, Gusella JF, Aronin N, DiFiglia M. Immunohistochemical localization of the D1 dopamine receptor in rat brain reveals its axonal transport, pre- and postsynaptic localization, and prevalence in the basal ganglia, limbic system, and thalamic reticular nucleus. Proc Natl Acad Sci U S A. 1992;89:11988–92.PubMedPubMedCentralCrossRef Huang Q, Zhou D, Chase K, Gusella JF, Aronin N, DiFiglia M. Immunohistochemical localization of the D1 dopamine receptor in rat brain reveals its axonal transport, pre- and postsynaptic localization, and prevalence in the basal ganglia, limbic system, and thalamic reticular nucleus. Proc Natl Acad Sci U S A. 1992;89:11988–92.PubMedPubMedCentralCrossRef
103.
go back to reference Mansour A, Meador-Woodruff JH, Bunzow JR, Civelli O, Akil H, Watson SJ. Localization of dopamine D2 receptor mRNA and D1 and D2 receptor binding in the rat brain and pituitary: an in situ hybridization-receptor autoradiographic analysis. J Neurosci. 1990;10(8):2587–600.PubMed Mansour A, Meador-Woodruff JH, Bunzow JR, Civelli O, Akil H, Watson SJ. Localization of dopamine D2 receptor mRNA and D1 and D2 receptor binding in the rat brain and pituitary: an in situ hybridization-receptor autoradiographic analysis. J Neurosci. 1990;10(8):2587–600.PubMed
104.
go back to reference Day HE, Campeau S, Watson SJ Jr, Akil H. Distribution of alpha 1a-, alpha 1b- and alpha 1d-adrenergic receptor mRNA in the rat brain and spinal cord. J Chem Neuroanat. 1997;13(2):115–39.PubMedCrossRef Day HE, Campeau S, Watson SJ Jr, Akil H. Distribution of alpha 1a-, alpha 1b- and alpha 1d-adrenergic receptor mRNA in the rat brain and spinal cord. J Chem Neuroanat. 1997;13(2):115–39.PubMedCrossRef
105.
go back to reference Weil ZM, Zhang Q, Hornung A, Blizard D, Pfaff DW. Impact of generalized brain arousal on sexual behavior. Proc Natl Acad Sci U S A. 2010;107(5):2265–70.PubMedPubMedCentralCrossRef Weil ZM, Zhang Q, Hornung A, Blizard D, Pfaff DW. Impact of generalized brain arousal on sexual behavior. Proc Natl Acad Sci U S A. 2010;107(5):2265–70.PubMedPubMedCentralCrossRef
106.
go back to reference Schober J, Weil Z, Pfaff D. How generalized CNS arousal strengthens sexual arousal (and vice versa). Horm Behav. 2011;59(5):689–95.PubMedCrossRef Schober J, Weil Z, Pfaff D. How generalized CNS arousal strengthens sexual arousal (and vice versa). Horm Behav. 2011;59(5):689–95.PubMedCrossRef
107.
go back to reference Thorp J, Simon J, Dattani D, Taylor L, Kimura T, Garcia M Jr, et al. Treatment of hypoactive sexual desire disorder in premenopausal women: efficacy of flibanserin in the DAISY study. J Sex Med. 2012;9(3):793–804.PubMedCrossRef Thorp J, Simon J, Dattani D, Taylor L, Kimura T, Garcia M Jr, et al. Treatment of hypoactive sexual desire disorder in premenopausal women: efficacy of flibanserin in the DAISY study. J Sex Med. 2012;9(3):793–804.PubMedCrossRef
108.
go back to reference Mendelson SD, Gorzalka BB. 5-HT1A receptors: differential involvement in female and male sexual behavior in the rat. Physiol Behav. 1986;37(2):345–51.PubMedCrossRef Mendelson SD, Gorzalka BB. 5-HT1A receptors: differential involvement in female and male sexual behavior in the rat. Physiol Behav. 1986;37(2):345–51.PubMedCrossRef
109.
go back to reference Fernandez-Guasti A, Ahlenius S, Hjorth S, Larsson K. Separation of dopaminergic and serotonergic inhibitory mechanisms in the mediation of estrogen-induced lordosis behavior in the rat. Pharmacol Biochem Behav. 1987;27:93–8.PubMedCrossRef Fernandez-Guasti A, Ahlenius S, Hjorth S, Larsson K. Separation of dopaminergic and serotonergic inhibitory mechanisms in the mediation of estrogen-induced lordosis behavior in the rat. Pharmacol Biochem Behav. 1987;27:93–8.PubMedCrossRef
110.
go back to reference Mendelson SD, Gorzalka BB. A facilitatory role for serotonin in the sexual behavior of the female rat. Pharmacol Biochem Behav. 1985;22(6):1025–33.PubMedCrossRef Mendelson SD, Gorzalka BB. A facilitatory role for serotonin in the sexual behavior of the female rat. Pharmacol Biochem Behav. 1985;22(6):1025–33.PubMedCrossRef
111.
go back to reference Borsini F, Evans K, Jason K, Rohde F, Alexander B, Pollentier S. Pharmacology of flibanserin. CNS Drug Rev. 2002;8(2):117–42.PubMedCrossRef Borsini F, Evans K, Jason K, Rohde F, Alexander B, Pollentier S. Pharmacology of flibanserin. CNS Drug Rev. 2002;8(2):117–42.PubMedCrossRef
112.
go back to reference Segraves RT, Clayton A, Croft H, Wolf A, Warnock J. Bupropion sustained release for the treatment of hypoactive sexual desire disorder in premenopausal women. J Clin Psychopharmacol. 2004;24(3):339–42.PubMedCrossRef Segraves RT, Clayton A, Croft H, Wolf A, Warnock J. Bupropion sustained release for the treatment of hypoactive sexual desire disorder in premenopausal women. J Clin Psychopharmacol. 2004;24(3):339–42.PubMedCrossRef
113.
go back to reference Caruso S, Agnello C, Intelisano G, Farina M, Di Mari L, Cianci A. Placebo-controlled study on efficacy and safety of daily apomorphine SL intake in premenopausal women affected by hypoactive sexual desire disorder and sexual arousal disorder. Urology. 2004;63(5):955–9.PubMedCrossRef Caruso S, Agnello C, Intelisano G, Farina M, Di Mari L, Cianci A. Placebo-controlled study on efficacy and safety of daily apomorphine SL intake in premenopausal women affected by hypoactive sexual desire disorder and sexual arousal disorder. Urology. 2004;63(5):955–9.PubMedCrossRef
Metadata
Title
The Role of Ovarian Hormones and the Medial Amygdala in Sexual Motivation
Authors
Mary K. Holder
Jessica A. Mong
Publication date
01-12-2017
Publisher
Springer US
Published in
Current Sexual Health Reports / Issue 4/2017
Print ISSN: 1548-3584
Electronic ISSN: 1548-3592
DOI
https://doi.org/10.1007/s11930-017-0131-4

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