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Published in: Neuroscience Bulletin 3/2024

Open Access 28-08-2023 | Neuropathic Pain | Original Article

Cytochrome P450 26A1 Contributes to the Maintenance of Neuropathic Pain

Authors: De-Li Cao, Ling-Jie Ma, Bao-Chun Jiang, Qiang Gu, Yong-Jing Gao

Published in: Neuroscience Bulletin | Issue 3/2024

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Abstract

The cytochrome P450 proteins (CYP450s) have been implicated in catalyzing numerous important biological reactions and contribute to a variety of diseases. CYP26A1, a member of the CYP450 family, carries out the oxidative metabolism of retinoic acid (RA), the active metabolite of vitamin A. Here we report that CYP26A1 was dramatically upregulated in the spinal cord after spinal nerve ligation (SNL). CYP26A1 was mainly expressed in spinal neurons and astrocytes. HPLC analysis displayed that the content of all-trans-RA (at-RA), the substrate of CYP26A1, was reduced in the spinal cord on day 7 after SNL. Inhibition of CYP26A1 by siRNA or inhibition of CYP26A1-mediated at-RA catabolism by talarozole relieved the SNL-induced mechanical allodynia during the maintenance phase of neuropathic pain. Talarozole also reduced SNL-induced glial activation and proinflammatory cytokine production but increased anti-inflammatory cytokine (IL-10) production. The RA receptors RARα, RXRβ, and RXRγ were expressed in spinal neurons and glial cells. The promoter of Il-10 has several binding sites for RA receptors, and at-RA directly increased Il-10 mRNA expression in vitro. Finally, intrathecal IL-10 attenuated SNL-induced neuropathic pain and reduced the activation of astrocytes and microglia. Collectively, the inhibition of CYP26A1-mediated at-RA catabolism alleviates SNL-induced neuropathic pain by promoting the expression of IL-10 and suppressing glial activation. CYP26A1 may be a potential therapeutic target for the treatment of neuropathic pain.
Literature
1.
go back to reference Nelson DR, Koymans L, Kamataki T, Stegeman JJ, Feyereisen R, Waxman DJ. P450 superfamily: Update on new sequences, gene mapping, accession numbers and nomenclature. Pharmacogenetics 1996, 6: 1–42.PubMed Nelson DR, Koymans L, Kamataki T, Stegeman JJ, Feyereisen R, Waxman DJ. P450 superfamily: Update on new sequences, gene mapping, accession numbers and nomenclature. Pharmacogenetics 1996, 6: 1–42.PubMed
2.
go back to reference Guengerich FP. Comparisons of catalytic selectivity of cytochrome P450 subfamily enzymes from different species. Chem Biol Interact 1997, 106: 161–182.PubMed Guengerich FP. Comparisons of catalytic selectivity of cytochrome P450 subfamily enzymes from different species. Chem Biol Interact 1997, 106: 161–182.PubMed
3.
go back to reference Nebert DW, Gonzalez FJ. P450 genes: Structure, evolution, and regulation. Annu Rev Biochem 1987, 56: 945–993.PubMed Nebert DW, Gonzalez FJ. P450 genes: Structure, evolution, and regulation. Annu Rev Biochem 1987, 56: 945–993.PubMed
5.
go back to reference Rasheed MSU, Mishra AK, Singh MP. Cytochrome P450 2D6 and parkinson’s disease: Polymorphism, metabolic role, risk and protection. Neurochem Res 2017, 42: 3353–3361. Rasheed MSU, Mishra AK, Singh MP. Cytochrome P450 2D6 and parkinson’s disease: Polymorphism, metabolic role, risk and protection. Neurochem Res 2017, 42: 3353–3361.
6.
go back to reference Song BJ, Abdelmegeed MA, Cho YE, Akbar M, Rhim JS, Song MK, et al. Contributing roles of CYP2E1 and other cytochrome P450 isoforms in alcohol-related tissue injury and carcinogenesis. Adv Exp Med Biol 2019, 1164: 73–87.PubMed Song BJ, Abdelmegeed MA, Cho YE, Akbar M, Rhim JS, Song MK, et al. Contributing roles of CYP2E1 and other cytochrome P450 isoforms in alcohol-related tissue injury and carcinogenesis. Adv Exp Med Biol 2019, 1164: 73–87.PubMed
7.
go back to reference Gilroy DW, Edin ML, De Maeyer RP, Bystrom J, Newson J, Lih FB, et al. CYP450-derived oxylipins mediate inflammatory resolution. Proc Natl Acad Sci U S A 2016, 113: E3240–E3249.PubMedPubMedCentral Gilroy DW, Edin ML, De Maeyer RP, Bystrom J, Newson J, Lih FB, et al. CYP450-derived oxylipins mediate inflammatory resolution. Proc Natl Acad Sci U S A 2016, 113: E3240–E3249.PubMedPubMedCentral
8.
go back to reference Lutz JD, Dixit V, Yeung CK, Dickmann LJ, Zelter A, Thatcher JE, et al. Expression and functional characterization of cytochrome P450 26A1, a retinoic acid hydroxylase. Biochem Pharmacol 2009, 77: 258–268.PubMed Lutz JD, Dixit V, Yeung CK, Dickmann LJ, Zelter A, Thatcher JE, et al. Expression and functional characterization of cytochrome P450 26A1, a retinoic acid hydroxylase. Biochem Pharmacol 2009, 77: 258–268.PubMed
9.
go back to reference Ross AC, Zolfaghari R. Cytochrome P450s in the regulation of cellular retinoic acid metabolism. Annu Rev Nutr 2011, 31: 65–87.PubMedPubMedCentral Ross AC, Zolfaghari R. Cytochrome P450s in the regulation of cellular retinoic acid metabolism. Annu Rev Nutr 2011, 31: 65–87.PubMedPubMedCentral
12.
go back to reference Maden M. Retinoic acid in the development, regeneration and maintenance of the nervous system. Nat Rev Neurosci 2007, 8: 755–765.PubMed Maden M. Retinoic acid in the development, regeneration and maintenance of the nervous system. Nat Rev Neurosci 2007, 8: 755–765.PubMed
13.
go back to reference Gudas LJ. Emerging roles for retinoids in regeneration and differentiation in normal and disease states. Biochim Biophys Acta 2012, 1821: 213–221.PubMed Gudas LJ. Emerging roles for retinoids in regeneration and differentiation in normal and disease states. Biochim Biophys Acta 2012, 1821: 213–221.PubMed
14.
go back to reference Abu-Abed S, Dollé P, Metzger D, Beckett B, Chambon P, Petkovich M. The retinoic acid-metabolizing enzyme, CYP26A1, is essential for normal hindbrain patterning, vertebral identity, and development of posterior structures. Genes Dev 2001, 15: 226–240.PubMedPubMedCentral Abu-Abed S, Dollé P, Metzger D, Beckett B, Chambon P, Petkovich M. The retinoic acid-metabolizing enzyme, CYP26A1, is essential for normal hindbrain patterning, vertebral identity, and development of posterior structures. Genes Dev 2001, 15: 226–240.PubMedPubMedCentral
15.
go back to reference Bowles J, Knight D, Smith C, Wilhelm D, Richman J, Mamiya S, et al. Retinoid signaling determines germ cell fate in mice. Science 2006, 312: 596–600.ADSPubMed Bowles J, Knight D, Smith C, Wilhelm D, Richman J, Mamiya S, et al. Retinoid signaling determines germ cell fate in mice. Science 2006, 312: 596–600.ADSPubMed
16.
go back to reference Koubova J, Menke DB, Zhou Q, Capel B, Griswold MD, Page DC. Retinoic acid regulates sex-specific timing of meiotic initiation in mice. Proc Natl Acad Sci U S A 2006, 103: 2474–2479.ADSPubMedPubMedCentral Koubova J, Menke DB, Zhou Q, Capel B, Griswold MD, Page DC. Retinoic acid regulates sex-specific timing of meiotic initiation in mice. Proc Natl Acad Sci U S A 2006, 103: 2474–2479.ADSPubMedPubMedCentral
17.
go back to reference Sakai Y, Meno C, Fujii H, Nishino J, Shiratori H, Saijoh Y, et al. The retinoic acid-inactivating enzyme CYP26 is essential for establishing an uneven distribution of retinoic acid along the anterio-posterior axis within the mouse embryo. Genes Dev 2001, 15: 213–225.PubMedPubMedCentral Sakai Y, Meno C, Fujii H, Nishino J, Shiratori H, Saijoh Y, et al. The retinoic acid-inactivating enzyme CYP26 is essential for establishing an uneven distribution of retinoic acid along the anterio-posterior axis within the mouse embryo. Genes Dev 2001, 15: 213–225.PubMedPubMedCentral
18.
go back to reference Ricard MJ, Gudas LJ. Cytochrome p450 cyp26a1 alters spinal motor neuron subtype identity in differentiating embryonic stem cells. J Biol Chem 2013, 288: 28801–28813.PubMedPubMedCentral Ricard MJ, Gudas LJ. Cytochrome p450 cyp26a1 alters spinal motor neuron subtype identity in differentiating embryonic stem cells. J Biol Chem 2013, 288: 28801–28813.PubMedPubMedCentral
19.
go back to reference Larsen R, Proue A, Scott EP, Christiansen M, Nakagawa Y. The thalamus regulates retinoic acid signaling and development of parvalbumin interneurons in postnatal mouse prefrontal cortex. eNeuro 2019, 6: ENEURO.0018-ENEURO.0019.2019.PubMed Larsen R, Proue A, Scott EP, Christiansen M, Nakagawa Y. The thalamus regulates retinoic acid signaling and development of parvalbumin interneurons in postnatal mouse prefrontal cortex. eNeuro 2019, 6: ENEURO.0018-ENEURO.0019.2019.PubMed
20.
go back to reference Wang Y, Zolfaghari R, Ross AC. Cloning of rat cytochrome P450RAI (CYP26) cDNA and regulation of its gene expression by all-trans-retinoic acid in vivo. Arch Biochem Biophys 2002, 401: 235–243.PubMed Wang Y, Zolfaghari R, Ross AC. Cloning of rat cytochrome P450RAI (CYP26) cDNA and regulation of its gene expression by all-trans-retinoic acid in vivo. Arch Biochem Biophys 2002, 401: 235–243.PubMed
21.
go back to reference Xi J, Yang Z. Expression of RALDHs (ALDH1As) and CYP26s in human tissues and during the neural differentiation of P19 embryonal carcinoma stem cell. Gene Expr Patterns 2008, 8: 438–442.PubMed Xi J, Yang Z. Expression of RALDHs (ALDH1As) and CYP26s in human tissues and during the neural differentiation of P19 embryonal carcinoma stem cell. Gene Expr Patterns 2008, 8: 438–442.PubMed
22.
go back to reference White JA, Ramshaw H, Taimi M, Stangle W, Zhang A, Everingham S, et al. Identification of the human cytochrome P450, P450RAI-2, which is predominantly expressed in the adult cerebellum and is responsible for all-trans-retinoic acid metabolism. Proc Natl Acad Sci U S A 2000, 97: 6403–6408.ADSPubMedPubMedCentral White JA, Ramshaw H, Taimi M, Stangle W, Zhang A, Everingham S, et al. Identification of the human cytochrome P450, P450RAI-2, which is predominantly expressed in the adult cerebellum and is responsible for all-trans-retinoic acid metabolism. Proc Natl Acad Sci U S A 2000, 97: 6403–6408.ADSPubMedPubMedCentral
23.
go back to reference Reijntjes S, Gale E, Maden M. Generating gradients of retinoic acid in the chick embryo: Cyp26C1 expression and a comparative analysis of the Cyp26 enzymes. Dev Dyn 2004, 230: 509–517.PubMed Reijntjes S, Gale E, Maden M. Generating gradients of retinoic acid in the chick embryo: Cyp26C1 expression and a comparative analysis of the Cyp26 enzymes. Dev Dyn 2004, 230: 509–517.PubMed
24.
go back to reference Tahayato A, Dolle P, Petkovich M. Cyp26C1 encodes a novel retinoic acid-metabolizing enzyme expressed in the hindbrain, inner ear, first branchial arch and tooth buds during murine development. Gene Expr Patterns 2003, 3: 449–454.PubMed Tahayato A, Dolle P, Petkovich M. Cyp26C1 encodes a novel retinoic acid-metabolizing enzyme expressed in the hindbrain, inner ear, first branchial arch and tooth buds during murine development. Gene Expr Patterns 2003, 3: 449–454.PubMed
25.
go back to reference Zhang Y, Crofton EJ, Smith TES, Koshy S, Li D, Green TA. Manipulation of retinoic acid signaling in the nucleus accumbens shell alters rat emotional behavior. Behav Brain Res 2019, 376: 112177.PubMedPubMedCentral Zhang Y, Crofton EJ, Smith TES, Koshy S, Li D, Green TA. Manipulation of retinoic acid signaling in the nucleus accumbens shell alters rat emotional behavior. Behav Brain Res 2019, 376: 112177.PubMedPubMedCentral
26.
go back to reference Donnelly CR, Andriessen AS, Chen G, Wang K, Jiang C, Maixner W, et al. Central nervous system targets: Glial cell mechanisms in chronic pain. Neurotherapeutics 2020, 17: 846–860.PubMedPubMedCentral Donnelly CR, Andriessen AS, Chen G, Wang K, Jiang C, Maixner W, et al. Central nervous system targets: Glial cell mechanisms in chronic pain. Neurotherapeutics 2020, 17: 846–860.PubMedPubMedCentral
27.
go back to reference Lu HJ, Gao YJ. Astrocytes in chronic pain: Cellular and molecular mechanisms. Neurosci Bull 2023, 39: 425–439.PubMed Lu HJ, Gao YJ. Astrocytes in chronic pain: Cellular and molecular mechanisms. Neurosci Bull 2023, 39: 425–439.PubMed
28.
go back to reference Jiang BC, Liu T, Gao YJ. Chemokines in chronic pain: Cellular and molecular mechanisms and therapeutic potential. Pharmacol Ther 2020, 212: 107581.PubMed Jiang BC, Liu T, Gao YJ. Chemokines in chronic pain: Cellular and molecular mechanisms and therapeutic potential. Pharmacol Ther 2020, 212: 107581.PubMed
29.
go back to reference van Neerven S, Nemes A, Imholz P, Regen T, Denecke B, Johann S, et al. Inflammatory cytokine release of astrocytes in vitro is reduced by all-trans retinoic acid. J Neuroimmunol 2010, 229: 169–179.PubMed van Neerven S, Nemes A, Imholz P, Regen T, Denecke B, Johann S, et al. Inflammatory cytokine release of astrocytes in vitro is reduced by all-trans retinoic acid. J Neuroimmunol 2010, 229: 169–179.PubMed
30.
go back to reference van Neerven S, Regen T, Wolf D, Nemes A, Johann S, Beyer C, et al. Inflammatory chemokine release of astrocytes in vitro is reduced by all-trans retinoic acid. J Neurochem 2010, 114: 1511–1526.PubMed van Neerven S, Regen T, Wolf D, Nemes A, Johann S, Beyer C, et al. Inflammatory chemokine release of astrocytes in vitro is reduced by all-trans retinoic acid. J Neurochem 2010, 114: 1511–1526.PubMed
31.
go back to reference Kampmann E, Johann S, van Neerven S, Beyer C, Mey J. Anti-inflammatory effect of retinoic acid on prostaglandin synthesis in cultured cortical astrocytes. J Neurochem 2008, 106: 320–332.PubMed Kampmann E, Johann S, van Neerven S, Beyer C, Mey J. Anti-inflammatory effect of retinoic acid on prostaglandin synthesis in cultured cortical astrocytes. J Neurochem 2008, 106: 320–332.PubMed
32.
go back to reference Wang X, Allen C, Ballow M. Retinoic acid enhances the production of IL-10 while reducing the synthesis of IL-12 and TNF-α from LPS-stimulated monocytes/macrophages. J Clin Immunol 2007, 27: 193–200.PubMed Wang X, Allen C, Ballow M. Retinoic acid enhances the production of IL-10 while reducing the synthesis of IL-12 and TNF-α from LPS-stimulated monocytes/macrophages. J Clin Immunol 2007, 27: 193–200.PubMed
33.
go back to reference Dheen ST, Jun Y, Yan Z, Tay SS, Ling EA. Retinoic acid inhibits expression of TNF-alpha and iNOS in activated rat microglia. Glia 2005, 50: 21–31.PubMed Dheen ST, Jun Y, Yan Z, Tay SS, Ling EA. Retinoic acid inhibits expression of TNF-alpha and iNOS in activated rat microglia. Glia 2005, 50: 21–31.PubMed
34.
go back to reference Zhang ZJ, Cao DL, Zhang X, Ji RR, Gao YJ. Chemokine contribution to neuropathic pain: Respective induction of CXCL1 and CXCR2 in spinal cord astrocytes and neurons. Pain 2013, 154: 2185–2197.PubMedPubMedCentral Zhang ZJ, Cao DL, Zhang X, Ji RR, Gao YJ. Chemokine contribution to neuropathic pain: Respective induction of CXCL1 and CXCR2 in spinal cord astrocytes and neurons. Pain 2013, 154: 2185–2197.PubMedPubMedCentral
35.
go back to reference Hylden JL, Wilcox GL. Intrathecal morphine in mice: A new technique. Eur J Pharmacol 1980, 67: 313–316.PubMed Hylden JL, Wilcox GL. Intrathecal morphine in mice: A new technique. Eur J Pharmacol 1980, 67: 313–316.PubMed
36.
go back to reference Jiang BC, Zhang WW, Yang T, Guo CY, Cao DL, Zhang ZJ, et al. Demethylation of G-protein-coupled receptor 151 promoter facilitates the binding of Krüppel-like factor 5 and enhances neuropathic pain after nerve injury in mice. J Neurosci 2018, 38: 10535–10551.PubMedPubMedCentral Jiang BC, Zhang WW, Yang T, Guo CY, Cao DL, Zhang ZJ, et al. Demethylation of G-protein-coupled receptor 151 promoter facilitates the binding of Krüppel-like factor 5 and enhances neuropathic pain after nerve injury in mice. J Neurosci 2018, 38: 10535–10551.PubMedPubMedCentral
37.
go back to reference Sakhi AK, Gundersen TE, Ulven SM, Blomhoff R, Lundanes E. Quantitative determination of endogenous retinoids in mouse embryos by high-performance liquid chromatography with on-line solid-phase extraction, column switching and electrochemical detection. J Chromatogr A 1998, 828: 451–460.PubMed Sakhi AK, Gundersen TE, Ulven SM, Blomhoff R, Lundanes E. Quantitative determination of endogenous retinoids in mouse embryos by high-performance liquid chromatography with on-line solid-phase extraction, column switching and electrochemical detection. J Chromatogr A 1998, 828: 451–460.PubMed
38.
go back to reference Jiang BC, Cao DL, Zhang X, Zhang ZJ, He LN, Li CH, et al. CXCL13 drives spinal astrocyte activation and neuropathic pain via CXCR5. J Clin Invest 2016, 126: 745–761.PubMedPubMedCentral Jiang BC, Cao DL, Zhang X, Zhang ZJ, He LN, Li CH, et al. CXCL13 drives spinal astrocyte activation and neuropathic pain via CXCR5. J Clin Invest 2016, 126: 745–761.PubMedPubMedCentral
39.
go back to reference Chaplan SR, Bach FW, Pogrel JW, Chung JM, Yaksh TL. Quantitative assessment of tactile allodynia in the rat paw. J Neurosci Methods 1994, 53: 55–63.PubMed Chaplan SR, Bach FW, Pogrel JW, Chung JM, Yaksh TL. Quantitative assessment of tactile allodynia in the rat paw. J Neurosci Methods 1994, 53: 55–63.PubMed
40.
go back to reference Thatcher JE, Zelter A, Isoherranen N. The relative importance of CYP26A1 in hepatic clearance of all-trans retinoic acid. Biochem Pharmacol 2010, 80: 903–912.PubMedPubMedCentral Thatcher JE, Zelter A, Isoherranen N. The relative importance of CYP26A1 in hepatic clearance of all-trans retinoic acid. Biochem Pharmacol 2010, 80: 903–912.PubMedPubMedCentral
41.
42.
go back to reference Zhuang ZY, Gerner P, Woolf CJ, Ji RR. ERK is sequentially activated in neurons, microglia, and astrocytes by spinal nerve ligation and contributes to mechanical allodynia in this neuropathic pain model. Pain 2005, 114: 149–159.PubMed Zhuang ZY, Gerner P, Woolf CJ, Ji RR. ERK is sequentially activated in neurons, microglia, and astrocytes by spinal nerve ligation and contributes to mechanical allodynia in this neuropathic pain model. Pain 2005, 114: 149–159.PubMed
43.
go back to reference Jin SX, Zhuang ZY, Woolf CJ, Ji RR. p38 mitogen-activated protein kinase is activated after a spinal nerve ligation in spinal cord microglia and dorsal root ganglion neurons and contributes to the generation of neuropathic pain. J Neurosci 2003, 23: 4017–4022.PubMedPubMedCentral Jin SX, Zhuang ZY, Woolf CJ, Ji RR. p38 mitogen-activated protein kinase is activated after a spinal nerve ligation in spinal cord microglia and dorsal root ganglion neurons and contributes to the generation of neuropathic pain. J Neurosci 2003, 23: 4017–4022.PubMedPubMedCentral
44.
go back to reference Chambon P. A decade of molecular biology of retinoic acid receptors. FASEB J 1996, 10: 940–954.PubMed Chambon P. A decade of molecular biology of retinoic acid receptors. FASEB J 1996, 10: 940–954.PubMed
45.
go back to reference Bastien J, Rochette-Egly C. Nuclear retinoid receptors and the transcription of retinoid-target genes. Gene 2004, 328: 1–16.PubMed Bastien J, Rochette-Egly C. Nuclear retinoid receptors and the transcription of retinoid-target genes. Gene 2004, 328: 1–16.PubMed
46.
go back to reference Blomhoff R, Blomhoff HK. Overview of retinoid metabolism and function. J Neurobiol 2006, 66: 606–630.PubMed Blomhoff R, Blomhoff HK. Overview of retinoid metabolism and function. J Neurobiol 2006, 66: 606–630.PubMed
47.
go back to reference Sisignano M, Angioni C, Park CK, Meyer Dos Santos S, Jordan H, Kuzikov M, et al. Targeting CYP2J to reduce paclitaxel-induced peripheral neuropathic pain. Proc Natl Acad Sci U S A 2016, 113: 12544.ADSPubMedPubMedCentral Sisignano M, Angioni C, Park CK, Meyer Dos Santos S, Jordan H, Kuzikov M, et al. Targeting CYP2J to reduce paclitaxel-induced peripheral neuropathic pain. Proc Natl Acad Sci U S A 2016, 113: 12544.ADSPubMedPubMedCentral
48.
go back to reference Li F, Zhu W, Gonzalez FJ. Potential role of CYP1B1 in the development and treatment of metabolic diseases. Pharmacol Ther 2017, 178: 18–30.PubMedPubMedCentral Li F, Zhu W, Gonzalez FJ. Potential role of CYP1B1 in the development and treatment of metabolic diseases. Pharmacol Ther 2017, 178: 18–30.PubMedPubMedCentral
49.
go back to reference Lim S, Alshagga M, Ong CE, Chieng JY, Pan Y. Cytochrome P450 4B1 (CYP4B1) as a target in cancer treatment. Hum Exp Toxicol 2020, 39: 785–796.PubMed Lim S, Alshagga M, Ong CE, Chieng JY, Pan Y. Cytochrome P450 4B1 (CYP4B1) as a target in cancer treatment. Hum Exp Toxicol 2020, 39: 785–796.PubMed
50.
go back to reference Priyanka SH, Thushara AJ, Rauf AA, Indira M. All trans retinoic acid attenuates markers of neuroinflammation in rat brain by modulation of SIRT1 and NFκB. Neurochem Res 2018, 43: 1791–1801.PubMed Priyanka SH, Thushara AJ, Rauf AA, Indira M. All trans retinoic acid attenuates markers of neuroinflammation in rat brain by modulation of SIRT1 and NFκB. Neurochem Res 2018, 43: 1791–1801.PubMed
51.
go back to reference Behairi N, Belkhelfa M, Rafa H, Labsi M, Deghbar N, Bouzid N, et al. All-trans retinoic acid (ATRA) prevents lipopolysaccharide-induced neuroinflammation, amyloidogenesis and memory impairment in aged rats. J Neuroimmunol 2016, 300: 21–29.PubMed Behairi N, Belkhelfa M, Rafa H, Labsi M, Deghbar N, Bouzid N, et al. All-trans retinoic acid (ATRA) prevents lipopolysaccharide-induced neuroinflammation, amyloidogenesis and memory impairment in aged rats. J Neuroimmunol 2016, 300: 21–29.PubMed
52.
go back to reference Romero-Sandoval EA, Alique M, Moreno-Manzano V, Molina C, Lucio FJ, Herrero JF. The oral administration of retinoic acid enhances nociceptive withdrawal reflexes in rats with soft-tissue inflammation. Inflamm res 2004, 53: 297–303.PubMed Romero-Sandoval EA, Alique M, Moreno-Manzano V, Molina C, Lucio FJ, Herrero JF. The oral administration of retinoic acid enhances nociceptive withdrawal reflexes in rats with soft-tissue inflammation. Inflamm res 2004, 53: 297–303.PubMed
53.
go back to reference Hamed EA, Mohamed Farghaly HS, Abdel Mola AF, Fahmi MK, Makhlouf MM, Balfas MA. Role of monocyte chemoattractant protein-1, stromal derived factor-1 and retinoic acid in pathophysiology of neuropathic pain in rats. J Basic Clin Physiol Pharmacol 2016, 27: 411–424.PubMed Hamed EA, Mohamed Farghaly HS, Abdel Mola AF, Fahmi MK, Makhlouf MM, Balfas MA. Role of monocyte chemoattractant protein-1, stromal derived factor-1 and retinoic acid in pathophysiology of neuropathic pain in rats. J Basic Clin Physiol Pharmacol 2016, 27: 411–424.PubMed
54.
go back to reference Stoppie P, Borgers M, Borghgraef P, Dillen L, Goossens J, Sanz G, et al. R115866 inhibits all-trans-retinoic acid metabolism and exerts retinoidal effects in rodents. J Pharmacol Exp Ther 2000, 293: 304–312.PubMed Stoppie P, Borgers M, Borghgraef P, Dillen L, Goossens J, Sanz G, et al. R115866 inhibits all-trans-retinoic acid metabolism and exerts retinoidal effects in rodents. J Pharmacol Exp Ther 2000, 293: 304–312.PubMed
55.
go back to reference Verfaille CJ, Coel M, Boersma IH, Mertens J, Borgers M, Roseeuw D. Oral R115866 in the treatment of moderate to severe facial acne vulgaris: An exploratory study. Br J Dermatol 2007, 157: 122–126.PubMed Verfaille CJ, Coel M, Boersma IH, Mertens J, Borgers M, Roseeuw D. Oral R115866 in the treatment of moderate to severe facial acne vulgaris: An exploratory study. Br J Dermatol 2007, 157: 122–126.PubMed
56.
go back to reference Verfaille CJ, Thissen CA, Bovenschen HJ, Mertens J, Steijlen PM, van de Kerkhof PC. Oral R115866 in the treatment of moderate to severe plaque-type psoriasis. J Eur Acad Dermatol Venereol 2007, 21: 1038–1046.PubMed Verfaille CJ, Thissen CA, Bovenschen HJ, Mertens J, Steijlen PM, van de Kerkhof PC. Oral R115866 in the treatment of moderate to severe plaque-type psoriasis. J Eur Acad Dermatol Venereol 2007, 21: 1038–1046.PubMed
57.
go back to reference Schrage K, Koopmans G, Joosten EA, Mey J. Macrophages and neurons are targets of retinoic acid signaling after spinal cord contusion injury. Eur J Neurosci 2006, 23: 285–295.PubMed Schrage K, Koopmans G, Joosten EA, Mey J. Macrophages and neurons are targets of retinoic acid signaling after spinal cord contusion injury. Eur J Neurosci 2006, 23: 285–295.PubMed
58.
go back to reference Aoto J, Nam CI, Poon MM, Ting P, Chen L. Synaptic signaling by all-trans retinoic acid in homeostatic synaptic plasticity. Neuron 2008, 60: 308–320.PubMedPubMedCentral Aoto J, Nam CI, Poon MM, Ting P, Chen L. Synaptic signaling by all-trans retinoic acid in homeostatic synaptic plasticity. Neuron 2008, 60: 308–320.PubMedPubMedCentral
59.
go back to reference Chen N, Napoli JL. All-trans-retinoic acid stimulates translation and induces spine formation in hippocampal neurons through a membrane-associated RARalpha. FASEB J 2008, 22: 236–245.PubMed Chen N, Napoli JL. All-trans-retinoic acid stimulates translation and induces spine formation in hippocampal neurons through a membrane-associated RARalpha. FASEB J 2008, 22: 236–245.PubMed
60.
go back to reference Stoney PN, Fragoso YD, Saeed RB, Ashton A, Goodman T, Simons C, et al. Expression of the retinoic acid catabolic enzyme CYP26B1 in the human brain to maintain signaling homeostasis. Brain Struct Funct 2016, 221: 3315–3326.PubMed Stoney PN, Fragoso YD, Saeed RB, Ashton A, Goodman T, Simons C, et al. Expression of the retinoic acid catabolic enzyme CYP26B1 in the human brain to maintain signaling homeostasis. Brain Struct Funct 2016, 221: 3315–3326.PubMed
61.
go back to reference Zhang ZJ, Jiang BC, Gao YJ. Chemokines in neuron-glial cell interaction and pathogenesis of neuropathic pain. Cell Mol Life Sci 2017, 74: 3275–3291.PubMed Zhang ZJ, Jiang BC, Gao YJ. Chemokines in neuron-glial cell interaction and pathogenesis of neuropathic pain. Cell Mol Life Sci 2017, 74: 3275–3291.PubMed
62.
go back to reference Tsuda M, Inoue K. Neuron-microglia interaction by purinergic signaling in neuropathic pain following neurodegeneration. Neuropharmacology 2016, 104: 76–81.PubMed Tsuda M, Inoue K. Neuron-microglia interaction by purinergic signaling in neuropathic pain following neurodegeneration. Neuropharmacology 2016, 104: 76–81.PubMed
63.
go back to reference Zhuang ZY, Kawasaki Y, Tan PH, Wen YR, Huang J, Ji RR. Role of the CX3CR1/p38 MAPK pathway in spinal microglia for the development of neuropathic pain following nerve injury-induced cleavage of fractalkine. Brain Behav Immun 2007, 21: 642–651.PubMed Zhuang ZY, Kawasaki Y, Tan PH, Wen YR, Huang J, Ji RR. Role of the CX3CR1/p38 MAPK pathway in spinal microglia for the development of neuropathic pain following nerve injury-induced cleavage of fractalkine. Brain Behav Immun 2007, 21: 642–651.PubMed
64.
go back to reference Milligan ED, Zapata V, Chacur M, Schoeniger D, Biedenkapp J, O’Connor KA, et al. Evidence that exogenous and endogenous fractalkine can induce spinal nociceptive facilitation in rats. Eur J Neurosci 2004, 20: 2294–2302.PubMed Milligan ED, Zapata V, Chacur M, Schoeniger D, Biedenkapp J, O’Connor KA, et al. Evidence that exogenous and endogenous fractalkine can induce spinal nociceptive facilitation in rats. Eur J Neurosci 2004, 20: 2294–2302.PubMed
65.
go back to reference Nam Y, Kim JH, Kim JH, Jha MK, Jung JY, Lee MG, et al. Reversible induction of pain hypersensitivity following optogenetic stimulation of spinal astrocytes. Cell Rep 2016, 17: 3049–3061.PubMed Nam Y, Kim JH, Kim JH, Jha MK, Jung JY, Lee MG, et al. Reversible induction of pain hypersensitivity following optogenetic stimulation of spinal astrocytes. Cell Rep 2016, 17: 3049–3061.PubMed
66.
go back to reference Milligan ED, Sloane EM, Langer SJ, Hughes TS, Jekich BM, Frank MG, et al. Repeated intrathecal injections of plasmid DNA encoding interleukin-10 produce prolonged reversal of neuropathic pain. Pain 2006, 126: 294–308.PubMed Milligan ED, Sloane EM, Langer SJ, Hughes TS, Jekich BM, Frank MG, et al. Repeated intrathecal injections of plasmid DNA encoding interleukin-10 produce prolonged reversal of neuropathic pain. Pain 2006, 126: 294–308.PubMed
67.
go back to reference Ledeboer A, Jekich BM, Sloane EM, Mahoney JH, Langer SJ, Milligan ED, et al. Intrathecal interleukin-10 gene therapy attenuates paclitaxel-induced mechanical allodynia and proinflammatory cytokine expression in dorsal root Ganglia in rats. Brain Behav Immun 2007, 21: 686–698.PubMed Ledeboer A, Jekich BM, Sloane EM, Mahoney JH, Langer SJ, Milligan ED, et al. Intrathecal interleukin-10 gene therapy attenuates paclitaxel-induced mechanical allodynia and proinflammatory cytokine expression in dorsal root Ganglia in rats. Brain Behav Immun 2007, 21: 686–698.PubMed
68.
go back to reference Kim WM, Jeong CW, Lee SH, Kim YO, Cui JH, Yoon MH. The intrathecally administered kappa-2 opioid agonist GR89696 and interleukin-10 attenuate bone cancer-induced pain through synergistic interaction. Anesth Analg 2011, 113: 934–940.PubMed Kim WM, Jeong CW, Lee SH, Kim YO, Cui JH, Yoon MH. The intrathecally administered kappa-2 opioid agonist GR89696 and interleukin-10 attenuate bone cancer-induced pain through synergistic interaction. Anesth Analg 2011, 113: 934–940.PubMed
69.
go back to reference Zhou Z, Peng X, Hao S, Fink DJ, Mata M. HSV-mediated transfer of interleukin-10 reduces inflammatory pain through modulation of membrane tumor necrosis factor alpha in spinal cord microglia. Gene Ther 2008, 15: 183–190.PubMed Zhou Z, Peng X, Hao S, Fink DJ, Mata M. HSV-mediated transfer of interleukin-10 reduces inflammatory pain through modulation of membrane tumor necrosis factor alpha in spinal cord microglia. Gene Ther 2008, 15: 183–190.PubMed
70.
go back to reference Ma L, Peng S, Wei J, Zhao M, Ahmad KA, Chen J, et al. Spinal microglial β-endorphin signaling mediates IL-10 and exenatide-induced inhibition of synaptic plasticity in neuropathic pain. CNS Neurosci Ther 2021, 27: 1157–1172.PubMedPubMedCentral Ma L, Peng S, Wei J, Zhao M, Ahmad KA, Chen J, et al. Spinal microglial β-endorphin signaling mediates IL-10 and exenatide-induced inhibition of synaptic plasticity in neuropathic pain. CNS Neurosci Ther 2021, 27: 1157–1172.PubMedPubMedCentral
71.
go back to reference Milligan ED, Penzkover KR, Soderquist RG, Mahoney MJ. Spinal interleukin-10 therapy to treat peripheral neuropathic pain. Neuromodulation 2012, 15: 520–526;discussion526. Milligan ED, Penzkover KR, Soderquist RG, Mahoney MJ. Spinal interleukin-10 therapy to treat peripheral neuropathic pain. Neuromodulation 2012, 15: 520–526;discussion526.
72.
go back to reference Lu Y, Jiang BC, Cao DL, Zhang ZJ, Zhang X, Ji RR, et al. TRAF6 upregulation in spinal astrocytes maintains neuropathic pain by integrating TNF-α and IL-1β signaling. Pain 2014, 155: 2618–2629.PubMedPubMedCentral Lu Y, Jiang BC, Cao DL, Zhang ZJ, Zhang X, Ji RR, et al. TRAF6 upregulation in spinal astrocytes maintains neuropathic pain by integrating TNF-α and IL-1β signaling. Pain 2014, 155: 2618–2629.PubMedPubMedCentral
73.
go back to reference Kawasaki Y, Zhang L, Cheng JK, Ji RR. Cytokine mechanisms of central sensitization: Distinct and overlapping role of interleukin-1beta, interleukin-6, and tumor necrosis factor-alpha in regulating synaptic and neuronal activity in the superficial spinal cord. J Neurosci 2008, 28: 5189–5194.PubMedPubMedCentral Kawasaki Y, Zhang L, Cheng JK, Ji RR. Cytokine mechanisms of central sensitization: Distinct and overlapping role of interleukin-1beta, interleukin-6, and tumor necrosis factor-alpha in regulating synaptic and neuronal activity in the superficial spinal cord. J Neurosci 2008, 28: 5189–5194.PubMedPubMedCentral
Metadata
Title
Cytochrome P450 26A1 Contributes to the Maintenance of Neuropathic Pain
Authors
De-Li Cao
Ling-Jie Ma
Bao-Chun Jiang
Qiang Gu
Yong-Jing Gao
Publication date
28-08-2023
Publisher
Springer Nature Singapore
Published in
Neuroscience Bulletin / Issue 3/2024
Print ISSN: 1673-7067
Electronic ISSN: 1995-8218
DOI
https://doi.org/10.1007/s12264-023-01101-1

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