Effects of estrogen on the serotonergic system and calcitonin gene-related peptide in trigeminal ganglia of rats

Milan Aggarwal, Veena Puri, Sanjeev Puri, Milan Aggarwal, Veena Puri, Sanjeev Puri

Abstract

Background: The prevalence of migraine is 3-folds higher in females than in males, and it is intricately related to the levels of estrogen. Estrogen may regulate the expression of metabolic enzymes and receptors of serotonin and also calcitonin gene-related peptide (CGRP), which are implicated in migraine pathogenesis.

Purpose: To study the effects of estrogen on the components of serotonin system and CGRP in trigeminal ganglia of ovariectomized (OVX) rats.

Methods: OVX rats were administered estrogen in silastic tubes and after 48 h, serum estrogen levels were determined. Trigeminal ganglia tissues were used for RT-PCRs of tryptophan hydroxylase (TPH), monoamine oxidase (MAO), serotonin receptors (5-HT1A, 5-HT1B, 5-HT2A), estrogen receptor (ER) and CGRP. Western blots of TPH and MAO were performed.

Results: Estradiol administration to OVX rats increased TPH mRNA levels, while decreased MAO mRNA levels in trigeminal ganglia tissue. Western blot data correlate with the gene expression results. The decreased mRNA levels of serotonin receptors following ovariectomy were restored in estrogen-replenished rats. The induced gene expression of ER in OVX rats was restored following estrogen replenishment.

Conclusion: Estrogen levels affect the levels of serotonin metabolizing enzymes and its receptors besides CGRP levels. Since TPH and MAO levels regulate circulating and physiologically available serotonin content, the regulation of serotonin metabolizing enzymes suggest a plausible mechanism by which estrogen alleviates migraine in women.

Keywords: 17β-estradiol; Migraine; Ovariectomy; Serotonin.

Conflict of interest statement

Competing interests: None

Figures

Fig. 1:
Fig. 1:
Expression of genes of the components of serotonin system, estrogen receptor and CGRP in trigeminal ganglia. (a) Ethidium bromide-stained agarose gels of RT-PCRs of tryptophan hydroxylase, monoamine oxidase, 5-HT1A, 5-HT1B, 5-HT2A, estrogen receptor and Rig/S15. Each gel depicts representative data from cycling (control), sham-operated, ovariectomized and estrogen-replenished ovariectomized rats. (b) Quantitation of RT-PCR data demonstrates significant changes in various genes expression. The ordinate represents the ratio of the intensity of the gene of interest to the housekeeping gene (Rig/S15), mean + standard error (n=5). *Means differ from control, P<0.05. $Means differ from OVX, P<0.05.
Fig. 2:
Fig. 2:
Western blot analysis of proteins in trigeminal ganglia of cycling (control), sham-operated, ovariectomized and estrogen-replenished ovariectomized rats. (a) Western blot of TPH, MAO and GAPDH proteins. (b) Quantitaion of proteins using chemiluminescence, mean ± standard error (n=5). *Means differ from control, P&0.05. $Means differ from OVX, P

Fig. 3:

Expression of CGRP gene in…

Fig. 3:

Expression of CGRP gene in trigeminal ganglia. (a) Ethidium bromide-stained agarose gels of…

Fig. 3:
Expression of CGRP gene in trigeminal ganglia. (a) Ethidium bromide-stained agarose gels of RT-PCRs of CGRP and Rig/S15. Each gel depicts representative data from cycling (control), sham-operated, ovariectomized and estrogen-replenished ovariectomized rats. (b) Quantitation of RT-PCR data demonstrates significant changes in gene expression. The ordinate represents the ratio of the intensity of CGRP gene to the housekeeping gene (Rig/S15), mean + standard error (n=5). *Means differ from control, P
Similar articles
Cited by
References
    1. Martin VT, Lipton RB. Epidemiology and biology of menstrual migraine. Headache. 2008;48:S124–S130. - PubMed
    1. Cairns BE. The influence of gender and sex steroids on craniofacial nociception. Headache Currents. 2007;47:319–324. - PubMed
    1. Sances G, Granella F, Nappi RE et al. Course of migraine during pregnancy and postpartum: a prospective study. Cephalalgia. 2003;23:197–205. - PubMed
    1. Martin VT, Behbehani M. Ovarian hormones and migraine headache: understanding mechanisms and pathogenesis- part 2. Headache. 2006;46:365–386. - PubMed
    1. Aegidius K, Zwart JA, Hagen K et al. Oral contraceptives and increased headache prevalence: the head-hunt study. Neurol. 2006;66:349–353. - PubMed
Show all 53 references
Full text links [x]
[x]
Cite
Copy Download .nbib
Format: AMA APA MLA NLM
Fig. 3:
Fig. 3:
Expression of CGRP gene in trigeminal ganglia. (a) Ethidium bromide-stained agarose gels of RT-PCRs of CGRP and Rig/S15. Each gel depicts representative data from cycling (control), sham-operated, ovariectomized and estrogen-replenished ovariectomized rats. (b) Quantitation of RT-PCR data demonstrates significant changes in gene expression. The ordinate represents the ratio of the intensity of CGRP gene to the housekeeping gene (Rig/S15), mean + standard error (n=5). *Means differ from control, P

References

    1. Martin VT, Lipton RB. Epidemiology and biology of menstrual migraine. Headache. 2008;48:S124–S130.
    1. Cairns BE. The influence of gender and sex steroids on craniofacial nociception. Headache Currents. 2007;47:319–324.
    1. Sances G, Granella F, Nappi RE et al. Course of migraine during pregnancy and postpartum: a prospective study. Cephalalgia. 2003;23:197–205.
    1. Martin VT, Behbehani M. Ovarian hormones and migraine headache: understanding mechanisms and pathogenesis- part 2. Headache. 2006;46:365–386.
    1. Aegidius K, Zwart JA, Hagen K et al. Oral contraceptives and increased headache prevalence: the head-hunt study. Neurol. 2006;66:349–353.
    1. Moskowitz MA. Defining a pathway from bench to bedside: the trigeminovascular system and sensitization. Headache. 2008;48:688–690.
    1. Welch KM, Choudhuri R, Cui L et al. Estrogen regulation of gene expression in cortical spreading depression: relevance to menstrual migraine. Headache. 2002;42
    1. Puri V, Puri S, Svojanovsky SR et al. Effects of oestrogen on trigeminal ganglia in culture: implications for hormonal effects on migraine. Cephalalgia. 2005;36:33–42.
    1. Berman NEJ, Puri V, Chandrala S et al. Serotonin in trigeminal ganglia of female rodents: relevance to menstrual migraine. Headache. 2006;46:1230–1245.
    1. Bolay H, Reuter U, Dunn AK et al. Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model. Nat Med. 2002;8:136–142.
    1. Brewerton TD, Murphy DL, Meuller EA et al. Induction of migraine-like headaches by the serotonin agonist, m-chlorophenylpiperazine. Clin Pharmacol Ther. 1988;43:605–609.
    1. Ferrari MD, Melamed E, Gawel MJ et al. Treatment of migraine attacks with sumatriptan. The subcutaneous sumatriptan international study group. N Engl J Med. 1991;325:316–321.
    1. Ferrari MD, Roon KI, Lipton RB et al. Oral triptans (5-HT(1B/1D) agonists) in acute migraine treatment: A meta-analysis of 53 trials. Lancet. 2001;358:1668–1675.
    1. Hiroi R, McDevitt RA, Neumaier JF. Estrogen selectively increases tryptophan hydroxylase-2 mRNA expression in distinct subregions of rat midbrain raphe nucleus: association between gene expression and anxiety behavior in the open field. Biol Psychiatry. 2006;60(3):288–295.
    1. Gangula PR, Lanlua P, Wimalawansa S et al. Regulation of calcitonin gene-related peptide expression in dorsal root ganglia of rats by female sex steroid hormones. Biol Reprod. 2000;62:1033–1039.
    1. Pecins-Thompson M, Brown NA, Kohama SG et al. Ovarian steroid regulation of tryptophan hydroxylase mRNA expression in rhesus macaques. J Neurosci. 1996;16:7021–7029.
    1. Pecins-Thompson M, Brown NA, Bethea CL. Regulation of serotonin re-uptake transporter mRNA expression by ovarian steroids in rhesus macaques. Brain Res Mol Brain Res. 1998;53:120–129.
    1. Smith LJ, Henderson JA, Abell CW et al. Effects of ovarian steroids and raloxifene on proteins that synthesize, transport and degrade serotonin in the raphe region of macaques. Neuropsychopharmacol. 2004;29:2035–2045.
    1. Bethea CL, Lu NZ, Gundlah C et al. Diverse actions of ovarian steroids in the serotonin neural system. Front Endocrinol. 2002;23:41–100.
    1. Yang Y, Ozawa H, Kawata M et al. Immunocytochemical analysis of sex differences in calcitonin gene-related peptide in the rat dorsal root ganglion, with special reference to estrogen and its receptor. Brain Res. 1998;791:35–42.
    1. Lowry OH, Rosebrough NJ, Farr AL et al. Protein measurement with the folin phenol reagent. J Biol Chem. 1951;193:265–275.
    1. Zhang X, Beaulieu JM, Gainetdinov RR et al. Functional polymorphisms of the brain serotonin synthesizing enzyme tryptophan hydroxylase-2. Cell Mol Life Sci. 2006;63(1):6–11.
    1. Bianchi P, Kunduzova O, Masini E et al. Oxidative stress by monoamine oxidase mediates receptor-independent cardiomyocyte apoptosis by serotonin and postischemic myocardial injury. Circulation. 2005;112(21):3297–3305.
    1. Cohen PE, Mlligan SR. Silastic implants for delivery of oestradiol to mice. J Reprod Fertility. 1993;99:219–223.
    1. Nelson LR, Bulun SE. Estrogen production and action. J Am Acad Dermatol. 2001;45(3):S116–S124.
    1. Charoenphandhu J, Teerapornpuntakit J, Nuntapornsak A et al. Anxiety-like behaviors and expression of SERT and TPH in the dorsal raphe of estrogen- and fluoxetine-treated ovariectomized rats. Pharmacol Biochem Behavior. 2011;98:503–510.
    1. Ma ZQ, Violani E, Villa F et al. Estrogenic control of monoamine oxidase A activity in human neuroblastoma cells expressing physiological concentrations of estrogen receptor. Eur J Pharmacol. 1995;284:71–76.
    1. Meneses A. Physiological, pathophysiological and therapeutic roles of 5-HT systems in learning and memory. Terapeutica Experimental Rev Neurosci. 1998;9(4):275–289.
    1. Schmuck K, Ullmer C, Kalkman HO et al. Activation of meningeal 5-HT2B receptors: an early step in the generation of migraine headache? Eur J Neurosci. 1996;8(5):959–967.
    1. Hamel E. The biology of serotonin receptors: focus on migraine pathophysiology and treatment. Can J Neurol Sci. 1999;26(3):S2–S6.
    1. Moskowitz MA, Buzi MG. Neuroeffector functions of sensory fibres: implications for headache mechanisms and drug actions. J Neurol. 1991;238:S18–S22.
    1. Bruinvels AT, Landwerhmeyer B, Moskowitz MA et al. Evidence for the presence of 5HT1B receptor messenger RNA in neurons of the rat trigeminal ganglia. Eur J Pharmacol. 1992;227:357–359.
    1. Sumner BEH, Fink G. Effects of acute estradiol on 5-hydroxytryptamine and dopamine receptor subtype mRNA expression in female rat brain. Mol Cellular Neurosci. 1993;4:83–92.
    1. Sumner BEH, Fink G. Estrogen increases the density of 5-hydroxytryptamine(2A) receptors in cerebral cortex and nucleus accumbens in the female rat. J Steroid Biochem Mol Biol. 1995;54(1–2):15–20.
    1. Osterlund MK, Hurd YL. Acute 17 beta-estradiol treatment down-regulates serotonin 5HT1A receptor mRNA expression in the limbic system of female rats. Brain Res Mol Brain Res. 1998;55:169–172.
    1. D’Souza DN, Zhang Y, Damjanoska KJ et al. Estrogen reduces serotonin-1A receptor-mediated oxytocin release and Galpha (i/o/z) proteins in the hypothalamus of ovariectomized rats. Neuroendocrinol. 2004;80:31–41.
    1. Birzniece V, Johansson IM, Wang MD et al. Serotonin 5-HT(1A) receptor mRNA expression in dorsal hippocampus and raphe nuclei after gonadal hormone manipulation in female rats. Neuroendocrinol. 2001;74:135–142.
    1. Lu NZ, Bethea CL. Ovarian steroid regulation of 5-HT1A receptor binding and G protein activation in female monkeys. Neuropsychopharmacol. 2002;27:12–24.
    1. Hay DL, Poyner DR. Calcitonin gene-related peptide, adrenomedullin and flushing. Maturitas. 2009;64:104–108.
    1. Osterlund MK, Halldin C, Hurd YL. Effects of chronic 17β-estradiol treatment on the serotonin 5-HT1A receptor mRNA and binding levels in the rat brain. Synapse. 2000;35:39–44.
    1. Amin Z, Canli T, Epperson CN. Effect of estrogen–serotonin interactions on mood and cognition. Behav Cogn Neurosci Rev. 2005;4:43–58.
    1. Puri V, Cui L, Liverman CS et al. Ovarian steroids regulate neuropeptides in the trigeminal ganglion. Neuropeptides. 2005;40:35–46.
    1. Schreihofer DA, Rowe DF, Rissman EF et al. Estrogen receptor-alpha (ERalpha), but not ERbeta, modulates estrogen stimulation of the ERalpha-truncated variant, TERP-1. Endocrinol. 2002;143:4196–4202.
    1. Shughrue PJ, Bushnell CD, Dorsa DM. Estrogen receptor messenger ribonucleic acid in female rat brain during the estrous cycle: a comparison with ovariectomized females and intact males. Endocrinol. 1992;131:381–388.
    1. Yang Y, Ozawa H, Kawata M et al. Immunocytochemical analysis of sex differences in calcitonin gene-related peptide in the rat dorsal root ganglion, with special reference to estrogen and its receptor. Brain Res. 1998;791:35–42.
    1. Wyon Y, Frisk J, Lundeberg T et al. Postmenopausal women with vasomotor symptoms have increased urinary excretion of calcitonin gene-related peptide. Maturitas. 1998;30:289–294.
    1. Goadsby PJ, Edvinsson L, Ekman R. Vasoactive peptide release in the extracerebral circulation of humans during migraine headache. Ann Neurol. 1990;28:183–7.
    1. Juhasz G, Zsombok T, Jakab B et al. Sumatriptan causes parallel decrease in plasma calcitonin gene-related peptide (CGRP) concentration and migraine headache during nitroglycerin induced migraine attack. Cephalalgia. 2005;25:179–83.
    1. Levy D, Burstein R, Kainz V et al. Mast cell degranulation activates a pain pathway underlying migraine headache. Pain. 2007;130:166–76.
    1. Sarajari S, Oblinger MM. Estrogen effects on pain sensitivity and neuropeptide expression in rat sensory neurons. Experimental Neurol. 2010;224:163–169.
    1. Ma QL, Zhou HY, Sun M. Relationship between sex hormone levels and blood calcitonin gene-related peptide/endothelin-1 in postmenopausal women with coronary heart disease. Hunan Yi Ke Da Xue Xue Bao. 2001;26:146–148.
    1. Corominas R, Sobrido MJ, Ribasés M et al. Association study of the serotoninergic system in migraine in the Spanish population. Am J Med Genet B Neuropsychiatr Genet. 2010;153B(1):177–84.
    1. Ishii M, Shimizu S, Sakairi Y et al. MAOA, MTHFR, and TNF-β genes polymorphisms and personality traits in the pathogenesis of migraine. Mol Cell Biochem. 2012;1–2;363:357–66.

Source: PubMed

3
Subskrybuj