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2014 | 74 | 2 |

Tytuł artykułu

Gender differences in the neurochemical response of trigeminal ganglion neurons to peripheral inflammation in mice

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
It is well established that the majority of headache and other trigeminal nerve-associated disorders have higher prevalence in females than in males. However, the pathogenesis of many chronic trigeminal pain conditions, such as trigeminal neuralgia, migraine and temporo-mandibular disorders, is still not known. One of the proposed mechanisms involve calcitonin gene-related peptide (CGRP), which is considered the most important neuropeptide in the trigeminal system. In various animal models of trigeminal nerve-associated disorders concentration of CGRP has been shown to be increased in trigeminal ganglia (TG). Moreover, intraganglionic release of CGRP has been shown to modulate neuronal transmission of pain signals. In most of these models, pathological changes in the trigeminal system are accompanied by inflammation within peripheral endings of TG neurons. The aim of the present study was to investigate the relation between gender and neurochemical changes in trigeminal ganglia evoked by peripheral inflammation, induced by Complete Freund Adjuvant (CFA) administration. Our studies show significant increase in CGRP expression in female mice, comparing to male mice. Furthermore, we demonstrate, that activation of trigeminal nociceptors by peripheral inflammation causes significant increase in expression of IL-ip, IL-6, TNF and BDNF in male mice, comparing to female mice. This phenomenon may be involved in clinically observed gender-dependent differences in the frequency of both migraine and other trigeminal nerve- related facial pain disorders.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

74

Numer

2

Opis fizyczny

p.227-232,fig.,ref.

Twórcy

  • Department of Experimental and Clinical Pharmacology, Medical University of Warsaw, Warsaw, Poland
  • Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, Warsaw, Poland
autor
  • Department of Experimental and Clinical Pharmacology, Medical University of Warsaw, Warsaw, Poland
autor
  • Department of Experimental and Clinical Pharmacology, Medical University of Warsaw, Warsaw, Poland
  • Department of Experimental and Clinical Pharmacology, Medical University of Warsaw, Warsaw, Poland
  • Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, Warsaw, Poland

Bibliografia

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  • Bałkowiec-Iskra E, Vermehren-Schmaedick A, Balkowiec A (2011) Tumor necrosis factor-a increases brain-derived neurotrophic factor expression in trigeminal ganglion neurons in an activity-dependent manner. Neuroscience 180: 322-333.
  • Bigal ME, Walter S, Rapaport AM (2013) Calcitonin gene- related peptide (CGRP) and migraine current understand¬ing and state of development. Headache 53: 1230-1244.
  • Binshtok AM, Wang H, Zimmermann K, Amaya F, Vardeh D, Shi L, Brenner GJ, Ji RR, Bean BP, Woolf CJ, Samad TA (2008) Nociceptors are interleukin-1beta sensors. J Neurosci 28: 14062-14073.
  • Bowen EJ, Schmidt TW, Firm CS, Russo AF, Durham PL (2006) Tumor necrosis factor-alpha stimulation of calcitonin gene-related peptide expression and secretion from rat trigeminal ganglion neurons. J Neurochem 96: 65-77.
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  • Buse DC, Loder EW, Gorman JA, Stewart WF, Reed ML, Fanning KM, Serrano D, Lipton RB (2013) Sex differ¬ences in the prevalence, symptoms and associated fea¬tures of migraine, prabable migraine and other severe headache: results of the American Migraine Prevalence and Prevention (AMPP) Study. Headache 53: 1278¬1299.
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  • Flake NM, Gold MS (2005) Inflammation alters sodium cur¬rents and excitability of temporomandibular joint affer¬ents. Neurosci Lett 384: 294-299.
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  • Gupta S, Mehrotra, Villalon C, Vries RD, Garrelds I, Saxena P, VanDenBrink AM (2007b) Effects of female sex hor¬mones on responses to CGRP, acetylcholine and 5-HT in rat isolated arteries. Headache 47: 564-575.
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  • Krzyżanowska A, Pittolo S, Cabrerizo M, Sanchez-Lopez J, Krishnasamy S, Venero C, Avendano C (2011) Assessing nociceptive sensitivity in mouse models of inflammatory and neuropathic trigeminal pain. J Neurosci Meth 201: 46-54.
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  • Lazarov NE (2002) Comparative analysis of the chemical neuroanatomy of the mammalian trigeminal ganglion and mesencephalic trigeminal nucleus. Prog Neurobiol 66: 19-59.
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  • Messlinger K, Lennerz JK, Eberhardt M, Fischer MJ (2012) CGRP and NO in the trigeminal system: mechanisms and role in headache generation. Headache 52: 1411-1427.
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  • Tarsa L, Balkowiec-Iskra E, Kratochvil FJ, III, Jenkins VK, McLean A, Brown AL, Smith JA, Baumgartner JC, Balkowiec A (2010) Tooth pulp inflammation increases brain-derived neurotrophic factor expression in rodent trigeminal ganglion neurons. Neuroscience 167: 1205¬1215.
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Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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