The role of calcitonin gene-related peptide on the increase in transient receptor potential vanilloid-1 levels in trigeminal ganglion and trigeminal nucleus caudalis activation of rat

被引:19
作者
Chatchaisak, Duangthip [1 ]
Srikiatkhachorn, Anan [2 ]
Maneesri-le Grand, Supang [3 ]
Govitrapong, Piyarat [1 ,4 ,5 ]
Chetsawang, Banthit [1 ]
机构
[1] Mahidol Univ, Inst Mol Biosci, Res Ctr Neurosci, Salaya 73170, Nakhonpathom, Thailand
[2] Chulalongkorn Univ, Fac Med, Dept Physiol, Bangkok 10330, Thailand
[3] Chulalongkorn Univ, Fac Med, Dept Pathol, Bangkok 10330, Thailand
[4] Mahidol Univ, Fac Sci, Ctr Neurosci, Bangkok 10400, Thailand
[5] Mahidol Univ, Fac Sci, Dept Pharmacol, Bangkok 10400, Thailand
关键词
Migraine; CGRP; TRPV1; c-Fos; Trigeminal ganglion; Trigeminal nucleus caudalis; ACTIVITY-MODIFYING PROTEIN-1; PRIMARY AFFERENT NEURONS; TRIGEMINOVASCULAR SYSTEM; SUBSTANCE-P; KINASE-C; CGRP; MIGRAINE; EXPRESSION; RELEASE; SENSITIZATION;
D O I
10.1016/j.jchemneu.2012.09.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Calcitonin gene-related peptide (CGRP) and transient receptor potential vanilloid-1 (TRPV1) play an important role in the development of pain and migraine pathogenesis. Increase in plasma CGRP levels is associated with delayed migraine-like attacks in migraine patients. Although several lines of evidence have indicated a key role of CGRP in migraine pain, its mechanisms remain unclear. In this study, we aimed to investigate the functional role of CGRP on trigeminal nociceptive pathway by determining the alteration in TRPV1 levels in trigeminal ganglion (TG) and the activation of trigeminal nucleus caudalis (TNC) of rat. Post intravenous injection of CGRP (600 ng/kg) at 60 min significantly increased the levels of TRPV1, CGRP, phosphorylated protein kinase C and phosphorylated cyclic AMP responsive element-binding protein in TG of rats. The number of small and medium TRPV1 and CGRP positive immunostaining neurons accompanying with co-localization of TRPV1 with CGRP neurons were significantly increased in TG of CGRP-injected rats. The sustained increase in c-Fos expression in TNC neurons was also observed in CGRP-injected rats. These results indicate that CGRP may participate in trigeminal nociceptive system sensitization by induced increase in TRPV1 and CGRP levels in TG neurons and activation of the central neurons in TNC. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:50 / 56
页数:7
相关论文
共 39 条
[1]   Effect of CGRP and sumatriptan on the BOLD response in visual cortex [J].
Asghar, Mohammad S. ;
Hansen, Adam E. ;
Larsson, Henrik B. W. ;
Olesen, Jes ;
Ashina, Messoud .
JOURNAL OF HEADACHE AND PAIN, 2012, 13 (02) :159-166
[2]   Expression of vanilloid receptor TRPV1 in the rat trigentinal sensory nuclei [J].
Bae, YC ;
Oh, JM ;
Hwang, SJ ;
Shigenaga, Y ;
Valtschanoff, JG .
JOURNAL OF COMPARATIVE NEUROLOGY, 2004, 478 (01) :62-71
[3]   Vascular actions of calcitonin gene-related peptide and adrenomedullin [J].
Brain, SD ;
Grant, AD .
PHYSIOLOGICAL REVIEWS, 2004, 84 (03) :903-934
[4]   Calcitonin Gene-Related Peptide Promotes Cellular Changes in Trigeminal Neurons and Glia Implicated in Peripheral and Central Sensitization [J].
Cady, Ryan J. ;
Glenn, Joseph R. ;
Smith, Kael M. ;
Durham, Paul L. .
MOLECULAR PAIN, 2011, 7
[5]   Calcitonin gene-related peptide (CGRP) increases intracellular free Ca2+ concentrations but not cyclic AMP formation in CGRP receptor-positive osteosarcoma cells (OHS-4) [J].
Drissi, H ;
Lieberherr, M ;
Hott, M ;
Marie, PJ ;
Lasmoles, F .
CYTOKINE, 1999, 11 (03) :200-207
[6]  
Durham P.L., 2010, The Open Pain Journal, V8, P3, DOI DOI 10.2174/1876386301003010003
[7]  
Durham Paul L, 2004, Curr Opin Investig Drugs, V5, P731
[8]   Neurobiology in primary headaches [J].
Edvinsson, L ;
Uddman, R .
BRAIN RESEARCH REVIEWS, 2005, 48 (03) :438-456
[9]   NEUROPEPTIDES IN THE CEREBRAL-CIRCULATION - RELEVANCE TO HEADACHE [J].
EDVINSSON, L ;
GOADSBY, PJ .
CEPHALALGIA, 1995, 15 (04) :272-276
[10]   Plasma calcitonin gene-related peptide in diagnosing and predicting paediatric migraine [J].
Fan, P-C ;
Kuo, P-H ;
Chang, S-H ;
Lee, W-T ;
Wu, R-M ;
Chiou, L-C .
CEPHALALGIA, 2009, 29 (08) :883-890