Increase of Capsaicin-Induced Trigeminal Fos-Like Immunoreactivity by 5-HT7 Receptors

被引:11
作者
Martinez-Garcia, Esther [1 ]
Leopoldo, Marcello [2 ]
Lacivita, Enza [2 ]
Terron, Jose A. [1 ]
机构
[1] Cinvestav IPN, Dept Pharmacol, Mexico City 07360, DF, Mexico
[2] Univ Bari, Dipartimento Farmacochim, Bari, Italy
来源
HEADACHE | 2011年 / 51卷 / 10期
关键词
5-hydroxytryptamine7; receptor; Fos-like immunoreactivity; trigeminal nucleus caudalis; capsaicin; cephalic pain; rat; RAT DURA-MATER; POLYMERASE-CHAIN-REACTION; MESSENGER-RNA EXPRESSION; GENE-RELATED PEPTIDE; NUCLEUS CAUDALIS; SPINAL-CORD; INTRACISTERNAL CAPSAICIN; BLOOD-VESSELS; MAST-CELLS; IN-VIVO;
D O I
10.1111/j.1526-4610.2011.02011.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective. To explore whether pharmacological stimulation of the 5-hydroxytryptamine7 (5-HT7) receptor modulates Fos-like immunoreactivity in the trigeminal nucleus caudalis of rats.
引用
收藏
页码:1511 / 1519
页数:9
相关论文
共 48 条
[1]   Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model [J].
Bolay, H ;
Reuter, U ;
Dunn, AK ;
Huang, ZH ;
Boas, DA ;
Moskowitz, MA .
NATURE MEDICINE, 2002, 8 (02) :136-142
[2]   5-HYDROXYTRYPTAMINE RECEPTOR AGONISTS FOR THE ABORTIVE TREATMENT OF VASCULAR HEADACHES BLOCK MAST-CELL, ENDOTHELIAL AND PLATELET ACTIVATION WITHIN THE RAT DURA-MATER AFTER TRIGEMINAL STIMULATION [J].
BUZZI, MG ;
DIMITRIADOU, V ;
THEOHARIDES, TC ;
MOSKOWITZ, MA .
BRAIN RESEARCH, 1992, 583 (1-2) :137-149
[3]   5HT increases excitability of nociceptor-like rat dorsal root Na+ channels [J].
Cardenas, LM ;
Cardenas, CG ;
Scroggs, RS .
JOURNAL OF NEUROPHYSIOLOGY, 2001, 86 (01) :241-248
[4]   Attenuation by valproate of c-fos immunoreactivity in trigeminal nucleus caudalis induced by intracisternal capsaicin [J].
Cutrer, FM ;
Limmroth, V ;
Ayata, G ;
Moskowitz, MA .
BRITISH JOURNAL OF PHARMACOLOGY, 1995, 116 (08) :3199-3204
[5]   SUPPRESSION BY THE SUMATRIPTAN ANALOG, CP-122,288 OF C-FOS IMMUNOREACTIVITY IN TRIGEMINAL NUCLEUS CAUDALIS INDUCED BY INTRACISTERNAL CAPSAICIN [J].
CUTRER, FM ;
SCHOENFELD, D ;
LIMMROTH, V ;
PANAHIAN, N ;
MOSKOWITZ, MA .
BRITISH JOURNAL OF PHARMACOLOGY, 1995, 114 (05) :987-992
[6]   THE NONPEPTIDE NEUROKININ-1 ANTAGONIST, RPR-100893, DECREASES C-FOS EXPRESSION IN TRIGEMINAL NUCLEUS CAUDALIS FOLLOWING NOXIOUS CHEMICAL MENINGEAL STIMULATION [J].
CUTRER, FM ;
MOUSSAOUI, S ;
GARRET, C ;
MOSKOWITZ, MA .
NEUROSCIENCE, 1995, 64 (03) :741-750
[7]  
DIMITRIADOU V, 1991, NEUROSCIENCE, V44, P97
[8]   EFFECTS OF THE PUTATIVE 5-HT1A RECEPTOR AGONIST 8-OH-2-(DI-N-PROPYLAMINO) TETRALIN ON NOCICEPTIVE SENSITIVITY IN MICE [J].
FASMER, OB ;
BERGE, OG ;
POST, C ;
HOLE, K .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1986, 25 (04) :883-888
[9]   SB-656104-A:: A novel 5-HT7 receptor antagonist with improved in vivo properties [J].
Forbes, IT ;
Douglas, S ;
Gribble, AD ;
Ife, RJ ;
Lightfoot, AP ;
Garner, AE ;
Riley, GJ ;
Jeffrey, P ;
Stevens, AJ ;
Stean, TO ;
Thomas, DR .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2002, 12 (22) :3341-3344
[10]   LP-211 is a brain penetrant selective agonist for the serotonin 5-HT7 receptor [J].
Hedlund, Peter B. ;
Leopoldo, Marcello ;
Caccia, Silvio ;
Sarkisyan, Gor ;
Fracasso, Claudia ;
Martelli, Giuliana ;
Lacivita, Enza ;
Berardi, Francesco ;
Perrone, Roberto .
NEUROSCIENCE LETTERS, 2010, 481 (01) :12-16