Substance P: A new era, a new role

被引:106
作者
DeVane, CL [1 ]
机构
[1] Med Univ S Carolina, Dept Psychiat & Behav Sci, Charleston, SC 29425 USA
来源
PHARMACOTHERAPY | 2001年 / 21卷 / 09期
关键词
D O I
10.1592/phco.21.13.1061.34612
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Substance P has been extensively studied and is considered the prototypic neuropeptide of the more than 50 known neuroactive molecules. The understanding of substance P has evolved beyond the original concept as the pain transmitter of the dorsal horn. Animal and genetic research, recent developments of nonpeptide substance P antagonists, and important changes in the understanding of neuro transmission have each contributed to the current understanding of substance P. After 7 decades, the physiologic role of substance P is known as a modulator of nociception, involved in signaling the intensity of noxious or aversive stimuli. Genetic studies in mice and development of substance P antagonists provide more recent results that support the redefinition of the central role of substance P. Evidence suggests that this neuropeptide is an integral part of central nervous system pathways involved in psychologic stress.
引用
收藏
页码:1061 / 1069
页数:9
相关论文
共 41 条
[1]   Effects of microinjections of the neuropeptide substance P in the dorsal periaqueductal gray on the behaviour of rats in the plus-maze test [J].
Aguiar, MS ;
Brandao, ML .
PHYSIOLOGY & BEHAVIOR, 1996, 60 (04) :1183-1186
[2]   ROLE OF ENDOGENOUS SUBSTANCE-P IN STRESS-INDUCED ACTIVATION OF MESOCORTICAL DOPAMINE NEURONS [J].
BANNON, MJ ;
ELLIOTT, PJ ;
ALPERT, JE ;
GOEDERT, M ;
IVERSEN, SD ;
IVERSEN, LL .
NATURE, 1983, 306 (5945) :791-792
[3]   INVIVO INHIBITION OF THE PREOVULATORY LH SURGE BY SUBSTANCE-P AND INVITRO MODULATION OF GONADOTROPIN-RELEASING HORMONE-INDUCED LH-RELEASE BY SUBSTANCE-P, ESTRADIOL AND PROGESTERONE IN THE FEMALE RAT [J].
BATTMANN, T ;
PARSADANIANTZ, SM ;
JEANJEAN, B ;
KERDELHUE, B .
JOURNAL OF ENDOCRINOLOGY, 1991, 130 (02) :169-175
[4]   Neurogenic amplification of immune complex inflammation [J].
Bozic, CR ;
Lu, B ;
Hopken, UE ;
Gerard, C ;
Gerard, NP .
SCIENCE, 1996, 273 (5282) :1722-1725
[5]   Primary afferent tachykinins are required to experience moderate to intense pain [J].
Cao, YQ ;
Mantyh, PW ;
Carlson, EJ ;
Gillespie, AM ;
Epstein, CJH ;
Basbaum, AI .
NATURE, 1998, 392 (6674) :390-394
[6]  
CHARNEY DS, 2000, 10 AM PSYCH ASS S CH
[7]   CENTRAL TACHYKININS - MEDIATORS OF DEFENSE REACTION AND STRESS REACTIONS [J].
CULMAN, J ;
UNGER, T .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 1995, 73 (07) :885-891
[8]   Altered nociception, analgesia and aggression in mice lacking the receptor for substance P [J].
De Felipe, C ;
Herrero, JF ;
O'Brien, JA ;
Palmer, JA ;
Doyle, CA ;
Smith, AJH ;
Laird, JMA ;
Belmonte, C ;
Cervero, F ;
Hunt, SP .
NATURE, 1998, 392 (6674) :394-397
[9]   Potential of substance P antagonists as antiemetics [J].
Diemunsch, P ;
Grélot, L .
DRUGS, 2000, 60 (03) :533-546
[10]   NK1 receptor antagonist blocks angiotensin II responses in renin transgenic rat medulla oblongata [J].
Diz, DI ;
Westwood, B ;
Bosch, SM ;
Ganten, D ;
Ferrario, C .
HYPERTENSION, 1998, 31 (01) :473-479