Nocistatin reverses the effect of orphanin FQ/nociceptin in antagonizing morphine analgesia

被引:39
作者
Zhao, CS
Li, BS
Zhao, GY
Liu, HX
Luo, F
Wang, Y
Tian, JH
Chang, JK
Han, JS [1 ]
机构
[1] Beijing Med Univ, Neurosci Res Inst, Beijing 100083, Peoples R China
[2] Phoenix Pharmaceut Inc, Mt View, CA USA
关键词
allodynia; hyperalgesia; morphine; nociceptive; nocistatin;
D O I
10.1097/00001756-199902050-00017
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
NOCISTATIN is a recently characterized neuropeptide derived from the preprohormone containing nociceptin (Orphanin FQ, OFQ). Nocistatin was reported to antagonize OFQ induced allodynia, hyperalgesia and prostaglandin E-2-elicited pain responses. The aim of the present study was to determine whether nocistatin, injected intracerebroventricularly (i.c.v.), would reverse the anti-morphine effect of OFQ in rats using the tail-flick latency (TFL) as the nociceptive index. I.c.v. injection of nocistatin at doses of 0.005, 0.05, 0.5, 5, 50, and 500 ng produced no significant changes in the basal TFL, nor did it affect morphine analgesia. However, it significantly reversed the antagonistic effect of OFQ on morphine analgesia when co-injected i.c.v. at doses of 0.05, 0.5, 5, 50 and 500 ng per rat with OFQ. The dose-response curve was bell-shaped and the most effective dose was 0.5 ng. The results suggest that nocistatin can reverse the anti-morphine effect of OFQ in rat brain. (C) 1999 Lippincott Williams & Wilkins.
引用
收藏
页码:297 / 299
页数:3
相关论文
共 21 条
[1]   MOLECULAR-CLONING AND TISSUE DISTRIBUTION OF A PUTATIVE MEMBER OF THE RAT OPIOID RECEPTOR GENE FAMILY THAT IS NOT A MU-OPIOID, DELTA-OPIOID OR KAPPA-OPIOID RECEPTOR-TYPE [J].
BUNZOW, JR ;
SAEZ, C ;
MORTRUD, M ;
BOUVIER, C ;
WILLIAMS, JT ;
LOW, M ;
GRANDY, DK .
FEBS LETTERS, 1994, 347 (2-3) :284-288
[2]  
FUKEDA K, 1994, FEBS LETT, V343, P42
[3]  
HAN JS, 1995, PHARMACOLOGICAL SCIENCES: PERSPECTIVES FOR RESEARCH AND THERAPY IN THE LATE 1990S, P199
[4]   Characterization of nociceptin hyperalgesia and allodynia in conscious mice [J].
Hara, N ;
Minami, T ;
OkudaAshitaka, E ;
Sugimoto, T ;
Sakai, M ;
Onaka, M ;
Mori, H ;
Imanishi, T ;
Shingu, K ;
Ito, S .
BRITISH JOURNAL OF PHARMACOLOGY, 1997, 121 (03) :401-408
[5]   ISOLATION AND STRUCTURE OF THE ENDOGENOUS AGONIST OF OPIOID RECEPTOR-LIKE ORL(1) RECEPTOR [J].
MEUNIER, JC ;
MOLLEREAU, C ;
TOLL, L ;
SUAUDEAU, C ;
MOISAND, C ;
ALVINERIE, P ;
BUTOUR, JL ;
GUILLEMOT, JC ;
FERRARA, P ;
MONSARRAT, B ;
MAZARGUIL, H ;
VASSART, G ;
PARMENTIER, M ;
COSTENTIN, J .
NATURE, 1995, 377 (6549) :532-535
[6]   Orphanin FQ is a functional anti-opioid peptide [J].
Mogil, JS ;
Grisel, JE ;
Reinscheid, RK ;
Civelli, O ;
Belknap, JK ;
Grandy, DK .
NEUROSCIENCE, 1996, 75 (02) :333-337
[7]  
MOGIL JS, 1996, NEUROSCI LETT, V214, P1
[8]   ORL1, A NOVEL MEMBER OF THE OPIOID RECEPTOR FAMILY - CLONING, FUNCTIONAL EXPRESSION AND LOCALIZATION [J].
MOLLEREAU, C ;
PARMENTIER, M ;
MAILLEUX, P ;
BUTOUR, JL ;
MOISAND, C ;
CHALON, P ;
CAPUT, D ;
VASSART, G ;
MEUNIER, JC .
FEBS LETTERS, 1994, 341 (01) :33-38
[9]   Nocistatin, a peptide that blocks nociceptin action in pain transmission [J].
Okuda-Ashitaka, E ;
Minami, T ;
Tachibana, S ;
Yoshihara, Y ;
Nishiuchi, Y ;
Kimura, T ;
Ito, S .
NATURE, 1998, 392 (6673) :286-289
[10]   Identification and characterization of an endogenous ligand for opioid receptor homologue ROR-C: Its involvement in allodynic response to innocuous stimulus [J].
OkudaAshitaka, E ;
Tachibana, S ;
Houtani, T ;
Minami, T ;
Masu, Y ;
Nishi, M ;
Takeshima, H ;
Sugimoto, T ;
Ito, S .
MOLECULAR BRAIN RESEARCH, 1996, 43 (1-2) :96-104