INHIBITION OF THE ANTIANALGESIC ACTION OF DYNORPHIN-A IN MICE BY CHOLERA-TOXIN

被引:13
作者
ARTS, KS
FUJIMOTO, JM
CRAIN, SM
机构
[1] VET ADM MED CTR,RES SERV IST,MILWAUKEE,WI 53295
[2] YESHIVA UNIV ALBERT EINSTEIN COLL MED,DEPT NEUROSCI,BRONX,NY 10461
[3] YESHIVA UNIV ALBERT EINSTEIN COLL MED,DEPT PHYSIOL BIOPHYS,BRONX,NY 10461
[4] VET ADM MED CTR,DEPT PHARMACOL & TOXICOL,MILWAUKEE,WI 53295
[5] MED COLL WISCONSIN,MILWAUKEE,WI 53295
关键词
DYNORPHIN; ANTIANALGESIA; CHOLERA TOXIN; G(S); MORPHINE; CLONIDINE;
D O I
10.1016/0091-3057(93)90553-6
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Dynorphin A-(1-17) (Dyn A) administered intrathecally (IT) or released spinally in the mouse produces an antianalgesic action. The present experiments indicate that IT administration of cholera toxin inhibited the antianalgesic action of Dyn A. When clonidine was administered intracerebroventricularly (ICV) to release spinal Dyn A, IT cholera toxin inhibited the antianalgesic action of Dyn A so that the analgesic component of action of clonidine became evident. Dyn A given IT inhibited the analgesic action of morphine given ICV. Cholera toxin given IT eliminated the antagonistic action of Dyn A. These results, in addition to others, indicate that IT cholera toxin antagonized the action of Dyn A. When the antianalgesic action of Dyn A was attenuated by pretreatment with dynorphin antiserum or by pretreatment that produced desensitization to Dyn A, cholera toxin had no effect. These results suggested that the antianalgesic action of Dyn A is mediated by activation of opioid receptors that are positively coupled to adenylate cyclase through a G(s) regulatory protein.
引用
收藏
页码:623 / 629
页数:7
相关论文
共 37 条
[1]   OPIOID ANTAGONISTS - INDIRECT ANTAGONISM OF MORPHINE ANALGESIA BY SPINAL DYNORPHIN-A [J].
AKSU, F ;
HOLMES, BB ;
FUJIMOTO, JM .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1993, 45 (02) :409-418
[2]  
ARTS KS, 1992, J PHARMACOL EXP THER, V261, P643
[3]   BLOCKADE OF MORPHINE ANALGESIA BY BOTH PERTUSSIS AND CHOLERA TOXINS IN THE PERIAQUEDUCTAL GRAY AND LOCUS-CERULEUS [J].
BODNAR, RJ ;
PAUL, D ;
ROSENBLUM, M ;
LIU, L ;
PASTERNAK, GW .
BRAIN RESEARCH, 1990, 529 (1-2) :324-328
[4]   INHIBITOR OF CYCLIC AMP-DEPENDENT PROTEIN-KINASE BLOCKS OPIOID-INDUCED PROLONGATION OF THE ACTION-POTENTIAL OF MOUSE SENSORY GANGLION NEURONS IN DISSOCIATED CELL-CULTURES [J].
CHEN, GG ;
CHALAZONITIS, A ;
SHEN, KF ;
CRAIN, SM .
BRAIN RESEARCH, 1988, 462 (02) :372-377
[5]   OPIOIDS CAN EVOKE DIRECT RECEPTOR-MEDIATED EXCITATORY EFFECTS ON SENSORY NEURONS [J].
CRAIN, SM ;
SHEN, KF .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1990, 11 (02) :77-81
[6]   PERTUSSIS TOXIN BLOCKS DEPRESSANT EFFECTS OF OPIOID, MONOAMINERGIC AND MUSCARINIC AGONISTS ON DORSAL-HORN NETWORK RESPONSES IN SPINAL CORD-GANGLION CULTURES [J].
CRAIN, SM ;
CRAIN, B ;
MAKMAN, MH .
BRAIN RESEARCH, 1987, 400 (01) :185-190
[7]   OPIOIDS EXCITE RATHER THAN INHIBIT SENSORY NEURONS AFTER CHRONIC OPIOID EXPOSURE OF SPINAL CORD-GANGLION CULTURES [J].
CRAIN, SM ;
SHEN, KF ;
CHALAZONITIS, A .
BRAIN RESEARCH, 1988, 455 (01) :99-109
[8]  
D'amour FE, 1941, J PHARMACOL EXP THER, V72, P74
[9]  
DEWEY WL, 1970, J PHARMACOL EXP THER, V175, P435
[10]   OPIOIDS AT LOW CONCENTRATION DECREASE OPENINGS OF K+ CHANNELS IN SENSORY GANGLION NEURONS [J].
FAN, SF ;
SHEN, KF ;
CRAIN, SM .
BRAIN RESEARCH, 1991, 558 (01) :166-170