1,3-DI-O-TOLYLGUANIDINE (DTG) DIFFERENTIALLY AFFECTS ACUTE AND TONIC FORMALIN PAIN - ANTAGONISM BY RIMCAZOLE

被引:11
作者
KEST, B
MOGIL, JS
STERNBERG, WF
PECHNICK, RN
LIEBESKIND, JC
机构
[1] UNIV CALIF LOS ANGELES,DEPT PSYCHOL,LOS ANGELES,CA 90024
[2] UNIV CALIF LOS ANGELES,BRAIN RES INST,LOS ANGELES,CA 90024
[3] UNIV CALIF LOS ANGELES,INST NEUROPSYCHIAT,DEPT PSYCHIAT & BIOBEHAV SCI,LOS ANGELES,CA 90024
[4] VET ADM MED CTR,RES SERV 151W,PORTLAND,OR 97201
[5] LOUISIANA STATE UNIV,MED CTR,DEPT PHARMACOL,NEW ORLEANS,LA 70119
关键词
SIGMA RECEPTOR; ANTINOCICEPTION; HYPERALGESIA; MICE;
D O I
10.1016/0091-3057(95)00085-B
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
The role of the sigma receptor in prolonged pain was examined by assessing the effects of 1,3,di-o-tolylguanidine (DTG), a selective sigma receptor ligand, on the formalin test in mice. Formalin injected subcutaneously into the hindpaw produces a biphasic pain response: an acute phase of short duration followed by a longer-lasting tonic phase. DTG (10 mg/kg, IP) potently reduced pain behavior in the acute phase but increased pain behavior in the tonic phase. Rimcazole (5 and 10 mg/kg, IP), a selective sigma receptor antagonist, blocked both the DTG-induced decrease and increase in pain behavior observed in the acute and tonic phases, respectively. These data support previous findings indicating a modulatory role for the sigma receptor in nociceptive processes, and suggest that this receptor differentially modulates acute vs. tonic pain.
引用
收藏
页码:175 / 178
页数:4
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