CALCIUM-CHANNEL ANTAGONISTS AND ADENOSINE-ANALOGS DECREASE TOLERANCE TO OPIATE PENTAZOCINE AND U-50488H

被引:8
作者
CONTRERAS, E [1 ]
QUIJADA, L [1 ]
GERMANY, A [1 ]
FLECKENSTEIN, R [1 ]
HERNANDEZ, A [1 ]
机构
[1] UNIV CHILE, INST NUTR & FOOD TECHNOL, NEUROPHYSIOL & BIOPHYS UNIT, SANTIAGO, CHILE
来源
GENERAL PHARMACOLOGY-THE VASCULAR SYSTEM | 1993年 / 24卷 / 05期
关键词
D O I
10.1016/0306-3623(93)90369-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. A single dose of pentazocine induces cross-tolerance the analgesic effects of the kappa agonist U 50488H. Tolerance is observed by means of the hot plate test or by the i.p. administration of acetic acid 6 or 24 hr after the priming dose, respectively. 2. The administration of the calcium channel antagonists, diltiazem, nifedipine or verapamil, reduces the degree of tolerance as assessed by the hot plate test or acetic acid administration. 3. The adenosine agonist N6-cyclopentyl adenosine significantly reduced the intensity of the process; in contrast, N6-cyclohexyladenosine antagonized the analgesic response to the opiate obscuring its influence on the process. 4. The results are discussed in relation to the interaction of calcium channel function in the analgesic response to the kappa opiates.
引用
收藏
页码:1203 / 1206
页数:4
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