L-740,093, a new antagonist of the CCK-B receptor, potentiates the antinociceptive effect of morphine: Electrophysiological and behavioural studies

被引:6
作者
Xu, XJ
Hoffmann, O
WiesenfeldHallin, Z
机构
[1] HUDDINGE UNIV HOSP,KAROLINSKA INST,DEPT MED LAB SCI & TECHNOL,CLIN NEUROPHYSIOL SECT,S-14186 HUDDINGE,SWEDEN
[2] SABBATSBERGS HOSP,DRUG ABUSE CLIN,S-11382 STOCKHOLM,SWEDEN
关键词
D O I
10.1016/S0143-4179(96)90088-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The interaction between morphine and L740,093, a newly developed highly potent antagonist of cholecystokinin-B receptors, was examined in electrophysiological and behavioural studies. intravenous L740, 093 at 0.01 mg/kg had no effect on its own, but significantly potentiated the depressive effect of 1 mg/kg morphine on the nociceptive flexor reflex in decerebrate, spinalized rats. Similarly, subcutaneous L740, 093 at 0.03 mg/kg significantly prolonged the duration of antinociception induced by 10 mg/kg morphine in the rat hotplate test. A bell shaped dose-response curve was noted in the behavioural studies with respect to the interaction between L740,094 and morphine. L740,093, which has excellent CNS penetration, may represent a new tool in studying the involvement of the endogenous cholecystokinin system in the modulation of opioid analgesia and in exploring novel analgesics.
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收藏
页码:203 / 206
页数:4
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