ASSOCIATION OF THE PEPTIDASE INHIBITOR RB-101 AND A CCK-B ANTAGONIST STRONGLY ENHANCES ANTINOCICEPTIVE RESPONSES

被引:52
作者
MALDONADO, R [1 ]
DERRIEN, M [1 ]
NOBLE, F [1 ]
ROQUES, BP [1 ]
机构
[1] UNIV PARIS 05,FAC SCI PHARMACEUT & BIOL,CNRS,URA D1500,INSERM,U266,F-75270 PARIS 06,FRANCE
关键词
RB-101; L-365,260; ENDOGENOUS ENKEPHALINS; CHOLECYSTOKININ; CCK-B RECEPTORS; ANTINOCICEPTION;
D O I
10.1097/00001756-199307000-00028
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
THE brain peptide cholecystokinin (CCK) has been shown to counteract the analgesic effects of morphine suggesting a physiological antagonism between opioid and CCK neural systems. This has been definitely demonstrated in this study by co-administration of the CCK-B selective antagonist L-365,260 with RB 101, a systemically active inhibitor of peptidases, which fully protects the endogenous opioids, the enkephalins, from their inactivation. The naloxone reversible analgesic effects induced by RB 101 in the mouse hot-plate and rat tail-flick tests were strongly increased by low doses of L-365,260. These results could have important clinical applications by reducing the efficient dose of RB 101, which has recently been shown to be practically devoid of morphine-like side-effects.
引用
收藏
页码:947 / 950
页数:4
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