The partial agonist properties of levocabastine in neurotensin-induced analgesia

被引:38
作者
Dubuc, I [1 ]
Remande, S [1 ]
Costentin, J [1 ]
机构
[1] Fac Med & Pharm, Int Fed Rech Multidisciplinaire Peptides, Unit Neuropsychopharmacol Expt, CNRS,UPRESA 6036,IFRMP 23, F-76800 St Etienne, France
关键词
levocabastine; neurotensin; analgesia; neurotensin low affinity receptor; hypothermia;
D O I
10.1016/S0014-2999(99)00554-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The antihistaminic drug levocabastine is a ligand for the low affinity neurotensin receptor (NTS2). Its intracerebroventricular administration to mice induced a significant analgesia in the writhing test but not in the hot plate test. In the writhing test, levocabastine decreased neurotensin-induced analgesia to a level not significantly different from the effects of levocabastine alone. In the hot plate test, levocabastine had no analgesic effect but completely reversed the neurotensin-induced analgesia. Mepyramine, another antihistaminic drug, did not share these levocabastine effects. Neither levocabastine nor mepyramine modified the colonic temperature or reversed the neurotensin-induced hypothermia. Thus, levocabastine behaves as a partial agonist at neurotensin NTS2 receptors, which are involved in visceral nociception, but not at yet unidentified neurotensin receptors involved in hypothermia. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:9 / 12
页数:4
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