Narita M, Suzuki T, Misawa M, Nagase H
Department of Pharmacology, School of Pharmacy, Hoshi University, Tokyo, Japan.
Psychopharmacology (Berl). 1993;110(1-2):254-6. doi: 10.1007/BF02246982.
The Straub tail reaction (STR) induced by intracerebroventricular injection (ICV) of morphine was significantly antagonized by beta-funaltrexamine (beta-FNA, mu antagonist), given intracerebroventricularly (ICV), but not naltrindole given ICV (NTI, delta antagonist) or SC norbinaltorphimine given subcutaneously (SC) (nor-BNI, kappa antagonist). When given either SC or ICV the kappa-agonist, U-50,488 H markedly suppressed the STR elicited by ICV morphine; these effects were reversed by nor-BNI. These results suggest that the activation of supraspinal kappa receptors can inhibit the ICV morphine-induced STR which results from activation of supraspinal mu receptors.
脑室内注射吗啡所诱导的斯特劳布尾反应(STR),可被脑室内注射的β-氟纳曲酮(β-FNA,μ受体拮抗剂)显著拮抗,但不能被脑室内注射的纳曲吲哚(NTI,δ受体拮抗剂)或皮下注射的norbinaltorphimine(nor-BNI,κ受体拮抗剂)所拮抗。当κ受体激动剂U-50,488 H皮下或脑室内给药时,可显著抑制脑室内注射吗啡所诱发的STR;这些效应可被nor-BNI逆转。这些结果表明,脊髓上κ受体的激活可抑制由脊髓上μ受体激活所导致的脑室内注射吗啡诱发的STR。