Capasso Anna, Loizzo Alberto
Department of Pharmaceutical Sciences, University of Salerno, Fisciano (Salerno), Italy.
Phytother Res. 2003 Aug;17(7):774-7. doi: 10.1002/ptr.1234.
In the present work the effect of papaverine, a non specific smooth muscle relaxant, was investigated on the naloxone-precipitated withdrawal contracture of the acute morphine-dependent guinea-pig ileum in vitro. Furthermore, the effect of papaverine was also considered on DAGO (highly selective mu -agonist) and U50-488H (highly selective k-agonist) withdrawal to test whether the possible interaction of papaverine on opioid withdrawal involves mu - and/or k-opioid receptors. Following a 4 min in vitro exposure to opioid agonist, the guinea-pig isolated ileum exhibited a strong contracture after the addition of naloxone. Papaverine treatment (1 x 10(-7) - 5 x 10(-7) - 1 x 10(-6) M) before or after the opioid agonists was able of both preventing and reversing the naloxone-induced contracture after exposure to mu (morphine and DAGO) or k (U50-488H) opiate agonists in a concentration-dependent fascion. Both acetylcholine response and electrical stimulation were not affected by papaverine treatment whereas the final opiate withdrawal was still reduced. The results of the present study indicate that papaverine was able to produce significative influence on the opiate withdrawal in vitro and papaverine was able to exert its effect both at mu and k opioid agonists.
在本研究中,研究了非特异性平滑肌松弛剂罂粟碱对急性吗啡依赖的豚鼠离体回肠中纳洛酮诱发的戒断挛缩的影响。此外,还考察了罂粟碱对DAGO(高选择性μ激动剂)和U50-488H(高选择性κ激动剂)戒断的影响,以测试罂粟碱对阿片类药物戒断的可能相互作用是否涉及μ和/或κ阿片受体。在体外暴露于阿片类激动剂4分钟后,加入纳洛酮后,豚鼠离体回肠出现强烈挛缩。在阿片类激动剂之前或之后进行罂粟碱处理(1×10⁻⁷ - 5×10⁻⁷ - 1×10⁻⁶ M),能够在浓度依赖性方式下预防和逆转在暴露于μ(吗啡和DAGO)或κ(U50-488H)阿片类激动剂后纳洛酮诱导的挛缩。罂粟碱处理对乙酰胆碱反应和电刺激均无影响,而最终的阿片类药物戒断仍有所减轻。本研究结果表明,罂粟碱能够在体外对阿片类药物戒断产生显著影响,并且罂粟碱能够在μ和κ阿片类激动剂上发挥其作用。