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左诺曲朵对大鼠海马体和纹状体中乙酰胆碱周转的抑制作用。

Levonantradol-induced inhibition of acetylcholine turnover in rat hippocampus and striatum.

作者信息

Costa E, Cheney D L, Murray T F

出版信息

J Clin Pharmacol. 1981 Aug-Sep;21(S1):256S-261S. doi: 10.1002/j.1552-4604.1981.tb02603.x.

Abstract

The effects of levonantradol, a structural novel cannabinoid-related analgesic, on the turnover rate of acetylcholine (TRACh) have been studied in various regions of the rat brain. Levonantradol (0.3 mg/kg subcutaneously) decreases the tRACh in the hippocampus and striatum by 53 and 30 per cent, respectively. The extent of the reduction in TRACh is dose dependent, with a maximal decrease of 80 per cent in the hippocampus and 57 per cent in the striatum following the 3 mg/kg dose. In contrast, cortical TRACh is not affected by any dose of levonantradol. This pattern of activity on cholinergic dynamics elicited by levonantradol is qualitatively similar to that of cannabinoids but differs from that previously reported for narcotic analgesics. Moreover naltrexone (2 mg/kg intraperitoneally) does not reverse the effects of levonantradol on striatal or hippocampal TRACh. This pattern of activity on cholinergic dynamics elicited by levonantradol is consistent with a cannabinoid-like rather than an opioid-like mode of action.

摘要

新型结构大麻素类镇痛药左南曲朵对大鼠脑不同区域乙酰胆碱周转率(TRACh)的影响已得到研究。左南曲朵(皮下注射0.3毫克/千克)使海马体和纹状体中的TRACh分别降低53%和30%。TRACh的降低程度呈剂量依赖性,3毫克/千克剂量后,海马体中最大降幅为80%,纹状体中为57%。相比之下,任何剂量的左南曲朵均不影响皮质TRACh。左南曲朵引发的这种胆碱能动力学活性模式在性质上与大麻素相似,但与先前报道的麻醉性镇痛药不同。此外,纳曲酮(腹腔注射2毫克/千克)不能逆转左南曲朵对纹状体或海马体TRACh的作用。左南曲朵引发的这种胆碱能动力学活性模式与类大麻素而非类阿片样作用模式一致。

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