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大麻提取物而非Δ1-四氢大麻酚可抑制人脑和肝脏中的单胺氧化酶。

Cannabis extract, but not delta 1-tetrahydrocannabinol, inhibits human brain and liver monoamine oxidase.

作者信息

Schurr A, Rigor B M

出版信息

Gen Pharmacol. 1984;15(2):171-4. doi: 10.1016/0306-3623(84)90104-6.

Abstract

Mitochondrial monoamine oxidase (MAO) of human brain and liver was inhibited by low concentrations of cannabis extract (CE) and a cannabinoid fraction isolated from it. delta 1-Tetrahydrocannabinol (THC) did not elicit any inhibitory effect on the enzyme. The inhibition of MAO activity by CE and by its active fraction was more pronounced when the monoamine substrates 2-phenylethylamine (PEA) and benzylamine (BA) were used, as compared to the inhibition of the enzyme activity when 5-hydroxytryptamine was the substrate. The active cannabinoid fraction was found to be more potent than CE in inhibiting the activity of MAO with either substrate. The isolated fraction contains at least two cannabinoids with Rf values of 0.67 and 0.71 on silica gel thin layer chromatography (TLC), as determined with toluene/chloroform/methanol (100:10:1, by volume) as the solvent system. The findings of this study emphasize the need for further exploration of the potential of cannabis as a source for therapeutic agents.

摘要

人脑和肝脏中的线粒体单胺氧化酶(MAO)受到低浓度大麻提取物(CE)及其分离出的大麻素组分的抑制。δ1-四氢大麻酚(THC)对该酶没有任何抑制作用。与以5-羟色胺为底物时对酶活性的抑制相比,当使用单胺底物2-苯乙胺(PEA)和苄胺(BA)时,CE及其活性组分对MAO活性的抑制作用更明显。发现活性大麻素组分在抑制两种底物的MAO活性方面比CE更有效。在以甲苯/氯仿/甲醇(体积比为100:10:1)为溶剂系统的硅胶薄层色谱(TLC)上,分离出的组分含有至少两种大麻素,其Rf值分别为0.67和0.71。本研究结果强调有必要进一步探索大麻作为治疗药物来源的潜力。

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