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大麻素对突触膜酶的影响。I. 对从大鼠脑部分离出的突触膜的体外研究。

Effects of cannabinoids on synaptic membrane enzymes. I. In vitro studies on synaptic membranes isolated from rat brain.

作者信息

Olmsted C A

出版信息

Am J Drug Alcohol Abuse. 1976;3(3):485-505. doi: 10.3109/00952997609014289.

Abstract

The understanding of the effects of cannabinoids in human subjects has been obscured by a lack of knowledge about how the various active principles from marijuana act at the cellular level in the brain. For this reason the present study was undertaken to determine the effects of cannabinoids on the enzymes associated with the synaptic membranes. Electron micrographic analysis was performed to determine the purity of synaptic membrane preparations from rat brain, and subsequently such preparations were subjected to additions of ethanol, Tween-80, 80% glycerol, and either delta-tetrahydrocannabinol, 11-hydroxy-delta-tetrahydrocannabinol, or cannabinol. Both sodium and potassium activated ATPase (Na, K-ATPase), and Mg-ATPase were measured as the micrometer orthophosphate (P) released per minute per microgram membrane protein and these specific activities of the enzymes expressed as absolute values and as the percentage depression brought about by the cannabinoids. The ATPase spcific activities are taken from the rate curve over a 30-min incubation time. Additionally, synaptic membrane acetylcholineesterase specific activity was measured by continuous rate enzyme assay. While as low as 10 M delta-tetrahydrocannabinol showed appreciable decrements in both the membrane-bound ATPases, the other cannabinoids did not show such a great depression in enzyme activity. The specific activity of acetylcholinesterase, which is weakly bound to the membrane, showed only slight or no changes in activity with the various cannabinoids. It was additionally shown that the cannabinoids, delta-tetrahydrocannabinol in particular, bound to the synaptic membranes almost irreversibly in the in vitro system, and that the vehicle for dissolving the cannabinoids, while used as background control values when calculating the percentage decrements in enzyme specific activity, did vary the effects on the ATPase enzymes in particular. These data are discussed in relation to psychotomimetic activity of the cannabinoids.

摘要

由于缺乏关于大麻中各种活性成分如何在大脑细胞水平发挥作用的知识,人们对大麻素在人体中的作用的理解一直受到阻碍。因此,开展了本研究以确定大麻素对与突触膜相关的酶的影响。进行电子显微镜分析以确定大鼠脑突触膜制剂的纯度,随后将这些制剂添加乙醇、吐温 - 80、80%甘油,以及Δ - 四氢大麻酚、11 - 羟基 - Δ - 四氢大麻酚或大麻酚。钠钾激活的ATP酶(Na,K - ATPase)和镁ATP酶的活性通过每分钟每微克膜蛋白释放的微摩尔正磷酸盐(P)来测定,这些酶的比活性以绝对值以及大麻素引起的抑制百分比来表示。ATP酶的比活性取自30分钟孵育时间内的速率曲线。此外,通过连续速率酶测定法测量突触膜乙酰胆碱酯酶的比活性。虽然低至10 μM的Δ - 四氢大麻酚就使两种膜结合ATP酶的活性显著下降,但其他大麻素并未使酶活性出现如此大幅度的降低。与膜结合较弱的乙酰胆碱酯酶的比活性在使用各种大麻素时仅显示出轻微变化或无变化。此外还表明,大麻素,尤其是Δ - 四氢大麻酚,在体外系统中几乎不可逆地与突触膜结合,并且在计算酶比活性的降低百分比时用作背景对照值的溶解大麻素的载体,确实会特别改变对ATP酶的影响。这些数据结合大麻素的拟精神病活性进行了讨论。

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