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δ9-四氢大麻酚及其他大麻素对突触体中环磷酸腺苷积累的影响。

The effects of delta 9-tetrahydrocannabinol and other cannabinoids on cAMP accumulation in synaptosomes.

作者信息

Little P J, Martin B R

机构信息

Department of Pharmacology and Toxicology, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298-0613.

出版信息

Life Sci. 1991;48(12):1133-41. doi: 10.1016/0024-3205(91)90450-p.

Abstract

The effects of delta 9-THC and other cannabinoids on cAMP levels in synaptosomes from mouse brains were investigated in order to determine whether cannabinoids produced their behavioral effects through alterations in adenylate cyclase. delta 9-THC (0.01-10 microM) did not significantly alter basal cAMP levels, whereas delta 9-THC and other cannabinoids were able to alter forskolin-stimulated cAMP levels in synaptosomes. In general, three kinds of responses were observed. Some cannabinoids displayed a modest, concentration-dependent decrease in cAMP levels, producing significant inhibition between 1-10 microM. Other cannabinoids, including delta 9-THC and delta 8-THC, appeared to produce a biphasic effect in that inhibition of cAMP was observed only at a single concentration. Finally, some analogs were unable to significantly alter forskolin-stimulated cAMP. There was not a clear relationship between the ability of the cannabinoids to alter cAMP levels in synaptosomes and the behavioral effects observed in mice. However, it was demonstrated that the analogs which are the most potent in producing cannabimimetic effects in mice were the analogs which inhibited cAMP in a concentration-dependent manner. While cannabinoids were able to alter cAMP levels in synaptosomes, the ability to alter cAMP levels does not appear to be absolutely necessary for the production of cannabinoid effects in mice.

摘要

为了确定大麻素是否通过改变腺苷酸环化酶来产生其行为效应,研究了δ9-四氢大麻酚(delta 9-THC)和其他大麻素对小鼠脑突触体中cAMP水平的影响。δ9-四氢大麻酚(0.01 - 10微摩尔)并未显著改变基础cAMP水平,而δ9-四氢大麻酚和其他大麻素能够改变突触体中福司可林刺激的cAMP水平。一般来说,观察到三种反应。一些大麻素表现出适度的、浓度依赖性的cAMP水平降低,在1 - 10微摩尔之间产生显著抑制。其他大麻素,包括δ9-四氢大麻酚和δ8-四氢大麻酚,似乎产生双相效应,即仅在单一浓度下观察到对cAMP的抑制。最后,一些类似物无法显著改变福司可林刺激的cAMP。大麻素改变突触体中cAMP水平的能力与在小鼠中观察到的行为效应之间没有明确的关系。然而,已证明在小鼠中产生大麻模拟效应最有效的类似物是以浓度依赖性方式抑制cAMP的类似物。虽然大麻素能够改变突触体中的cAMP水平,但改变cAMP水平的能力似乎并非小鼠产生大麻素效应所绝对必需的。

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