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胆碱能磷脂酰肌醇对抑制性G蛋白偶联神经递质作用的调节:大鼠海马体的电生理研究

Cholinergic phosphatidylinositol modulation of inhibitory, G protein-linked neurotransmitter actions: electrophysiological studies in rat hippocampus.

作者信息

Worley P F, Baraban J M, McCarren M, Snyder S H, Alger B E

出版信息

Proc Natl Acad Sci U S A. 1987 May;84(10):3467-71. doi: 10.1073/pnas.84.10.3467.

Abstract

In electrophysiological studies using the rat hippocampal slice preparation, cholinergic agonists and phorbol 12,13-diacetate, a stimulator of protein kinase C, block the inhibitory actions of baclofen, a gamma-aminobutyric acid B receptor agonist, and adenosine. Relative potencies of cholinergic agonists in stimulating the phosphatidylinositol system, as measured biochemically, parallel their activity in blocking adenosine assessed electrophysiologically. Electrical stimulation of cholinergic afferents also reverses adenosine's inhibitory action. These findings indicate that stimulation of protein kinase C by the phosphatidylinositol system mediates cholinergic blockade of adenosine and baclofen. As these inhibitory agonists act by way of receptors linked to GTP-binding proteins, protein kinase C's inactivation of the GTP-binding protein involved may account for this cholinergic action.

摘要

在使用大鼠海马脑片标本的电生理研究中,胆碱能激动剂以及蛋白激酶C的激活剂佛波酯12,13 - 二乙酸酯,可阻断γ-氨基丁酸B受体激动剂巴氯芬和腺苷的抑制作用。通过生化方法测定,胆碱能激动剂刺激磷脂酰肌醇系统的相对效能,与其在电生理实验中阻断腺苷的活性平行。胆碱能传入纤维的电刺激也可逆转腺苷的抑制作用。这些发现表明,磷脂酰肌醇系统对蛋白激酶C的刺激介导了胆碱能系统对腺苷和巴氯芬的阻断作用。由于这些抑制性激动剂通过与鸟苷酸结合蛋白相连的受体发挥作用,蛋白激酶C使相关鸟苷酸结合蛋白失活可能是这种胆碱能作用的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ed/304892/b2ec06aa1c53/pnas00275-0397-a.jpg

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