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抗抑郁药对大鼠大脑皮质细胞膜中腺苷酸环化酶的GTP结合蛋白的直接影响。

Direct influence of antidepressants on GTP binding protein of adenylate cyclase in cell membranes of the cerebral cortex of rats.

作者信息

Yamaoka K, Nanba T, Nomura S

机构信息

Department of Neuropsychiatry, Fujita-Gakuen Health University, School of Medicine, Aichi, Japan.

出版信息

J Neural Transm. 1988;71(3):165-75. doi: 10.1007/BF01245710.

Abstract

Recently, it has been suggested that antidepressant drugs exert their pharmacological action through functional changes in the adrenergic-receptor coupled adenylate cyclase system. In the present research, we examined the direct effects of antidepressants on adenylate cyclase (A-cyclase) activity by in vitro incubation of cell membranes from the cerebral cortex of rats with these drugs. All antidepressants examined, such as imipramine, clomipramine, amitriptyline, desipramine, mianserin and zimelidine inhibited A-cyclase in a dose dependent manner. Antidepressants did not exert any influence on Mn2+-induced elevation of A-cyclase, but significantly suppressed F(-)-stimulated A-cyclase activity. GTP-induced elevation of A-cyclase was completely inhibited by prior incubation with antidepressants. Our conclusion, therefore, is that antidepressants may reduce A-cyclase activity not by inhibiting the function of the catalytic unit of A-cyclase, but by suppressing the N-protein function.

摘要

最近,有人提出抗抑郁药物通过肾上腺素能受体偶联腺苷酸环化酶系统的功能变化发挥其药理作用。在本研究中,我们通过用这些药物体外孵育大鼠大脑皮质细胞膜来检测抗抑郁药对腺苷酸环化酶(A-环化酶)活性的直接影响。所检测的所有抗抑郁药,如丙咪嗪、氯米帕明、阿米替林、地昔帕明、米安色林和齐美利定,均以剂量依赖的方式抑制A-环化酶。抗抑郁药对锰离子诱导的A-环化酶升高没有任何影响,但显著抑制氟离子刺激的A-环化酶活性。预先用抗抑郁药孵育可完全抑制鸟苷三磷酸(GTP)诱导的A-环化酶升高。因此,我们的结论是,抗抑郁药可能不是通过抑制A-环化酶催化单位的功能,而是通过抑制N蛋白功能来降低A-环化酶活性。

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