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刺激剥夺会增加松果体的Gsα和Gβ。

Stimulus deprivation increases pineal Gs alpha and G beta.

作者信息

Babila T, Klein D C

机构信息

Section on Neuroendocrinology, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

J Neurochem. 1992 Oct;59(4):1356-62. doi: 10.1111/j.1471-4159.1992.tb08448.x.

Abstract

Denervation and other forms of stimulus deprivation cause an increase in the magnitude of subsequent responses, a phenomenon commonly referred to as denervation supersensitivity. This has been well demonstrated with the cyclic AMP response to norepinephrine in the pineal gland. In the present report, we address the question of whether stimulus deprivation alters alpha and beta subunits of the GTP binding regulatory protein that stimulates adenylyl cyclase activity (Gs). Stimulus deprivation of the pineal gland was produced by denervation (superior cervical ganglionectomy), decentralization of the superior cervical ganglia, or by exposure of the animal to continuous lighting. All increased both the alpha and beta subunits of Gs (Gs alpha and G beta) by up to fourfold, as estimated using semiquantitative western blot technology. These effects were detectable after 1 day of stimulus deprivation and were sustained for 2 weeks. The stimulatory effects of constant light-induced stimulus deprivation were also apparent by measuring cholera toxin-dependent ADP-ribosylation of Gs alpha, which revealed a four-fold increase in the amount of labeled substrate. The results of in vivo studies were confirmed with in vitro studies, which demonstrated a spontaneous increase in both Gs alpha and G beta during 72 h of organ culture. The constant light-induced increases in both Gs alpha and G beta were prevented by continuous administration of isoproterenol (0.3 mg/kg/day), supporting the suggestion that adrenergic stimulation controls the levels of Gs alpha and G beta. These studies indicate that stimulus deprivation increases both Gs alpha and G beta.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

去神经支配及其他形式的刺激剥夺会导致后续反应强度增加,这一现象通常被称为去神经超敏反应。这已在松果体中去甲肾上腺素引起的环磷酸腺苷(cAMP)反应中得到充分证明。在本报告中,我们探讨刺激剥夺是否会改变刺激腺苷酸环化酶活性的GTP结合调节蛋白(Gs)的α和β亚基。松果体的刺激剥夺通过去神经支配(颈上神经节切除术)、颈上神经节分散或使动物持续暴露于光照来产生。使用半定量蛋白质免疫印迹技术估计,所有这些方法均使Gs的α和β亚基(Gsα和Gsβ)增加了四倍之多。这些效应在刺激剥夺1天后即可检测到,并持续2周。通过测量霍乱毒素依赖的Gsα的ADP核糖基化,也可明显看出持续光照诱导的刺激剥夺的刺激作用,这显示标记底物的量增加了四倍。体内研究结果在体外研究中得到证实,体外研究表明在器官培养72小时期间Gsα和Gsβ均自发增加。持续给予异丙肾上腺素(0.3毫克/千克/天)可防止持续光照诱导的Gsα和Gsβ增加,这支持了肾上腺素能刺激控制Gsα和Gsβ水平的观点。这些研究表明,刺激剥夺会使Gsα和Gsβ均增加。(摘要截选至250字)

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