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氟化物抑制激动剂诱导的大鼠皮质中肌醇磷酸的形成。

Fluoride inhibits agonist-induced formation of inositol phosphates in rat cortex.

作者信息

Godfrey P P, Watson S P

机构信息

Department of Clinical Pharmacology, Radcliffe Infirmary, Oxford, United Kingdom.

出版信息

Biochem Biophys Res Commun. 1988 Sep 15;155(2):664-9. doi: 10.1016/s0006-291x(88)80546-1.

Abstract

Sodium fluoride inhibited carbachol, 5-hydroxytryptamine and noradrenaline stimulated formation of inositol phosphates in rat cerebral cortex. For example, carbachol (1 mM) induced a 337% increase of inositol phosphates above basal in 30 min which was reduced to 69% in the presence of NaF (10 mM). The IC50 for NaF was approximately 1.5 mM and inhibition was mediated by a decrease in maxima of the carbachol dose response curve rather than a shift to the right. This inhibitory action was not mimicked by NaBr or NaI, or by agents which increase cAMP. Inhibition did not appear to result from a toxic action of NaF since it had no effect on the formation of inositol phosphates by high K+; moreover, in higher concentrations NaF stimulated phospholipase C activity. Since fluoride ions are known to activate G-proteins in the concentrations used in this study, these results may indicate the existence of a novel G-protein linked to receptor inhibition of phospholipase C.

摘要

氟化钠抑制了大鼠大脑皮层中由卡巴胆碱、5-羟色胺和去甲肾上腺素刺激形成的肌醇磷酸。例如,卡巴胆碱(1 mM)在30分钟内使肌醇磷酸的生成量比基础水平增加了337%,而在存在氟化钠(10 mM)的情况下,这一增加量降至69%。氟化钠的IC50约为1.5 mM,其抑制作用是通过降低卡巴胆碱剂量反应曲线的最大值来介导的,而不是向右移动。溴化钠、碘化钠或增加环磷酸腺苷(cAMP)的试剂均不能模拟这种抑制作用。抑制作用似乎并非由氟化钠的毒性作用引起,因为它对高钾诱导的肌醇磷酸生成没有影响;此外,在更高浓度下,氟化钠会刺激磷脂酶C的活性。由于已知氟离子在本研究使用的浓度下会激活G蛋白,这些结果可能表明存在一种与受体抑制磷脂酶C相关的新型G蛋白。

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