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星形胶质细胞中环磷酸腺苷(cAMP)依赖性牛磺酸释放的失活。

Inactivation of cyclic AMP-dependent taurine release from astroglia.

作者信息

Shain W, Madelian V, Martin D L

机构信息

Laboratory of Neurotoxicology and Nervous System Disorders, Wadsworth Center for Laboratories and Research, Albany NY 12201.

出版信息

J Neurochem. 1989 May;52(5):1455-60. doi: 10.1111/j.1471-4159.1989.tb09193.x.

DOI:10.1111/j.1471-4159.1989.tb09193.x
PMID:2540271
Abstract

When astroglial cells are exposed to beta-adrenergic agonists for long periods of time (greater than 20 min), transient increases in taurine release and intracellular cyclic AMP (cAMP) are observed. Three phases of taurine release can be distinguished: activation, inactivation, and an elevated steady state. In this article, we present data describing the relationship between intracellular cAMP levels and inactivation of taurine release. To do this, we compared the apparent first-order rate constants for the inactivation of taurine release (ktau) with the apparent first-order rate constant for the decline of intracellular cAMP (kcAMP). We also measured ktau under experimental conditions that were chosen to provide a wide range of intracellular cAMP concentrations or to stimulate release without the involvement of the beta-adrenergic receptor and adenylate cyclase. When taurine release was stimulated with a saturating concentration of isoproterenol, the inactivation of release was significantly faster than the decline of intracellular cAMP. Furthermore, there were no significant differences in ktau measured under any of the experimental conditions used. Thus, inactivation of taurine release does not involve changes in the activity of the beta-adrenergic receptor and adenylate cyclase, i.e., desensitization, and appears to be independent of the intracellular concentration of cAMP. These results indicate that cAMP-mediated events can be regulated by mechanism(s) in addition to those that control receptor-adenylate cyclase interactions and the synthesis of cAMP.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

当星形胶质细胞长时间(超过20分钟)暴露于β-肾上腺素能激动剂时,可观察到牛磺酸释放和细胞内环磷酸腺苷(cAMP)的短暂增加。牛磺酸释放可分为三个阶段:激活、失活和升高的稳态。在本文中,我们展示了描述细胞内cAMP水平与牛磺酸释放失活之间关系的数据。为此,我们将牛磺酸释放失活的表观一级速率常数(ktau)与细胞内cAMP下降的表观一级速率常数(kcAMP)进行了比较。我们还在选择用于提供广泛细胞内cAMP浓度范围或在不涉及β-肾上腺素能受体和腺苷酸环化酶的情况下刺激释放的实验条件下测量了ktau。当用饱和浓度的异丙肾上腺素刺激牛磺酸释放时,释放的失活明显快于细胞内cAMP的下降。此外,在所使用的任何实验条件下测量的ktau均无显著差异。因此,牛磺酸释放的失活不涉及β-肾上腺素能受体和腺苷酸环化酶的活性变化,即脱敏,并且似乎与细胞内cAMP浓度无关。这些结果表明,除了控制受体-腺苷酸环化酶相互作用和cAMP合成的机制外,cAMP介导的事件还可由其他机制调节。(摘要截短于250字)

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