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成年大鼠α1 - 肾上腺素能受体刺激的和匀浆心肌细胞中肌醇磷酸的代谢

Metabolism of inositol phosphates in alpha 1-adrenoceptor-stimulated and homogenized cardiac myocytes of adult rats.

作者信息

Guse A H, Berg I, Gercken G

机构信息

Institute of Biochemistry and Food Chemistry, Department of Biochemistry, Hamburg, Federal Republic of Germany.

出版信息

Biochem J. 1989 Jul 1;261(1):89-92. doi: 10.1042/bj2610089.

Abstract

Previous studies demonstrated the accumulation of inositol mono- and poly-phosphates in carbamoylcholine-stimulated cultured cardiac ventricular myocytes of adult rats [Berg, Guse & Gercken (1989) Biochim. Biophys. Acta 1010, 100-107]. Stimulation with noradrenaline (50 microM) in the presence of propranolol (10 microM) led to a time-dependent pattern of inositol mono- and poly-phosphates in cultured cardiac-ventricular myocytes. Ins(1,4,5)P3 and Ins(1,3,4,5)P4 increased in a rapid initial phase. The degradation products of Ins(1,4,5)P3, namely Ins(1,4)P2 and Ins(4)P, accumulated between 1 and 15 min. Ins(1,3,4,5)P4 was rapidly dephosphorylated to Ins(1,3,4)P3, which was then metabolized to Ins(1,3)P2 and Ins(3,4)P2. The last two InsP2 isomers and their degradation products, Ins(1)P and Ins(3)P (determined as an enantiomeric mixture), increased at extended stimulation periods. To confirm the pathway of Ins(1,3,4,5)P4 degradation, homogenates of isolated ventricular myocytes were incubated with [3H]INs(1,3,4,5)P4. The subsequent products were Ins(1,3,4)P3, Ins(3,4)P2, Ins(1,3)P2 and InsP. The effect of noradrenaline was antagonized by prazosin (0.1 microM), but not by yohimbine (0.1 microM), indicating phosphoinositidase activation via the alpha 1-adrenoceptor.

摘要

先前的研究表明,在成年大鼠的氨甲酰胆碱刺激的培养心室肌细胞中,肌醇单磷酸和多磷酸会积累[伯格、古斯和格肯(1989年),《生物化学与生物物理学报》1010卷,第100 - 107页]。在普萘洛尔(10微摩尔)存在的情况下,用去甲肾上腺素(50微摩尔)刺激培养的心室肌细胞,会导致肌醇单磷酸和多磷酸出现时间依赖性模式。肌醇-1,4,5-三磷酸(Ins(1,4,5)P3)和肌醇-1,3,4,5-四磷酸(Ins(1,3,4,5)P4)在初始快速阶段增加。Ins(1,4,5)P3的降解产物,即肌醇-1,4-二磷酸(Ins(1,4)P2)和肌醇-4-磷酸(Ins(4)P),在1至15分钟之间积累。Ins(1,3,4,5)P4迅速去磷酸化为肌醇-1,3,4-三磷酸(Ins(1,3,4)P3),然后再代谢为肌醇-1,3-二磷酸(Ins(1,3)P2)和肌醇-3,4-二磷酸(Ins(3,4)P2)。最后这两种InsP2异构体及其降解产物,肌醇-1-磷酸(Ins(1)P)和肌醇-3-磷酸(Ins(3)P,以对映体混合物形式测定),在延长刺激期时增加。为了证实Ins(1,3,4,5)P4的降解途径,将分离的心室肌细胞匀浆与[3H]Ins(1,3,4,5)P4一起孵育。随后的产物是Ins(1,3,4)P3、Ins(3,4)P2、Ins(1,3)P2和肌醇磷酸(InsP)。去甲肾上腺素的作用被哌唑嗪(0.1微摩尔)拮抗,但不被育亨宾(0.1微摩尔)拮抗,这表明通过α1-肾上腺素能受体激活了磷酸肌醇酶。

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