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[环核苷酸对离体兔主动脉完整内皮细胞膜电位的影响]

[The effect of cyclic nucleotides on the membrane potential of intact endothelium of isolated rabbit aorta].

作者信息

Iarots'kyĭ V V, Sahach V F, Marchenko S M

机构信息

A. A. Bogomoletz Institute of Physiology, National Academy of Science of Ukraine, Kiev.

出版信息

Fiziol Zh (1994). 2001;47(6):3-9.

Abstract

The influence of intracellular cyclic nucleotides concentration increase on the membrane potential of intact endothelium of isolated rabbit aorta has been investigated. Both applications of bucladesine, an adenosine 3',5'-cyclic monophosphate (cAMP) membrane permeable analogue, and phoshophodiesterase blockers 3-isobutyl-1-methylxanthine (IBMX) and theophylline depolarized endothelial membrane. IBMX-induced depolarization was significantly smaller then theophylline-induced depolarization. It could be explained by the existence of IBMX-insensitive phosphodiesterases. Non-selective protein kinase blocker H-7 did not affect on the both IBMX-stimulated and non-stimulated membrane potential of aortic endothelium. It has been shown that the IBMX-induced depolarization and ATP-induced depolarization correlate with high correlation coefficient.

摘要

研究了细胞内环核苷酸浓度增加对离体兔主动脉完整内皮细胞膜电位的影响。应用双丁酰环磷腺苷(一种腺苷3',5'-环磷酸(cAMP)膜可渗透类似物)以及磷酸二酯酶阻滞剂3-异丁基-1-甲基黄嘌呤(IBMX)和茶碱均使内皮细胞膜去极化。IBMX诱导的去极化明显小于茶碱诱导的去极化。这可以用存在对IBMX不敏感的磷酸二酯酶来解释。非选择性蛋白激酶阻滞剂H-7对主动脉内皮细胞的IBMX刺激和未刺激的膜电位均无影响。已表明,IBMX诱导的去极化和ATP诱导的去极化具有高度相关系数。

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