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海参毒素:一种牛脑3'-5'磷酸二酯酶的激活剂。

Holothurin: an activator of bovine brain 3'-5' phosphodiesterase.

作者信息

Vig P J, Mehrotra B D, Desaiah D

机构信息

Department of Neurology, University of Mississippi Medical Center, Jackson 39216.

出版信息

Res Commun Chem Pathol Pharmacol. 1990 Mar;67(3):419-22.

PMID:1693008
Abstract

The effect of marine toxin, holothurin A, on calmodulin(CaM)-dependent bovine brain 3'-5' phosphodiesterase (PDE) was studied. Holothurin stimulated CaM-depleted PDE in a concentration dependent manner and this interaction was independent of Ca2+ concentrations. Activation of PDE by holothurin was pH and incubation temperature dependent. Heat treatment of holothurin (at 95 degrees C) at various time intervals (2-8 min) decreased its ability to stimulate PDE. CaM-dependent dependent PDE activity was decreased by holothurin. CaM antagonist W-7 and an organochlorine compound chlordecone significantly inhibited holothurin stimulated PDE. These data indicate that holothurin activates CaM-deficient 3'-5' PDE which is antagonized by classical CaM antagonists.

摘要

研究了海洋毒素海参毒素A对钙调蛋白(CaM)依赖性牛脑3'-5'磷酸二酯酶(PDE)的影响。海参毒素以浓度依赖性方式刺激CaM缺失的PDE,且这种相互作用与Ca2+浓度无关。海参毒素对PDE的激活作用依赖于pH值和孵育温度。在不同时间间隔(2 - 8分钟)对海参毒素进行热处理(95摄氏度)会降低其刺激PDE的能力。CaM依赖性PDE活性被海参毒素降低。CaM拮抗剂W - 7和有机氯化合物开蓬显著抑制海参毒素刺激的PDE。这些数据表明,海参毒素激活CaM缺陷的3'-5' PDE,而经典的CaM拮抗剂可拮抗这种激活作用。

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