新型房钠肽受体非肽拮抗剂HS-142-1的分离纯化。

Y. Morishita, Mitsuru Takahashi, T. Sano, I. Kawamoto, K. Ando, H. Sano, Y. Saitoh, H. Kase, Y. Matsuda
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引用次数: 18

摘要

在筛选微生物来源的心房利钠肽(ANP)受体配体的过程中,我们从金黄色担子菌(Aureo-basidium pullulans vars . melanigenum)培养液中分离出一种新的非肽类ANP拮抗剂HS-142-1。结构分析表明,HS-142-1由20 ~ 30种经己基酯化的β-1,6-葡聚糖组成;每种成分的效力几乎相等。HS-142-1抑制兔肾皮质膜[125I]-rANP与其受体结合的IC50为0.3μg/ml,并呈剂量依赖性地拮抗anp诱导的牛肺膜cGMP产生。这种非肽类ANP拮抗剂HS-142-1的发现将为研究利钠肽系统的生理意义提供有用的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolation and Purification of HS-142-1, a Novel Nonpeptide Antagonist for the Atrial Natriuretic Peptide Receptor, from Aureobasidium sp.
During the screening program for atrial natriuretic peptide (ANP) receptor ligands of microbial origin, we isolated a novel nonpeptide ANP antagonist, HS-142-1, from a culture broth of Aureo-basidium pullulans var. melanigenum. Structural analysis showed that HS-142-1 was composed of 20–30 kinds of β-1,6-glucan esterified by caproyl groups; each component had an almost equal potency. HS-142-1 inhibited [125I]-rANP binding to its receptor in rabbit kidney cortex membranes with an IC50 of 0.3μg/ml and antagonized ANP-induced cGMP production by bovine lung membranes in a dose-dependent fashion. The discovery of this nonpeptide ANP antagonist, HS-142-1, will provide a useful tool to study the physiological significance of natriuretic peptide system.
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