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HS-142-1是一种新型的微生物来源多糖,它能特异性识别大鼠肾小球中与鸟苷酸环化酶相连的心房钠尿肽受体。

HS-142-1, a novel polysaccharide of microbial origin, specifically recognizes guanylyl cyclase-linked ANP receptor in rat glomeruli.

作者信息

Sano T, Imura R, Morishita Y, Matsuda Y, Yamada K

机构信息

Tokyo Research Laboratories, Kyowa Hakko Kogyo Co., Ltd., Japan.

出版信息

Life Sci. 1992;51(18):1445-51. doi: 10.1016/0024-3205(92)90539-2.

DOI:10.1016/0024-3205(92)90539-2
PMID:1357523
Abstract

HS-142-1, a novel polysaccharide, of microbial origin had been characterized as a specific antagonist of guanylyl cyclase-linked atrial natriuretic peptide (ANP) receptors (ANP-GC receptor) in bovine adrenal cortex. The effect of HS-142-1 on ANP receptors of rat glomeruli were examined. HS-142-1 blocked rat ANP (r-ANP)-stimulated cGMP production in a concentration-dependent manner, although it caused only slight inhibition in the specific binding of [125I]-rANP to the glomeruli where only a small portion of the binding sites are coupled to guanylyl cyclase. HS-142-1 recognized the 135K ANP receptor which is thought to be ANP-GC receptors but did not recognized 60K receptor, guanylyl cyclase-free type from affinity cross-linking studies with glomerular membranes. These results indicate that HS-142-1 is a specific antagonist for the ANP-GC receptor in rat glomeruli, and that it will be a powerful tool for understanding the physiological roles of ANP in renal responses.

摘要

HS - 142 - 1是一种源自微生物的新型多糖,已被鉴定为牛肾上腺皮质中鸟苷酸环化酶连接型心钠素(ANP)受体(ANP - GC受体)的特异性拮抗剂。研究了HS - 142 - 1对大鼠肾小球ANP受体的作用。HS - 142 - 1以浓度依赖性方式阻断大鼠ANP(r - ANP)刺激的cGMP生成,尽管它对[125I] - rANP与肾小球的特异性结合仅产生轻微抑制,而在肾小球中只有一小部分结合位点与鸟苷酸环化酶偶联。通过与肾小球膜的亲和交联研究,HS - 142 - 1识别被认为是ANP - GC受体的135K ANP受体,但不识别60K受体(无鸟苷酸环化酶型)。这些结果表明,HS - 142 - 1是大鼠肾小球中ANP - GC受体的特异性拮抗剂,并且它将成为理解ANP在肾脏反应中的生理作用的有力工具。

相似文献

1
HS-142-1, a novel polysaccharide of microbial origin, specifically recognizes guanylyl cyclase-linked ANP receptor in rat glomeruli.HS-142-1是一种新型的微生物来源多糖,它能特异性识别大鼠肾小球中与鸟苷酸环化酶相连的心房钠尿肽受体。
Life Sci. 1992;51(18):1445-51. doi: 10.1016/0024-3205(92)90539-2.
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Inhibition by HS-142-1, a novel nonpeptide atrial natriuretic peptide antagonist of microbial origin, of atrial natriuretic peptide-induced relaxation of isolated rabbit aorta through the blockade of guanylyl cyclase-linked receptors.HS-142-1(一种新型的源自微生物的非肽类心房利钠肽拮抗剂)通过阻断鸟苷酸环化酶连接受体,抑制心房利钠肽诱导的离体兔主动脉舒张。
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HS-142-1, a novel nonpeptide atrial natriuretic peptide (ANP) antagonist, blocks ANP-induced renal responses through a specific interaction with guanylyl cyclase-linked receptors.HS-142-1是一种新型非肽类心房利钠肽(ANP)拮抗剂,它通过与鸟苷酸环化酶连接受体的特异性相互作用来阻断ANP诱导的肾脏反应。
Eur J Pharmacol. 1992 Mar 12;225(3):203-7. doi: 10.1016/0922-4106(92)90021-m.
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Pharmacological profile of HS-142-1, a novel nonpeptide atrial natriuretic peptide antagonist of microbial origin. I. Selective inhibition of the actions of natriuretic peptides in anesthetized rats.HS-142-1的药理学特性,一种新型的微生物来源的非肽类心房利钠肽拮抗剂。I. 对麻醉大鼠中利钠肽作用的选择性抑制
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Microbial polysaccharide, HS-142-1, competitively and selectively inhibits ANP binding to its guanylyl cyclase-containing receptor.微生物多糖HS-142-1竞争性且选择性地抑制心钠素与其含鸟苷酸环化酶的受体的结合。
Biochem Biophys Res Commun. 1991 May 15;176(3):949-57. doi: 10.1016/0006-291x(91)90374-g.
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Maturation of A71915-dependent inhibition of atrial natriuretic peptide-stimulated cyclic GMP production in isolated rat glomeruli.A71915依赖性抑制心房利钠肽刺激的离体大鼠肾小球中环鸟苷酸生成的成熟过程。
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Increased cyclic guanosine monophosphate production and overexpression of atrial natriuretic peptide A-receptor mRNA in spontaneously hypertensive rats.自发性高血压大鼠中环磷酸鸟苷生成增加及心钠素A受体mRNA过表达
J Clin Invest. 1993 Nov;92(5):2499-508. doi: 10.1172/JCI116858.
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Identification of renal natriuretic peptide receptor subpopulations by use of the non-peptide antagonist, HS-142-1.使用非肽拮抗剂HS-142-1鉴定肾钠尿肽受体亚群。
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Role of endogenous atrial natriuretic peptide in DOCA-salt hypertensive rats. Effects of a novel nonpeptide antagonist for atrial natriuretic peptide receptor.内源性心房利钠肽在去氧皮质酮盐高血压大鼠中的作用。一种新型心房利钠肽受体非肽拮抗剂的作用
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Stable expression of natriuretic peptide receptors: effects of HS-142-1, a non-peptide ANP antagonist.利钠肽受体的稳定表达:非肽类心房钠尿肽拮抗剂HS-142-1的作用
Biochem Biophys Res Commun. 1992 Nov 30;189(1):336-42. doi: 10.1016/0006-291x(92)91563-6.

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