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首页> 外文期刊>Life sciences >SPECIFIC POTENTIATION BY CYCLIC AMP OF NATRIURETIC PEPTIDE-MEDIATED CYCLIC GMP PRODUCTION IN ADIPOSE TISSUE
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SPECIFIC POTENTIATION BY CYCLIC AMP OF NATRIURETIC PEPTIDE-MEDIATED CYCLIC GMP PRODUCTION IN ADIPOSE TISSUE

机译:脂肪组织中钠尿肽介导的循环GMP产生的循环AMP强化作用

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摘要

Adipose tissue of the mesenteric territory contains large quantities of natriuretic peptide receptors (NPR) mainly of the NPR-C subtype. Guanylyl cyclase-bound receptors are also present since atrial natriuretic peptide (ANP) and C-type natriuretic peptide (CNP) are equally potent in activating this enzyme. While searching for a potential biological role for NP in adipocytes we observed that ANP-mediated generation of cyclic GMP (cGMP) was potentiated when the cells were simultaneously treated with isoproterenol. Indeed, isoproterenol, a beta-adrenergic agonist, and forskolin, an activator of adenylyl cyclase, can both double oi triple cGMP production in response to ANF stimulation. There was a direct correlation between the level of cyclic AMP (cAMP) generated and the level of NP-mediated cGMP production suggesting that a cAMP-dependent mechanism may be responsible of this potentiation. To determine whether or not this phenomenon was unique to adipocytes, NPR subtypes were characterized in 4 established cell lines and their cAMP-dependent cGMP behavior examined. A10 and A7r5 smooth muscle cells showed identical ratio of NPR subtypes with about 95% NPR-C and 5% NPR-B. PC12 cells presented 100% NPR-A and NIH 3T3 fibroblasts 50% NPR-C and 50% NPR-B. Regardless of the NPR subtype, forskolin could not potentiate the cGMP generation in these cell lines. These data indicate that the cAMP-dependent potentiation of the NP-mediated cGMP production is unique to adipocytes, appears independent of the guanylyl cyclase-linked NPR subtypes and may be involved in the sensitization of the guanylyl cyclase domain of NPR for a potential biological role of NP in the adipose tissue. [References: 32]
机译:肠系膜区域的脂肪组织包含大量的利尿钠肽受体(NPR),主要是NPR-C亚型。由于房利钠肽(ANP)和C型利钠肽(CNP)在激活该酶方面同样有效,因此也存在与胍基环化酶结合的受体。在寻找脂肪细胞中NP的潜在生物学作用时,我们观察到,当同时用异丙肾上腺素处理细胞时,ANP介导的环状GMP(cGMP)生成被增强。实际上,β-肾上腺素能激动剂异丙肾上腺素和腺苷酸环化酶的活化剂福斯高林都可以对ANF刺激产生两倍的cGMP产量。产生的环状AMP(cAMP)的水平与NP介导的cGMP产生的水平之间存在直接的相关性,表明cAMP依赖性机制可能是这种增强的原因。为了确定这种现象是否是脂肪细胞所独有的,在4种已建立的细胞系中鉴定了NPR亚型,并研究了其cAMP依赖性cGMP行为。 A10和A7r5平滑肌细胞显示出相同比例的NPR亚型,其中NPR-C约为95%,NPR-B约为5%。 PC12细胞呈现100%NPR-A和NIH 3T3成纤维细胞50%NPR-C和50%NPR-B。无论NPR亚型如何,福司柯林都不能在这些细胞系中增强cGMP的产生。这些数据表明,NP介导的cGMP产生的cAMP依赖性增强是脂肪细胞所独有的,独立于鸟苷酸环化酶连接的NPR亚型而出现,并且可能参与NPR鸟苷酸环化酶结构域的致敏作用,从而具有潜在的生物学作用。脂肪组织中的NP含量。 [参考:32]

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