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用心房利钠肽或C型利钠肽孵育的脑片中环磷酸鸟苷的生成:反应幅度和细胞分布的比较

Generation of cyclic guanosine monophosphate in brain slices incubated with atrial or C-type natriuretic peptides: comparison of the amplitudes and cellular distribution of the responses.

作者信息

Gonçalves J, Grove K L, Deschepper C F

机构信息

Neurobiology and Vasoactive Peptide Laboratory, Institut de Recherches Cliniques de Montréal (IRCM), Québec, Canada.

出版信息

Regul Pept. 1995 May 4;57(1):55-63. doi: 10.1016/0167-0115(95)00018-7.

Abstract

Natriuretic peptides have been demonstrated to induce a variety of effects when administered into the brain. Most studies to date have tested the effects of 'atrial' natriuretic peptide (ANP), but C-type natriuretic peptide (CNP) has recently been suggested to be the predominant form of natriuretic peptides within the brain. We therefore have compared the amplitudes of the cyclic guanosine monophosphate (cGMP) responses induced by either ANP or CNP in slices form different rat brain regions. Whereas both peptides induced the generation of cGMP, CNP-evoked responses were never greater than those obtained with ANP, regardless of the brain region used or the age of the animal. In diencephalon, ANP even induced a significantly higher cGMP response than CNP. To test which cells were targets to the actions of the peptides, brain slices were incubated with fluorocitrate (a drug that selectively blocks the metabolism of glial cells). Fluorocitrate totally blocked the ANP-evoked cGMP responses in brain slices. In contrast, fluorocitrate reduced only partially the responses evoked by sodium nitroprusside (a drug that stimulates soluble guanylate cyclase, which is contained predominantly in neurons). Likewise, the cGMP response induced by CNP was only partially affected by fluorocitrate. These results indicate that: (1) CNP is not more potent than ANP in terms of its ability to generate cGMP in rat brains; (2) brain cells generating cGMP upon exposure to ANP are predominantly glial; and (3) CNP-responsive cells are partly glial, but belong at least in part to a different compartment than ANP-responsive cells.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

利钠肽注入脑内时已被证明能产生多种效应。迄今为止,大多数研究测试的是“心房”利钠肽(ANP)的作用,但最近有人提出C型利钠肽(CNP)是脑内利钠肽的主要形式。因此,我们比较了ANP或CNP在不同大鼠脑区切片中诱导的环磷酸鸟苷(cGMP)反应的幅度。尽管两种肽都能诱导cGMP的产生,但无论使用的脑区或动物年龄如何,CNP引起的反应从未大于ANP所获得的反应。在间脑中,ANP诱导的cGMP反应甚至显著高于CNP。为了测试哪些细胞是这些肽作用的靶点,将脑切片与氟代柠檬酸(一种选择性阻断神经胶质细胞代谢的药物)一起孵育。氟代柠檬酸完全阻断了脑切片中ANP诱导的cGMP反应。相反,氟代柠檬酸仅部分降低了硝普钠(一种刺激可溶性鸟苷酸环化酶的药物,主要存在于神经元中)诱导的反应。同样,CNP诱导的cGMP反应仅受到氟代柠檬酸的部分影响。这些结果表明:(1)就其在大鼠脑中产生cGMP的能力而言,CNP并不比ANP更有效;(2)暴露于ANP时产生cGMP的脑细胞主要是神经胶质细胞;(3)对CNP有反应的细胞部分是神经胶质细胞,但至少部分属于与对ANP有反应的细胞不同的细胞区室。(摘要截短于250字)

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