Suppr超能文献

衰老对大鼠心脏中A1-腺苷受体介导的去甲肾上腺素释放抑制作用的影响。

Effect of aging on A1-adenosine receptor-mediated inhibition of norepinephrine release in the rat heart.

作者信息

Snyder D L, Wang W, Pelleg A, Friedman E, Horwitz J, Roberts J

机构信息

Department of Pharmacology, MCP-Hahnemann School of Medicine, Allegheny University of the Health Sciences, Philadelphia, Pennsylvania 19129, USA.

出版信息

J Cardiovasc Pharmacol. 1998 Mar;31(3):352-8. doi: 10.1097/00005344-199803000-00004.

Abstract

Adenosine inhibits norepinephrine (NE) release from cardiac adrenergic nerves and reduces the postsynaptic beta-adrenergic mediated actions of NE, leading to decreased myocardial force of contraction. The actions of adenosine are mediated by pre- and postsynaptic adenosine A1 receptors (A1-AdoR). We reported that adenosine inhibition of postsynaptic beta-adrenergic receptor-mediated cyclic adenosine monophosphate (cAMP) production declines with age in male F344 rat hearts. In this study, cardiac synaptosomes, isolated intact adrenergic nerve terminals, were used to examine the effect of age on adenosine inhibition of NE release. Cardiac synaptosomes were prepared from the hearts of 6- and 24-month-old male F344 rats, loaded with [3H]NE, and placed in a superfusion system. [3H]NE release was induced by high [K+] exposure in the presence of varying concentrations of adenosine or the specific A1-AdoR agonist, N6-p-sulfophenyladenosine (SPA). [3H]NE release was significantly reduced in old rats compared with young rats. Inhibition of [3H]NE release by adenosine and SPA was significantly greater in young rats compared with old rats. The A1-AdoR antagonist, 8-(p-sulfophenyl)-theophylline, blocked the actions of adenosine on [3H]NE release, and the specific adenosine A2-receptor agonist, cyclopropylcarboxamidoadenosine, had no effect on [3H]NE release. Our data suggest that presynaptic A1-AdoR-mediated inhibition of NE release in the rat heart declines with age.

摘要

腺苷可抑制心脏肾上腺素能神经释放去甲肾上腺素(NE),并降低NE的突触后β-肾上腺素能介导的作用,从而导致心肌收缩力下降。腺苷的作用由突触前和突触后的腺苷A1受体(A1-AdoR)介导。我们报道,在雄性F344大鼠心脏中,腺苷对突触后β-肾上腺素能受体介导的环磷酸腺苷(cAMP)生成的抑制作用随年龄增长而下降。在本研究中,心脏突触体(分离出的完整肾上腺素能神经末梢)被用于研究年龄对腺苷抑制NE释放的影响。从6个月和24个月大的雄性F344大鼠心脏中制备心脏突触体,用[3H]NE加载,并置于灌流系统中。在不同浓度的腺苷或特异性A1-AdoR激动剂N6-p-磺基苯腺苷(SPA)存在的情况下,通过高[K+]暴露诱导[3H]NE释放。与年轻大鼠相比,老年大鼠的[3H]NE释放显著减少。与老年大鼠相比,腺苷和SPA对[3H]NE释放的抑制作用在年轻大鼠中显著更大。A1-AdoR拮抗剂8-(p-磺基苯基)茶碱可阻断腺苷对[3H]NE释放的作用,而特异性腺苷A2受体激动剂环丙基甲酰胺腺苷对[3H]NE释放无影响。我们的数据表明,大鼠心脏中突触前A1-AdoR介导的NE释放抑制作用随年龄增长而下降。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验