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哺乳动物心肌细胞中β1肾上腺素能受体脱敏的机制和时间进程。

Mechanisms and time course of beta 1 adrenoceptor desensitisation in mammalian cardiac myocytes.

作者信息

Karliner J S, Simpson P C, Honbo N, Woloszyn W

出版信息

Cardiovasc Res. 1986 Mar;20(3):221-8. doi: 10.1093/cvr/20.3.221.

Abstract

To study the mechanisms and time course of beta1 adrenoceptor desensitisation in mammalian heart tissue neonatal rat cardiac myocytes (greater than 90% pure) were cultured in serum free medium. Cells were exposed to 1 mumol X litre-1 (-)-isoprenaline for 30 min, 4 h, and 16 h. In myocyte membranes mean(SEM)) 125I-iodocyanopindolol binding was 167(46) pmol X litre-1 (n = 5) and did not differ at 30 min, 4 h, or 16 h in control compared with (-)-isoprenaline treated cells. The maximum number of binding sites was 84(32) fmol X mg protein-1 and was unchanged at 30 min, but (-)-isoprenaline stimulated adenylate cyclase activity significantly decreased from 221(62) to 103(37) pmol X mg protein-1 30 min-1. (-)-Isoprenaline competition curves at 30 min showed a significant increase in the proportion of low affinity binding sites from 46% to 62% (n = 5). By 4 h the maximum number of binding sites was significantly decreased by 54%, adenylate cyclase activity remained depressed, and agonist affinity decreased threefold in the (-)-isoprenaline treated cells. At 16 h (-)-isoprenaline treated cells showed alterations similar to the 4 h values in the maximum number of binding sites, adenylate cyclase activity, and affinity for (-)-isoprenaline. (-)-Isoprenaline stimulated adenylate cyclase activity took 72 h to recover after desensitisation. Overnight ultracentrifugation of the cytosol showed a significant 40% increase in beta adrenoceptor density in cells exposed to (-)-isoprenaline for 4 h (n = 5), suggesting receptor internalisation.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为研究哺乳动物心脏组织中β1肾上腺素能受体脱敏的机制和时间进程,将新生大鼠心肌细胞(纯度大于90%)在无血清培养基中培养。细胞分别用1 μmol/L(-)-异丙肾上腺素处理30分钟、4小时和16小时。在心肌细胞膜中,(均值(标准误))125I-碘氰吲哚洛尔结合量为167(46)pmol/L(n = 5),与(-)-异丙肾上腺素处理的细胞相比,对照组在30分钟、4小时或16小时时无差异。结合位点的最大数量为84(32)fmol/mg蛋白质-1,在30分钟时无变化,但(-)-异丙肾上腺素刺激的腺苷酸环化酶活性从221(62)显著降至103(37)pmol/mg蛋白质-1·30分钟-1。30分钟时(-)-异丙肾上腺素的竞争曲线显示低亲和力结合位点的比例从46%显著增加到62%(n = 5)。到4小时时,结合位点的最大数量显著减少54%,腺苷酸环化酶活性仍受抑制,且(-)-异丙肾上腺素处理的细胞中激动剂亲和力降低了三倍。在16小时时,(-)-异丙肾上腺素处理的细胞在结合位点的最大数量、腺苷酸环化酶活性以及对(-)-异丙肾上腺素的亲和力方面表现出与4小时时相似的变化。脱敏后,(-)-异丙肾上腺素刺激的腺苷酸环化酶活性需要72小时才能恢复。对细胞溶质进行过夜超速离心显示,暴露于(-)-异丙肾上腺素4小时的细胞中β肾上腺素能受体密度显著增加40%(n = 5),提示受体内化。(摘要截断于250字)

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