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绵羊心肌和浦肯野纤维中哇巴因受体的比较。

Comparison of ouabain receptors in sheep myocardium and Purkinje fibres.

作者信息

Brown L, Hug E, Wagner G, Erdmann E

出版信息

Biochem Pharmacol. 1985 Oct 15;34(20):3701-10. doi: 10.1016/0006-2952(85)90234-5.

Abstract

The conducting system of the heart has been reported to be more sensitive to the toxic effects of digitalis than the working myocardium. To investigate the molecular basis of these observations, we have characterized the ouabain receptor in Purkinje fibres and ventricular muscle of the digitalis-sensitive sheep heart using cell membrane preparations, crude homogenates and contracting heart tissues. [3H]-Ouabain binding has the following characteristics: in sheep left ventricular cell membranes, specific binding was of high affinity (KD 1.9 X 10(-9) M at 37 degrees); was co-incident with an inhibition of (Na+ + K+)-ATPase activity; and was inhibited by K+ and unlabelled cardiotonic steroids; in crude homogenates, the maximal binding capacity but not the affinity for ouabain varied in different parts of the sheep heart with Purkinje fibres containing markedly fewer binding sites (0.33 X 10(14)/g wet weight; left ventricle, 1.3 X 10(14)/g wet weight) and in isolated, contracting Purkinje fibres and right ventricular moderator band strips, concentration-response curves for [3H]-ouabain binding, increase in force of contraction and inhibition of [86Rb+]-uptake were co-incident. In both contracting tissues, a ouabain concentration of 3 X 10(-7) M occupied about 50% of the specific binding sites, gave the maximal inotropic effect without toxicity and inhibited [86Rb+]-uptake by about 50%. The maximal binding capacity was lower in contracting Purkinje fibres (2 X 10(14) binding sites/g wet weight) than in contracting moderator band strips (3.9 X 10(14) binding sites/g wet weight). The maximal inotropic effects were reached slightly faster in Purkinje fibres but toxicity also occurred faster in these fibers. We conclude that the specific ouabain binding site is the receptor mediating positive inotropy and inhibition of (Na+ + K+)-ATPase in the sheep heart. Further, this receptor is identical in both the conducting system and working myocardium but the conducting system contains many fewer receptors. This change in receptor number, rather than affinity, may underlie the increased ouabain toxicity observed in Purkinje fibres.

摘要

据报道,心脏传导系统比工作心肌对洋地黄的毒性作用更敏感。为了研究这些观察结果的分子基础,我们使用细胞膜制剂、粗匀浆和收缩的心脏组织,对洋地黄敏感的绵羊心脏的浦肯野纤维和心室肌中的哇巴因受体进行了表征。[3H] - 哇巴因结合具有以下特征:在绵羊左心室细胞膜中,特异性结合具有高亲和力(37℃时KD为1.9×10(-9)M);与(Na + + K +)-ATP酶活性的抑制同时发生;并且被K +和未标记的强心甾类抑制;在粗匀浆中,绵羊心脏不同部位对哇巴因的最大结合容量而不是亲和力有所不同,浦肯野纤维含有的结合位点明显较少(0.33×10(14)/克湿重;左心室,1.3×10(14)/克湿重),并且在分离的收缩的浦肯野纤维和右心室节制索条带中,[3H] - 哇巴因结合的浓度 - 反应曲线、收缩力增加和[86Rb +]摄取抑制是同时发生的。在两种收缩组织中,3×10(-7)M的哇巴因浓度占据约50%的特异性结合位点,产生最大的正性肌力作用且无毒性,并抑制[86Rb +]摄取约50%。收缩的浦肯野纤维中的最大结合容量(2×10(14)个结合位点/克湿重)低于收缩的节制索条带中的最大结合容量(3.9×10(14)个结合位点/克湿重)。浦肯野纤维中最大正性肌力作用达到得稍快,但这些纤维中毒性也更快出现。我们得出结论,特异性哇巴因结合位点是介导绵羊心脏正性肌力作用和抑制(Na + + K +)-ATP酶的受体。此外,该受体在传导系统和工作心肌中是相同的,但传导系统含有的受体要少得多。受体数量的这种变化而非亲和力的变化,可能是浦肯野纤维中观察到的哇巴因毒性增加的基础。

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