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噻二嗪酮衍生物对哺乳动物心室收缩参数和蛋白质磷酸化的立体选择性作用比较。

Comparison of the stereoselective effects of a thiadiazinone derivative on contractile parameters and protein phosphorylation in the mammalian ventricle.

作者信息

Neumann J, Bokník P, Schmitz W, Scholz H, Zimmermann N

机构信息

Abteilung Allgemeine Pharmakologie, Universitäts-Krankenhaus Eppendorf, Hamburg, Germany.

出版信息

J Cardiovasc Pharmacol. 1995 May;25(5):789-93. doi: 10.1097/00005344-199505000-00015.

Abstract

In papillary muscles from reserpinized guinea pigs, EMD 57033, the most potent Ca(2+)-sensitizer known, effectively increased force of contraction (FOC) and concomitantly increased duration of contraction. In isolated 32P-labeled guinea pig ventricular cardiomyocytes, EMD 57033 increased the phosphorylation state of phospholamban as well as the inhibitory subunit of troponin, which are usually linked to reductions in contraction time. Therefore, EMD 57033 dissociates phospholamban-phosphorylation and effects on contractile parameters, probably owing to its strong Ca(2+)-sensitizing properties.

摘要

在利血平化豚鼠的乳头肌中,已知最强效的钙敏化剂EMD 57033可有效增加收缩力(FOC),并同时延长收缩持续时间。在分离的32P标记的豚鼠心室心肌细胞中,EMD 57033增加了受磷蛋白以及肌钙蛋白抑制亚基的磷酸化状态,而这通常与收缩时间的缩短有关。因此,EMD 57033使受磷蛋白磷酸化与对收缩参数的影响相分离,这可能归因于其强大的钙敏化特性。

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