匹莫苯丹直接致敏重组细丝在心肌肌球蛋白上滑动

Masataka Sata , Seiryo Sugiura, Hiroshi Yamashita, Teruhiko Aoyagi, Shin-ichi Momomura, Takashi Serizawa
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引用次数: 14

摘要

为了阐明匹莫苯丹Ca2+增敏作用的机制,用肌动蛋白和原肌凝蛋白-肌钙蛋白复合物重建心脏细丝,并使其在肌凝蛋白层上滑动。虽然细丝在Ca2+浓度较低时表现为布朗运动,但在Ca2+浓度一定水平以上,细丝以恒定速度滑动,表明在较窄的pCa范围内,这种滑动受Ca2+的调节。酸中毒、无机磷酸盐的添加和肌钙蛋白I的磷酸化增加了Ca2+的阈值浓度。添加匹莫苯丹逆转了这些脱敏作用。这些结果清楚地表明,匹莫苯丹直接增加Ca2+细丝的敏感性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pimobendan directly sensitizes reconstituted thin filament to slide on cardiac myosin

To elucidate the mechanism of the Ca2+-sensitizing action of pimobendan, cardiac thin filaments were reconstituted from actin and tropomyosin-troponin complex and made to slide on a myosin layer. Although filaments showed Brownian movement with a low Ca2+ concentration, they slid at a constant velocity above a certain level of Ca2+ concentration, showing that the sliding was regulated by Ca2+ within a narrow pCa range. Acidosis, addition of inorganic phosphate, and phosphorylation of troponin I increased the threshold Ca2+ concentration. Addition of pimobendan reversed these desensitization effects. These results clearly demonstrated that pimobendan directly increases the Ca2+ sensitivity of thin filament.

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