传统中药欣麦隆注射液改善心功能的作用机制。

Zhengtao Li, Sujuan Li, Lin Hu, Fang Li, Alex Chun Cheung, Weizai Shao, Yuling Que, George Pek-Heng Leung, Cui Yang
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引用次数: 0

摘要

背景:欣麦隆注射液(XML)是从美洲大蠊中提取的一种生物活性复合物,在中国被用于治疗充血性心力衰竭(CHF)。临床数据证明,XML 具有正性肌力特性。本研究旨在评估XML对充血性心力衰竭的治疗作用机制:测量 XML 对离体大鼠心脏功能的影响。在大鼠心肌细胞(H9c2 细胞)中使用 Ca2+ 成像技术来揭示 XML 对 Ca2+ 通道的作用。同时,还测定了 XML 对 Na+/K+ ATPase 和钠/钙交换子活性的影响。此外,还测定了心肌细胞中活性氧的水平以及超氧化物歧化酶和血红素氧化酶的蛋白表达量:结果表明:XML 增加了电脉冲诱导的 H9c2 细胞中的[Ca2+]i,这依赖于细胞外 Ca2+,并被 ML218-HCl(一种 T 型 Ca2+ 通道拮抗剂)而非尼莫地平(一种 L 型 Ca2+ 通道拮抗剂)所取消。Na+/K+-ATP酶抑制剂欧阿巴因能增加电脉冲诱导的[Ca2+]i,而XML能显著抑制这种增加。此外,XML 还能明显抑制 H9c2 细胞中 Na+/K+ ATPase 的活性。此外,XML 还明显减少了活性氧的产生,并增强了 H9c2 细胞中超氧化物歧化酶 1、超氧化物歧化酶 2 和血红素氧合酶 1 等抗氧化酶的蛋白表达:我们的研究结果为更好地理解 XML 对心血管系统的治疗作用铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

MECHANISMS UNDERLYING ACTION OF <i>XINMAILONG</i> INJECTION, A TRADITIONAL CHINESE MEDICINE IN CARDIAC FUNCTION IMPROVEMENT.

MECHANISMS UNDERLYING ACTION OF <i>XINMAILONG</i> INJECTION, A TRADITIONAL CHINESE MEDICINE IN CARDIAC FUNCTION IMPROVEMENT.

MECHANISMS UNDERLYING ACTION OF <i>XINMAILONG</i> INJECTION, A TRADITIONAL CHINESE MEDICINE IN CARDIAC FUNCTION IMPROVEMENT.

MECHANISMS UNDERLYING ACTION OF XINMAILONG INJECTION, A TRADITIONAL CHINESE MEDICINE IN CARDIAC FUNCTION IMPROVEMENT.

Background: As a bioactive composite extracted from American cockroach, Xinmailong injection (XML) is used for the treatment of congestive heart failure (CHF) in China. Clinical data has provided evidence that XML has positive inotropic properties. The objective of this study was to assess the mechanisms involved in the therapeutical effect of XML on CHF.

Materials and methods: The effects of XML on the cardiac function in isolated rat heart were measured. A Ca2+ imaging technology was used in rat cardiomyocytes (H9c2 cells) to reveal the role of XML on Ca2+ channels. Meanwhile, the effects of XML on the activities of Na+/K+ ATPase and sodium/calcium exchanger were measured. In addition, the level of reactive oxygen species and the protein expressions for the superoxide dismutase and hemeoxygenase were determined in the cardiomyocytes.

Results: The results showed that XML increased the electrical impulse-induced [Ca2+]i in H9c2 cells, which was dependant on extracellular Ca2+ and was abolished by ML218-HCl (a T-type Ca2+channels antagonist) but not nimodipine (a L-type Ca2+channels antagonist). Ouabain, a Na+/K+-ATPase inhibitor, increased the electrical impulse-induced [Ca2+]i, which was significantly inhibited by XML. Moreover, XML markedly inhibited the Na+/K+ ATPase activity in H9c2 cells. In addition, XML notably reduced the production of reactive oxygen species and enhanced the protein expressions of antioxidant enzymes including superoxide dismutase 1, superoxide dismutase 2 and hemeoxygenase 1 in H9c2 cell.

Conclusion: Our findings pave the ways to the better understandings of the therapeutic effects of XML on cardiovascular system.

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