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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Angiotensin II as a stimulator of Na(+)-dependent Ca2+ efflux from freshly isolated adult rat cardiomyocytes.
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Angiotensin II as a stimulator of Na(+)-dependent Ca2+ efflux from freshly isolated adult rat cardiomyocytes.

机译:血管紧张素II作为从新鲜分离的成年大鼠心肌细胞中Na(+)依赖的Ca2 +外排的刺激物。

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摘要

In cardiac tissues, angiotensin II causes inotropic and chronotropic effects on the heart. It is indicated that the mechanism of the inotropic effect of angiotensin II is attributed to an increase in cytosolic free calcium ([Ca2+]i) in cardiomyocytes. However, increased [Ca2+]i should be restored to a physiological level because cumulative elevation in [Ca2+]i leads to irreversible injury in cardiomyocytes. Whereas it is known that angiotensin II causes the increase in [Ca2+]i in cardiac cells, little is known about the mechanisms of decrease in [Ca2+]i in cardiomyocytes upon angiotensin II stimulation. In the present study, we examined the effect of angiotensin II on Ca2+ efflux from freshly isolated adult rat cardiomyocytes. Angiotensin II stimulated the efflux of 45Ca2+ from the cells in a concentration-dependent manner (10(-7)-10(-5) M). The 45Ca2+ efflux from the cells was inhibited by type 1 angiotensin II receptor inhibitor. The angiotensin II-stimulated 45Ca2+ efflux was not affected by deprivation of the extracellular Ca2+, but was dependent on the presence of extracellular Na+. These results indicate that angiotensin II stimulates extracellular Na(+)-dependent 45Ca2+ efflux from freshly isolated adult rat cardiomyocytes, probably through its stimulatory effect on the plasma membrane type 1 angiotensin II receptors which may couple to Na+/Ca2+ exchange.
机译:在心脏组织中,血管紧张素II对心脏产生正性变力和变时性作用。结果表明,血管紧张素II的正性肌力作用的机制归因于心肌细胞中胞质游离钙([Ca2 +] i)的增加。但是,增加的[Ca2 +] i应该恢复到生理水平,因为[Ca2 +] i的累积升高会导致心肌细胞不可逆转的损伤。尽管已知血管紧张素II引起心肌细胞中[Ca 2+] i的增加,但是对于血管紧张素II刺激后心肌细胞中[Ca 2+] i减少的机制知之甚少。在本研究中,我们检查了血管紧张素II对新鲜分离的成年大鼠心肌细胞Ca2 +外流的影响。血管紧张素II以浓度依赖性方式(10(-7)-10(-5)M)刺激45Ca2 +从细胞中流出。来自细胞的45Ca 2+外排被1型血管紧张素II受体抑制剂抑制。血管紧张素II刺激的45Ca2 +流出不受细胞外Ca2 +剥夺的影响,但取决于细胞外Na +的存在。这些结果表明,血管紧张素II可能是通过刺激对质膜1型血管紧张素II受体的刺激作用而刺激的,该刺激作用可能与Na + / Ca2 +交换耦合,血管紧张素II刺激了新鲜分离的成年大鼠心肌细胞的Na(+)依赖性45Ca2 +外流。

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