Suppr超能文献

血管紧张素II对成年大鼠新鲜分离心肌细胞Ca2+外流的影响:钠/钙交换体的可能作用

Effect of angiotensin II on Ca2+ efflux from freshly isolated adult rat cardiomyocytes: possible involvement of Na+/Ca2+ exchanger.

作者信息

Fukuta Y, Yoshizumi M, Kitagawa T, Hori T, Katoh I, Houchi H, Tamaki T

机构信息

Department of Cardiovascular Surgery, School of Medicine, The University of Tokushima, Japan.

出版信息

Biochem Pharmacol. 1998 Feb 15;55(4):481-7. doi: 10.1016/s0006-2952(97)00496-6.

Abstract

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, at least in pharmacological doses of 10(-8) M to 10(-5) M. The 45Ca2+ efflux was inhibited by the type 1 angiotensin II receptor antagonist losartan, but not by the type 2 antagonist PD 123319. Angiotensin II also induced an increase in cytosolic free calcium ([Ca2+]i) and inositol trisphosphate formation within the cardiomyocytes. Angiotensin II-induced 45Ca2+ efflux and the increase in [Ca2+]i were both inhibited by thapsigargin, a specific inhibitor of the sarcoplasmic reticulum Ca2+ pump. The 45Ca2+ efflux was not affected by removal of the extracellular Ca2+ but was dependent on the presence of extracellular Na+. In addition, angiotensin II caused 22Na+ influx into the cells. These results indicate that angiotensin II stimulates Na+-dependent 45Ca2+ efflux from freshly isolated adult rat cardiomyocytes, probably through its stimulatory effect on the plasma membrane type 1 angiotensin II receptors. Angiotensin II-induced increase in [Ca2+]i may cause an activation of Na+/Ca2+ exchange which finally results in the stimulation of 45Ca2+ efflux from the cells. Since it is reported that Na+/Ca2+ exchange is important in calcium homeostasis within the cells, angiotensin II may play some role in the reduction of intracellular Ca2+ from isolated adult rat cardiomyocytes.

摘要

在本研究中,我们检测了血管紧张素II对新鲜分离的成年大鼠心肌细胞钙外流的影响。血管紧张素II以浓度依赖的方式刺激细胞中45Ca2+的外流,至少在10(-8)M至10(-5)M的药理剂量下如此。45Ca2+外流受到1型血管紧张素II受体拮抗剂氯沙坦的抑制,但不受2型拮抗剂PD 123319的抑制。血管紧张素II还诱导心肌细胞内细胞溶质游离钙([Ca2+]i)增加和肌醇三磷酸生成。血管紧张素II诱导的45Ca2+外流和[Ca2+]i增加均受到毒胡萝卜素(肌浆网钙泵的特异性抑制剂)的抑制。45Ca2+外流不受细胞外钙去除的影响,但依赖于细胞外钠的存在。此外,血管紧张素II导致22Na+流入细胞。这些结果表明,血管紧张素II刺激新鲜分离的成年大鼠心肌细胞中依赖钠的45Ca2+外流,可能是通过其对质膜1型血管紧张素II受体的刺激作用。血管紧张素II诱导的[Ca2+]i增加可能导致钠/钙交换激活,最终导致细胞中45Ca2+外流受到刺激。由于据报道钠/钙交换在细胞内钙稳态中很重要,血管紧张素II可能在分离的成年大鼠心肌细胞内钙减少中发挥某种作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验