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尼索地平可阻止非胰岛素依赖型糖尿病(NIDDM)患者红细胞内与钠-锂逆向转运活性升高相关的细胞内游离钙离子浓度增加。

Nisoldipine blocks the increase of intracellular free calcium-ion concentration associated with elevated sodium-lithium countertransport activity in erythrocytes in patients with NIDDM.

作者信息

Fujita J, Tsuda K, Obayashi H, Fukui I, Ishida H, Seino Y

机构信息

Department of Metabolism and Clinical Nutrition, Kyoto University Faculty of Medicine, Sakyo-ku, Japan.

出版信息

Diabet Med. 1997 Jun;14(6):499-502. doi: 10.1002/(SICI)1096-9136(199706)14:6<499::AID-DIA366>3.0.CO;2-B.

Abstract

To understand the mechanism by which elevated sodium-lithium countertransport activity (SLC) associates with increased intracellular free calcium-ion concentration ([Ca2+]i), we investigated the relationship between SLC and the effects of the extracellular Ca2+ concentration ([Ca2+]o) and a Ca2(+)-channel blocker, nisoldipine, on [Ca2+]i in erythrocytes from 48 patients with non-insulin-dependent (Type 2) diabetes mellitus (NIDDM). There was a significant correlation between SLC and [Ca2+]i. Nisoldipine in the incubation medium significantly decreased [Ca2+]i, and there was a significant positive correlation between SLC and the degree of [Ca2+]i decrease. When the [Ca2+]o was elevated, [Ca2+]i was significantly increased, but nisoldipine almost completely suppressed this increase of [Ca2+]i. There was a significant positive correlation between SLC and the degree of the suppression. These data suggest that elevated SLC correlates with increased [Ca2+]i, and that the increased [Ca2i]i might be due to the increased Ca2+ influx through a dihydropyridine-sensitive Ca2+ pathway.

摘要

为了解钠-锂逆向转运活性(SLC)升高与细胞内游离钙离子浓度([Ca2+]i)增加相关的机制,我们研究了48例非胰岛素依赖型(2型)糖尿病(NIDDM)患者红细胞中SLC与细胞外钙离子浓度([Ca2+]o)及钙通道阻滞剂尼索地平对[Ca2+]i影响之间的关系。SLC与[Ca2+]i之间存在显著相关性。孵育培养基中的尼索地平显著降低[Ca2+]i,且SLC与[Ca2+]i降低程度之间存在显著正相关。当[Ca2+]o升高时,[Ca2+]i显著增加,但尼索地平几乎完全抑制了[Ca2+]i的这种增加。SLC与抑制程度之间存在显著正相关。这些数据表明,升高的SLC与增加的[Ca2+]i相关,且增加的[Ca2+]i可能是由于通过二氢吡啶敏感的钙途径增加了钙离子内流。

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