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兔肾小动脉钠钙交换的特性

Characterization of sodium-calcium exchange in rabbit renal arterioles.

作者信息

Fowler B C, Carmines P K, Nelson L D, Bell P D

机构信息

Department of Physiology and Biophysics, University of Alabama at Birmingham, USA.

出版信息

Kidney Int. 1996 Dec;50(6):1856-62. doi: 10.1038/ki.1996.506.

Abstract

Experiments were performed to test the hypothesis that renal arterioles exhibit Na-Ca exchange capability and that this process is regulated by protein kinase C (PKC). Glomeruli with attached arterioles were dissected from rabbit kidney and loaded with fura-2 for measurement of intracellular calcium concentration ([Ca2+]i) using microscope-based photometry. In tissue bathed in Ringer's solution containing 150 mM Na+ and 1.5 mM Ca2+, afferent and efferent arteriolar [Ca2+]i averaged 136 +/- 6 and 154 +/- 7 nM, respectively. Removal of extracellular Na+ increased afferent arteriolar [Ca2+]i by 70 +/- 7 mM, while efferent arteriolar [Ca2+]i only increased by 39 +/- 5 nM (P < 0.01 vs. afferent arteriole). These responses were inhibited by 6 nM Ni2+ and required extracellular Ca2+, but were unaffected by 10 microM diltiazem. After incubation in 500 microM ouabain, 5 microM monensin, and 5 microM nigericin, [Ca2+]i responses to removal of extracellular Na+ were exaggerated significantly, averaging 174 +/- 50 nM in afferent arterioles and 222 +/- 82 nM in efferent arterioles (NS vs. afferent arterioles). Moreover, responses to removal of extracellular Na+ were enhanced by 100 nM phorbol 12-myristate 13-acetate, an affect which was blocked by PKC inhibition (25 nM K252b). These data indicate that both afferent and efferent arterioles express the Na-Ca exchanger, and that PKC activity impacts on exchange capacity in these vessels.

摘要

进行实验以验证以下假设

肾小动脉具有钠钙交换能力,且该过程受蛋白激酶C(PKC)调节。从兔肾中分离出带有相连小动脉的肾小球,并用fura-2进行负载,以便使用基于显微镜的光度法测量细胞内钙浓度([Ca2+]i)。在含有150 mM Na+和1.5 mM Ca2+的林格氏溶液中孵育的组织中,传入和传出小动脉的[Ca2+]i平均分别为136±6 nM和154±7 nM。去除细胞外Na+使传入小动脉的[Ca2+]i增加70±7 nM,而传出小动脉的[Ca2+]i仅增加39±5 nM(与传入小动脉相比,P<0.01)。这些反应被6 nM Ni2+抑制且需要细胞外Ca2+,但不受10 μM地尔硫䓬影响。在500 μM哇巴因、5 μM莫能菌素和5 μM尼日利亚菌素中孵育后,对去除细胞外Na+的[Ca2+]i反应显著增强,传入小动脉平均为174±50 nM,传出小动脉平均为222±82 nM(与传入小动脉相比无显著差异)。此外,100 nM佛波醇12-肉豆蔻酸酯13-乙酸盐增强了对去除细胞外Na+的反应,该作用被PKC抑制(25 nM K252b)阻断。这些数据表明,传入和传出小动脉均表达钠钙交换体,且PKC活性影响这些血管中的交换能力。

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