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近端肾小管钠/氢交换受α1A -和α1B -肾上腺素能受体亚型调节。

Proximal nephron Na+/H+ exchange is regulated by alpha 1A- and alpha 1B-adrenergic receptor subtypes.

作者信息

Liu F, Nesbitt T, Drezner M K, Friedman P A, Gesek F A

机构信息

Department of Pharmacology and Toxicology, Dartmouth Medical School, Hanover, New Hampshire 03755, USA.

出版信息

Mol Pharmacol. 1997 Dec;52(6):1010-8. doi: 10.1124/mol.52.6.1010.

Abstract

Activation of alpha 1-adrenergic receptors (alpha 1-AR) increases Na+/H+ exchange (NHE) in proximal tubule. NHE mediates the majority of active Na+ absorption in the proximal tubule. Three alpha 1-AR subtypes have been detected in kidney by molecular and binding techniques. We detected message for all three alpha 1-AR subtypes in mouse proximal tubule cells through reverse transcription-polymerase chain reaction and Northern analysis. To determine the alpha 1-AR subtypes that regulate NHE in mouse proximal tubule cells, two strategies were used: (i) antisense oligodeoxynucleotides (ODNs) to selectively inhibit expression of alpha 1A-, alpha 1B-, and alpha 1D-AR subtypes and (ii) subtype-selective alpha 1-AR antagonists. Streptolysin-O permeabilization was used to introduce antisense and sense ODNs into cells three times over 72 hr. Western blot analysis of membranes prepared from cells treated with alpha 1B-AR antisense ODN demonstrated that alpha 1B-AR protein expression was reduced by 90% at 72 hr compared with control or sense ODN treatments. Functional regulation of NHE by alpha 1-ARs was determined by alpha 1-AR agonist changes in intracellular pH (pHi) in cells grown on coverslips and loaded with 2',7'-bis(2-carboxyethyl)-5(6)carboxyfluorescein-acetoxymethyl ester. Antisense ODNs for alpha 1B-AR significantly reduced phenylephrine (PHE)-induced maximal changes in pHi by 49%. The PHE-induced changes in pHi observed in cells treated with alpha 1A-AR antisense ODNs was reduced by 42%. The selective alpha 1A-AR antagonist WB-4101 and the alpha 1B-AR antagonist spiperone reduce PHE-induced pHi increases to a comparable extent. No significant changes in pHi were observed with cells treated with alpha 1D-AR antisense ODNs or the alpha 1D-AR antagonist BMY 7378 compared with untreated cells. Combined treatment with alpha 1A- and alpha 1B-AR antisense ODNs and antagonists additively inhibits PHE-induced delta pHi by 90%. We conclude that alpha 1A and alpha 1B-AR but not alpha 1D-ARs regulate NHE in proximal tubule cells.

摘要

α1 - 肾上腺素能受体(α1 - AR)的激活会增加近端小管中的钠氢交换(NHE)。NHE介导近端小管中大部分的钠主动重吸收。通过分子和结合技术在肾脏中检测到了三种α1 - AR亚型。我们通过逆转录 - 聚合酶链反应和Northern分析在小鼠近端小管细胞中检测到了所有三种α1 - AR亚型的信息。为了确定调节小鼠近端小管细胞中NHE的α1 - AR亚型,采用了两种策略:(i)反义寡脱氧核苷酸(ODN)以选择性抑制α1A -、α1B - 和α1D - AR亚型的表达,以及(ii)亚型选择性α1 - AR拮抗剂。使用链球菌溶血素 - O通透化技术在72小时内分三次将反义ODN和正义ODN导入细胞。对用α1B - AR反义ODN处理的细胞制备的膜进行蛋白质印迹分析表明,与对照或正义ODN处理相比,在72小时时α1B - AR蛋白表达降低了90%。通过α1 - AR激动剂对生长在盖玻片上并加载了2',7' - 双(2 - 羧乙基) - 5(6) - 羧基荧光素 - 乙酰氧基甲酯的细胞内pH(pHi)的变化来确定α1 - AR对NHE的功能调节。α1B - AR的反义ODN使去氧肾上腺素(PHE)诱导的pHi最大变化显著降低了49%。在用α1A - AR反义ODN处理的细胞中观察到的PHE诱导的pHi变化降低了42%。选择性α1A - AR拮抗剂WB - 4101和α1B - AR拮抗剂螺哌隆将PHE诱导的pHi升高降低到了相当的程度。与未处理的细胞相比,用α1D - AR反义ODN或α1D - AR拮抗剂BMY 7378处理的细胞中未观察到pHi的显著变化。用α1A - 和α1B - AR反义ODN及拮抗剂联合处理可累加性地将PHE诱导的ΔpHi抑制90%。我们得出结论,α1A和α1B - AR而非α1D - AR调节近端小管细胞中的NHE。

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