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缓激肽B2受体拮抗剂增加大鼠髓质集合管中氯离子和水的重吸收。

Bradykinin B2 receptor antagonist increases chloride and water absorption in rat medullary collecting duct.

作者信息

Mukai H, Fitzgibbon W R, Bozeman G, Margolius H S, Ploth D W

机构信息

Department of Medicine, Medical University of South Carolina, Charleston 29425, USA.

出版信息

Am J Physiol. 1996 Aug;271(2 Pt 2):R352-60. doi: 10.1152/ajpregu.1996.271.2.R352.

Abstract

This study tested the hypothesis that intrarenal kinins play a regulatory role in electrolyte excretion by altering Cl- absorption in the collecting duct. We measured Cl- and insulin concentrations in tubular fluid samples obtained from medullary collecting ducts (MCD) of Dahl/Rapp salt-resistant (SR/ Jr) rats by microcatheterization of ducts of Bellini before and after treatment with the bradykinin receptor antagonist HOE-140. Tubular fluid was obtained from paired terminal inner medullary (t-IMCD) and outer medullary (OMCD) collecting duct sites of the left kidney. HOE-140 (n = 7) or vehicle (n = 5) was infused intravenously, and the collections were repeated. HOE-140 did not alter glomerular filtration rate but decreased urine flow rate (P < 0.05) and absolute and fractional Cl- excretion (P < 0.01). HOE-140 did not alter the fraction of filtered Cl- delivered (FDCl) to the OMCD but decreased FDCl to the t-IMCD from 2.3 +/- 0.3 to 1.3 +/- 0.3% (P < 0.05). The fraction of filtered Cl- absorbed per millimeter between the collection sites was increased from 0.2 +/- 0.1 to 0.6 +/- 0.1% (P < 0.05). Fractional absorption of water along the MCD was also increased (P < 0.05). No changes in excretory function or tubular Cl- or water absorption were observed in vehicle-treated rats. These studies show that kinin B2 receptor blockade enhances Cl- and water absorption in the MCD, a finding that supports a role of renal kinins in the regulation of NaCl and water excretion.

摘要

本研究检验了如下假设

肾内激肽通过改变集合管中氯离子的重吸收,在电解质排泄中发挥调节作用。我们通过微导管插入贝氏管,在给达氏/拉普耐盐(SR/Jr)大鼠的髓质集合管(MCD)用缓激肽受体拮抗剂HOE - 140治疗前后,测量了肾小管液样本中的氯离子和胰岛素浓度。肾小管液取自左肾成对的终末内髓(t - IMCD)和外髓(OMCD)集合管部位。静脉注射HOE - 140(n = 7)或赋形剂(n = 5),然后重复收集样本。HOE - 140不改变肾小球滤过率,但降低尿流率(P < 0.05)以及氯离子的绝对排泄量和排泄分数(P < 0.01)。HOE - 140不改变输送至OMCD的滤过氯离子分数(FDCl),但使输送至t - IMCD的FDCl从2.3±0.3%降至1.3±0.3%(P < 0.05)。两个收集部位之间每毫米滤过氯离子的重吸收分数从0.2±0.1%增至0.6±0.1%(P < 0.05)。沿MCD的水重吸收分数也增加(P < 0.05)。在接受赋形剂治疗的大鼠中未观察到排泄功能、肾小管氯离子或水重吸收的变化。这些研究表明,激肽B2受体阻断增强了MCD中氯离子和水的重吸收,这一发现支持肾内激肽在氯化钠和水排泄调节中的作用。

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