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大鼠皮质集合管的主细胞不是跨上皮氯离子转运的途径。

Principal cells of cortical collecting ducts of the rat are not a route of transepithelial Cl- transport.

作者信息

Schlatter E, Greger R, Schafer J A

机构信息

Physiologisches Institut, Albert-Ludwigs-Universität, Freiburg, Federal Republic of Germany.

出版信息

Pflugers Arch. 1990 Nov;417(3):317-23. doi: 10.1007/BF00370998.

Abstract

The rat cortical collecting duct (CCD) exhibits high rates of NaCl reabsorption when stimulated by mineralocorticoid and antidiuretic hormone (ADH). The present study was undertaken to determine if there is significant transcellular Cl- movement across the principal cells of the rat CCD. CCDs were dissected from kidneys of rats that had been injected with deoxycorticosterone (5 mg, i.m.) 2-9 days prior to the experiment. The ducts were perfused in vitro with identical perfusing and bathing solutions, except that 200 pmol.l-1 ADH was added to the bathing solutions. The basolateral membrane voltage (PDbl) of principal cells was -77 +/- 1 mV and the luminal membrane voltage (PD1) was -68 +/- 1 mV (mean +/- SEM, n = 124). Separate impalements with single-barrelled Cl(-)-selective microelectrodes gave an apparent intracellular Cl- activity of principal cells of 17 +/- 2 mmol.l-1. Transepithelial PD and PDbl were unaffected by luminal furosemide, hydrochlorothiazide (HCT), 4-acetamido-4-isothiocyanostilbene2,2-disulphonic acid, (SITS), or the Cl- channel blocker 5-nitro-2-(3-phenylpropylamino)-benzoic acid (NPPB); bath addition of SITS or the Cl- channel blocker diphenylamino-2-carboxylic acid; or replacement of bath HCO3- by Cl-. The intracellular Cl- activity (a(cell)Cl) also remained unchanged with the addition of HCT, SITS or the Cl- channel blockers to either the perfusing or bathing solutions, or with replacement of the bathing solution HCO3-.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

当受到盐皮质激素和抗利尿激素(ADH)刺激时,大鼠皮质集合管(CCD)表现出较高的氯化钠重吸收率。本研究旨在确定是否存在显著的跨细胞氯离子转运穿过大鼠CCD的主细胞。从实验前2 - 9天注射脱氧皮质酮(5毫克,肌肉注射)的大鼠肾脏中分离出CCD。除了在浴液中添加200皮摩尔/升的ADH外,体外使用相同的灌注液和浴液灌注这些导管。主细胞的基底外侧膜电压(PDbl)为 -77 ± 1毫伏,管腔膜电压(PD1)为 -68 ± 1毫伏(平均值 ± 标准误,n = 124)。用单管氯离子选择性微电极进行单独穿刺,得出主细胞的表观细胞内氯离子活性为17 ± 2毫摩尔/升。管腔呋塞米、氢氯噻嗪(HCT)、4 - 乙酰氨基 - 4 - 异硫氰基芪 - 2,2 - 二磺酸(SITS)或氯离子通道阻滞剂5 - 硝基 - 2 -(3 - 苯丙基氨基) - 苯甲酸(NPPB)对跨上皮PD和PDbl无影响;浴液中添加SITS或氯离子通道阻滞剂二苯胺 - 2 - 羧酸;或将浴液中的HCO3-替换为Cl-。向灌注液或浴液中添加HCT、SITS或氯离子通道阻滞剂,或替换浴液中的HCO3-,细胞内氯离子活性(a(cell)Cl)也保持不变。(摘要截断于250字)

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