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小鼠髓袢升支粗段中的氯化钠转运。II. 抗利尿激素对跨细胞氯化钠协同转运的增强作用;跨上皮电压的起源。

NaCl transport in mouse medullary thick ascending limbs. II. ADH enhancement of transcellular NaCl cotransport; origin of transepithelial voltage.

作者信息

Hebert S C, Culpepper R M, Andreoli T E

出版信息

Am J Physiol. 1981 Oct;241(4):F432-42. doi: 10.1152/ajprenal.1981.241.4.F432.

Abstract

We measured the relations between tubular perfusion rate and the rate of net NaCl transport in medullary thick ascending limbs of Henle (mTALH) either in the presence or absence of ADH. These data, together with the known Na+, Cl-, and water permeability characteristics of the mTALH, were used to calculate tau NaCl (mol . s-1 . cm-2), the rate of conservative Cl- transport from lumen through cells to interspaces; and CNaCl, the effective NaCl concentration in lateral intercellular spaces. The experimental results indicate that in these tubules the rate of net Cl- absorption increases monotonically with perfusion rate, and that at a given perfusion rate ADH increases the rate of net salt absorption. The theoretical calculations show clearly that the ADH-mediated increase in salt absorption depends on an increase in the rate of conservative transcellular Cl- transport. However, the present analytical data do not permit a distinction between wholly electroneutral apical membrane NaCl entry with respect to a process in which apical membrane Na+/Cl- entry has a stoichiometry less than unity, and electrogenic Na+ transport accounts for the remaining component of net Na+ absorption. Identification of the stoichiometry of the Na+/Cl- apical membrane entry step will depend, among other factors, on identifying explicitly the diffusion resistance of paracellular fluid and the mode of passive ion transport across junctional complexes.

摘要

我们测量了在有或没有抗利尿激素(ADH)的情况下,髓袢升支粗段(mTALH)中肾小管灌注率与净NaCl转运率之间的关系。这些数据,连同已知的mTALH的Na⁺、Cl⁻和水通透性特征,被用于计算τNaCl(mol·s⁻¹·cm⁻²),即从管腔通过细胞到细胞间隙的保守性Cl⁻转运速率;以及CNaCl,即细胞间外侧间隙中的有效NaCl浓度。实验结果表明,在这些肾小管中,净Cl⁻吸收速率随灌注率单调增加,并且在给定的灌注率下,ADH会增加净盐吸收速率。理论计算清楚地表明,ADH介导的盐吸收增加取决于保守性跨细胞Cl⁻转运速率的增加。然而,目前的分析数据无法区分完全电中性的顶端膜NaCl进入过程与顶端膜Na⁺/Cl⁻进入化学计量比小于1的过程,以及电生性Na⁺转运占净Na⁺吸收其余部分的过程。确定顶端膜Na⁺/Cl⁻进入步骤的化学计量比,除其他因素外,将取决于明确确定细胞旁液的扩散阻力以及跨连接复合体的被动离子转运模式。

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