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远端小管的电中性氯化钠转运:Na⁺/H⁺-Cl⁻/HCO₃⁻交换的证据

Electroneutral NaCl transport by distal tubule: evidence for Na+/H+-Cl-/HCO3- exchange.

作者信息

Stanton B A

机构信息

Department of Physiology, Dartmouth Medical School, Hanover, New Hampshire 03756.

出版信息

Am J Physiol. 1988 Jan;254(1 Pt 2):F80-6. doi: 10.1152/ajprenal.1988.254.1.F80.

Abstract

The mechanisms, of electrolyte transport by isolated and perfused late distal tubules of the salamander, Amphiuma, were investigated by electrophysiological and transport techniques. The tubules absorbed Na+, HCO3-, and Cl- but not K+. The transepithelial voltage (VT) was not different from zero. Amiloride (10(-3) M) in the perfusion fluid reduced sodium absorption by 43% and HCO3- absorption by 49% without changing VT. This and previous data are consistent with the presence of a Na+/H+ antiporter in the apical membrane. Hydrochlorothiazide (HCTZ, 10(-4) M) in the perfusion fluid inhibited Na+ absorption by 48% but had no effect on HCO3- absorption or VT. Thus HCTZ reduced NaCl absorption. Intracellular microelectrode techniques were used to examine the cellular mechanisms of ion transport and sites of action of amiloride and HCTZ. Two cell types were identified by their electrophysiological properties. Neither amiloride nor HCTZ appreciably altered the electrical properties of cell type I, a cell previously identified as being involved in H+ secretion. In contrast, both diuretics hyperpolarized the basolateral membrane voltage (Vbl) of cell type II. Additional studies of cell type II showed that the removal of Cl- from the lumen hyperpolarized Vbl, as did the addition to the lumen of the Cl-/HCO3- exchange inhibitor 4,4'-diisothiocyanostilbene-2-2'-disulphonic acid. Finally, reducing the [HCO3-] of the lumen depolarized Vbl.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

通过电生理学和转运技术,对两栖动物鳗螈分离并灌注的远端肾小管晚期电解质转运机制进行了研究。肾小管吸收Na⁺、HCO₃⁻和Cl⁻,但不吸收K⁺。跨上皮电压(VT)与零无差异。灌注液中加入氨氯吡咪(10⁻³M)可使钠吸收减少43%,HCO₃⁻吸收减少49%,而VT不变。这一结果和之前的数据与顶端膜中存在Na⁺/H⁺反向转运体一致。灌注液中加入氢氯噻嗪(HCTZ,10⁻⁴M)可使Na⁺吸收减少48%,但对HCO₃⁻吸收或VT无影响。因此,HCTZ减少了NaCl的吸收。采用细胞内微电极技术研究离子转运的细胞机制以及氨氯吡咪和HCTZ的作用位点。根据电生理特性鉴定出两种细胞类型。氨氯吡咪和HCTZ均未明显改变I型细胞的电特性,I型细胞之前被确定参与H⁺分泌。相反,两种利尿剂均使II型细胞的基底外侧膜电压(Vbl)超极化。对II型细胞的进一步研究表明,从管腔中去除Cl⁻可使Vbl超极化,向管腔中加入Cl⁻/HCO₃⁻交换抑制剂4,4'-二异硫氰基芪-2,2'-二磺酸也有同样效果。最后,降低管腔中[HCO₃⁻]可使Vbl去极化。(摘要截选至250词)

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