耦合NaCl输运:共输运还是平行离子交换?

Kroc Foundation series Pub Date : 1984-01-01
D W Powell, C C Fan
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引用次数: 0

摘要

近年来,人们发现至少部分钠离子和氯离子的跨细胞运动是通过一个或多个过程连接起来的,这些过程将钠离子穿过肠细胞的顶细胞膜进入到氯离子中。在某些组织中,如胆囊和肾小管,钠和氯的这种耦合运输可能是主要的电解质运输机制。对家兔回肠刷边膜囊泡的研究表明,NaCl耦合过程具有相同的离子特异性和相似的动力学,与通过完整上皮顶膜的内流技术所证明的过程相同。然而,囊泡也表现出Na:H和Cl:HCO3交换过程,而抑制剂被认为是NaCl共转运系统(环利尿剂)、Na:H交换(大剂量氨酰)或Cl:HCO3交换(二磺酸二苯乙烯,如sit或DIDS)的特异性,但事实并非如此。这三个过程可能都存在于肠刷缘膜中。此外,分离囊泡的技术可以解偶联或抑制耦合的NaCl过程。尽管如此,目前的大量证据表明,正如Turnberg等人[4]最初提出的那样,平行离子交换剂Na:H和Cl:HCO3可以解释兔子回肠中NaCl的耦合运输。需要进一步的研究来确定这是否是肠顶端膜的唯一机制,以及这一结论是否适用于其他组织,如胆囊和肾小管。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Coupled NaCl transport: cotransport or parallel ion exchange?

In recent years it has become apparent that at least part of the transcellular movements of Na and Cl are linked by a process or processes which couple the entry of Na to Cl across the apical cell membrane of the intestinal cell. In some tissues, eg, gallbladder and renal tubule, this coupled transport of Na and Cl may be the predominant electrolyte-transporting mechanism. Studies in rabbit ileal brush-border membrane vesicles present evidence for a coupled NaCl process that has the same ionic specificities and similar kinetics as the processes demonstrated by influx techniques across the apical membrane of the intact epithelium. However, the vesicles also exhibit Na:H and Cl:HCO3 exchange processes and the inhibitors thought to be specific for either the NaCl cotransport system (loop diuretics), for the Na:H exchange (high-dose amiloride), or for the Cl:HCO3 exchange (disulfonic stilbenes such as SITS or DIDS), do not prove to be so. It is possible that all three processes could be present in intestinal brush-border membranes. Furthermore, the techniques of isolating vesicles could uncouple or otherwise inhibit the coupled NaCl process. Nonetheless, the preponderance of evidence at this time indicates that parallel ion exchangers of Na:H and Cl:HCO3, as initially suggested by Turnberg et al [4], account for coupled NaCl transport in rabbit ileum. Additional studies will be necessary to determine if this is the only mechanism in the intestinal apical membrane and whether this conclusion applies to other tissues such as gallbladder and renal tubule.

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