Marunaka Y
Laboratory of Cellular and Molecular Physiology, Division of Respiratory Research, The Hospital for Sick Children and Institute of Medical Science, University of Toronto, Toronto, ON M5G 1X8, Canada.
Jpn J Physiol. 1997 Dec;47(6):499-511. doi: 10.2170/jjphysiol.47.499.
One of the most important factors controlling blood pressure is the total body Na+ content, which depends upon Na+ intake and excretion. The kidney influences body Na+ content by regulating the tubular absorption of the Na+ filtered through the glomeruli. Thus, the regulation of Na+ absorption in the tubules of the kidney plays an important role in controlling blood pressure. More than 99% of the Na+ passing through the glomerulus is reabsorbed in the kidney. About 90% of the filtered Na+ through the glomerulus is reabsorbed in the proximal tubule and the ascending limb of the loop of Henle. The remainder of the Na+ absorption occurs in the distal nephron. This process is regulated by hormones such as aldosterone and antidiuretic hormone (ADH), and also by the osmolality of the plasma. These observations suggest that the regulation of Na+ transport in the distal nephron by hormones and osmolality plays an important role in the control of blood pressure. The distal nephron is composed of two different types of epithelial cells: the principal cell and the intercalated cell. The latter is also composed of two types of cells: alpha and beta intercalated cells. In addition to Na+ absorption, the distal-nephron epithelial cells also participate in K+ and H+ secretion. Na+ absorption is mediated through the principal cell, which also contributes to K+ secretion, whereas H+ is secreted through both types of intercalated cells, alpha and beta, in different ways. There are, in general, two steps in the transepithelial ion movement across the epithelium, including the distal-nephron epithelium. For example, in the case of Na+ absorption, one is the entry step of Na+ across the apical membrane and the other is the extrusion step of Na+ across the basolateral membrane. This means that there are two major regulatory sites of transepithelial Na+ absorption: namely, regulation of the entry and extrusion steps of Na+. It is generally thought that the entry step of Na+ across the apical membrane is the rate-limiting step in the transepithelial Na+ transport and that Na+ channels in the apical membrane play an important role as an entry step of Na+ and are regulated by hormones and plasma osmolality. In this review, we describe the regulatory mechanisms of Na+ absorption in renal distal-nephron epithelium by aldosterone, ADH and osmolality. Further, we will review the regulatory mechanisms of Cl- transport, which also plays an important role in Na+ transport as a major counter ion, and discuss other roles of Cl- in the active regulation of Na+ transport.
控制血压的最重要因素之一是机体总钠含量,它取决于钠的摄入与排泄。肾脏通过调节经肾小球滤过的钠在肾小管的重吸收来影响机体钠含量。因此,肾脏肾小管中钠重吸收的调节在控制血压方面发挥着重要作用。超过99%经肾小球滤过的钠在肾脏中被重吸收。约90%经肾小球滤过的钠在近端小管和髓袢升支被重吸收。其余的钠重吸收发生在远端肾单位。这个过程受醛固酮和抗利尿激素(ADH)等激素以及血浆渗透压的调节。这些观察结果表明,激素和渗透压对远端肾单位钠转运的调节在血压控制中起重要作用。远端肾单位由两种不同类型的上皮细胞组成:主细胞和闰细胞。后者又由两种细胞组成:α和β闰细胞。除了钠重吸收外,远端肾单位上皮细胞还参与钾和氢离子的分泌。钠重吸收通过主细胞介导,主细胞也参与钾的分泌,而氢离子通过α和β两种闰细胞以不同方式分泌。一般来说,跨上皮(包括远端肾单位上皮)的离子移动有两个步骤。例如,就钠重吸收而言,一个是钠穿过顶端膜的进入步骤,另一个是钠穿过基底外侧膜的排出步骤。这意味着跨上皮钠重吸收有两个主要调节位点:即钠进入和排出步骤的调节。一般认为,钠穿过顶端膜的进入步骤是跨上皮钠转运的限速步骤,顶端膜中的钠通道作为钠的进入步骤起重要作用,并受激素和血浆渗透压调节。在本综述中,我们描述了醛固酮、ADH和渗透压对肾远端肾单位上皮钠重吸收的调节机制。此外,我们将综述氯转运的调节机制,氯作为主要的抗衡离子在钠转运中也起重要作用,并讨论氯在钠转运的主动调节中的其他作用。