Féraille E
Division de néphrologie, Hôpital cantonal universitaire, Genève.
Nephrologie. 1994;15(4):301-5.
Na-K-ATPase is an ubiquitous enzyme involved in the tubular reabsorption process. Na-K-ATPase is specifically controlled in each nephron segment. Sodium retention is one of the main features of the nephrotic syndrome. Hypervolemia is found in most of the nephrotic syndromes in adults, suggesting a primary renal origin. In the puromycin-induced nephrotic syndrome in rats, the collecting duct is the site of sodium retention. We have shown that Na-K-ATPase activity is specifically enhanced in collecting ducts from rats with puromycin-induced nephrotic syndrome. The stimulation of Na-K-ATPase activity was independent of aldosterone and endogenous inhibitors of the Na-K-ATPase, suggesting a primary paracrin or cellular mechanism. We have demonstrated that two different isoforms of the Na-K-ATPase are coexpressed all along the rat nephron. In the puromycin-induced nephrotic syndrome, the activity of one isoform is specifically enhanced. These results demonstrate that the different isoforms of the Na-K-ATPase can be individually controlled.
钠钾ATP酶是一种参与肾小管重吸收过程的普遍存在的酶。钠钾ATP酶在每个肾单位节段受到特异性调控。钠潴留是肾病综合征的主要特征之一。大多数成人肾病综合征患者存在血容量过多,提示其主要源于肾脏。在嘌呤霉素诱导的大鼠肾病综合征中,集合管是钠潴留的部位。我们已经表明,在嘌呤霉素诱导的肾病综合征大鼠的集合管中,钠钾ATP酶活性特异性增强。钠钾ATP酶活性的刺激独立于醛固酮和钠钾ATP酶的内源性抑制剂,提示存在一种主要的旁分泌或细胞机制。我们已经证明,钠钾ATP酶的两种不同同工型在大鼠整个肾单位中共同表达。在嘌呤霉素诱导的肾病综合征中,一种同工型的活性特异性增强。这些结果表明,钠钾ATP酶的不同同工型可以分别受到调控。