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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Ouabain-insensitive Na~+-ATPase of proximal tubules is an effector for urodilatin and atrial natriuretic peptide
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Ouabain-insensitive Na~+-ATPase of proximal tubules is an effector for urodilatin and atrial natriuretic peptide

机译:近端小管对哇巴因不敏感的Na〜+ -ATPase是尿嘧啶和心钠素的效应子

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摘要

In the present paper we studied the effect of urodilatin and atrial natriuretic peptide (ANP) on the proximal tubule Na+-ATPase and (Na~+K~+)ATPase activities. Urodilatin and ANP inhibit the Na~+-ATPase activity but not the (Na+K+)ATPase activity. Maximal effect was observed at a concentration of 10?11 M for both peptides. In this condition, the enzyme activity decreases from 10.8±1.6 (control) to 5.7±0.9 or 6.1±0.7 nmol Pi mg~(-1) min~(-1) in the presence of urodilatin or ANP, respectively. This effect was completely reversed by 10?6 M LY83583, a guanylyl cyclase inhibitor, and mimicked by 10 nM cGMP. Furthermore, both ANP and urodilatin increase cGMP production by 33% and 49%, respectively. This is the first demonstration that it was shown that urodilatin and ANP directly modulate primary active sodium transport in the proximal tubule. The data obtained indicate that this effect is mediated by the activation of the NPR-A/guanylate cyclase/cGMP pathway.
机译:在本文中,我们研究了urodilatin和心钠素对近端小管Na + -ATPase和(Na〜+ K〜+)ATPase活性的影响。 Urodilatin和ANP抑制Na〜+ -ATPase活性,但不抑制(Na + K +)ATPase活性。两种肽在10?11 M的浓度下都能观察到最大的效果。在这种条件下,在存在urodilatin或ANP的条件下,酶活性分别从10.8±1.6(对照组)降至5.7±0.9或6.1±0.7 nmol Pi mg·(-1)min〜(-1)。这种作用被鸟苷酸环化酶抑制剂10-6M LY83583完全逆转,并被10nM cGMP模仿。此外,ANP和urodilatin均可将cGMP产量分别提高33%和49%。这是第一个证明,证明urodilatin和ANP直接调节近端小管中的主要活性钠转运。获得的数据表明该作用是由NPR-A /鸟苷酸环化酶/ cGMP途径的激活介导的。

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