Ouabain-insensitive Na+-ATPase of proximal tubules is an effector for urodilatin and atrial natriuretic peptide

被引:22
作者
Caruso-Neves, C [1 ]
Vives, D [1 ]
Dantas, C [1 ]
Albino, CM [1 ]
Fonseca, LM [1 ]
Lara, LS [1 ]
Iso, M [1 ]
Lopes, AG [1 ]
机构
[1] Univ Fed Rio de Janeiro, Inst Biofis Carlos Chagas Filho, BR-21949900 Rio De Janeiro, RJ, Brazil
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2004年 / 1660卷 / 1-2期
基金
巴西圣保罗研究基金会;
关键词
Na+-ATPase; urodilatin; ANP; furosemide; proximal tubule;
D O I
10.1016/j.bbamem.2003.11.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:93 / 98
页数:6
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