High salt differentially regulates surface NKCC2 expression in thick ascending limbs of Dahl salt-sensitive and salt-resistant rats

被引:42
|
作者
Haque, Mohammed Ziaul [1 ]
Ares, Gustavo Rosier [1 ]
Caceres, Paulo Sebastian [1 ,2 ]
Ortiz, Pablo Alfredo [1 ,2 ]
机构
[1] Henry Ford Hosp, Dept Internal Med Hypertens & Vasc Res, Detroit, MI 48202 USA
[2] Wayne State Univ, Dept Physiol, Detroit, MI USA
基金
美国国家卫生研究院;
关键词
Na-K-2Cl cotransporter; nephron; salt-sensitive hypertension; trafficking; CL COTRANSPORTER NKCC2; NA+-K+-2CL(-) COTRANSPORTER; NITRIC-OXIDE; CHLORIDE REABSORPTION; SS/JR RATS; TRANSPORT; PHOSPHORYLATION; PROTEIN; LOOP; HYPERTENSION;
D O I
10.1152/ajprenal.00600.2010
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Haque MZ, Ares GR, Caceres PS, Ortiz PA. High salt differentially regulates surface NKCC2 expression in thick ascending limbs of Dahl salt-sensitive and salt-resistant rats. Am J Physiol Renal Physiol 300: F1096-F1104, 2011. First published February 9, 2011; doi:10.1152/ajprenal.00600.2010.-NaCl reabsorption by the thick ascending limb of the loop of Henle (THAL) occurs via the apical Na-K-2Cl cotransporter, NKCC2. Overall, NKCC2 activity and NaCl reabsorption are regulated by the amount of NKCC2 at the apical surface, and also by phosphorylation. Dahl salt-sensitive rats (SS) exhibit higher NaCl reabsorption by the THAL compared with Dahl salt-resistant rats (SR), and they become hypertensive during high-salt (HS) intake. However, the effect of HS on THAL transport, surface NKCC2 expression, and NKCC2 NH2-terminus phosphorylation has not been studied. We hypothesized that HS enhances surface NKCC2 and its phosphorylation in THALs from Dahl SS. THAL suspensions were obtained from a group of SS and SR rats on normal-salt (NS) or HS intake. In SR rats THAL NaCl transport measured as furosemide-sensitive oxygen consumption was decreased by HS (-34%, P < 0.05). In contrast, HS did not affect THAL transport in SS rats. As expected, HS increased systolic blood pressure only in SS rats (Delta 23 +/- 2 mmHg, P < 0.002) but not in SR rats (Delta 5 +/- 3 mmHg). We next tested the effect of HS intake on apical surface NKCC2 and its NH2-terminus threonine phosphorylation (P-NKCC2) in SS and SR rats. HS intake decreased surface NKCC2 by 15 +/- 2% (P < 0.03) in THALs from SR without affecting total NKCC2 or NH2-terminus P-NKCC2. In contrast, in SS rats HS intake increased surface NKCC2 by 54 +/- 6% (P < 0.01) without affecting total NKCC2 expression or P-NKCC2. We conclude that HS intake causes different effects on surface NKCC2 in SS and SR rats. Our data suggest that enhanced surface NKCC2 in SS rats might contribute to enhanced NaCl reabsorption in SS rats during HS intake.
引用
收藏
页码:F1096 / F1104
页数:9
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