Expression of rat thick limb Na/H exchangers in potassium depletion and chronic metabolic acidosis

Details

Serval ID
serval:BIB_E5C19A3EA676
Type
Article: article from journal or magazin.
Collection
Publications
Title
Expression of rat thick limb Na/H exchangers in potassium depletion and chronic metabolic acidosis
Journal
Kidney Int
Author(s)
Laghmani K., Richer C., Borensztein P., Paillard M., Froissart M.
ISSN-L
0085-2538 (Print) 0085-2538 (Linking)
Publication state
Published
Issued date
2001
Volume
60
Number
4
Pages
1386-96
Notes
Laghmani, K
Richer, C
Borensztein, P
Paillard, M
Froissart, M
eng
Research Support, Non-U.S. Gov't
2001/09/29 10:00
Kidney Int. 2001 Oct;60(4):1386-96.
Abstract
BACKGROUND: Regulation of renal transporter expression has been shown to support adaptation of transporter activities in several chronic situations. Basolateral and apical Na/H exchangers (NHE) in medullary thick ascending limb (MTAL) are involved in NH4+ and HCO3+ absorption, respectively. The NH4+ absorption rate in Henle's loop is increased in chronic metabolic acidosis (CMA) and potassium depletion (KD), which may be secondary to the increased NH4+ concentration in luminal fluid and/or to an increased NH4+ absorptive capacity of MTAL. HCO3- absorptive capacity in Henle's loop is increased in CMA and decreased in metabolic alkalosis, but is unchanged in KD despite the presence of metabolic alkalosis. The present study compared the effects of NH4Cl-induced CMA and KD on the expression of basolateral NHE-1 and the effect of KD on the expression of apical NHE-3 in MTAL. METHODS: NHE-1 and NHE-3 mRNAs and proteins were assessed by a competitive reverse transcription-polymerase chain reaction (RT-PCR) method and semiquantitative immunoblots, respectively, in MTAL-purified suspensions from rats with CMA and KD. RESULTS: NHE-1 protein abundance was similarly increased (approximately 90%) at two and five weeks of KD, while NHE-1 mRNA amount in MTAL cells was increased at two weeks of KD and returned to normal values by five weeks of KD. In contrast, NHE-1 mRNA and protein abundance did not change in CMA. NHE-3 protein abundance remained unchanged in both two and five weeks of KD, while NHE-3 mRNA was unchanged by two weeks of KD and reduced by approximately 50% at five weeks of KD. CONCLUSIONS: The results suggest the following: (1) in KD, where the increased NH4+ concentration of luminal fluid that favors NH4+ absorption is counterbalanced by a decrease in BSC1 expression and activity, the increased NHE-1 expression may support an increased MTAL NH4+ absorptive capacity in CMA, NHE-1 expression is not specifically regulated and remains unchanged, suggesting that the increase in NH4+ concentration in luminal fluid is the main determinant of increased NH4+ absorption in MTAL. (2) In KD, NHE-3 expression did not decrease despite the presence of metabolic alkalosis, in agreement with the unchanged HCO3- absorptive capacity of Henle's loop.
Keywords
Acidosis/*metabolism, Animals, Chronic Disease, Loop of Henle/*metabolism, Male, Potassium, RNA, Messenger/metabolism, Rats, Rats, Sprague-Dawley, Sodium-Hydrogen Antiporter/genetics/*metabolism
Open Access
Yes
Create date
03/03/2016 17:49
Last modification date
21/08/2019 6:35
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