Chronic metabolic acidosis enhances NHE-3 protein abundance and transport activity in the rat thick ascending limb by increasing NHE-3 mRNA
Details
Serval ID
serval:BIB_445CFB2543CC
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Chronic metabolic acidosis enhances NHE-3 protein abundance and transport activity in the rat thick ascending limb by increasing NHE-3 mRNA
Journal
J Clin Invest
ISSN-L
0021-9738 (Print) 0021-9738 (Linking)
Publication state
Published
Issued date
1997
Volume
99
Number
1
Pages
24-30
Notes
Laghmani, K
Borensztein, P
Ambuhl, P
Froissart, M
Bichara, M
Moe, O W
Alpern, R J
Paillard, M
eng
DK-39298/DK/NIDDK NIH HHS/
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S.
1997/01/01
J Clin Invest. 1997 Jan 1;99(1):24-30.
Borensztein, P
Ambuhl, P
Froissart, M
Bichara, M
Moe, O W
Alpern, R J
Paillard, M
eng
DK-39298/DK/NIDDK NIH HHS/
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S.
1997/01/01
J Clin Invest. 1997 Jan 1;99(1):24-30.
Abstract
Chronic metabolic acidosis (CMA) is associated with an adaptive increase in the bicarbonate absorptive capacity of the rat medullary thick ascending limb (MTAL). To specify whether NHE-3, the apical MTAL Na/H exchanger, is involved in this adaptation, NHE-3 mRNA was quantified by a competitive RT-PCR using an internal standard which differed from the wild-type NHE-3 mRNA by an 80-bp deletion. CMA increased NHE-3 mRNA from 0.025+/-0.003 to 0.042+/-0.009 amol/ng total RNA (P < 0.005). NHE-3 transport activity was measured as the initial proton flux rate calculated from the Na-dependent cell pH recovery of Na-depleted acidified MTAL cells in the presence of 50 microM HOE694 which specifically blocks NHE-1, the basolateral MTAL NHE isoform. CMA caused a 68% increase in NHE-3 transport activity (P < 0.001). In addition, CMA was associated with a 71% increase in NHE-3 protein abundance (P < 0.05) as determined by Western blot analysis on MTAL membranes using a polyclonal antiserum directed against a cytoplasmic epitope of rat NHE-3. Thus, NHE-3 adapts to CMA in the rat MTAL via an increase in the mRNA transcript that enhances NHE-3 protein abundance and transport activity.
Keywords
Acidosis/*genetics/*metabolism, Ammonium Chloride/pharmacology, Animals, Bicarbonates/metabolism, Biological Transport, Blotting, Western, Cells, Cultured, Chronic Disease, Male, Medulla Oblongata/cytology/*metabolism, Polymerase Chain Reaction, Proton Pumps, RNA, Messenger/analysis, Rats, Rats, Sprague-Dawley, Sodium-Hydrogen Antiporter/genetics/*metabolism/physiology, Transcription, Genetic
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Open Access
Yes
Create date
03/03/2016 16:49
Last modification date
21/08/2019 5:35