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      Insulin Increases Acid Production and May Directly Stimulate Na +/H + Exchange Activity in Cultured Vascular Smooth Muscle Cells

      review-article
      , ,
      Journal of Vascular Research
      S. Karger AG
      Insulin, Intracellular pH, Smooth muscle cells, Vascular physiology

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          Abstract

          Insulin was reported to decrease Na<sup>+</sup>/H<sup>+</sup> exchange activity in murine vascular smooth muscle (VSM) tissue. In most other cells, insulin increases activity. We tested the effects of insulin on Na<sup>+</sup>/H<sup>+</sup> exchange activity in primary cultured canine VSM cells. Intracellular pH (pH<sub>i</sub>) was measured with 2′,7′-bis(2-carboxyethyl)-5-carboxyfluorescein fluorescence and Na<sup>+</sup> uptake by isotopic methods. Insulin alone did not significantly affect pH<sub>i</sub> (7.13 ± 0.05 vs. 7.10 ± 0.03 for control and insulin, respectively; p = not significant), and EIPA alone lowered it to 6.98 ± 0.04 (p < 0.05), upon which insulin lowered it further to 6.91 ± 0.04 (p < 0.05). In the presence of a pH<sub>i</sub> clamp, pH<sub>i</sub>/extracellular pH (pH<sub>o</sub>) 7.1/7.4, insulin increased amiloride-sensitive <sup>22</sup>Na uptake by 98 ± 25% (p < 0.05). At pH<sub>i</sub>/pH<sub>o</sub> 6.0/7.4 or 6.7/7.4, amiloride-sensitive <sup>22</sup>Na uptake was stimulated by 378 ± 59 and 105 ± 27%, respectively, compared to pH<sub>i</sub>/pH<sub>o</sub> 7.1/7.4 (p < 0.05 for all 3 versus each other), but was insulin insensitive. In acid-loaded cells (pH<sub>i</sub> 6.0), addition of extracellular Na<sup>+</sup> (pH<sub>o</sub> 7.4) caused rapid intracellular alkalinization, and the initial rate was not affected by insulin. It is concluded that insulin stimulates acid accumulation in VSM cells that is normally effluxed by increased Na<sup>+</sup>/H<sup>+</sup> exchange activity, and insulin may directly stimulate Na<sup>+</sup>/H<sup>+</sup> exchange activity when cells are clamped at resting pH<sub>i</sub> but not at acidic pH<sub>i</sub>.

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          Most cited references15

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          Impaired insulin-mediated skeletal muscle blood flow in patients with NIDDM.

          Patients with non-insulin-dependent diabetes mellitus (NIDDM) exhibit decreased rates of skeletal muscle insulin-mediated glucose uptake (IMGU). Because IMGU is equal to the product of the arteriovenous glucose difference (AVG delta) across and blood flow (F) into muscle (IMGU = AVG delta x F), reduced tissue permeability (AVG delta) and/or glucose and insulin delivery (F) can potentially lead to decreased IMGU. The components of skeletal muscle IMGU were studied in six obese NIDDM subjects (103 +/- 9 kg) and compared with those previously determined in six lean (weight 68 +/- 3 kg), and six obese (94 +/- 3 kg) with normal glucose tolerance. The insulin dose-response curves for whole body and leg muscle IMGU were constructed using the combined euglycemic clamp and leg balance techniques during sequential insulin infusions (range of serum insulin 130-80,000 pmol/L). In lean, obese, and NIDDM subjects, whole body IMGU, femoral AVG delta, and leg IMGU increased in a dose-dependent fashion over the range of insulin with an ED50 of 400-500 pmol/L in lean, 1000-1200 pmol/L in obese, and 4000-7000 pmol/L in NIDDM subjects (P less than 0.01 lean vs. obese and NIDDM). In lean and obese subjects, maximally effective insulin concentrations increased leg blood flow approximately 2-fold from basal with an ED50 of 266 pmol/L and 957 pmol/L, respectively (P less than 0.01 lean vs. obese). In contrast, leg F did not increase from the basal value in NIDDM subjects (2.7 +/- 0.1 vs. 3.5 +/- 0.5 dl/min, NS).(ABSTRACT TRUNCATED AT 250 WORDS)
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            Intracellular Ph Regulation by Na+/H+ Exchange Requires Phosphatidylinositol 4,5-Bisphosphate

            The carrier-mediated, electroneutral exchange of Na+ for H+ across the plasma membrane does not directly consume metabolic energy. Nevertheless, acute depletion of cellular ATP markedly decreases transport. We analyzed the possible involvement of polyphosphoinositides in the metabolic regulation of NHE1, the ubiquitous isoform of the Na+/H+ exchanger. Depletion of ATP was accompanied by a marked reduction of plasmalemmal phosphatidylinositol 4,5-bisphosphate (PIP2) content. Moreover, sequestration or hydrolysis of plasmalemmal PIP2, in the absence of ATP depletion, was associated with profound inhibition of NHE1 activity. Examination of the primary structure of the COOH-terminal domain of NHE1 revealed two potential PIP2-binding motifs. Fusion proteins encoding these motifs bound PIP2 in vitro. When transfected into antiport-deficient cells, mutant forms of NHE1 lacking the putative PIP2-binding domains had greatly reduced transport capability, implying that association with PIP2 is required for optimal activity. These findings suggest that NHE1 activity is modulated by phosphoinositides and that the inhibitory effect of ATP depletion may be attributable, at least in part, to the accompanying net dephosphorylation of PIP2.
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              The regulation of ion channels and transporters by glycolytically derived ATP.

              Glycolysis is an evolutionary conserved metabolic pathway that provides small amounts of energy in the form of ATP when compared to other pathways such as oxidative phosphorylation or fatty acid oxidation. The ATP levels inside metabolically active cells are not constant and the local ATP level will depend on the site of production as well as the respective rates of ATP production, diffusion and consumption. Membrane ion transporters (pumps, exchangers and channels) are located at sites distal to the major sources of ATP formation (the mitochondria). We review evidence that the glycolytic complex is associated with membranes; both at the plasmalemma and with membranes of the endo/sarcoplasmic reticular network. We examine the evidence for the concept that many of the ion transporters are regulated preferentially by the glycolytic process. These include the Na(+)/K(+)-ATPase, the H(+)-ATPase, various types of Ca(2+)-ATPases, the Na(+)/H(+) exchanger, the ATP-sensitive K(+) channel, cation channels, Na(+) channels, Ca(2+) channels and other channels involved in intracellular Ca(2+) homeostasis. Regulation of these pumps, exchangers and ion channels by the glycolytic process has important consequences in a variety of physiological and pathophysiological processes, and a better understanding of this mode of regulation may have important consequences for developing future strategies in combating disease and developing novel therapeutic approaches.
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                Author and article information

                Journal
                JVR
                J Vasc Res
                10.1159/issn.1018-1172
                Journal of Vascular Research
                S. Karger AG
                1018-1172
                1423-0135
                2011
                October 2011
                11 August 2011
                : 48
                : 6
                : 505-512
                Affiliations
                Division of Nephrology and Hypertension, Department of Medicine, Medical School, University of Texas Health Science Center, Houston, Tex., USA
                Author notes
                *Dr. Andrew M. Kahn, Division of Nephrology and Hypertension, Department of Medicine, Medical School University of Texas Health Science Center, 6431 Fannin, MSB 5.134, Houston, TX 77030 (USA), Tel. +1 713 500 6868, E-Mail Andrew.M.Kahn@uth.tmc.edu
                Article
                329587 J Vasc Res 2011;48:505–512
                10.1159/000329587
                21832840
                46c52eec-c8a9-4f8c-9d1c-1122ce0e5a19
                © 2011 S. Karger AG, Basel

                Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher. Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug. Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.

                History
                : 07 December 2010
                : 20 May 2011
                Page count
                Figures: 4, Pages: 8
                Categories
                Research Paper

                General medicine,Neurology,Cardiovascular Medicine,Internal medicine,Nephrology
                Smooth muscle cells,Insulin,Intracellular pH,Vascular physiology

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