Different modulation of hepatocellular Na+/H+ exchange activity by insulin and EGF

Haimovici, J.; Beck, J.S.; Molla-Hosseini, C.; Vallerand, D.; Haddad, P.

American Journal of Physiology 267(3 Pt 1): G364-G370

1994


ISSN/ISBN: 0002-9513
PMID: 7943232
Document Number: 430226
Indirect evidence suggests that insulin, like epidermal growth factor (EGF), stimulates liver cell Na+/H+ exchange. We directly studied the effect of insulin on intracellular pH (pHi) and the Na+/H+ exchanger in isolated rat hepatocyte with the fluorescent probe, 2',7'-bis(2-carboxyethyl)-5(6)-carboxyfluorescein (BCECF). The effects of insulin were compared with those of EGF. Studies were carried out in the absence of HCO3- and in the presence of acetazolamide to isolate the Na+/H+ exchanger from other pH regulatory mechanisms. Insulin (9 nM) caused a reversible acidification of baseline pHi, whereas no significant effect was observed with EGF (30 nM). pHi was acidified by two different methods (NH4Cl pulse and external Na+ removal) to assess liver cell Na+/H+ exchange activity. In the NH4Cl pulse experiments, insulin had no significant effect on the Na+/H+ exchanger compared with the control (0.141 ± 0.009 pH units/min, n = 14, and 0.122 ± 0.023 pH units/min, n = 16, respectively). However, in the same conditions, EGF nearly doubled the rate of the Na+/H+ exchange activity (0.193 ± 0.015 pH units/min, P < 0.05, n = 6). In the Na+ removal experiments, EGF again significantly increased the pHi recovery rate (0.542 ± 0.032 pH units/min, n = 3) compared with the control (0.227 ± 0.028 pH units/min, n = 5) and insulin (0.245 ± 0.053 pH units/min, n = 5). Compared with control conditions, a subchronic administration of insulin (9 nM) in vitro had no significant effect on the Na+/H+ exchanger, nor did it affect baseline pHi. Results show that insulin, unlike EGF, does not stimulate liver cell Na+/H+ exchange, suggesting different modulation of the membrane transporter by different classes of receptor tyrosine kinase. Reprinted by permission of the publisher.

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