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J. Biol. Chem., Vol. 265, Issue 27, 16088-16095, 09, 1990
SC Lu, C Garcia-Ruiz, J Kuhlenkamp, M Ookhtens, M Salas-Prato and N Kaplowitz
The efflux of GSH has been shown previously to be a saturable process in
both isolated rat hepatocytes and perfused liver, suggesting a
carrier-mediated transport mechanism. The possibility in hormonal
regulation of this process has been raised by recent reports. Our present
work examined the role of hormones known to affect intracellular signal
transduction mechanisms on GSH efflux in cultured rat hepatocytes and
perfused rat livers. We found that cAMP-dependent factors, such as cholera
toxin (CT), dibutyryl cAMP, forskolin, and glucagon all stimulated GSH
efflux in cultured rat hepatocytes. The efflux kinetics were compared in
cultured cells incubated with or without CT; the stimulation of GSH efflux
was related to a near doubling of the Vmax while exhibiting no significant
alteration of the Km. The increase in intracellular cAMP level associated
with the threshold for this stimulatory effect was 25% above control. The
stimulatory effect of CT could not be blocked by cyclohexamide pretreatment
or reversed by colchicine treatment. The stimulatory effect of glucagon was
abolished in the presence of ouabain but not in the presence of barium. On
the other hand, hormones which act through Ca2+ and protein kinase C, such
as phenylephrine and vasopressin, had no effect on GSH efflux in the
cultured cells. In the perfused liver model, glucagon (10 nM) and dibutyryl
cAMP (8 microM) stimulated sinusoidal GSH efflux to 130 and 144% of control
values, respectively, and increased bile flow while not affecting biliary
GSH efflux. Finally, the physiological significance of glucagon-mediated
stimulation of sinusoidal GSH efflux was assessed by both plasma GSH and
glucose levels in response to in vivo glucagon infusion. The threshold dose
of glucagon for significant increase in plasma GSH (5.21 pmol/min) was
lower than for glucose (15.61 pmol/min). At the highest glucagon infusion
rate (261 pmol/min), plasma GSH level doubled while glucose level increased
80%. In conclusion, increased cAMP stimulates GSH efflux in cultured rat
hepatocytes and perfused livers. The stimulatory effect of cAMP is exerted
at the sinusoidal pole and appears to be mediated by hyperpolarization of
hepatocytes by stimulation of Na(+)-K(+)-ATPase. In vivo studies confirmed
the importance of cAMP-mediated stimulation of sinusoidal GSH efflux as it
resulted in significant elevation of the plasma GSH level.
Hormonal regulation of glutathione efflux
Department of Medicine, University of Southern California School of Medicine, Los Angeles 90033.
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