JBC Advanced Glycation Endproducts

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lu, S. C.
Right arrow Articles by Kaplowitz, N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lu, S. C.
Right arrow Articles by Kaplowitz, N.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

J. Biol. Chem., Vol. 265, Issue 27, 16088-16095, 09, 1990

Hormonal regulation of glutathione efflux

SC Lu, C Garcia-Ruiz, J Kuhlenkamp, M Ookhtens, M Salas-Prato and N Kaplowitz
Department of Medicine, University of Southern California School of Medicine, Los Angeles 90033.

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.
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
J. Physiol.Home page
B. Gonzalez and R. Manso
Induction, modification and accumulation of HSP70s in the rat liver after acute exercise: early and late responses
J. Physiol., April 15, 2004; 556(2): 369 - 385.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
F. Mariotti, K. L. Simbelie, L. Makarios-Lahham, J.-F. Huneau, B. Laplaize, D. Tome, and P. C. Even
Acute Ingestion of Dietary Proteins Improves Post-Exercise Liver Glutathione in Rats in a Dose-Dependent Relationship with their Cysteine Content
J. Nutr., January 1, 2004; 134(1): 128 - 131.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
P. Palestini, M. Pitto, G. Tedeschi, A. Ferraretto, M. Parenti, J. Brunner, and M. Masserini
Tubulin Anchoring to Glycolipid-enriched, Detergent-resistant Domains of the Neuronal Plasma Membrane
J. Biol. Chem., March 31, 2000; 275(14): 9978 - 9985.
[Abstract] [Full Text] [PDF]


Home page
FASEB J.Home page
S. C. LU
Regulation of hepatic glutathione synthesis: current concepts and controversies
FASEB J, July 1, 1999; 13(10): 1169 - 1183.
[Abstract] [Full Text]


Home page
J. Nutr.Home page
C. Leeuwenburgh and L. L. Ji
Glutathone and Glutathione Ethyl Ester Supplementation of Mice Alter Glutathione Homeostasis during Exercise
J. Nutr., December 1, 1998; 128(12): 2420 - 2426.
[Abstract] [Full Text]


Home page
Biol. Reprod.Home page
T. L. McNutt-Scott and C. Harris
Modulation of Intracellular Glutathione and Cysteine Metabolism in Bovine Oviduct Epithelial Cells Cultured In Vitro
Biol Reprod, August 1, 1998; 59(2): 314 - 320.
[Abstract] [Full Text]


Home page
J. Nutr.Home page
S.-T. Wang, H.-W. Chen, L.-Y. Sheen, and C.-K. Lii
Methionine and Cysteine Affect Glutathione Level, Glutathione-Related Enzyme Activities and the Expression of Glutathione S-Transferase Isozymes in Rat Hepatocytes
J. Nutr., November 1, 1997; 127(11): 2135 - 2141.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 All ASBMB Journals   Molecular and Cellular Proteomics 
 Journal of Lipid Research   ASBMB Today 
Copyright © 1990 by the American Society for Biochemistry and Molecular Biology.