Literature DB >> 4324309

Reduction in adipocyte ATP by lipolytic agents: relation to intracellular free fatty acid accumulation.

A Angel, K S Desai, M L Halperin.   

Abstract

Epinephrine, norepinephrine, ACTH, and dibutyryl 3',5'-cyclic AMP reduced adipocyte ATP levels during 60 min incubation; glucose displayed a protective effect. The reduction in adipocyte ATP levels could not be attributed solely to: a direct hormone effect, deficiency in metabolic substrate, activation of adenyl cyclase with ATP consumption, loss of adenine nucleotide from the cell or loss of cells during incubation, lipolytic rate per se, or extracellular accumulation of FFA or glycerol. To determine whether intracellular FFA accumulation was a causative factor, intracellular FFA levels were measured during hormone-stimulated lipolysis. This was accomplished by using sucrose-U-(14)C as a marker for the extracellular space to correct for contamination of cells by extracellular albumin-bound FFA. These experiments showed that the fall in adipocyte ATP correlated with FFA saturation of medium albumin and progressive accumulation of FFA within the adipocyte. Furthermore, the protective effect of glucose noted above was associated with a marked reduction in intracellular FFA as compared to the extracellular FFA pool. On the basis of these studies, combined with those in the literature, it is concluded that in vitro effects of lipolytic agents on adipocyte ATP levels are the net result of imparied ATP synthesis (uncoupled oxidative phosphorylation) in the face of normal or augmented ATP consumption.

Entities:  

Mesh:

Substances:

Year:  1971        PMID: 4324309

Source DB:  PubMed          Journal:  J Lipid Res        ISSN: 0022-2275            Impact factor:   5.922


  17 in total

1.  Relationship between lipolysis and calcium in epididymal adipose tissue of obese-hyperglycaemic mice.

Authors:  J P Dehaye; J Winand; P Poloczek; J Christophe
Journal:  Diabetologia       Date:  1979-06       Impact factor: 10.122

2.  Inhibition of hormone-stimulated lipolysis by clofibrate. A possible mechanism for its hypolipidemic action.

Authors:  M A D'Costa; A Angel
Journal:  J Clin Invest       Date:  1975-01       Impact factor: 14.808

3.  The effect of glucose, insulin and noradrenaline on lipolysis, and on the concentrations of adenosine 3':5'-cyclic monophosphate and adenosine 5'-triphosphate in adipose tissue.

Authors:  B L Knight; J Iliffe
Journal:  Biochem J       Date:  1973-01       Impact factor: 3.857

4.  Beta-adrenergic stimulation of adenine nucleotide catabolism and purine release in human adipocytes.

Authors:  H Kather
Journal:  J Clin Invest       Date:  1990-01       Impact factor: 14.808

5.  Adipose-tissue Mg2+-dependent phosphatidate phosphohydrolase. Control of activity and subcellular distribution in vitro and in vivo.

Authors:  S J Taylor; E D Saggerson
Journal:  Biochem J       Date:  1986-10-15       Impact factor: 3.857

6.  The regulation of glyceride synthesis in isolated white-fat cells. The effects of palmitate and lipolytic agents.

Authors:  E D Saggerson
Journal:  Biochem J       Date:  1972-08       Impact factor: 3.857

7.  The effect of beta-adrenergic agonists on the membrane potential of fat-cell mitochondria in situ.

Authors:  R J Davis; B R Martin
Journal:  Biochem J       Date:  1982-09-15       Impact factor: 3.857

8.  Triphenylmethylphosphonium cation distribution as a measure of hormone-induced alterations in white adipocyte membrane potential.

Authors:  M L Vallano; M Sonenberg
Journal:  J Membr Biol       Date:  1982       Impact factor: 1.843

9.  Extensive but reversible depletion of ATP via adenylate cyclase in rat adipocytes.

Authors:  F Z Chung; H W Weber; M M Appleman
Journal:  Proc Natl Acad Sci U S A       Date:  1985-03       Impact factor: 11.205

10.  Effect of insulin, catecholamines and calcium ions on phospholipid metabolism in isolated white fat-cells.

Authors:  J A García-Sáinz; J N Fain
Journal:  Biochem J       Date:  1980-03-15       Impact factor: 3.857

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.