The α1-adrenergic transduction system in hamster brown adipocytes. Release of arachidonic acid accompanies activation of phospholipase C

Author:

Schimmel R J1

Affiliation:

1. Department of Physiology, University of Medicine and Dentistry of New Jersey, Robert Wood Johnson Medical School, School of Osteopathic Medicine, Piscataway NJ, 08854 U.S.A.

Abstract

Previous studies of brown adipocytes identified an increased breakdown of phosphoinositides after selective alpha 1-adrenergic-receptor activation. The present paper reports that this response, elicited with phenylephrine in the presence of propranolol and measured as the accumulation of [3H]inositol phosphates, is accompanied by increased release of [3H]arachidonic acid from cells prelabelled with [3H]arachidonic acid. Differences between stimulated arachidonic acid release and formation of inositol phosphates included a requirement for extracellular Ca2+ for stimulated release of arachidonic acid but not for the formation of inositol phosphates and the preferential inhibition of inositol phosphate formation by phorbol 12-myristate 13-acetate. The release of arachidonic acid in response to phenylephrine was associated with an accumulation of [3H]arachidonic acid-labelled diacylglycerol, and this response was not dependent on extracellular Ca2+ but was partially prevented by treatment with the phorbol ester. The release of arachidonic acid was also stimulated by melittin, which increases the activity of phospholipase A2, by ionophore A23187, by lipolytic stimulation with forskolin and by exogenous phospholipase C. The arachidonic acid response to phospholipase C was completely blocked by RHC 80267, an inhibitor of diacylglycerol lipase, but this inhibitor had no effect on release stimulated with melittin or A23187 and inhibited phenylephrine-stimulated release by only 40%. The arachidonate response to forskolin was additive with the responses to either phenylephrine or exogenous phospholipase C. These data indicate that brown adipocytes are capable of releasing arachidonic acid from neutral lipids via triacylglycerol lipolysis, and from phospholipids via phospholipase A2 or by the sequential activities of phospholipase C and diacylglycerol lipase. Our findings also suggest that the action of phenylephrine to promote the liberation of arachidonic acid utilizes both of these reactions.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry

Cited by 14 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Arachidonic acid stimulates DNA synthesis in brown preadipocytes through the activation of protein kinase C and MAPK;Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids;2012-10

2. ATP and β-adrenergic stimulation enhance voltage-gated K current inactivation in brown adipocytes;American Journal of Physiology-Cell Physiology;2000-12-01

3. Effect of hypothyroidism on adenylyl cyclase activity and subtype gene expression in brown adipose tissue;American Journal of Physiology-Regulatory, Integrative and Comparative Physiology;1997-08-01

4. Metabotropic glutamate receptors, transmitter output and fatty acids: studies in rat brain slices;British Journal of Pharmacology;1996-01

5. Signaling Through G Protein-Coupled Receptors;G Protein-Coupled Receptors;1995

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