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Research Article Free access | 10.1172/JCI116791

Glucocorticoid deficiency increases phospholipase A2 activity in rats.

B S Vishwanath, F J Frey, M J Bradbury, M F Dallman, and B M Frey

Department of Medicine, University of Bern, Switzerland.

Find articles by Vishwanath, B. in: PubMed | Google Scholar

Department of Medicine, University of Bern, Switzerland.

Find articles by Frey, F. in: PubMed | Google Scholar

Department of Medicine, University of Bern, Switzerland.

Find articles by Bradbury, M. in: PubMed | Google Scholar

Department of Medicine, University of Bern, Switzerland.

Find articles by Dallman, M. in: PubMed | Google Scholar

Department of Medicine, University of Bern, Switzerland.

Find articles by Frey, B. in: PubMed | Google Scholar

Published October 1, 1993 - More info

Published in Volume 92, Issue 4 on October 1, 1993
J Clin Invest. 1993;92(4):1974–1980. https://doi.org/10.1172/JCI116791.
© 1993 The American Society for Clinical Investigation
Published October 1, 1993 - Version history
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Abstract

An important mechanism for the antiinflammatory effect of pharmacological doses of glucocorticoids is the inhibition of arachidonic acid release from phospholipids by phospholipase A2 (PLA2). As a corollary, one might predict that low endogenous concentrations of glucocorticoids favor inflammatory disease states. Indeed, clinical and experimental observations revealed an association between glucocorticoid deficiency and disease states caused by immunological and/or inflammatory mechanisms. The purpose of the present investigation was to study the regulation of PLA2 mRNA, protein, and enzyme activity in adrenalectomized (ADX) rats where glucocorticoid concentrations were below physiological levels. The mRNA of group I and II PLA2 were measured by PCR. Group II PLA2 mRNA was increased by 126 +/- 9% in lung tissue of ADX rats, whereas group I PLA2 was increased only by 27 +/- 1.5%. The increase in group II mRNA in ADX rats was reflected by a corresponding increase of group II PLA2 protein (70-100%) in lung, spleen, liver, and kidney. This increase was reversed by the administration of exogenous corticosterone. After ADX, the percentage increase in total PLA2 activity was higher than that of mRNA or PLA2 protein, suggesting that the activity of the enzyme was modulated by inhibitors or activators. The concentration of lipocortin-I, an inhibitor of PLA2 enzyme was strongly correlated with the activity of PLA2 in the tissues (lung, spleen, liver, and kidney). In all these tissues, the concentrations of lipocortin-I declined after ADX. Thus upregulation of PLA2 enzyme and downregulation of lipocortin-I might account for the enhanced inflammatory response in hypoglucocorticoid states.

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