1. Thiazolidinediones increase arachidonic acid release and subsequent prostanoid production in a peroxisome proliferator-activated receptor gamma-independent manner.
- Author
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Tsukamoto H, Hishinuma T, Suzuki N, Tayama R, Hiratsuka M, Yoshihisa T, Mizugaki M, and Goto J
- Subjects
- Animals, COS Cells, Cell Membrane drug effects, Cell Membrane metabolism, Chlorocebus aethiops, Cyclooxygenase 1, Cyclooxygenase 2, Humans, Lipopolysaccharides pharmacology, Membrane Proteins, Mice, NIH 3T3 Cells, PPAR gamma agonists, PPAR gamma antagonists & inhibitors, Phospholipases A metabolism, Phosphorylation, Pioglitazone, Prostaglandin-Endoperoxide Synthases metabolism, Rosiglitazone, U937 Cells, Arachidonic Acid biosynthesis, Dinoprostone biosynthesis, PPAR gamma physiology, Thiazolidinediones pharmacology, Thromboxane A2 biosynthesis
- Abstract
Thiazolidinedione, peroxisome proliferator-activated receptor gamma (PPARgamma) agonist, has been used as an anti-diabetic drug and as an useful tool to elucidate multiple PPARgamma functions by in vitro and in vivo studies. We investigated the effects of thiazolidinediones on prostanoid production in lipopolysaccharide-stimulated cells. The high concentrations (>10 microM) of rosiglitazone and pioglitazone significantly increased lipopolysaccharide-stimulated prostanoid production such as thromboxane A2 and prostaglandin E2. However, PPARgamma antagonist could not inhibit them. In PPARgamma-deficient cells, thiazolidinediones increased prostaglandin E2 production. Thiazolidinediones increased arachidonic acid (AA) release from the cell membrane by not stimulating AA releasing process involving several phospholipase A2s but inhibiting AA reuptaking process. The expression of cyclooxygenase-1 and cyclooxygenase-2 were not affected by thiazolidinediones. In this study, we demonstrated that high concentrations of TZDs increased AA release by the inhibition of AA reuptaking process, leading to subsequent increase in the prostanoid production in a PPARgamma-independent manner. This mechanism provides useful information for the elucidation of multiple PPARgamma functions and diabetic drug therapy.
- Published
- 2004
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