Troglitazone stimulates the insulin-induced tetrahydrobiopterin synthesis in vascular endothelial cells

被引:0
作者
Ishii, M [1 ]
Shimizu, S [1 ]
Shiota, K [1 ]
Kiuchi, Y [1 ]
Yamamoto, T [1 ]
机构
[1] Showa Univ, Sch Pharmaceut Sci, Dept Clin Pharm, Shinagawa Ku, Tokyo 1428555, Japan
关键词
insulin; tetrahydrobiopterin; GTP cyclohydrolase I; troglitazone; endothelial cell;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We investigated the effects of troglitazone, which is a ligand of nuclear transcription factor peroxisome proliferator-activated receptor-gamma (PPAR-gamma), on insulin-induced tetrahydrobiopterin (BH4) synthesis in mouse brain microvascular endothelial cells (MBMECs). BH, content was determined as biopterin, by reversed-phase high performance liquid chromatography using fluorometric detection. Measurement of mRNA level of GTP cydohydrolase I(GTPCH), which is a rate-limiting enzyme for de novo BH, synthesis, was performed by reverse transcription-polymerase chain reaction (RT-PCR). Addition of insulin (10 mug/ml) to endothelial cells increased intra cellular BH4 content and GTPCH mRNA level, and the insulin-induced increase in BH, content and GTPCH mRNA level was further stimulated by co-treatment with troglitazone (0.3-3 muN). However, the expression of PPAR-gamma mRNA in untreated and insulin-treated endothelial cells was not detected. Moreover, bezafibrate (1-10 muM), a ligand of PPAR-delta, did not affect BH4 synthesis in insulin-treated endothelial cells. These findings suggest that troglitazone stimulates insulin-induced BH4 synthesis in endothelial cells with the induction of GTPCH through PPAR-gamma- and PPAR-delta -independent mechanism.
引用
收藏
页码:137 / 141
页数:5
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