Troglitazone but not pioglitazone affects ATP-sensitive K+ channel activity

被引:18
作者
Sunaga, Y
Inagaki, N
Gonoi, T
Yamada, Y
Ishida, H
Seino, Y
Seino, S
机构
[1] Kyoto Univ, Grad Sch Med, Dept Metab & Clin Nutr, Sakyo Ku, Kyoto 6068501, Japan
[2] Chiba Univ, Sch Med, Dept Mol Med, Chuo Ku, Chiba 2608670, Japan
[3] Pathogen Fungi & Microbial Toxicoses Res Ctr, Chuo Ku, Chiba 2608670, Japan
关键词
K+ (K-ATP) channel; ATP-sensitive; sulfonylurea receptor; troglitazone; pioglitazone;
D O I
10.1016/S0014-2999(99)00539-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We compared the effects of the two thiazolidinedione derivatives, troglitazone and pioglitazone, on ATP-sensitive K+ (K-ATP) channel activities. Pancreatic beta-cell type and cardiac type K-ATP channels were reconstituted in COS-1 cells (SV 40-transformed African green monkey kidney (AGMK) cells) by heterologously expressing sulfonylurea receptor 1 (SUR1) plus Kir6.2 and sulfonylurea receptor 2A (SUR2A) plus Kir6.2, respectively. Troglitazone inhibited [Rb-86(+)] efflux in both K-ATP channel types in the presence of metabolic inhibitors, which was confirmed by electrophysiological techniques. The [Rb-86(+)] efflux increased by the channel openers diazoxide and pinacidil was abolished by troglitazone. In contrast, pioglitazone did not affect these channel activities in either type K-ATP channel. These results suggest that troglitazone modulates the various cellular functions including insulin secretion by inhibiting the K-ATP channels, while pioglitazone has no effect on K-ATP channel activity. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:71 / 76
页数:6
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