We compared the effects of the two thiazolidinedione derivatives, troglitaz
one and pioglitazone, on ATP-sensitive K+ (K-ATP) channel activities. Pancr
eatic 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 s
ulfonylurea receptor 2A (SUR2A) plus Kir6.2, respectively. Troglitazone inh
ibited [Rb-86(+)] efflux in both K-ATP channel types in the presence of met
abolic inhibitors, which was confirmed by electrophysiological techniques.
The [Rb-86(+)] efflux increased by the channel openers diazoxide and pinaci
dil was abolished by troglitazone. In contrast, pioglitazone did not affect
these channel activities in either type K-ATP channel. These results sugge
st that troglitazone modulates the various cellular functions including ins
ulin 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.