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- W2004668515 abstract "Novel non-thiazolidinedione, tyrosine-derived peroxisome proliferator-activated receptor γ agonists, GI 262570, GW 7845, GW 1929, developed by GlaxoSmithKline (GSK) along with pioglitazone and nisoldipine, were studied on currents through L-type voltage-dependent calcium channels (VDCC) in freshly isolated smooth muscle cells from mesenteric arteries, and on the diameter of pressurized mesenteric arteries in vitro. Using Ba<sup>2+</sup> (10 mmol/l) as the charge carrier through VDCC, the half-inhibition constants (IC<sub>50</sub>) for GI 262570, GW 7845, GW 1929, and pioglitazone were 2.0 ± 0.5, 3.0 ± 0.5, 5.0 ± 0.7, and 10.0 ± 0.8 µmol/l, respectively. For arterial diameter measurements the IC<sub>50</sub> values for GI 262570, GW 7845, GW 1929, and pioglitazone were 2.4, 4.1, 6.3, and 13.9 µmol/l, respectively. Each GSK compound and pioglitazone was effective at inhibiting VDCC and relaxing pressurized arteries, suggesting that the vasodilation of resistance arteries could be explained by the inhibition of calcium entry through VDCC." @default.
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- W2004668515 date "2004-12-03" @default.
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- W2004668515 title "Novel PPARγ Agonists GI 262570, GW 7845, GW 1929, and Pioglitazone Decrease Calcium Channel Function and Myogenic Tone in Rat Mesenteric Arteries" @default.
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- W2004668515 doi "https://doi.org/10.1159/000081070" @default.
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