Sato Toshiaki, Nakaya Haruaki
Department of Pharmacology, Chiba University Graduate School of Medicine, Chuo-ku, Chiba, Japan.
J Cardiovasc Pharmacol. 2006 Feb;47(2):165-8. doi: 10.1097/01.fjc.0000199224.40799.a4.
P-1075 was reported to be selective for sarcolemmal ATP-sensitive K (sarcKATP) channels because of its lack of mitochondria-oxidizing effect in isolated adult rabbit myocytes. Conflicting results however have been reported on the action of P-1075 on mitochondrial KATP (mitoKATP) channels. The aim of the present study was to reevaluate the effect of P-1075 on mitoKATP channels. Endogenous flavoprotein autofluorescence in isolated rabbit ventricular myocytes was measured to assay mitoKATP channel activity. The mitoKATP channel opener diazoxide (100 microM) oxidized the flavoprotein. P-1075 at a concentration of 30 microM significantly inhibited the oxidative effect of diazoxide from 48.6 +/- 7.1% to 28.2 +/- 5.2% of the maximum value induced by 2,4-dinitrophenol (DNP, 100 microM) (n = 4, P < 0.05). Additionally, P-1075 (30 microM) significantly inhibited the pinacidil (100 microM)-induced flavoprotein oxidation by 48.4 +/- 3.9% (n = 4, P < 0.05). The inhibitory effects of P-1075 on diazoxide-induced flavoprotein oxidation were observed in the micromolar range in a concentration dependent manner. P-1075 alone oxidized flavoprotein in the range 30 nM to 5 microM, and was nearly maximal at 150 nM (11.1 +/- 1.9% of the DN P value, n = 5). These results indicate that P-1075 exerts diverse effects on mitoKATP channel in rabbit ventricular myocytes: P-1075 has a partial agonist effect and weakly activates mitoKATP channels at low concentrations, whereas P-1075 rather inhibits the opening of mitoKATP channels in the micromolar concentration range.
据报道,P - 1075对肌膜ATP敏感性钾(sarcKATP)通道具有选择性,因为它在分离的成年兔心肌细胞中缺乏线粒体氧化作用。然而,关于P - 1075对线粒体ATP敏感性钾(mitoKATP)通道的作用,已有相互矛盾的报道。本研究的目的是重新评估P - 1075对mitoKATP通道的影响。通过测量分离的兔心室肌细胞中的内源性黄素蛋白自发荧光来检测mitoKATP通道活性。mitoKATP通道开放剂二氮嗪(100微摩尔)可氧化黄素蛋白。浓度为30微摩尔的P - 1075可将二氮嗪的氧化作用从2,4 - 二硝基苯酚(DNP,100微摩尔)诱导的最大值的48.6±7.1%显著抑制至28.2±5.2%(n = 4,P < 0.05)。此外,P - 1075(30微摩尔)可将吡那地尔(100微摩尔)诱导的黄素蛋白氧化作用显著抑制48.4±3.9%(n = 4,P < 0.05)。在微摩尔范围内观察到P -