Komjati M, Vierhapper H, Waldhäusl W
Life Sci. 1985 Nov 11;37(19):1829-33. doi: 10.1016/0024-3205(85)90226-7.
The effect of indomethacin (IND) on glucagon-induced hepatic glucose production (HGP) was studied in the isolated perfused livers of rats. Addition of IND (0.2 mM) to the perfusion medium had no effect on glucagon-stimulated HGP when compared to control experiments without added IND (1.02 +/- 0.17 vs. 1.00 +/- 0.26 mmol per (120 min X 100 g b.w.), respectively; NS). Intravenous pretreatment with both, IND (10 mg/kg b.w.), or vehicle resulted in a reduction in glucagon-induced HGP due to a decrease in hepatic glycogen content. A complete depletion of the hepatic glycogen pool and thus a lack in glucagon-stimulated HGP was observed when IND was given intraperitoneally. These results indicate that the changes in HGP observed after pretreatment with IND may largely if not completely be due to a non-specific depletion in hepatic glycogen content and that IND does not exert a direct influence on HGP.
在大鼠离体灌注肝脏中研究了吲哚美辛(IND)对胰高血糖素诱导的肝葡萄糖生成(HGP)的影响。与未添加IND的对照实验相比,向灌注培养基中添加IND(0.2 mM)对胰高血糖素刺激的HGP没有影响(分别为1.02±0.17与1.00±0.26 mmol/(120分钟×100克体重);无显著性差异)。用IND(10毫克/千克体重)或溶剂进行静脉预处理,由于肝糖原含量降低,导致胰高血糖素诱导的HGP减少。当腹腔注射IND时,观察到肝糖原池完全耗尽,因此缺乏胰高血糖素刺激的HGP。这些结果表明,IND预处理后观察到的HGP变化如果不是完全由肝糖原含量的非特异性消耗引起,也可能在很大程度上是由其引起的,并且IND对HGP没有直接影响。