Shin M, Iwamoto N, Yamashita M, Sano K, Umezawa C
School of Pharmacy, Kobe Gakuin University, Japan.
Biochem Pharmacol. 1998 Feb 1;55(3):367-71. doi: 10.1016/s0006-2952(97)00507-8.
Hepatic NAD+, NADH, and NADPH were increased significantly 3 days after feeding rats with a 0.25% clofibrate diet, increased further after 8 days, and stayed at the same levels 14 days after feeding the diet. The NAD+/NADH ratio was decreased significantly by feeding the clofibrate diet for 8 days, while the ratio remained unchanged with a 1% pyrazinamide diet. Hepatic quinolinate phosphoribosyltransferase (QAPRTase) (EC 2.4.2.19) activity was increased to 1.8 and 1.3 times that of the control animals in the clofibrate- and the pyrazinamide-fed rats, respectively, while hepatic aminocarboxymuconate-semialdehyde decarboxylase (ACMSDase) (EC 4.1.1.45) activity was decreased to 0 and 19% of that of the control animals. The heat-treated liver homogenate from the pyrazinamide-fed rats contained inhibitory activity toward ACMSDase, while no inhibitory activity was found in the liver homogenate of the clofibrate-fed animals. We conclude that these changes of enzyme activities, which seem due to different mechanisms, may contribute to the increase of pyridine nucleotides in the liver of rats fed clofibrate or pyrazinamide.
给大鼠喂食0.25%氯贝丁酯饮食3天后,肝脏中的NAD⁺、NADH和NADPH显著增加,8天后进一步增加,喂食该饮食14天后维持在相同水平。喂食氯贝丁酯饮食8天可显著降低NAD⁺/NADH比值,而喂食1%吡嗪酰胺饮食时该比值保持不变。在喂食氯贝丁酯和吡嗪酰胺的大鼠中,肝脏喹啉酸磷酸核糖基转移酶(QAPRTase)(EC 2.4.2.19)活性分别增加至对照动物的1.8倍和1.3倍,而肝脏氨基羧基粘康酸半醛脱羧酶(ACMSDase)(EC 4.1.1.45)活性分别降低至对照动物的0和19%。喂食吡嗪酰胺的大鼠经热处理的肝脏匀浆含有对ACMSDase的抑制活性,而在喂食氯贝丁酯的动物肝脏匀浆中未发现抑制活性。我们得出结论,这些酶活性的变化似乎是由不同机制引起的,可能有助于喂食氯贝丁酯或吡嗪酰胺的大鼠肝脏中吡啶核苷酸的增加。