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长期乙醇摄入对大鼠肝门周和肝静脉周围肝细胞呼吸及糖酵解活性的影响。

Effect of chronic ethanol consumption on respiratory and glycolytic activities of rat periportal and perivenous hepatocytes.

作者信息

Baio D L, Czyz C N, Van Horn C G, Ivester P, Cunningham C C

机构信息

Department of Biochemistry, Wake Forest University Medical Center, Winston-Salem, North Carolina 27157-1016, USA.

出版信息

Arch Biochem Biophys. 1998 Feb 15;350(2):193-200. doi: 10.1006/abbi.1997.0514.

Abstract

Previous studies (Ivester et al., Arch. Biochem. Biophys. 322, 14-21, 1995) have established that periportal and perivenous hepatocytes isolated from ethanol-fed rats demonstrate lower ATP concentrations than those in control preparations when the cells are maintained at very low oxygen tension. In the present investigation, experiments were implemented with periportal and perivenous hepatocytes to determine the effects of chronic ethanol consumption on cellular respiratory and glycolytic activities, since both contribute to maintenance of the energy state of the liver cell. Both periportal and perivenous hepatocytes from ethanol-fed rats demonstrated significantly increased, rather than decreased, respiratory activity when monitored with oxygen concentrations ranging from 16 to 140 microM. Whole liver hepatocytes from control and ethanol-fed animals demonstrated equivalent oxygen utilization, however. Glycolytic activity, monitored by lactate + pyruvate concentrations obtained after both anaerobic and aerobic incubation protocols, was decreased in both cell types from ethanol-fed animals. The glycogen concentrations in freshly isolated periportal and perivenous hepatocytes were also decreased eight- and sevenfold, respectively, as compared with control preparations. Incubation under anaerobic conditions resulted in almost complete depletion of glycogen in both cell types. These observations suggest the possibility that the decreased energy state observed in hepatocytes from ethanol-fed animals is related to a depression in anaerobic glycolysis due to depletion of the endogenous substrate, glycogen.

摘要

以往的研究(Ivester等人,《生物化学与生物物理学报》322卷,14 - 21页,1995年)已证实,当细胞维持在极低氧张力下时,从乙醇喂养大鼠分离出的门周和中央静脉周围肝细胞的ATP浓度低于对照制剂中的细胞。在本研究中,对门周和中央静脉周围肝细胞进行了实验,以确定长期摄入乙醇对细胞呼吸和糖酵解活性的影响,因为这两者都有助于维持肝细胞的能量状态。当用16至140微摩尔的氧浓度监测时,乙醇喂养大鼠的门周和中央静脉周围肝细胞的呼吸活性均显著增加,而非降低。然而,对照动物和乙醇喂养动物的全肝肝细胞的氧利用率相当。通过厌氧和好氧孵育方案后获得的乳酸 + 丙酮酸浓度监测的糖酵解活性,在乙醇喂养动物的两种细胞类型中均降低。与对照制剂相比,新鲜分离的门周和中央静脉周围肝细胞中的糖原浓度也分别降低了8倍和7倍。在厌氧条件下孵育导致两种细胞类型中的糖原几乎完全耗尽。这些观察结果表明,在乙醇喂养动物的肝细胞中观察到的能量状态降低可能与内源性底物糖原耗尽导致的厌氧糖酵解抑制有关。

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