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氟烷(2-溴-2-氯-1,1,1-三氟乙烷)对离体灌注大鼠肝脏糖酵解及生物合成过程的影响。

The effects of halothane (2-bromo-2-chloro-1,1,1-trifluoroethane) on glycolysis and biosynthetic processes of the isolated perfused rat liver.

作者信息

Biebuyck J F, Lund P, Krebs H A

出版信息

Biochem J. 1972 Jul;128(3):711-20. doi: 10.1042/bj1280711.

Abstract
  1. With reference to the post-operative dysfunction of the liver observed after halothane anaesthesia, the effects of the anaesthetic on some metabolic functions were studied in the isolated perfused rat liver. Oxygen uptake, glycolysis, gluconeogenesis and urea synthesis were affected by halothane at a concentration (2.5% of the gas phase) within the range used in clinical anaesthesia. 2. At this concentration of halothane uptake of oxygen was inhibited in livers from both fed and starved rats. 3. In livers from fed rats there was a 16-fold increase in lactate production. This was accompanied by a fivefold decrease in the tissue content of 2-oxoglutarate and a more than twofold decrease in citrate. The calculated [free NAD(+)]/[free NADH] ratio in both cytoplasm and mitochondria was lower in the halothane-exposed livers than in controls. 4. In livers of starved rats the rate of gluconeogenesis from lactate was decreased by halothane to 30% of the control rate. 5. Halothane inhibited gluconeogenesis from alanine and propionate to the same extent as from lactate, whereas glucose formation from dihydroxyacetone, glycerol, fructose and sorbitol was relatively unaffected. 6. During gluconeogenesis from 10mm-lactate the tissue content of ATP was decreased by 50%, glutamate by 50% and 2-oxoglutarate was decreased eightfold in the halothane-exposed livers. 7. Halothane decreased urea synthesis in the presence of 10mm-NH(4)Cl and 2mm-ornithine to 15% of the control rate. 8. The inhibitions of gluconeogenesis and urea synthesis were completely abolished within 15min of withdrawal of the anaesthetic. 9. The stimulation of uptake of oxygen brought about by the addition of lactate or precursors of urea was abolished by halothane. 10. Effects on gluconeogenesis similar to those of halothane occurred in livers exposed to the anaesthetic methoxyflurane, although normal rates were not restored on withdrawal of the drug. Other anaesthetic agents tested (ketamine-HCl and trichloroethylene) decreased gluconeogenesis to 66% of the control rate. 11. The inhibitory effects of halothane are consistent with an interference at the stage of the NADH dehydrogenase of the electron-transport chain.
摘要
  1. 关于氟烷麻醉后观察到的肝脏术后功能障碍,在离体灌注大鼠肝脏中研究了该麻醉剂对某些代谢功能的影响。在临床麻醉所用浓度范围内(气相的2.5%),氟烷影响氧摄取、糖酵解、糖异生和尿素合成。2. 在该氟烷浓度下,喂食大鼠和饥饿大鼠肝脏中的氧摄取均受到抑制。3. 在喂食大鼠的肝脏中,乳酸生成增加了16倍。同时,2-氧代戊二酸的组织含量下降了5倍,柠檬酸下降了两倍多。暴露于氟烷的肝脏中,细胞质和线粒体中计算出的[游离NAD(+)]/[游离NADH]比值均低于对照组。4. 在饥饿大鼠的肝脏中,氟烷使乳酸糖异生速率降至对照速率的30%。5. 氟烷抑制丙氨酸和丙酸的糖异生程度与抑制乳酸的相同,而二羟基丙酮、甘油、果糖和山梨醇生成葡萄糖的过程相对未受影响。6. 在由10mmol/L乳酸进行糖异生过程中,暴露于氟烷的肝脏中ATP的组织含量下降了50%,谷氨酸下降了50%,2-氧代戊二酸下降了8倍。7. 在存在10mmol/L NH(4)Cl和2mmol/L鸟氨酸的情况下,氟烷使尿素合成降至对照速率的15%。8. 停止麻醉后15分钟内,糖异生和尿素合成受到的抑制完全消除。9. 氟烷消除了添加乳酸或尿素前体所引起的氧摄取刺激。10. 暴露于麻醉剂甲氧氟烷的肝脏中,对糖异生的影响与氟烷相似,尽管停药后未恢复到正常速率。测试的其他麻醉剂(氯胺酮-HCl和三氯乙烯)使糖异生降至对照速率的66%。11. 氟烷的抑制作用与电子传递链中NADH脱氢酶阶段的干扰一致。

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