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本文引用的文献

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Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
2
Respiratory enzymes in oxidative phosphorylation. I. Kinetics of oxygen utilization.氧化磷酸化中的呼吸酶。I. 氧气利用动力学
J Biol Chem. 1955 Nov;217(1):383-93.
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Age- and sex-related differences in acetaminophen metabolism in the rat.
Life Sci. 1981 Dec 7;29(23):2421-8. doi: 10.1016/0024-3205(81)90479-3.
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Acetaminophen-induced hepatotoxicity.
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Selective interaction of D-beta-hydroxybutyrate dehydrogenase with intracellular membranes.
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Rapid colorimetric assay for acetaminophen without salicylate or phenylephrine interference.用于对乙酰氨基酚的快速比色测定法,无阿司匹林或去氧肾上腺素干扰。
Clin Chem. 1982 May;28(5):1171-3.
7
Paracetamol self-poisoning: diagnosis, management, and outcome.对乙酰氨基酚自服中毒:诊断、处理及转归
Med J Aust. 1982 Jan 23;1(2):77-9. doi: 10.5694/j.1326-5377.1982.tb132164.x.
8
Late presentation of acetaminophen hepatotoxicity. An unresolved problem.对乙酰氨基酚肝毒性的延迟表现。一个尚未解决的问题。
Dig Dis Sci. 1982 Apr;27(4):375-6. doi: 10.1007/BF01296761.
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Acetaminophen-induced hepatic glycogen depletion and hyperglycemia in mice.对乙酰氨基酚诱导的小鼠肝脏糖原耗竭和高血糖症。
Biochem Pharmacol. 1983 Jul 1;32(13):1979-88. doi: 10.1016/0006-2952(83)90415-x.
10
Acetaminophen nephrotoxicity in the rat. II. Strain differences in nephrotoxicity and metabolism of p-aminophenol, a metabolite of acetaminophen.对乙酰氨基酚在大鼠中的肾毒性。II. 对乙酰氨基酚代谢产物对氨基苯酚的肾毒性及代谢的品系差异
Toxicol Appl Pharmacol. 1983 Jun 30;69(2):307-18. doi: 10.1016/0041-008x(83)90312-5.

对乙酰氨基酚诱导大鼠肝毒性后线粒体氧化能量代谢受损。

Impaired mitochondrial oxidative energy metabolism following paracetamol-induced hepatotoxicity in the rat.

作者信息

Katyare S S, Satav J G

机构信息

Biochemistry Division, Bhabha Atomic Research Centre, Bombay, India.

出版信息

Br J Pharmacol. 1989 Jan;96(1):51-8. doi: 10.1111/j.1476-5381.1989.tb11783.x.

DOI:10.1111/j.1476-5381.1989.tb11783.x
PMID:2522334
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1854327/
Abstract
  1. Effects of paracetamol treatment in vivo at subtoxic (375 mg kg-1 body weight) and toxic (750 mg kg-1 body weight) doses on energy metabolism in rat liver mitochondria were examined. 2. Paracetamol treatment resulted in a significant loss in body weights without affecting the liver protein contents. Toxic doses, however, resulted in 21% decrease in the yield of mitochondrial proteins. 3. Subtoxic doses of paracetamol did not, in general, affect the respiratory parameters in the liver mitochondria except in the case of succinate where both the state 3 respiration and the ADP-phosphorylation rates increased by 28%. 4. Toxic doses of paracetamol caused 25 to 47% decrease in the state 3 respiration rates depending on the substrate used. ADP/O ratios also decreased significantly with pyruvate + malate and succinate as the substrates. Consequently, ADP-phosphorylation was impaired significantly from 20 to 63%. 5. Subtoxic doses of paracetamol resulted in increased contents of cytochrome c + c1 while the toxic doses caused lowering of the cytochromes aa3 and b contents. 6. Glutamate and succinate dehydrogenase activities decreased in both the experimental groups while Mg2+-ATPase activity was impaired only after toxic dose-treatment. 7. The results show that toxic doses of paracetamol result in impaired energy coupling in the liver mitochondria. Effects of subtoxic doses were also demonstrable in terms of impaired dehydrogenases activities.
摘要
  1. 研究了对乙酰氨基酚在亚毒性(375毫克/千克体重)和毒性(750毫克/千克体重)剂量下对大鼠肝脏线粒体能量代谢的体内作用。2. 对乙酰氨基酚处理导致体重显著下降,但不影响肝脏蛋白质含量。然而,毒性剂量导致线粒体蛋白质产量下降21%。3. 一般来说,亚毒性剂量的对乙酰氨基酚不会影响肝脏线粒体的呼吸参数,除了琥珀酸的情况,在琥珀酸实验中,状态3呼吸和ADP磷酸化率均提高了28%。4. 根据所使用的底物不同,毒性剂量的对乙酰氨基酚会使状态3呼吸率下降25%至47%。以丙酮酸+苹果酸和琥珀酸为底物时,ADP/O比值也显著下降。因此,ADP磷酸化显著受损20%至63%。5. 亚毒性剂量的对乙酰氨基酚导致细胞色素c + c1含量增加,而毒性剂量导致细胞色素aa3和b含量降低。6. 两个实验组的谷氨酸和琥珀酸脱氢酶活性均降低,而Mg2 + -ATP酶活性仅在毒性剂量处理后受损。7. 结果表明,毒性剂量的对乙酰氨基酚会导致肝脏线粒体能量偶联受损。亚毒性剂量的影响在脱氢酶活性受损方面也很明显。