Literature DB >> 1192708

Hepatic glutathione depletion and impaired bromosulphthalein clearance early after paracetamol overdose in man and the rat.

M Davis, G Ideo, N G Harrison, R Williams.   

Abstract

1. Plasma clearance of bromosulphthalein was impaired in patients within 8 h, and in rats within 2 h , of paracetamol overdose, before biochemical signs of liver damage had appeared. 2. Paracetamol and bromosulphthalein competed for uptake into the liver and excretion into the bile. Impaired hepatic uptake of bromosulphthalein could also be demonstrated in man at doses of the drug within the therapeutic range. 3. In patients studied a smaller proportion of bromosulphthalein was retained in the plasma as the glutathione conjugate after an overdose than after therapeutic doses. This effect could be reproduced in the rat and shown to be due to depletion of hepatic glutathione and to impairment in the activity of the enzyme glutathione-S-aryl transferase. 4. These studies provide further evidence that depletion of hepatic glutathione occurs after paracetamol overdose in man, as in the experimental animal, allowing the subsequent accumulation and binding of a toxic metabolite of the drug within liver cells. Impaired enzymic conjugation of the toxic metabolite with hepatic reduced glutathione may also be important in this situation.

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Year:  1975        PMID: 1192708     DOI: 10.1042/cs0490495

Source DB:  PubMed          Journal:  Clin Sci Mol Med        ISSN: 0301-0538


  8 in total

Review 1.  Paracetamol overdosage. Pharmacological considerations and clinical management.

Authors:  L F Prescott
Journal:  Drugs       Date:  1983-03       Impact factor: 9.546

2.  Serum mitochondrial biomarkers and damage-associated molecular patterns are higher in acetaminophen overdose patients with poor outcome.

Authors:  Mitchell R McGill; Vincent S Staggs; Matthew R Sharpe; William M Lee; Hartmut Jaeschke
Journal:  Hepatology       Date:  2014-08-25       Impact factor: 17.425

Review 3.  Animal models of drug-induced liver injury.

Authors:  Mitchell R McGill; Hartmut Jaeschke
Journal:  Biochim Biophys Acta Mol Basis Dis       Date:  2018-09-03       Impact factor: 5.187

4.  Structural and kinetic analyses of macrophage migration inhibitory factor active site interactions.

Authors:  Gregg V Crichlow; Jodi B Lubetsky; Lin Leng; Richard Bucala; Elias J Lolis
Journal:  Biochemistry       Date:  2009-01-13       Impact factor: 3.162

Review 5.  Metabolism and disposition of acetaminophen: recent advances in relation to hepatotoxicity and diagnosis.

Authors:  Mitchell R McGill; Hartmut Jaeschke
Journal:  Pharm Res       Date:  2013-03-06       Impact factor: 4.200

Review 6.  Mechanistic biomarkers in acetaminophen-induced hepatotoxicity and acute liver failure: from preclinical models to patients.

Authors:  Mitchell R McGill; Hartmut Jaeschke
Journal:  Expert Opin Drug Metab Toxicol       Date:  2014-05-16       Impact factor: 4.481

7.  Circulating acylcarnitines as biomarkers of mitochondrial dysfunction after acetaminophen overdose in mice and humans.

Authors:  Mitchell R McGill; Feng Li; Matthew R Sharpe; C David Williams; Steven C Curry; Xiaochao Ma; Hartmut Jaeschke
Journal:  Arch Toxicol       Date:  2013-08-25       Impact factor: 5.153

Review 8.  Extrahepatic toxicity of acetaminophen: critical evaluation of the evidence and proposed mechanisms.

Authors:  Stefanie Kennon-McGill; Mitchell R McGill
Journal:  J Clin Transl Res       Date:  2017-11-18
  8 in total

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