Glutathione Turnover Is Increased during the Acute Phase of Sepsis in Rats

التفاصيل البيبلوغرافية
العنوان: Glutathione Turnover Is Increased during the Acute Phase of Sepsis in Rats
المؤلفون: Pierre Capitan, T. Malmezat, Philippe Patureau Mirand, Denis Breuille, Christiane Obled
المصدر: The Journal of Nutrition. 130:1239-1246
بيانات النشر: Elsevier BV, 2000.
سنة النشر: 2000
مصطلحات موضوعية: Male, medicine.medical_specialty, Glutamate-Cysteine Ligase, Glutathione reductase, Medicine (miscellaneous), Spleen, Biology, Rats, Sprague-Dawley, Sepsis, chemistry.chemical_compound, Internal medicine, medicine, Animals, Large intestine, Cysteine, Intestinal Mucosa, Infusions, Intravenous, Cysteine metabolism, Nutrition and Dietetics, Body Weight, Organ Size, Glutathione, medicine.disease, Small intestine, Rats, Glutathione Reductase, medicine.anatomical_structure, Endocrinology, Liver, chemistry, Biochemistry
الوصف: Glutathione metabolism during infection has been poorly documented. Glutathione concentrations and synthesis rates were studied in infected rats (2 d after infection) and in pair-fed controls. Glutathione synthesis rates were determined in liver, spleen, lung, small and large intestine, skeletal muscle, heart and blood by a 4-h or 6-h (15)N cysteine infusion. The activities of four hepatic enzymes involved in glutathione metabolism were also determined. Glutathione synthesis rates were significantly greater in liver (+465%), spleen (+388%), large intestine (+109%), lung (+100%), muscle (+91%) and heart (+80%) of infected rats compared with pair-fed controls. Glutathione concentrations were also greater in these tissues but were unaffected in small intestine and lower in blood. In keeping with the stimulation of liver glutathione synthesis, the activities of liver gamma-glutamyl-cysteine synthetase and glutathione reductase were significantly greater in liver of infected rats than of pair-fed rats. From the present study, we estimate that glutathione synthesis accounts for at least 40% of the enhanced cysteine utilization during infection. This increased utilization may be the primary cause of an enhanced cysteine requirement in infection.
تدمد: 0022-3166
DOI: 10.1093/jn/130.5.1239
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fedc865b61cda09d955d63c545cea085
https://doi.org/10.1093/jn/130.5.1239
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....fedc865b61cda09d955d63c545cea085
قاعدة البيانات: OpenAIRE
الوصف
تدمد:00223166
DOI:10.1093/jn/130.5.1239