Fasting augments lipid peroxidation during reperfusion after ischemia in the perfused rat liver
OBJECTIVETo test the hypothesis that fasting would aggravate postischemic lipid peroxidation in a perfused rat liver model. DESIGNProspective, randomized study in a rat perfused liver model. SUBJECTSMale Sprague-Dawley rats. INTERVENTIONSLivers isolated from fed and fasted male Sprague-Dawley rats (...
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Published in: | Critical care medicine Vol. 27; no. 2; pp. 401 - 406 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
Hagerstown, MD
Lippincott Williams & Wilkins, Inc
01-02-1999
Lippincott |
Subjects: | |
Online Access: | Get full text |
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Summary: | OBJECTIVETo test the hypothesis that fasting would aggravate postischemic lipid peroxidation in a perfused rat liver model.
DESIGNProspective, randomized study in a rat perfused liver model.
SUBJECTSMale Sprague-Dawley rats.
INTERVENTIONSLivers isolated from fed and fasted male Sprague-Dawley rats (n = 16) were exposed to 2.5 hrs of normothermic (38[degree sign]C) ischemia followed by 2 hrs of reperfusion.
MEASUREMENTS AND MAIN RESULTSLipid peroxidation was measured by chemiluminescence and thiobarbituric acid reactive substances (TBARS). Injury parameters, potassium, lactate dehydrogenase efflux, and oxygen extraction were measured every 30 mins. Chemiluminescence and TBARS were greater in the fasted ischemic group during reperfusion. (fasted vs. fedchemiluminescence, 946.8 +/- 205.5 [SEM] vs. 98.1 +/- 8.2 counts per second, p = .0004; thiobarbituric acid reactive substances, 1.11 +/- 0.25 vs. 0.21 +/- 0.032 nM/g of liver wt/min, p = .0019). Potassium efflux in the fasted group was greater than in the fed group. (1.568 +/- 0.082 vs. 1.28 +/- 0.079 [micro sign]Eq/g liver weight/min, p = .0184). Fasted livers extracted less oxygen after ischemia (1.94 +/- 0.22 vs. 1.14 +/- 0.46 microM/g liver wt/min, p = .0048). Lactate dehydrogenase levels showed no significant differences.
CONCLUSIONFasting augmented lipid peroxidation markedly. Nutrition may be an important mechanism that protects organs from oxidative injury. (Crit Care Med 1999; 27:401-406) |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0090-3493 1530-0293 |
DOI: | 10.1097/00003246-199902000-00049 |