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Diabetes and hypertriglyceridemia modify the mode of acetaminophen-induced hepatotoxicity and nephrotoxicity in rats and mice.
- Source :
-
The Journal of toxicological sciences [J Toxicol Sci] 2009 Feb; Vol. 34 (1), pp. 1-11. - Publication Year :
- 2009
-
Abstract
- Certain disease conditions can modify drug-induced toxicities, which, in turn, may cause a medication-related health crisis. Therefore, preclinical investigations into the alterations in drug-induced toxicities using appropriate disease animal models are very important. This paper reviews the reported data related to the effects of diabetes and hypertriglyceridemia, common lifestyle-related diseases in a modern society, on acetaminophen (APAP)-induced hepatotoxicity and nephrotoxicity in rats and mice. It has generally been reported that diabetes protects rats and mice from APAP-induced hepatotoxicity and there are several reports that help to speculate on the effects of diabetes on APAP-induced nephrotoxicity. In fructose-induced hypertriglyceridemic rats, hepatotoxicity of APAP becomes apparently less severe, whereas nephrotoxicity of APAP becomes significantly more severe. The mechanisms of alteration of APAP-induced hepatorenal toxicity under diabetic and hypertriglyceridemic conditions are also discussed in this paper.
- Subjects :
- Acetaminophen antagonists & inhibitors
Acetaminophen metabolism
Analgesics, Non-Narcotic antagonists & inhibitors
Analgesics, Non-Narcotic metabolism
Animals
Diabetes Mellitus physiopathology
Disease Models, Animal
Humans
Hypertriglyceridemia physiopathology
Inactivation, Metabolic physiology
Mice
Rats
Acetaminophen toxicity
Analgesics, Non-Narcotic toxicity
Chemical and Drug Induced Liver Injury
Diabetes Mellitus metabolism
Hypertriglyceridemia metabolism
Kidney Diseases chemically induced
Subjects
Details
- Language :
- English
- ISSN :
- 1880-3989
- Volume :
- 34
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- The Journal of toxicological sciences
- Publication Type :
- Academic Journal
- Accession number :
- 19182431
- Full Text :
- https://doi.org/10.2131/jts.34.1