Effects of alpha-lipoic acid on high fructose induced hepatic pathology
Autor: | M Ozgocmen, Senay Topsakal, Ozlem Ozmen |
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Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
antioxidant Animals Antioxidants/*pharmacology Apoptosis/drug effects Chemical and Drug Induced Liver Injury/*prevention & control Female Hepatocytes/drug effects High Fructose Corn Syrup/*toxicity Random Allocation Rats Rats Wistar Sweetening Agents/*toxicity Thioctic Acid/administration & dosage/*pharmacology Alpha-Lipoic Acid Apoptosis Pharmacology Wistar rat medicine.disease_cause Antioxidants fructose Pathogenesis chemistry.chemical_compound 0302 clinical medicine corn syrup thioctic acid hepatic damage oxidative stress rat animal Thioctic Acid drug effect liver cell food and beverages General Medicine toxic hepatitis Corn syrup Medical Laboratory Technology female 030220 oncology & carcinogenesis Chemical and Drug Induced Liver Injury Alpha-lipoic acid Histology food.ingredient randomization liver 03 medical and health sciences food medicine 030102 biochemistry & molecular biology High-fructose corn syrup Fructose Hepatic toxicity chemistry Sweetening Agents High fructose Hepatocytes pathology sweetening agent High Fructose Corn Syrup Oxidative stress |
Zdroj: | Biotechnichistochemistry : official publication of the Biological Stain Commission. 94(4) |
ISSN: | 1473-7760 |
Popis: | Little is known about the pathogenesis of high fructose corn syrup (HFCS) induced hepatic toxicity. We investigated hepatic lesions induced by chronic HFCS consumption and the protective effects of alpha-lipoic acid (ALA) on liver pathology. We used 24 rats allocated randomly into three groups of eight. The HFCS group was given in drinking water for 10 weeks. The ALA + HFCS group was given the same dose of HFCS and ALA also was administered during the last 6 weeks of the experiment. The control group was untreated. The rats were euthanized at the end of 10 weeks and 24 h after the last ALA administration. A significant increase was observed in the serum aspartate aminotransferase (AST) level of the HFCS group compared to controls. Tissue malondialdehyde (MDA) levels also increased significantly and catalase (CAT) activity decreased significantly in the HFCS group. Caspase-3 expression increased significantly in the HFCS group compared to controls. In the ALA treated group, the levels of MDA, CAT and caspase-3 returned to near control levels. HFCS caused hepatic toxicity by increasing oxidative stress and apoptosis. ALA administration ameliorated the pathological changes. © 2018, © 2018 The Biological Stain Commission. |
Databáze: | OpenAIRE |
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