Protective effects of whey on rat liver damage induced by chronic alcohol intake

Author:

Radic I1,Mijovic M2,Tatalovic N3,Mitic M4ORCID,Lukic V5,Joksimovic B6,Petrovic Z4,Ristic S6,Velickovic S1,Nestorovic V7,Corac A8,Miric M1,Adzic M4,Blagojevic DP3,Popovic L1ORCID,Hudomal SJ9

Affiliation:

1. Institute of Pathological Physiology, Faculty of Medical Science, University of Priština, City of Kosovska Mitrovica, Serbia

2. Institute of Pathology, Faculty of Medical Science, University of Priština, City of Kosovska Mitrovica, Serbia

3. Department of Physiology, Institute for Biological Research “Siniša Stanković,” University of Belgrade, Belgrade, Serbia

4. Laboratory of Molecular Biology and Endocrinology, VINČA Institute of Nuclear Sciences, University of Belgrade, Belgrade, Serbia

5. Institute of Forensic Medicine, Faculty of Medicine, University of Belgrade, Belgrade, Serbia

6. Department of Preclinical sciences, Faculty of Medicine in Foča, University of East Sarajevo, Republic of Srpska, Bosnia and Herzegovina

7. Institute of Physiology, Faculty of Medical Science, University of Priština, City of Kosovska Mitrovica, Serbia

8. Institute of Hygiene, University of Priština, City of Kosovska Mitrovica, Serbia

9. Institute of Pharmacology and toxicology, University of Priština, City of Kosovska Mitrovica, Serbia

Abstract

In 2012, alcohol liver disease resulted in 3.3 million—5.9% of global deaths. This study introduced whey protection capacity against chronic alcohol-induced liver injury. Rats were orally administered to 12% ethanol solution in water (ad libitum, average 8.14 g of ethanol/kg body weight (b.w.)/day) alone or combined with whey ( per os, 2 g/kg b.w./day). After 6-week treatment, chronic ethanol consumption induced significant histopathological liver changes: congestion, central vein dilation, hepatic portal vein branch dilation, Kupffer cells hyperplasia, fatty liver changes, and hepatocytes focal necrosis. Ethanol significantly increased liver catalase activity and glutathione reductase protein expression without significant effects on antioxidative enzymes: glutathione peroxidase (GPx), copper–zinc-containing superoxide dismutase (CuZnSOD) and manganese-containing superoxide dismutase (MnSOD). Co-treatment with whey significantly attenuated pathohistological changes induced by ethanol ingestion and increased GSH-Px and nuclear factor kappa B (NF-κB) protein expression. Our results showed positive effects of whey on liver chronically exposed to ethanol, which seem to be associated with NF-κB-GPx signaling.

Funder

Ministry of Education, Science and Technological Development, Republic of Serbia

Publisher

SAGE Publications

Subject

Health, Toxicology and Mutagenesis,Toxicology,General Medicine

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