The antioxidant and antiapoptotic effect of boric acid on hepatoxicity in chronic alcohol-fed rats

Author:

Sogut Ibrahim1,Paltun Sıla Ozlem2,Tuncdemir Matem3,Ersoz Melike4,Hurdag Canan2

Affiliation:

1. Vocational School of Health Services, Istanbul Bilim University, Istanbul, Turkey.

2. Department of Histology and Embryology, Faculty of Medicine, Istanbul Bilim University, Istanbul, Turkey.

3. Department of Medical Biology, Faculty of Medicine, Istanbul University, Istanbul, Turkey.

4. Department of Molecular Biology and Genetics, Faculty of Arts and Sciences, Istanbul Bilim University, Istanbul, Turkey.

Abstract

The harmful use of alcohol is a worldwide problem involving all ages. This study aims to investigate chronic alcohol exposure related hepatotoxicity on the rat liver and possible hepatoprotective effects of boric acid. Rats were separated into 4 different groups: control, ethanol, ethanol+boric acid, and boric acid. We measured (i) malondialdehyde (MDA), total sialic acid (TSA), superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx) levels, which are known to be the markers of alcohol damage; and also (ii) caspase-3, tumor necrosis factor-alpha (TNF-α), and the terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) as the markers of apoptosis. In the ethanol group, MDA, TSA, and TNF-α levels increased whereas SOD and CAT levels decreased compared with the control group. Ethanol+boric acid group MDA, TSA, caspase-3, and TNF-α levels decreased whereas SOD and CAT levels increased compared with the ethanol group. Using histopathological evaluation of light microscope images, immunohistochemical caspase-3 and TNF-α activity in the ethanol+boric acid group were shown to be decreased compared with that in the ethanol group. Our results revealed that ethanol is capable of triggering oxidative stress and apoptosis in the rat liver. We propose that boric acid is an effective compound in protecting the rat liver against ethanol.

Publisher

Canadian Science Publishing

Subject

Physiology (medical),Pharmacology,General Medicine,Physiology

Reference44 articles.

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5. Boron attenuates malathion-induced oxidative stress and acetylcholinesterase inhibition in rats

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