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The Effect of Curcumin and Exercise Rehabilitation on Liver Paraoxonase-1 and NF-kβ Gene Expression in the Rat Induced by Forced Drinking of Ethanol

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Specialty Gastroenterology
Date 2020 Mar 14
PMID 32166124
Citations 1
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Abstract

Aim Of The Study: Binge ethanol drinking causes liver damage and decreased paraoxonase-1 (PON-1) gene expression. On the other hand, regular physical activity and curcumin consumption as non-invasive interventions can have liver protective effects through enhancing antioxidant defense, and improving PON-1 and NF-kβ (nuclear factor kappa B) gene expression. The aim of this study was to investigate the interactive effect of exercise rehabilitation and curcumin consumption on hepatocyte damage as well as NF-kβ and PON-1 gene expression in rats.

Material And Methods: Fifty-six male Wistar rats were randomly selected and equally divided into seven groups: dextrose-control (Dext-Con), ethanol-control (Eth-Con), ethanol-saline (Eth-sal), ethanol-DMSO (Eth-DMSO), ethanol-curcumin (Eth-Cur), ethanol-swimming training (Eth-SWT) and ethanol-SWT + curcumin (Eth-SWT + Cur). After four days of the binge drinking protocol followed by six days of quitting, the interventions of SWT and curcumin (50 mg/kg) were employed for 14 days. Afterwards, the rats' liver tissues were collected and sent to the laboratory for biochemical assays.

Results: The interaction of SWT and curcumin caused an increase in PON-1 gene expression ( = 0.02). In addition, curcumin consumption ( = 0.003) and its interaction with SWT ( = 0.004) resulted in a reduction in NF-kβ gene expression. Also, liver tissue damage was observed in the Eth-Con group compared to other groups.

Conclusions: The combination of curcumin and SWT may be used to reduce the side effects of binge ethanol drinking and improve recovery in the quitting period.

Citing Articles

Phytochemicals as Modulators of Paraoxonase-1 in Health and Diseases.

Arab Z, Khayatan D, Razavi S, Zare K, Kheradkhah E, Momtaz S Antioxidants (Basel). 2022; 11(7).

PMID: 35883764 PMC: 9311866. DOI: 10.3390/antiox11071273.

References
1.
Sorenson R, Teiber J, La Du B . The human serum paraoxonase/arylesterase gene (PON1) is one member of a multigene family. Genomics. 1996; 33(3):498-507. DOI: 10.1006/geno.1996.0225. View

2.
Tomas M, Elosua R, Senti M, Molina L, Vila J, Anglada R . Paraoxonase1-192 polymorphism modulates the effects of regular and acute exercise on paraoxonase1 activity. J Lipid Res. 2002; 43(5):713-20. View

3.
Sun Y, Peng M . [Recent advances in curcumin and its derivatives for treatment of liver diseases]. Yao Xue Xue Bao. 2015; 49(11):1483-90. View

4.
Casella-Filho A, Chagas A, Maranhao R, Trombetta I, Cesena F, Silva V . Effect of exercise training on plasma levels and functional properties of high-density lipoprotein cholesterol in the metabolic syndrome. Am J Cardiol. 2011; 107(8):1168-72. DOI: 10.1016/j.amjcard.2010.12.014. View

5.
Samuhasaneeto S, Thong-Ngam D, Kulaputana O, Suyasunanont D, Klaikeaw N . Curcumin decreased oxidative stress, inhibited NF-kappaB activation, and improved liver pathology in ethanol-induced liver injury in rats. J Biomed Biotechnol. 2009; 2009:981963. PMC: 2709731. DOI: 10.1155/2009/981963. View