Betaine Protects Chronic Alcohol and ω-3 PUFA-Mediated Down-Regulations of PON1 Gene, Serum PON1 and Homocysteine Thiolactonase Activities With Restoration of Liver GSH

• Published in: Alcoholism, clinical and experimental research Vol. 34; no. 3; pp. 424 - 431
• Main Authors: Varatharajalu, Ravi, Garige, Mamatha, Leckey, Leslie C., Gong, Maokai, Lakshman, M. Raj
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01-03-2010; Wiley
• Subjects: Alanine Transaminase - blood; Alcoholism and acute alcohol poisoning; Animals; Aryldialkylphosphatase - blood; Aryldialkylphosphatase - genetics; Betaine - administration & dosage; Biological and medical sciences; Body Weight - drug effects; Central Nervous System Depressants - administration & dosage; Down-Regulation - drug effects; Ethanol; Ethanol - administration & dosage; Fatty Acids, Omega-3 - administration & dosage; Female; Fish Oil; Glutathione; Glutathione - metabolism; Homocysteine Thiolactonase; Lipid Metabolism - drug effects; Liver - drug effects; Liver - metabolism; Medical sciences; Organ Size - drug effects; Paraoxonase; Rats; Rats, Wistar; RNA, Messenger - metabolism; Toxicology; Biological fluid; Thiol; Ethanol; Digestive system; Enzyme; Hepatoprotector; Liver; Esterases; Paraoxonase; Fish oil; Homocysteine Thiolactonase; Biological activity; Sulfur containing aminoacid; Prevention; Phosphoric triester hydrolases; Alcoholic beverage; Chronic; Gene; Homocystein; Betaine; Hydrolases; Serum; Aryldialkylphosphatase; Glutathione
• ISSN: 0145-6008; 1530-0277
• DOI: 10.1111/j.1530-0277.2009.01107.x

Background:  Paraoxonase (PON1) is an antioxidant enzyme that prevents LDL oxidation as well as detoxifies homocysteine thiolactone (HCTL), both of which can cause atherosclerosis. Chronic alcohol (ETOH) and high ω‐3 polyunsaturated fatty acids (ω‐3 PUFA) consumption may affect PON1 status presumably via reactive oxygen species by depleting liver glutathione (GSH), whereas betaine may counter their effects. Therefore, we investigated the influence of ETOH, ω‐3 PUFA, and betaine on liver GSH, PON1 expression, lipid score, as well as serum PON1 and HCTLase activities.
Methods:  Experimental rats belonging to various dietary groups were pair‐fed with Lieber‐DeCarli low (2.8% the dietary calories as ω3‐fatty acids) and high (13.8% the dietary calories as ω3‐fatty acids) menhaden fish alcohol‐liquid diets with and without betaine (10 g/l diet) for 8 weeks after which liver PON1 mRNA, GSH, lipid score, and serum PON1, HCTLase, and ALT activities were measured.
Results:  High ω‐3 PUFA decreased liver PON1 mRNA expression, serum PON1, and HCTLase activity by 23% (p < 0.01), 20% (p < 0.05), and 28% (p < 0.05), respectively compared to the low ω‐3 PUFA group. ETOH decreased PON1 mRNA expression by 25 and 30% (p < 0.01) with concomitant 27% (p < 0.05) and 38% (p < 0.01), decrease in liver GSH levels in low and high ω‐3 PUFA groups, respectively. Correspondingly, serum PON1 activity decreased by 23% (p < 0.05) and 58% (p < 0.01) while serum HCTLase activity decreased by 25% (p < 0.05) and 59% (p < 0.01) in the low and high ω‐3 PUFA ETOH groups, respectively. Betaine restored liver PON1 mRNA expressions in low and high ω‐3 PUFA ETOH groups with parallel restorations of PON1 activity and liver GSH. Concomitantly, betaine reduced hepatosteatosis accompanied by alleviation of liver injury caused by chronic alcohol and high ω‐3 PUFA.
Conclusions:  Based on these results, we conclude that dietary betaine not only atheroprotective by restoring liver GSH that quenches free radicals, but also may alleviate liver injury by reducing hepatosteatosis.