Hossain Shahdat, Chowdhury Imrul Hasan, Basunia Mafroz Ahmed, Nahar Taslima, Rahaman Asiqur, Choudhury Bazlur Karim, Choudhuri Shahabuddin Kabir, Mahmud Ishtiaq, Uddin Borhan
Department of Biochemistry and Molecular Biology, Jahangirnagar University, Dhaka, Bangladesh.
J Complement Integr Med. 2011 Jan;8. doi: 10.2202/1553-3840.1445.
The in vitro oxidative stress induced by ethanol/Fenton's reaction in rat liver homogenates decreased significantly in the presence of Syzygium cumini seed extract, suggesting the protective effect of the seed extract against the oxidative stress in liver. To corroborate the in vitro effects by an in vivo experiment, 24 rats were divided into four groups: control, S. cumini seed-extract-administered (SE), 15% ethanol-fed (Alc) and Alc+SE rats. The oral administration of the extract (400 mg/kg BW.day) for 7 weeks significantly decreased the levels of liver LPO in the Alc+SE rats, suggesting that S. cumini seed not only obstructed the in vitro free radical production and subsequent oxidative stress, but also inhibited their in vivo formation. The oral administration of extract also reduced the enzyme activities of serum gammaglutamyl transferase, glutamate oxaloacetate transaminase and glutamate pyruvate transaminase and the levels of serum creatinine and blood urea nitrogen, serum/liver triglycerides and total cholesterol of the alcoholic rats. The levels of fecal cholesterol were increased by the extract. Fatty degenerations in liver and kidney were absent with S. cumini seed extract treatment. The results suggest that S. cumini seed may be a potential therapy for alcoholics and related dysfunctions by restraining oxidative stress.
在大鼠肝脏匀浆中,乙醇/芬顿反应诱导的体外氧化应激在存在蒲桃种子提取物的情况下显著降低,这表明该种子提取物对肝脏氧化应激具有保护作用。为了通过体内实验证实体外效应,将24只大鼠分为四组:对照组、给予蒲桃种子提取物(SE)组、喂食15%乙醇(Alc)组和Alc + SE组大鼠。连续7周口服提取物(400 mg/kg体重·天)可显著降低Alc + SE组大鼠肝脏脂质过氧化(LPO)水平,这表明蒲桃种子不仅在体外阻碍自由基产生及随后的氧化应激,还能在体内抑制其形成。口服提取物还降低了酒精性大鼠血清γ-谷氨酰转移酶、谷氨酸草酰乙酸转氨酶和谷氨酸丙酮酸转氨酶的酶活性,以及血清肌酐、血尿素氮、血清/肝脏甘油三酯和总胆固醇水平。提取物使粪便胆固醇水平升高。蒲桃种子提取物处理后,肝脏和肾脏未出现脂肪变性。结果表明,蒲桃种子可能通过抑制氧化应激成为治疗酗酒者及相关功能障碍的潜在疗法。