青光眼甲醇叶提取物诱导血脂异常相关心血管疾病指标及其对抗氧化蛋白的影响

S. Osagie-Eweka, N. Orhue, E. Omogbai, E. G. Moke
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引用次数: 1

摘要

本研究主要研究了青花香茅甲醇叶提取物(MESG)对雄性Wistar大鼠血脂、胆固醇及氧化应激生物标志物的影响。根据经济合作与发展组织(OECD)第425号准则对MESG的毒理学调查进行了评估。采用雄性Wistar大鼠24只;分为四组,每组6只,包括对照组。实验大鼠分别给予MESG 500、1000和2000 mg/kg体重,每天30天。研究结束后禁食过夜,处死大鼠,评价生化指标。结果显示,总胆固醇在MESG 2000 mg/kg时显著升高(p小于0.05);在所有剂量下,高密度脂蛋白胆固醇和甘油三酯分别减少和增加(p小于0.05);低密度脂蛋白胆固醇在MESG 2000 mg/kg时升高(p小于0.05)。附加数据显示丙二醛水平无变化(p > 0.05);在MESG 500和2000 mg/kg剂量下,肝脏过氧化氢酶显著表达(p小于0.05),肾脏CAT显著表达(p小于0.05)。MESG 1000、2000 mg/kg时肝脏超氧化物歧化酶(SOD)显著表达(p小于0.05);MESG值为500和2000 mg/kg时,肾脏和心脏超氧化物歧化酶(SOD)也显著表达(P小于0.05)。血浆GSH-PX在MESG 1000 mg/kg时显著(P小于0.05)表达;500mg /kg时肝脏和心脏GSH-PX分别显著表达(P小于0.05)和抑制(P < 0.05)。综上所述,MESG引起了明显的血脂异常;伴随着内源性氧化应激生物标志物的显著改变。
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Methanol leaf extract of Simarouba glauca induced dyslipidemia-linked cardiovascular disease indicators and its effect on antioxidant proteins
The study focused on the effect of methanol leaf extract of Simarouba glauca (MESG) on lipoproteins cholesterols and oxidative stress biomarkers in male Wistar rat. Toxicological inquest of MESG was evaluated as prescribed in the guidelines of organization for economic co-operation and development (OECD), No. 425. A total of twenty-four male Wistar rats were used; divided into four groups of six rats each, including the control. Test rats were given MESG 500, 1000 and 2000 mg/kg body weight respectively, daily for thirty (30) days. At the end of the study, the rats were fasted overnight and sacrificed and biochemical indicators were evaluated. Results showed marked increase (p ˂ 0.05) in Total Cholesterol at MESG 2000 mg/kg; a reduction and increase (p ˂ 0.05) in High-Density Lipoprotein Cholesterol and Triglycerides respectively, at all doses; an increase (p ˂ 0.05) in Low- Density Lipoprotein Cholesterol at MESG 2000 mg/kg. Additional data indicated no changes (p ˃ 0.05) in Malondialdehyde levels; liver Catalase was significantly (p ˂ 0.05) expressed at MESG 500 and 2000 mg/kg, kidney CAT was significantly (P ˂ 0.05) expressed at all doses. The liver Superoxide Dismutase (SOD) was significantly (p ˂ 0.05) expressed at MESG 1000 and 2000 mg/kg; the kidney and heart SOD were also significantly (P ˂ 0.05) expressed at MESG 500 and 2000 mg/kg respectively. The plasma GSH-PX was significantly (P ˂ 0.05) expressed at MESG 1000 mg/kg; while the liver and heart GSH-PX were significantly (P ˂ 0.05) expressed and repressed at 500 mg/kg respectively. Conclusively, MESG elicited obvious dyslipidemia; accompanied by marked alterations in selected endogenous oxidative stress biomarkers.
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