Effects of Aqueous Leaf Extract of Simarouba glauca DC (Simaroubaceae) on Lipoprotein Homeostasis and Oxidative Stress Biomarkers

S. E. Osagie-Eweka, N. Orhue, Eric K. I. Omogbai
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Abstract

Background and Purpose: Simarouba glauca is widely reported to contain a number of biologically active compounds with potentials in the treatment of numerous diseases. The study was conducted to evaluate the sub-acute effects of the aqueous leaf extract of Simarouba glauca (AESG) on lipoproteins and oxidative stress biomarkers in male Wistar rats. Methods: Oral administration of AESG was carried out in line with the guidelines of the Organization for Economic Co-operation and Development (OECD), No. 425 using a total of 24 male Wistar rats allotted to four groups (n=6); given distilled water, 500, 1000, and 2000 mg/kg/day of AESG respectively for 30 days. Results: In plasma, there was a significant reduction (P?0.05) in HDL-cholesterol; elevated (P?0.05) triglycerides (TG) at 1000 and 2000 mg/kg/day; elevated (P?0.05), and LDL-cholesterol at 500 and 1000 mg/kg/day, relative to the control. While the level of liver total cholesterol (TC) reduced significantly, it increased in the heart. Catalase (CAT) activity in the liver increased significantly (P?0.05) at all doses. The dose of 1000 mg/kg/day significantly (P?0.05) elevated kidney CAT activity. The activities of superoxide dismutase (SOD) in liver and heart reduced (P?0.05) at 500 mg/kg/day. At all doses, the levels of reduced glutathione (GSH) in plasma, liver and heart were comparable with the control. Although, there were no significant changes in plasma and liver glutathione peroxidase (GSH-PX) activity at all doses, animals given 500 mg/kg had reduction (P?0.05) in the heart GSH-PX activity compared to the control. Conclusion: Oral sub-acute AESG at high doses altered lipid homeostasis in plasma and heart without lipid peroxidation or oxidative stress. The extract has the potential to cause hyperlipidemia.
水仙花叶提取物对脂蛋白稳态和氧化应激生物标志物的影响
背景与目的:据广泛报道,青花香茅含有多种生物活性化合物,具有治疗多种疾病的潜力。本研究旨在评价青叶水提物(AESG)对雄性Wistar大鼠脂蛋白和氧化应激生物标志物的亚急性影响。方法:按照经济合作与发展组织(OECD)第425号指南,将24只雄性Wistar大鼠分为4组(n=6),口服AESG;分别给予蒸馏水500、1000、2000 mg/kg/天的AESG,连续30天。结果:血浆中高密度脂蛋白胆固醇水平显著降低(P?0.05);甘油三酯(TG)在1000和2000 mg/kg/d时升高(P?0.05);在500和1000 mg/kg/d时,ldl -胆固醇相对于对照组升高(P?0.05)。肝脏总胆固醇(TC)水平显著降低,但心脏总胆固醇水平升高。各剂量下肝脏过氧化氢酶(CAT)活性均显著升高(P?0.05)。1000mg /kg/d显著提高了肾CAT活性(P?0.05)。500mg /kg/d组肝脏和心脏超氧化物歧化酶(SOD)活性降低(P > 0.05)。在所有剂量下,血浆、肝脏和心脏中的还原型谷胱甘肽(GSH)水平与对照组相当。虽然在所有剂量下,血浆和肝脏谷胱甘肽过氧化物酶(GSH-PX)活性没有显著变化,但与对照组相比,500 mg/kg的动物心脏GSH-PX活性降低(P?0.05)。结论:大剂量口服亚急性AESG可改变血浆和心脏脂质稳态,无脂质过氧化或氧化应激。这种提取物有可能引起高脂血症。
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