Effect of Methanolic Extract of Platycerium angolence on Aluminium Chloride-induced Neurotoxicity in Rats

A. Olowoyeye, O. Osukoya, T. Obafemi, J. A. Akinyemi, O. Molehin
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引用次数: 1

Abstract

The aim of this study is to determine the ameliorative effects of methanolic extract of Platycerium angolence (MEPA)on aluminium chloride (AlCl3)-induced neurotoxicity in rats. Rats were randomly separated into five groups containing four rats each. Group 1 serves as the control group and received normal saline, group 2 rats were administered with 100 mg/kg body weight of AlCl3 orally for 28 days to induce neuronal damage, while groups 3 and 4 rats received 250 mg/kg and 500 mg/kg of MEPA for 7days after induction of neuronal damage by AlCl3 for 28 days. Group 5 rats were administered donepezil drug (0.2 mg/kg) which served as reference drug. Behavioural study such as elevated plus maze, Y-maze and open field tests were investigated on the rats. Biochemical assays such as lipid peroxidation, acetylcholinesterase activities, and metal concentration in the whole brain homogenates were estimated using standard procedures. Results revealed a significant (p<0.05) increase in the memory index (MI), lipid peroxidation of animals in the AlCl3 group when compared with the control and the MEPA treated groups. The significant (p<0.05) decrease on lipid peroxidation MEPA was dose dependent. The acetylcholinesterase activities observed in the brain of 250 mg/kg (0.49 μmol acetylcholine/hr/mg protein) group and 500 mg/kg of extract (0.66 μmol acetylcholine/hr/mg protein) has comparative effect with the group treated with the standard drug donepezil when compared with AlCl3 induced group (1.31 μmol acetylcholine/hr/mg protein). This study revealed that both doses of 250 and 500 mg/kg of MEPA has ameliorative potential against AlCl3-induced neurotoxicity in rats but 500 mg/kg of the extract shows better protection.
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桔梗甲醇提取物对氯化铝致大鼠神经毒性的影响
本研究旨在探讨桔梗甲醇提取物(MEPA)对氯化铝(AlCl3)诱导的大鼠神经毒性的改善作用。将大鼠随机分为5组,每组4只。第1组作为对照组,给予生理盐水;第2组大鼠给予100 mg/kg体重的AlCl3,连续28天诱导神经元损伤;第3、4组大鼠在AlCl3诱导神经元损伤28天后,分别给予250 mg/kg、500 mg/kg的MEPA,连续7天。5组大鼠给予多奈哌齐药物0.2 mg/kg作为对照药。对大鼠进行了高架+迷宫、y型迷宫和野外实验等行为学研究。生化测定如脂质过氧化、乙酰胆碱酯酶活性和全脑匀浆中的金属浓度使用标准程序进行估计。结果显示,与对照组和MEPA处理组相比,AlCl3组动物的记忆指数(MI)、脂质过氧化率显著(p<0.05)升高。MEPA对脂质过氧化的影响呈剂量依赖性(p<0.05)。250 mg/kg (0.49 μmol乙酰胆碱/hr/mg蛋白)组和500 mg/kg (0.66 μmol乙酰胆碱/hr/mg蛋白)提取物脑内乙酰胆碱酯酶活性与标准药物多奈哌齐组比较,与AlCl3诱导组(1.31 μmol乙酰胆碱/hr/mg蛋白)脑内乙酰胆碱酯酶活性比较。本研究发现,250和500 mg/kg剂量的MEPA对alcl3诱导的大鼠神经毒性均有改善潜力,但500 mg/kg的MEPA提取物具有更好的保护作用。
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