Effect of Spirulina Platensis on Liver Malondialdehyde Levels of Male White Rat Induced by High Dose Paracetamol

Anggilia Vanny, Sihning E. J. Tehupuring, Indri Ngesti Rahayu, Roostantia Indrawati
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Abstract

Paracetamol is widely used in therapy, yet it becomes hepatotoxic agent in a high dose using. The CYP450 enzyme metabolizes a small portion of paracetamol to a reactive substance, NAPQI. High dose of paracetamol causes an extensive increase in NAPQI levels. NAPQI then binds to hepatocytes conditions of oxidative stress. Spirulina platensis contains C-phycocyanin, flavonoids, and phenolics that inhibit lipid peroxidation and reduce oxidative stress. This study aims to determine the effect of Spirulina platensis on MDA levels in the liver tissue of male Wistar rats induced by high dose of paracetamol. This research was experimental with a Randomized Post-test Only Control Group design using 24 white male rats divided into three groups; negative control group (G-), positive control group (G+) was given paracetamol at a dose of 1,250 mg/kg on the 8th day, and treatment group (Gt) was given an amount of Spirulina platensis extract 360 mg/kg BW/day for ten days from 1st until 10th day and paracetamol at a single dose of 1,250 mg/kg BW on the 8th. At the 10th day of the treatment, all groups were terminated for liver tissue collection. TBA test was used to calculate MDA levels. Statistical tests analyzed the results of the data. This statistical tests by SPSS software: MDA levels in the treatment group did not significantly differ (p = 0.144) compared to the negative control group. There was a significant difference of liver tissue MDA levels in the treatment group (p = 0.016) compared to the positive control group. This study concludes that administering Spirulina platensis at a dose of 360 mg/kg/day for ten days can help prevent on increase in tissue MDA levels and maintain liver conditions close to their original state.
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螺旋藻对大剂量对乙酰氨基酚诱导的雄性大鼠肝脏丙二醛水平的影响
对乙酰氨基酚广泛应用于治疗,但在高剂量使用时成为肝毒性药物。CYP450酶将一小部分扑热息痛代谢为活性物质NAPQI。高剂量扑热息痛可引起NAPQI水平的广泛增加。NAPQI随后与氧化应激条件下的肝细胞结合。螺旋藻含有c -藻蓝蛋白、类黄酮和酚类物质,可抑制脂质过氧化和减少氧化应激。本研究旨在探讨螺旋藻对大剂量扑热息痛诱导的雄性Wistar大鼠肝组织MDA水平的影响。本研究采用随机后验对照组设计,24只雄性白种大鼠分为三组;阴性对照组(G-)、阳性对照组(G+)于第8天给予剂量为1250 mg/kg的扑热息痛,治疗组(Gt)于第1 ~ 10天连续10天给予剂量为360 mg/kg BW的螺旋藻提取物,第8天给予单剂量1250 mg/kg BW的扑热息痛。在治疗第10天,所有组均终止,收集肝组织。采用TBA试验计算MDA水平。统计测试分析了数据的结果。采用SPSS软件进行统计学检验:治疗组MDA水平与阴性对照组比较差异无统计学意义(p = 0.144)。治疗组肝组织MDA水平与阳性对照组比较差异有统计学意义(p = 0.016)。本研究提示,连续10天给药360 mg/kg/d的螺旋藻可以防止组织MDA水平的升高,使肝脏状况接近于原来的状态。
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审稿时长
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