对乙酰氨基酚对白化病大鼠肝、肾功能的影响及余甘子乙醇提取物的植物化学成分测定

M. O. Enemali, Ikonomopoulos John, Muhammed H. Abdullahi, H. Sunday, Iko A. Danjuma, Ejiogu I. Chibueze
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引用次数: 0

摘要

本研究以白化病大鼠为实验动物,研究了叶前叶乙醇提取物的植物化学成分及对肝脏和肾脏的影响。所有的分析都按照标准的实验室方法和程序进行。将15只大鼠随机分为3组,每组5只,第一组为对照组,试验组分别给予1000mg/kg体重(b.w)和500mg/kg体重(b.w),连续14 d,随后给予高剂量扑热息痛(200mg/kg b.w)进行系统毒理学挑战。这样做是为了通过测定血清生物标记物来观察连续服用多日提取物是否会保护肝脏和肾脏免受扑热息痛的侵害。结果表明:皂苷(8.84 g/100g)、单宁(1.32 g/100g)、酚类(0.11 g/100g)、黄酮类(0.512 g/100g)和生物碱(0.038 g/100g)均未检出;心苷、树脂、萜类和甾体均未检出。1000mg/kg体重和500mg/kg体重组ALT活性均显著(p < 0.05)升高,1000mg/kg体重组ALT活性不显著(p>0.05)降低,500mg/kg体重组ALT活性显著(p>0.05)升高。500mg/kg体重组血清ALB显著(p > 0.05)升高,1000mg/kg体重组和500mg/kg体重组血清HCO3-均显著(p > 0.05)升高,1000mg/kg体重组血清HCO3-均无显著降低。1000mg/kg体重和500mg/kg体重时,尿素浓度均不显著降低,肌酐浓度在1000mg/kg体重和500mg/kg体重时均显著升高。与对照相比,在1000mg/kg b.w和500mg/kg b.w时Na+含量增加不显著。尽管存在一些植物化学物质,但提取物可能没有保护肝脏和肾脏免受扑热息痛的侵害,因此建议对肝脏和肾脏进行组织学检查,以便更清楚地了解所观察到的效果。
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Determination of Phytochemical Composition and the Effects of Ethanol Extract of Phyllanthus urinaria on the Liver and Kidney Function Parameters in Paracetamol-Administered Albino Rat Models
The current study was aimed at determining the phytochemical composition and the effects of Phyllantus urinaria Ethanol extract on the liver and kidneys by using albino rats as the animal models. All the analyses were carried out following standard laboratory methods and procedures. A total of fifteen rats were randomly distributed into three groups of five rats in each group where group one served as the control while the test groups comprise of 1000mg/kg body weight (b.w) and 500mg/kg b.w administered daily for fourteen days and followed by administration of a high dose of paracetamol (200mg/kg b.w) to challenge the system toxicologically. This was deliberately done to note whether the extract having administered for many days will protect the liver and kidneys against the paracetamol by determining the serum biomarkers. The results showed the presence of saponins (8.84 g/100g), tannins (1.32 g/100g), phenols (0.11 g/100g), flavonoids (0.512 g/100g) and alkaloids (0.038 g/100g) while cardiac glycosides, Resins, terpenoids and steroids were not detected. The activity of ALP was significantly (p < 0.05) higher in both the 1000mg/kg b.w and 500mg/kg b.w. There was no significant (p>0.05) decrease in ALT activity of 1000mg/kg b.w and at 500mg/kg b.w. the activity of ALT significant (p>0.05) increased when compared with the control. There was a significant (p<0.05) decrease in AST activity of 1000mg/kg b.w and 500mg/kg b.w when compared with the control. Bilirubin concentration significantly (p< 0.05) decreased at 1000mg/kg b.w and non-significantly (p>0.05) increased at 500mg/kg b.w. ALB significantly (p > 0.05) increased at 1000mg/kg b.w and 500mg/kg b.w. A non-significant decrease in Serum HCO3- in both 1000mg/kg/b.w and 500mg/kg b.w. Urea non-significantly decreased at both 1000mg/kg b.w and 500mg/kg b.w. Creatinine significantly increased at both 1000mg/kg b.w and 500mg/kg b.w concentration when compared to the control. Na+ showed a non-significant increase at 1000mg/kg b.w and 500mg/kg b.w when compared to the control. The extract may not have protected the liver and kidneys against paracetamol despite the presence of some phytochemicals, a histological examination of the liver and kidneys is therefore recommended so as to have a clearer picture of the effects observed.
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