Acute, Sub-acute and Chronic Toxicity Evaluation of Aqueous Extract of the Aerial Parts of Leonurus cardiaca in Normal Non-pregnant Female Wistar Albino Rats per OECD 425 TG

E. O. Wellington, E. N. Onyeike, D. Peters, M. B. Otobo, D. Félix, S. J. Ogbomade
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Abstract

This study graded the acute, sub-acute, and chronic toxicity of aqueous extract of the aerial parts of Leonurus cardiaca in non-pregnant female wistar rats. Fifty wistar albino rats weighing between 180 and 200g were used for this study. The rats were grouped into 10 groups of five rats per group. Group 1 served as control while group 2-11 were orally administered aqueous extract of Leonurus cardiaca at 166, 250, and 500mg/kg for 7, 14, and 21 days. All haematological and biochemical parameters were determined based on standard methods. The plasma RBC, Hb, MCV, and WBC of the control were 5.33±0.01 x 1012/L, 13.54±0.01 g/dl, 42.16±0.01 fl, and 1.83±0.01 X 109/L respectively. The plasma RBC, Hb, MCV, and WBC of the rats treated with 500mg/kg of the extract for 21 days were 10.93±0.01x 1012/L, 19.24±0.01g/dl, 28.33±0.01fl, and 1.41±0.01 x 109/L respectively and were significantly different from the control at p≤0.05. The plasma Na+, K+ , Cl-, HCO3 , creatinine, and urea levels treated with extract at 500mg/kg for 21 days were 167.97±0.01 01mmol/l, 7.85±0.0101mmol/l, 164.24±0.0101mmol/l, 40.84±0.0101mmol/l, 1.16±0.0101mmol/l, and 5.68±0.02 01mmol/l respectively, were significantly different from the control at p≤0.05. The plasma ALT, ALP, and AST activities treated with extract at 500mg/kg for 21 days were 146.24±0.02U/L, 77.33±0.01U/L, and 168.71±0.01U/L respectively, were significantly different from the control at p≤0.05. Enhancement on architecture of the heart, kidney and liver tissues occurred after treatment with 500mg/kg of the extract for 21 days in comparison to the control. The significantly improved effects observed on all assayed parameters were expressive that the extract of the aerial parts of Leonurus cardiaca is safe at 500 mg/Kg.
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益母草地上部分水提物对正常未怀孕雌性Wistar白化大鼠急性、亚急性和慢性毒性评价(OECD 425 TG
本研究对益母草地上部分水提物对未怀孕雌性wistar大鼠的急性、亚急性和慢性毒性进行了分级。50只体重在180到200克之间的wistar白化大鼠被用于这项研究。将大鼠分为10组,每组5只。1组作为对照组,2-11组分别以166、250、500mg/kg剂量口服益母草水提物,连续7、14、21 d。所有血液学和生化参数均按标准方法测定。对照组血浆RBC、Hb、MCV、WBC分别为5.33±0.01 × 1012/L、13.54±0.01 g/dl、42.16±0.01 fl、1.83±0.01 × 109/L。500mg/kg提取物作用21 d后,大鼠血浆RBC、Hb、MCV和WBC分别为10.93±0.01 × 1012/L、19.24±0.01g/dl、28.33±0.01fl和1.41±0.01 × 109/L,与对照组差异显著(p≤0.05)。500mg/kg提取物处理21 d血浆Na+、K+、Cl-、HCO3、肌酐和尿素水平分别为167.97±0.01 mmol/l、7.85±0.0101mmol/l、164.24±0.0101mmol/l、40.84±0.0101mmol/l、1.16±0.0101mmol/l和5.68±0.02 mmol/l,与对照组差异显著(p≤0.05)。500mg/kg提取物处理21 d后血浆ALT、ALP和AST活性分别为146.24±0.02U/L、77.33±0.01U/L和168.71±0.01U/L,与对照组差异显著(p≤0.05)。与对照组相比,500mg/kg的提取物治疗21天后,心脏、肾脏和肝脏组织的结构有所增强。结果表明,在500 mg/Kg的浓度下,益母草地上部位提取物是安全的。
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