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Paracetamol-induced nephrotoxicity and oxidative stress in rats: the protective role of Nigella sativa

机译:扑热息痛诱导的大鼠肾毒性和氧化应激:黑带草的保护作用

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Abstract Context Nigella sativa L. (Ranunculaceae) (NS) is traditionally used to treat many conditions such as inflammation. Objective This study evaluates the effects of NS seeds ethanol extract in paracetamol-induced acute nephrotoxicity in rats. Materials and methods Forty-eight female Wistar Albino rats were divided into eight groups: I?=?sham; II?=?sham?+?1000?mg/kg NS; III?=?sham?+?140?mg/kg (N-acetyl cysteine) NAC; IV?=?2?g/kg paracetamol; V?=?2?g/kg paracetamol?+?140?mg/kg NAC; VI, VII and VIII?=?2?g/kg paracetamol?+?250, 500 and 1000?mg/kg NS, respectively. Paracetamol administration (oral) was carried out 1?h after NS and NAC administrations (oral), and all animals were sacrificed 24?h later. Results Paracetamol administration significantly increased serum urea (88.05?U/L) and creatinine (0.80?U/L) when compared with the sham group (49.80 and 0.31?U/L, respectively). However, serum urea level was reduced to 65.60, 56.00 and 54.18?U/L, with 250, 500 and 1000?mg/kg doses of the extract, respectively. Also, serum creatinine level was reduced to 0.64, 0.57 and 0.52?U/L with 250, 500 and 1000?mg/kg doses of the extract, respectively. NS administration increased superoxide dismutase and glutathione, and decreased malondialdehyde levels in the kidneys. Kidney histopathological examinations showed that NS administration antagonized paracetamol-induced kidney pathological damage. Discussion and conclusions The results suggest NS has a significant nephroprotective activity on paracetamol-induced nephrotoxicity. It may be suggested that the antiinflammatory and antioxidant effects of NS ethanolic extract originated from different compounds of its black seeds.
机译:摘要背景传统黑毛病(Nanella sativa L.(Ranunculaceae)(NS)用于治疗多种疾病,例如炎症。目的研究NS种子乙醇提取物对扑热息痛所致大鼠急性肾毒性的作用。材料和方法48只Wistar Albino雌性大鼠分为八组: II?=?假?+?1000?mg / kg NS; Ⅲ==“假” + =140μmg/ kg(N-乙酰半胱氨酸)NAC。 IV ==2μg/ kg扑热息痛; V≥2?g / kg扑热息痛?+140?mg / kg NAC; Ⅵ,和?的△δ分别为〜2μg/ kg对乙酰氨基酚+250、500和1000μmg/ kg NS。在NS和NAC给药后1小时(口服)进行扑热息痛给药(口服),并在24小时后处死所有动物。结果与假手术组(分别为49.80和0.31?U / L)相比,扑热息痛的给药显着增加了血清尿素(88.05?U / L)和肌酐(0.80?U / L)。然而,分别以250、500和1000?mg / kg剂量的提取物将血清尿素水平降至65.60、56.00和54.18?U / L。同样,分别以250、500和1000?mg / kg剂量的提取物将血清肌酐水平降低至0.64、0.57和0.52?U / L。 NS给药增加了肾脏中的超氧化物歧化酶和谷胱甘肽,并降低了丙二醛水平。肾脏组织病理学检查显示,NS给药可拮抗扑热息痛引起的肾脏病理损害。讨论与结论结果表明,NS对扑热息痛引起的肾毒性具有明显的肾保护活性。可能暗示NS乙醇提取物的抗炎和抗氧化作用源自其黑种子的不同化合物。

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