首页> 外文期刊>Asian journal of biochemistry >Liver protective activity of the methanol extract of Crinum jagus bulb against acetaminophen-induced hepatic damage in wistar rats
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Liver protective activity of the methanol extract of Crinum jagus bulb against acetaminophen-induced hepatic damage in wistar rats

机译:crinum jagus bulb甲醇提取物对对乙酰氨基酚诱导的Wistar大鼠肝损伤的肝保护活性

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Hepatotoxins constitute a serious health concern in both rural and urban population globally. Despite advances in medical research, the discovery of an ideal hepatoprotective agent remains a challenge. The present research sought to evaluate the hepatoprotective activity of the crude methanol extract of Crinum jagus bulb as a step towards further detailed study to isolate the bioactive principles. Wistar rats were pre-challenged individually with a high dose of acetaminophen (paracetamol, 2000 mg kg ~(-1)) per os to induce hepatic damage prior to treatment. The control group was given distilled water (10 mL kg ~(-1), p.o.) while one out of the other experimental rat groups was either treated with silymarin (50 mg kg -1, p.o.) or with a dose of C. jagus bulb extract (75, 150 and 300 mg kg ~(-1)). Pentobarbitone-induced sleeping time, the mean relative liver weight of individual rats, biochemical assay and histopathological lesions in the liver of the separate rat groups were assessed and compared to determine the extent of hepatic damage. The prolonged paracetamol-induced pentobarbitone sleeping time in untreated, control rats (145.2±1.4 min) was most remarkably reduced to 122.5±2.1 and 109.5±0.4 min in rats which were treated orally with 150 and 300 mg kg ~(-1) of the extract respectively. The acetaminophen-mediated decrease in the mean relative liver weight of intoxicated rats was relatively reversed with 150 and 300 mg kg ~(-1) of the extract. C. jag us bulb extract also demonstrated significant (p<0.05) potency at 150 and 300 mg kg ~(-1) in reducing acetaminophen-induced increase in the rat serum transaminases (AST, ALT and ALP) and total bilirubin but with elevation in total serum protein values. Histopathology revealed that 2000 mg kg ~(-1) of paracetamol induced severe necrosis of hepatocytes in untreated control rats. Treatment of the acetaminophen-challenged rats with silymarin (50 mg kg ~(-1), p.o.) and C, jagus bulb extract (150 and 300 mg kg ~(-1), p.o.) gave a better protection with regeneration of hepatocytes relative to the untreated control. Crinum jagus bulb extract seemed to have multiplicity of effects in regenerating parenchymal cells, hepatic microsomal enzymes with high antioxidant and anti-inflammatory activities. The bulb of C. jagus could be a potential source of potent hepatoprotective agents.
机译:肝毒素对全球的农村和城市人口都构成严重的健康问题。尽管医学研究取得了进步,理想的肝保护剂的发现仍然是一个挑战。本研究试图评估Cri麻鳞茎粗甲醇提取物的保肝活性,作为进一步进一步研究以分离生物活性成分的一步。 Wistar大鼠在接受治疗前,先经大剂量对乙酰氨基酚(对乙酰氨基酚,对乙酰氨基酚,2000 mg kg〜(-1))进行预攻击,以引起肝损伤。对照组给予蒸馏水(10 mL kg〜(-1),口服),而其他实验大鼠组中的一组接受水飞蓟素(50 mg kg -1,口服)或一定剂量的美洲豹(C. jagus)治疗鳞茎提取物(75、150和300 mg kg〜(-1))。评估和比较戊巴比妥诱导的睡眠时间,每只大鼠的平均相对肝脏重量,生化分析和不同大鼠组肝脏中的组织病理学损害,并比较以确定肝损害的程度。在口服150和300 mg kg〜(-1)的大鼠中,未经对乙酰氨基酚诱导的戊巴比妥延长的睡眠时间(145.2±1.4分钟)最显着地降低至大鼠的122.5±2.1和109.5±0.4分钟。分别提取。对乙酰氨基酚介导的中毒大鼠平均相对肝脏重量的减少与150和300 mg kg〜(-1)的提取物相对逆转。 C. jag us bulb提取物还显示出在150和300 mg kg〜(-1)时具有显着(p <0.05)的效价,可降低对乙酰氨基酚诱导的大鼠血清转氨酶(AST,ALT和ALP)和总胆红素的增加,但升高总血清蛋白值组织病理学表明,在未处理的对照大鼠中,对乙酰氨基酚2000 mg kg〜(-1)引起肝细胞严重坏死。水飞蓟素(50 mg kg〜(-1),po)对乙酰氨基酚攻击的大鼠进行治疗,刺槐提取物(150和300 mg kg〜(-1),po)对肝细胞再生具有更好的保护作用到未经处理的对照。豆提取物似乎在再生实质细胞,具有高抗氧化和抗炎活性的肝微粒体酶方面具有多种作用。美洲印第安人球茎可能是有效的肝保护剂的潜在来源。

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