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鞣花酸和南瓜籽油对甲氨蝶呤诱导的大鼠小肠损伤的保护作用。

Protective effect of ellagic acid and pumpkin seed oil against methotrexate-induced small intestine damage in rats.

作者信息

El-Boghdady Noha A

机构信息

Biochemistry Department, Faculty of Pharmacy, Cairo University, Cairo 11562, Egypt.

出版信息

Indian J Biochem Biophys. 2011 Dec;48(6):380-7.

Abstract

Gastrointestinal toxicity is one of the most serious side effects in the methotrexate (MTX) treatment. This study was designed to investigate whether ellagic acid (EA) and/or pumpkin seed oil (PSO) had a protective effect on MTX-induced small intestine damage. Forty albino rats were randomized into five groups of 8 rats each. Group I served as a normal control group. In Group II, MTX was administered as a single dose (20 mg/kg) intraperitoneally. Groups III, IV and V were pre-treated respectively with either PSO (40 mg/kg), EA (10 mg/kg) or 0.2% DMSO (vehicle control) orally every day by gavage for 5 days and then they received MTX. All animals were sacrificed 5 days after the intraperitoneal injection of MTX for histopathological examination, estimation of serum prostaglandin E2 (PGE2) level, assay of tissue malondialdehyde (MDA), reduced glutathione (GSH) and nitric oxide (NO) levels and myloperoxidase (MPO), xanthine oxidase (XO) and adenosine deaminase (AD) activities. Administration of EA and/or PSO decreased the intestinal damage, PGE2, MDA and NO levels and MPO, XO and AD activities and increased GSH level. These results suggest that EA and PSO protect the small intestine of rats from MTX-induced damage through their antioxidant and anti-inflammatory effects and thus have potential as a promising drug in the prevention of undesired side effects of MTX.

摘要

胃肠道毒性是甲氨蝶呤(MTX)治疗中最严重的副作用之一。本研究旨在调查鞣花酸(EA)和/或南瓜籽油(PSO)是否对MTX诱导的小肠损伤具有保护作用。40只白化大鼠被随机分为5组,每组8只。第一组作为正常对照组。第二组腹腔注射单剂量MTX(20mg/kg)。第三组、第四组和第五组分别每天经口灌胃给予PSO(40mg/kg)、EA(10mg/kg)或0.2%二甲基亚砜(溶剂对照),持续5天,然后接受MTX。在腹腔注射MTX 5天后处死所有动物,进行组织病理学检查、血清前列腺素E2(PGE2)水平测定、组织丙二醛(MDA)、还原型谷胱甘肽(GSH)和一氧化氮(NO)水平检测以及髓过氧化物酶(MPO)、黄嘌呤氧化酶(XO)和腺苷脱氨酶(AD)活性测定。给予EA和/或PSO可减轻肠道损伤、降低PGE2、MDA和NO水平以及MPO、XO和AD活性,并提高GSH水平。这些结果表明,EA和PSO通过其抗氧化和抗炎作用保护大鼠小肠免受MTX诱导的损伤,因此在预防MTX的不良副作用方面具有作为一种有前景药物的潜力。

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