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维生素E对甲氨蝶呤诱导的大鼠空肠黏膜损伤的保护作用

Protective Effects of Vitamin E on Methotrexate-Induced Jejunal Mucosal Damage in Rats.

作者信息

Burcu Busra, Kanter Mehmet, Orhon Zeynep Nur, Yarali Oguzhan, Karabacak Rukiye

出版信息

Anal Quant Cytopathol Histpathol. 2016 Apr;38(2):87-94.

Abstract

OBJECTIVE

To investigate the possible protective effects of Vitamin E (Vit E) on oxidative stress and jejunal damage in the rat intestinal mucosa after methotrexate (MTX)-induced enterotoxicity.

STUDY DESIGN

Rats were divided into 3 groups: control, MTX, and MTX+ Vit E; each group contained 8 animals. The control group was given physiological serum in addition to sunflower oil for 3 days. The second group was given sunflower oil with intragastric tube daily, followed by MTX injection (20 mg/kg intraperitoneally). To the third group, starting 3 days before injection, Vit E was given dissolved in sunflower oil (600 mg/kg orally) in addition to MTX injection. Four days after MTX injection the anesthetized rats were sacrificed, and the tissue samples obtained from their jejunums were investigated for histological and biochemical analysis.

RESULTS

Vit E treatment significantly decreased the elevated tissue malondialdehyde levels and increased the reduced glutathione peroxidase and superoxide dismutase activities in comparison to the MTX-treated group. MTX treatment caused severe histopathological injury including mucosal erosions, inflammatory cell infiltration, necrosis, hemorrhage, and villous congestion. Vit E treatment significantly attenuated the severity of intestinal injury caused by MTX via inhibiting induced nitric oxide synthase levels and NF-κB p65 activation.

CONCLUSION

Because of its reconstructing and antioxidant effects, Vit E pretreatment may have protective effects in the intestinal tissue of MTX-treated rats.

摘要

目的

研究维生素E(Vit E)对甲氨蝶呤(MTX)诱导的肠毒性后大鼠肠黏膜氧化应激和空肠损伤的可能保护作用。

研究设计

将大鼠分为3组:对照组、MTX组和MTX + Vit E组;每组包含8只动物。对照组除给予葵花籽油外,还给予生理血清3天。第二组每天经胃管给予葵花籽油,随后腹腔注射MTX(20 mg/kg)。对于第三组,在注射前3天开始,除了MTX注射外,还给予溶解在葵花籽油中的Vit E(600 mg/kg口服)。MTX注射4天后,将麻醉的大鼠处死,从其空肠获取组织样本进行组织学和生化分析。

结果

与MTX治疗组相比,Vit E治疗显著降低了升高的组织丙二醛水平,并增加了降低的谷胱甘肽过氧化物酶和超氧化物歧化酶活性。MTX治疗导致严重的组织病理学损伤,包括黏膜糜烂、炎性细胞浸润、坏死、出血和绒毛充血。Vit E治疗通过抑制诱导型一氧化氮合酶水平和NF-κB p65激活,显著减轻了MTX引起的肠道损伤严重程度。

结论

由于其重建和抗氧化作用,Vit E预处理可能对MTX治疗的大鼠肠道组织具有保护作用。

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