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3,4-氧代异亚丙基莽草酸对大鼠三硝基苯磺酸诱导实验性结肠炎的保护作用。

Protective effects of 3,4-oxo-isopropylidene-shikimic acid on experimental colitis induced by trinitrobenzenesulfonic acid in rats.

机构信息

Department of Pharmacy, College of Medicine, Xi'an Jiaotong University, Xi'an 710061, China.

出版信息

Dig Dis Sci. 2012 Aug;57(8):2045-54. doi: 10.1007/s10620-012-2155-y. Epub 2012 Apr 3.

Abstract

BACKGROUND

3,4-Oxo-isopropylidene-shikimic acid (ISA) is a derivative of shikimic acid (SA). SA is extracted from Illicium verum Hook.fil., which has been used in traditional Chinese medicine and used for treating vomiting, stomach aches, insomnia, skin inflammation, and rheumatic pain.

AIMS

To investigate the effects and the protective mechanism of 3,4-oxo-isopropylidene-shikimic acid on experimental colitis model induced by 2,4,6-trinitrobenzenesulfonic acid (TNBS) in rats.

METHODS

Colitis in rats was induced by colonic administration with TNBS. ISA (50, 100, and 200 mg/kg) was administered for 12 days to experimental colitis rats. The inflammatory degree was assessed by macroscopic damage score, colon weight/length ratios (mg/cm), and myeloperoxidase (MPO) activity. Malondialdehyde (MDA), glutathione (GSH), and nitric oxide (NO) levels, and superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), inducible nitric oxide synthase (iNOS) activities were measured with biochemical methods.

RESULTS

ISA significantly ameliorated macroscopic damage, reduced colon weight/length ratios and the activity of MPO, depressed MDA and NO levels and iNOS activity, and enhanced GSH level, and GSH-Px and SOD activities in the colon tissues of experimental colitis in a dose-dependent manner. Moreover, the effect of ISA (200 mg/kg) was as effective as sulfasalazine (500 mg/kg).

CONCLUSIONS

The findings of this study demonstrate the protective effect of ISA on experimental colitis, probably due to an antioxidant action.

摘要

背景

3,4-氧代异亚丙基莽草酸(ISA)是莽草酸(SA)的衍生物。SA 从八角茴香 Illicium verum Hook.fil. 中提取,用于治疗呕吐、胃痛、失眠、皮肤炎症和风湿痛等传统中药。

目的

研究 3,4-氧代异亚丙基莽草酸对 2,4,6-三硝基苯磺酸(TNBS)诱导的大鼠实验性结肠炎模型的作用及其保护机制。

方法

通过结肠内给予 TNBS 诱导大鼠结肠炎。ISA(50、100 和 200mg/kg)连续 12 天给药于实验性结肠炎大鼠。通过宏观损伤评分、结肠重量/长度比(mg/cm)和髓过氧化物酶(MPO)活性评估炎症程度。采用生化方法测定丙二醛(MDA)、谷胱甘肽(GSH)、一氧化氮(NO)水平以及超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-Px)、诱导型一氧化氮合酶(iNOS)活性。

结果

ISA 显著改善了宏观损伤,降低了结肠重量/长度比和 MPO 活性,降低了 MDA 和 NO 水平以及 iNOS 活性,增强了 GSH 水平以及 GSH-Px 和 SOD 活性,呈剂量依赖性。此外,ISA(200mg/kg)的作用与柳氮磺胺吡啶(500mg/kg)相当。

结论

本研究结果表明 ISA 对实验性结肠炎具有保护作用,可能是由于其抗氧化作用。

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