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洋甘菊、花青素及其组合对博来霉素诱导的大鼠肺纤维化的抗氧化作用

The Antioxidative Effect of Chamomile, Anthocyanoside and their Combination on Bleomycin-induced Pulmonary Fibrosis in Rat.

作者信息

Javadi Iraj, Emami SeyedAlireza

机构信息

Azad University of Shahreza, Isfahan, Iran.

Alzahra Hospital, Isfahan University Of Medical Sciences, Isfahan, Iran.

出版信息

Med Arch. 2015 Aug;69(4):229-31. doi: 10.5455/medarh.2015.69.229-231. Epub 2015 Aug 4.

Abstract

INTRODUCTION

Bleomycin is a small peptide with 1500Daltun of molecular weight which has two junction areas in two molecule's opposite sides, one of them to relate to the DNA and the other to relate to the iron. Iron is a crucially important factor in free radical production and cytotoxic activity of bleomycin.

MATERIAL AND METHODS

The study attempts to study, and compare, the effect of using Chamomile, Anthocyanoside and their combination, as anti-inflammatory agent to ameliorates, to prevent or control the development of fibrosis due to Bleomycin (BLM). to prepare pulmonary fibrosis model, male Wistar rats weighting 180-220g were assigned to specific groups Rats of each group received intratracheally 1U/100 g of BLM. 20 rats were divided to five comparable groups, as(1) BLM group, (2) saline group, (3) Chamomile group, (4) Anthocyanoside group, (5) combination of Anthocyanoside and Chamomile group. Antioxidative combinations were given as pretreatment and treatment after the rats received Bleomycine.

RESULTS

After 3 week, Malondialdehyde (MDA)was measured for each rat's lung. After three weeks, MDA was reduced, compared to BLM group, to 44.27%, 37.80% and 46.07% in Anthocyanoside, Chamomiland combination group, respectively. It was concluded from the present study that administration of combination of Chamomile and Anthocyanoside lead to a significant reduction in Bleomycin-induced MDA.

CONCLUSION

The mechanism of the effect of these combinations is possibly the result of phenolic combinations as antioxidant and oxy free radical scavenger and inhibitor of lipid peroxidation.

摘要

引言

博来霉素是一种分子量为1500道尔顿的小肽,在两个分子的相对侧有两个连接区域,其中一个与DNA相关,另一个与铁相关。铁是博来霉素自由基产生和细胞毒性活性的关键重要因素。

材料与方法

本研究试图研究并比较使用洋甘菊、花青素及其组合作为抗炎剂来改善、预防或控制博来霉素(BLM)所致纤维化发展的效果。为制备肺纤维化模型,将体重180 - 220克的雄性Wistar大鼠分配到特定组。每组大鼠经气管内给予1U/100克的BLM。20只大鼠被分为五个可比组,即(1)BLM组,(2)生理盐水组,(3)洋甘菊组,(4)花青素组,(5)花青素与洋甘菊组合组。在大鼠接受博来霉素后,给予抗氧化组合作为预处理和治疗。

结果

3周后,测量每只大鼠肺中的丙二醛(MDA)。三周后,与BLM组相比,花青素组、洋甘菊组和组合组中的MDA分别降低了44.27%、37.80%和46.07%。本研究得出结论,洋甘菊和花青素组合给药可显著降低博来霉素诱导的MDA。

结论

这些组合的作用机制可能是酚类组合作为抗氧化剂、氧自由基清除剂和脂质过氧化抑制剂的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b043/4610652/543560d2497a/MA-69-229-g002.jpg

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