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首页> 外文期刊>Inflammopharmacology >Brazilian green propolis hydroalcoholic extract reduces colon damages caused by dextran sulfate sodium-induced colitis in mice
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Brazilian green propolis hydroalcoholic extract reduces colon damages caused by dextran sulfate sodium-induced colitis in mice

机译:巴西绿色蜂胶水醇提取物减少了由葡聚糖硫酸葡聚糖诱导的结肠炎造成的结肠损伤

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摘要

This study investigated the effects of Brazilian green propolis hydroalcoholic extract (BPE) in 3% w/v dextran sodium sulfate (DSS)-induced?colitis?in mice. The effects of BPE (3, 30 and 300?mg/kg, p.o, by 7?days) on the morphological (colon length and colon weight), clinical (disease activity index and weight loss), microscopic (histological score and mucin levels) and biochemical parameters were determined. The effects of BPE (300?mg/kg, p.o) in the gastrointestinal transit of mice were also evaluated. As expected, the DSS ingestion damaged the colonic tissue, lowered the body weight, decreased the mucin levels, increased MPO activity,?reduced SOD activity and GSH amount. In contrast, the treatment with BPE (300?mg/kg) significantly reduced macroscopic colonic injury and the mucosal damage in colon on histopathological examination and reversed the decrease in mucin levels induced by?DSS. It also significantly normalized the SOD activity and the levels of GSH, but did not elicit any effect on MPO activity in the colon. In addition, BPE did not change the gastric emptying or the intestinal transit rate of mice. Together, these results suggested that BPE reduced the signs of DSS-induced colitis in mice through maintenance of intestinal mucin barrier and favoring intestinal antioxidant defenses.
机译:本研究调查了巴西绿色蜂胶水醇提取物(BPE)在3%w / v葡聚糖硫酸钠(dss)中的影响 - 诱导的α结肠炎α。 BPE(3,30和300×mg / kg,PO,7?天)对形态(结肠长度和结肠重量)的影响,临床(疾病活动指数和体重减轻),微观(组织学评分和粘蛋白水平)确定生化参数。还评估了BPE(300?Mg / kg,p.o)在小鼠胃肠道转发中的影响。如预期的那样,DSS摄入损坏结肠组织,降低体重,降低粘蛋白水平,增加MPO活性,α减少了SOD活性和GSH量。相比之下,用BPE(300×mg / kg)的处理显着降低了宏观结肠损伤和结肠粘膜损伤,对组织病理学检查进行了粘附性,并逆转了βDSS诱导的粘蛋白水平的降低。它也显着归一化了SOD活性和GSH的水平,但并未引发对结肠中MPO活性的任何影响。此外,BPE没有改变胃排空或小鼠的肠道转运率。这些结果表明,BPE通过维持肠粘粘蛋白屏障和有利于肠抗氧化防御,降低了小鼠中DSS诱导的结肠炎的迹象。

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