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A Sulfated-Polysaccharide Fraction from Seaweed Gracilaria birdiae Prevents Naproxen-Induced Gastrointestinal Damage in Rats

机译:海藻石cil的硫酸多糖成分可预防萘普生对大鼠胃肠道的损害

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Red seaweeds synthesize a great variety of sulfated galactans. Sulfated polysaccharides (PLSs) from seaweed are comprised of substances with pharmaceutical and biomedical potential. The aim of the present study was to evaluate the protective effect of the PLS fraction extracted from the seaweed Gracilaria birdiae in rats with naproxen-induced gastrointestinal damage. Male Wistar rats were pretreated with 0.5% carboxymethylcellulose (control group—vehicle) or PLS (10, 30, and 90 mg/kg, p.o.) twice daily (at 09:00 and 21:00) for 2 days. After 1 h, naproxen (80 mg/kg, p.o.) was administered. The rats were killed on day two, 4 h after naproxen treatment. The stomachs were promptly excised, opened along the greater curvature, and measured using digital calipers. Furthermore, the guts of the animals were removed, and a 5-cm portion of the small intestine (jejunum and ileum) was used for the evaluation of macroscopic scores. Samples of the stomach and the small intestine were used for histological evaluation, morphometric analysis and in assays for glutathione (GSH) levels, malonyldialdehyde (MDA) concentration, and myeloperoxidase (MPO) activity. PLS treatment reduced the macroscopic and microscopic naproxen-induced gastrointestinal damage in a dose-dependent manner. Our results suggest that the PLS fraction has a protective effect against gastrointestinal damage through mechanisms that involve the inhibition of inflammatory cell infiltration and lipid peroxidation.
机译:红海藻合成了各种各样的硫酸化半乳聚糖。海藻中的硫酸化多糖(PLS)由具有药物和生物医学潜力的物质组成。本研究的目的是评估从海藻Gracilaria birdiae提取的PLS组分对萘普生引起的胃肠道损伤的保护作用。雄性Wistar大鼠每天两次(分别在09:00和21:00)用0.5%羧甲基纤维素(对照组-车辆)或PLS(10、30和90 mg / kg,p.o。)进行预处理,持续2天。 1小时后,服用萘普生(80 mg / kg,p.o.)。萘普生治疗后第二天,4小时将大鼠处死。立即切除胃,沿更大的曲率张开胃,并使用数字卡尺进行测量。此外,去除动物的胆量,并且将5cm小肠部分(空肠和回肠)用于宏观评分的评估。胃和小肠的样品用于组织学评估,形态分析以及谷胱甘肽(GSH)水平,丙二醛(MDA)浓度和髓过氧化物酶(MPO)活性的测定。 PLS治疗以剂量依赖性方式减少了宏观和微观的萘普生引起的胃肠道损害。我们的结果表明,PLS组分通过抑制炎症细胞浸润和脂质过氧化的机制对胃肠道损害具有保护作用。

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