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首页> 外文期刊>Biochemical Pharmacology >Resveratrol, a polyphenol found in grapes, suppresses oxidative damage and stimulates apoptosis during early colonic inflammation in rats.
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Resveratrol, a polyphenol found in grapes, suppresses oxidative damage and stimulates apoptosis during early colonic inflammation in rats.

机译:白藜芦醇是葡萄中的一种多酚,可抑制大鼠早期结肠发炎期间的氧化损伤并刺激细胞凋亡。

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Oxidative stress, neutrophil infiltration, proinflammatory cytokines and eicosanoid generation are clearly involved in the pathogenesis of intestinal bowel disease. Resveratrol, a polyphenolic compound found in grapes and wine, has been shown to have anti-inflammatory, antioxidant, antitumour and immunomodulatory activities, however, its effects on experimental colitis remain unknown. We have investigated the effects of resveratrol on the colon injury caused by intracolonic instillation of trinitrobenzenesulphonic acid (TNBS) in rats. We determined the production of prostaglandin (PG)E(2) and PGD(2) in colon mucosa and the expression of cyclo-oxygenases (COX)-1 and -2 immunohistochemically. The inflammatory response was assessed by histology and myeloperoxidase activity, as an index of neutrophil infiltration. Interleukin-1 beta production, histological and histochemical analysis of the lesions were also carried out. Finally, since resveratrol has been found to modulate apoptosis we intended to elucidate its effects on colonic mucosa under early acute inflammatory conditions. Resveratrol (5-10mg/kg/day) significantly reduced the degree of colonic injury, the index of neutrophil infiltration and the levels of the cytokine. Resveratrol did not revert the increased PGE(2) levels but produced a significant fall in the PGD(2) concentration. Compared with inflamed colon, no changes in staining for COX-1 were observed in colon of resveratrol and TNBS-treated rats. In contrast, COX-2 expression was decreased. Furthermore, resveratrol enhanced apoptosis compared with already high level induced by TNBS. In conclusion, resveratrol reduces the damage in experimentally induced colitis, alleviates the oxidative events and stimulates apoptosis.
机译:氧化应激,中性粒细胞浸润,促炎性细胞因子和类花生酸的产生显然与肠道肠病的发病机理有关。白藜芦醇是一种在葡萄和葡萄酒中发现的多酚类化合物,已被证明具有抗炎,抗氧化,抗肿瘤和免疫调节活性,然而,其对实验性结肠炎的作用仍未知。我们研究了白藜芦醇对结肠内滴注三硝基苯磺酸(TNBS)引起的结肠损伤的影响。我们通过免疫组化测定了结肠粘膜中前列腺素(PG)E(2)和PGD(2)的产生以及环氧合酶(COX)-1和-2的表达。通过组织学和髓过氧化物酶活性评估炎症反应,作为中性粒细胞浸润的指标。还进行了白介素-1β的产生,病变的组织学和组织化学分析。最后,由于已经发现白藜芦醇可以调节细胞凋亡,因此我们打算阐明其在早期急性炎症条件下对结肠粘膜的作用。白藜芦醇(5-10mg / kg /天)显着降低结肠损伤程度,中性粒细胞浸润指数和细胞因子水平。白藜芦醇没有使增加的PGE(2)水平恢复原状,但使PGD(2)浓度显着下降。与发炎的结肠相比,在白藜芦醇和TNBS处理的大鼠结肠中未观察到COX-1染色的变化。相反,COX-2表达降低。此外,与已经由TNBS诱导的高水平白藜芦醇相比,白藜芦醇增强了细胞凋亡。总之,白藜芦醇减少了实验性结肠炎的损害,减轻了氧化事件并刺激了细胞凋亡。

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