首页> 美国卫生研究院文献>PLoS Clinical Trials >Comparison of anti-inflammatory activities of an anthocyanin-rich fraction from Portuguese blueberries (Vaccinium corymbosum L.) and 5-aminosalicylic acid in a TNBS-induced colitis rat model
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Comparison of anti-inflammatory activities of an anthocyanin-rich fraction from Portuguese blueberries (Vaccinium corymbosum L.) and 5-aminosalicylic acid in a TNBS-induced colitis rat model

机译:TNBS诱发的结肠炎大鼠模型中葡萄牙蓝莓(Vaccinium corymbosum L.)和5-氨基水杨酸中富含花青素的部分的抗炎活性比较

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摘要

Despite the actual therapeutic approaches for inflammatory bowel disease (IBD), efficient and secure alternative options remain a research focus. In this context, anthocyanins seem promising natural anti-inflammatory agents, but their action mechanisms and efficacy as compared with established drugs still require more clarification. The main aim of this study was to compare the anti-inflammatory action of a chemically characterized anthocyanin-rich fraction (ARF), obtained from Portuguese blueberries (Vaccinium corymbosum L.), with that of 5-aminosalicylic acid (5-ASA), a first-line drug in IBD, in a 2,4,6-trinitrobenzenesulfonic acid (TNBS)-induced colitis rat model. Such fraction showed a high content and great molecular diversity of anthocyanins, with malvidin-3-galactoside and petunidin-3-arabinoside in the highest concentrations. After daily administration by intragastric infusion for 8 days, ARF, at a molar anthocyanin concentration about 30 times lower than 5-ASA, showed a higher effectiveness in counteracting the intestinal inflammation, as assessed by i) body weight variation and colon damage score, ii) reduction in leukocyte infiltration, iii) increase in antioxidant defenses and iv) by downregulation of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) in colon tissue homogenates. The strong inhibition of COX-2 expression seems to be a crucial anti-inflammatory mechanism common to both ARF and 5-ASA, but the additional higher abilities of anthocyanins to downregulate iNOS and to decrease leukocytes infiltration and to increase antioxidant defenses in colon may account for the much higher anti-inflammatory action of anthocyanins. These data may contribute to the development of a promising natural approach in IBD management.
机译:尽管有针对炎症性肠病(IBD)的实际治疗方法,但是有效且安全的替代选择仍然是研究重点。在这种情况下,花色苷似乎是很有前途的天然抗炎药,但与已确立的药物相比,它们的作用机理和功效仍需要进一步阐明。这项研究的主要目的是比较从葡萄牙蓝莓(Vaccinium corymbosum L.)和5-氨基水杨酸(5-ASA)获得的具有化学特征的富含花青素的馏分(ARF)的抗炎作用, 2,4,6-三硝基苯磺酸(TNBS)诱导的结肠炎大鼠模型中IBD的一线药物。这样的馏分显示出高含量的花青素含量和很大的分子多样性,其中最高浓度的是malvidin-3-galactoside和petunidin-3-arabinoside。每天通过胃内输注给药8天后,ARF的花色苷摩尔浓度比5-ASA低约30倍,在抵抗肠道炎症方面显示出更高的有效性,方法如下:i)体重变化和结肠损伤评分,ii )白细胞浸润的减少,iii)抗氧化防御能力的增强,iv)结肠组织匀浆中诱导型一氧化氮合酶(iNOS)和环氧合酶-2(COX-2)的下调。 COX-2表达的强抑制似乎是ARF和5-ASA共同的关键抗炎机制,但花青素具有更高的下调iNOS并减少白细胞浸润和增强结肠抗氧化防御能力的能力。花青素具有更高的抗炎作用。这些数据可能有助于发展IBD管理中一种有前途的自然方法。

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