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Rutin modulates ASC expression in NLRP3 inflammasome: A study in alcohol and cerulein-induced rat model of pancreatitis

机译:芦丁调节NLRP3炎性小体中的ASC表达:酒精和青霉素诱导的胰腺炎大鼠模型的研究

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Inflammasomes are protein complexes formed in response to tissue injury and inflammation to regulate the formation of proinflammatory cytokines. Nod-like receptor pyrin domain containing 3 (NLRP3) is one such inflammasome involved in pancreatic inflammation. Caspase activation recruitment domain (CARD) is an interaction motif found in all the major components of NLRP3 inflammasome such as apoptosis associated speck-like CARD containing protein (ASC) and procaspase-1. NLRP3 activates procaspase-1 with the concerted action of CARD domain of ASC. In the present study, the effect of rutin, a natural flavonoid on the expression of ASC of NLRP3, was investigated in rats treated with ethanol (EtOH) and cerulein (Cer). Male albino Wistar rats were divided into four groups. Groups 1 and 2 rats were fed normal diet, whereas groups 3 and 4 rats were fed EtOH (36 % of total calories) containing diet for a total period of 5 weeks and also administered Cer (20 μg/kg body weight i.p.) thrice weekly for the last 3 weeks. In addition, groups 2 and 4 rats received daily 100 mg/kg body weight of rutin from third week. Rutin co-administration significantly decreased the level of pancreatic marker enzymes, oxidative stress markers, inflammatory markers, mRNA expression of caspase-1, cytokines, ASC-NLRP3, and protein expression of caspase-1 and ASC in rats received EtOH-Cer. The results of the study revealed that rutin can reduce inflammation in pancreas probably by influencing the down regulation of ASC-NLRP3 which might result in the reduced activation of caspase-1 and controlled cytokine production.
机译:炎性体是响应组织损伤和炎症而形成的蛋白复合物,以调节促炎性细胞因子的形成。包含3的Nod样受体吡啶结构域(NLRP3)是一种参与胰腺炎症的炎症小体。 Caspase激活募集结构域(CARD)是在NLRP3炎症小体的所有主要成分中发现的相互作用基序,例如凋亡相关的斑点样含CARD的蛋白质(ASC)和procaspase-1。 NLRP3在ASC的CARD结构域的协同作用下激活procaspase-1。在本研究中,研究了天然黄酮类芦丁对NLRP3 ASC表达的影响。将雄性白化Wistar大鼠分成四组。第1组和第2组大鼠接受正常饮食喂养,而第3组和第4组大鼠接受含饮食的EtOH(占总卡路里的36%),为期5周,并且每周三次给予Cer(20μg/ kg体重腹膜内)最近3周。另外,从第3周开始,第2和第4组大鼠每天接受100 mg / kg体重的芦丁。芦丁共同给药可显着降低大鼠接受EtOH-Cer的胰腺标志物酶,氧化应激标志物,炎症标志物,caspase-1 mRNA表达,细胞因子,ASC-NLRP3以及caspase-1和ASC蛋白表达。研究结果表明,芦丁可能通过影响ASC-NLRP3的下调来减轻胰腺的炎症,这可能导致caspase-1的激活减少和细胞因子的产生受到控制。

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