Nigella sativa Linn. seed extract modulates the activity of ASC complex of NLRP3 inflammasome in rats subjected to experimental pancreatitis

Periyanayagam Suguna , Arumugam Geetha , Ravikumar Aruna , Ganesan Vijaiyan Siva
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引用次数: 3

Abstract

NLRP3 inflammasome, a multi-protein complex containing ASC as a linker protein influences the process of inflammation and tissue injury in pancreas. In this study, the effect of methanolic seed extract of Nigella sativa (MENS) on the expression of ASC protein of NLRP3 inflammasome was investigated in rats subjected to experimental pancreatitis. Male albino Wistar rats were divided into 4 groups. Group 1 and 2 rats were fed with normal diet; group 3 and 4 rats were administered with ethanol (EtOH) and fed high fat diet (HFD) for 90 days. In addition, group 2 and 4 rats were administered orally with 200 mg/kg body weight of MENS for the last 60 days. We measured serum lipase and amylase activities, oxidative stress markers and inflammatory markers. The mRNA expression of caspase-1, ASC, pro-inflammatory cytokines, IL-1β, IL-18, TNF-α and protein expression of caspase-1 and ASC were determined in pancreas. Our study indicated that MENS co-administration significantly decreased the level of serum lipase and amylase activities, oxidative stress markers and inflammatory markers in EtOH and HFD fed rats. mRNA and protein level expression of caspase-1 and ASC were found to be downregulated in MENS co-administered rats. Spearman's rank correlation test showed that ASC mRNA expression has significant positive correlation with the serum levels of caspase-1 (rs = 0.885, P < 0.01), IL-1β (rs = 0.828, P < 0.05) and IL-18 (rs = 0.943, P = 0.01) in MENS co-administered rats. The present study showed that MENS exhibits anti-inflammatory activity probably by downregulating the expression of ASC protein of NLRP3 inflammasome in pancreas to minimize the activation of caspase-1.

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黑穗槐;种子提取物调节实验性胰腺炎大鼠NLRP3炎性体ASC复合物的活性
NLRP3炎性小体是一种以ASC为连接蛋白的多蛋白复合物,影响胰腺炎症和组织损伤的过程。本研究研究了黑Nigella sativa (MENS)甲醇籽提取物对实验性胰腺炎大鼠NLRP3炎性小体ASC蛋白表达的影响。雄性白化Wistar大鼠分为4组。1、2组大鼠饲喂正常日粮;第3、4组大鼠灌胃乙醇(EtOH)并饲喂高脂饲料(HFD) 90 d。最后60 d,第2组和第4组大鼠分别口服MENS 200 mg/kg体重。测定血清脂肪酶和淀粉酶活性、氧化应激标志物和炎症标志物。检测胰腺组织caspase-1、ASC mRNA表达、促炎因子、IL-1β、IL-18、TNF-α表达及caspase-1、ASC蛋白表达。我们的研究表明,MENS联合给药显著降低了EtOH和HFD喂养大鼠的血清脂肪酶和淀粉酶活性、氧化应激标志物和炎症标志物水平。MENS共给药大鼠caspase-1和ASC mRNA和蛋白水平表达下调。Spearman秩相关检验显示,ASC mRNA表达量与血清caspase-1水平呈显著正相关(rs = 0.885, P <0.01), IL-1β (rs = 0.828, P <0.05)和IL-18 (rs = 0.943, P = 0.01)。本研究表明,MENS可能通过下调胰腺NLRP3炎性小体ASC蛋白的表达来减少caspase-1的激活,从而具有抗炎活性。
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