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首页> 外文期刊>Molecular and Cellular Biochemistry: An International Journal for Chemical Biology >VSL#3 probiotics exerts the anti-inflammatory activity via PI3k/Akt and NF-κB pathway in rat model of DSS-induced colitis
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VSL#3 probiotics exerts the anti-inflammatory activity via PI3k/Akt and NF-κB pathway in rat model of DSS-induced colitis

机译:VSL#3益生菌通过PI3k / Akt和NF-κB途径在DSS诱发的结肠炎大鼠模型中发挥抗炎活性

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摘要

VSL#3 probiotics can be effective on induction and maintenance of the remission of clinical ulcerative colitis. However, the mechanisms are not fully understood. The aim of this study was to examine the effects of VSL#3 probiotics on dextran sulfate sodium (DSS)-induced colitis in rats. Acute colitis was induced by administration of DSS 3.5 % for 7 days in rats. Rats in two groups were treated with either 15 mg VSL#3 or placebo via gastric tube once daily after induction of colitis; rats in other two groups were treated with either the wortmannin (1 mg/kg) via intraperitoneal injection or the wortmannin + VSL#3 after induction of colitis. Anti-inflammatory activity was assessed by myeloperoxidase (MPO) activity. Expression of inflammatory related mediators (iNOS, COX-2, NF-κB, Akt, and p-Akt) and cytokines (TNF-α, IL-6, and IL-10) in colonic tissue were assessed. TNF-α, IL-6, and IL-10 serum levels were also measured. Our results demonstrated that VSL#3 and wortmannin have anti-inflammatory properties by the reduced disease activity index and MPO activity. In addition, administration of VSL#3 and wortmannin for 7 days resulted in a decrease of iNOS, COX-2, NF-κB, TNF-α, IL-6, and p-Akt and an increase of IL-10 expression in colonic tissue. At the same time, administration of VSL#3 and wortmannin resulted in a decrease of TNF-α and IL-6 and an increase of IL-10 serum levels. VSL#3 probiotics therapy exerts the anti-inflammatory activity in rat model of DSS-induced colitis by inhibiting PI3K/Akt and NF-κB pathway.
机译:VSL#3益生菌可以有效诱导和维持临床溃疡性结肠炎的缓解。但是,机制尚未完全了解。这项研究的目的是检查VSL#3益生菌对大鼠右旋糖酐硫酸钠(DSS)引起的结肠炎的作用。通过在大鼠中施用3.5%的DSS 7天来诱发急性结肠炎。两组大鼠在诱发结肠炎后每天一次通过胃管用15 mg VSL#3或安慰剂进行治疗;结肠炎诱发后,另两组大鼠腹膜内注射渥曼青霉素(1 mg / kg)或渥曼青霉素+ VSL#3。通过髓过氧化物酶(MPO)活性评估抗炎活性。评估结肠组织中炎性相关介质(iNOS,COX-2,NF-κB,Akt和p-Akt)和细胞因子(TNF-α,IL-6和IL-10)的表达。还测量了TNF-α,IL-6和IL-10血清水平。我们的结果表明,VSL#3和渥曼青霉素具有降低的疾病活动指数和MPO活性,具有抗炎特性。此外,施用VSL#3和渥曼青霉素7天导致结肠中iNOS,COX-2,NF-κB,TNF-α,IL-6和p-Akt减少,IL-10表达增加组织。同时,施用VSL#3和渥曼青霉素可导致TNF-α和IL-6降低,以及IL-10血清水平升高。 VSL#3益生菌疗法通过抑制PI3K / Akt和NF-κB途径在DSS诱导的结肠炎大鼠模型中发挥抗炎活性。

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