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益生菌混合物IRT5可改善大鼠年龄依赖性结肠炎。

The probiotic mixture IRT5 ameliorates age-dependent colitis in rats.

作者信息

Jeong Jin-Ju, Woo Jae-Yeon, Ahn Young-Tae, Shim Jae-Hun, Huh Chul-Sung, Im Sin-Heog, Han Myung Joo, Kim Dong-Hyun

机构信息

Department of Life and Nanopharmaceutical Sciences, College of Pharmacy, Kyung Hee University, Seoul 130-701, Republic of Korea.

R&B D Center, Korea Yakult Co., Ltd., Yongin 449-901, Republic of Korea.

出版信息

Int Immunopharmacol. 2015 Jun;26(2):416-22. doi: 10.1016/j.intimp.2015.04.021. Epub 2015 Apr 20.

Abstract

To investigate the anti-inflammatory effect of probiotics, we orally administered IRT5 (1×10(9)CFU/rat) for 8 weeks to aged (16 months-old) Fischer 344 rats, and measured parameters of colitis. The expression levels of the inflammatory markers' inducible NO synthase (iNOS), cyclooxygenase-2 (COX2), tumor necrosis factor (TNF)-α, and interleukin (IL)-1β were higher in the colons of normal aged rats (18 months-old) than in the colons of normal young rats (6 months-old). Treatment with IRT5 suppressed the age-associated increased expression of iNOS, COX2, TNF-α, and IL-1β, and activation of NF-κB and mitogen-activated protein kinases. In a similar manner, the expression of tight junction proteins in the colon of normal aged rats was suppressed more potently than in normal young rats, and treatment of aged rats with IRT5 decreased the age-dependent suppression of tight junction proteins ZO-1, occludin, and claudin-1. Treatment with IRT5 suppressed age-associated increases in expressions of senescence markers p16 and p53 in the colon of aged rats, but increased age-suppressed expression of SIRT1. However, treatment with IRT5 inhibited age-associated increased myeloperoxidase activity in the colon. In addition, treatment with IRT5 lowered the levels of LPS in intestinal fluid and blood of aged rats, as well as the reduced concentrations of reactive oxygen species, malondialdehyde, and C-reactive protein in the blood. These findings suggest that IRT5 treatment may suppress age-dependent colitis by inhibiting gut microbiota LPS production.

摘要

为了研究益生菌的抗炎作用,我们对16月龄的老年Fischer 344大鼠口服IRT5(1×10⁹CFU/大鼠),持续8周,并测量结肠炎相关参数。正常老年大鼠(18月龄)结肠中炎症标志物诱导型一氧化氮合酶(iNOS)、环氧化酶-2(COX2)、肿瘤坏死因子(TNF)-α和白细胞介素(IL)-1β的表达水平高于正常年轻大鼠(6月龄)结肠中的表达水平。IRT5处理抑制了与年龄相关的iNOS、COX2、TNF-α和IL-1β表达增加以及核因子κB(NF-κB)和丝裂原活化蛋白激酶的激活。同样,正常老年大鼠结肠中紧密连接蛋白的表达比正常年轻大鼠受到更强烈的抑制,用IRT5处理老年大鼠可减少年龄依赖性的紧密连接蛋白ZO-1、闭合蛋白和claudin-1的抑制。IRT5处理抑制了老年大鼠结肠中衰老标志物p16和p53表达与年龄相关的增加,但增加了年龄抑制的沉默信息调节因子1(SIRT1)的表达。然而,IRT5处理抑制了与年龄相关的结肠中髓过氧化物酶活性增加。此外,IRT5处理降低了老年大鼠肠液和血液中脂多糖(LPS)的水平,以及血液中活性氧、丙二醛和C反应蛋白浓度的降低。这些发现表明,IRT5处理可能通过抑制肠道微生物群LPS的产生来抑制年龄依赖性结肠炎。

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