Tan Fang, Zhou Xianrong, Ren Lixuan, Kong Chang-Suk
Department of Bioscience, Silla University, Busan 46958, Republic of Korea.
Department of Food and Nutrition, Silla University, Busan 46958, Republic of Korea.
Foods. 2024 May 12;13(10):1496. doi: 10.3390/foods13101496.
This study aimed to examine the potential impact of the intervention of HFY11 (LP-HFY11) on colitis using in vivo animal trials. The impact of LP-HFY11 intervention on colitis was determined by measuring the levels of relevant indicators in the intestine, colon, and blood after oxazolone-induced colitis in BALB/c mice. The results of the trial show that LP-HFY11 improved the colon weight-to-length ratio, reduced the colitis-induced colon length shortening, and reduced colonic abstinence. Furthermore, it decreased the levels of myeloperoxidase, nitric oxide, and malondialdehyde activities while increasing the glutathione content in the colon tissue of colitis-affected animals. LP-HFY11 lowered the interleukin-10 (IL-10) level and increased the IL-2 level in the serum of colitis mice. LP-HFY11 also upregulated the expression of neuronal nitric oxide synthase, endothelial nitric oxide synthase, c-Kit, and stem cell factor (SCF), and downregulated the expression of IL-8, C-X-C chemokine receptor type 2 (CXCR2), and inducible nitric oxide synthase (iNOS) in the colon tissue of mice with colitis. LP-HFY11 decreased the expression of in the gut while increasing the expression of , , and . This indicates that LP-HFY11 could control physiological alterations in the serum and colon tissue, as well as the expression of gut microorganism.
本研究旨在通过体内动物试验,探讨HFY11(LP - HFY11)干预对结肠炎的潜在影响。通过测量BALB/c小鼠在恶唑酮诱导的结肠炎后肠道、结肠和血液中相关指标的水平,来确定LP - HFY11干预对结肠炎的影响。试验结果表明,LP - HFY11改善了结肠重量与长度比,减少了结肠炎诱导的结肠长度缩短,并减轻了结肠炎症。此外,它降低了髓过氧化物酶、一氧化氮和丙二醛的活性水平,同时增加了受结肠炎影响动物结肠组织中的谷胱甘肽含量。LP - HFY11降低了结肠炎小鼠血清中的白细胞介素10(IL - 10)水平,并提高了IL - 2水平。LP - HFY11还上调了神经元型一氧化氮合酶、内皮型一氧化氮合酶、c - Kit和干细胞因子(SCF)的表达,并下调了结肠炎小鼠结肠组织中IL - 8、C - X - C趋化因子受体2(CXCR2)和诱导型一氧化氮合酶(iNOS)的表达。LP - HFY11降低了肠道中 的表达,同时增加了 、 和 的表达。这表明LP - HFY11可以控制血清和结肠组织中的生理变化以及肠道微生物的表达。