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紫苏油对高脂肪饮食诱导的葡聚糖硫酸钠诱导的结肠炎小鼠的保护作用。

Protective Effect of Perilla Oil Against Dextran Sodium Sulfate-Induced Colitis in Mice Challenged with a High-Fat Diet.

机构信息

Department of Food Science and Human Nutrition, Jeonbuk National University, Jeonju, Republic of Korea.

Obesity Research Center, Jeonbuk National University, Jeonju, Republic of Korea.

出版信息

J Med Food. 2022 Nov;25(11):1021-1028. doi: 10.1089/jmf.2022.K.0071. Epub 2022 Nov 1.

DOI:10.1089/jmf.2022.K.0071
PMID:36322892
Abstract

This study investigated the effect of perilla oil (PO) on an ulcerative colitis mouse model. Five-week-old male C57BL/6J mice were divided into HD (high-fat diet control), HDD (high-fat diet along with dextran sodium sulfate [DSS] administration), HDD + FO, HDD + PO, and HDD + OO where HDD + FO, HDD + PO, and HDD + OO groups were treated with fish oil (FO), PO, and olive oil (OO), respectively. Biochemical analysis of serum, quantitative polymerase chain reaction, and western blotting of colon tissue were conducted to measure inflammatory marker levels. Administration of DSS resulted in colon shortening and a higher disease activity score than HD group. These symptoms were significantly reversed in the oil-treated groups. The body weight loss after DSS administration was significantly lower in the HDD + PO and HDD + OO groups than in the HDD and HDD + FO groups. PO significantly attenuated the levels of tumor necrosis factor-, interleukin (IL)-6, and IL-1 in the serum and colon. The mRNA expression levels of proinflammatory markers in the colon were reduced, whereas those of tight junction proteins and epithelial defense barrier-associated markers were increased by PO treatment. The protein expression of p-p65 was significantly lower in the PO-treated group than the HDD group. In summary, this study revealed that PO improved colitis in the DSS-induced mouse model, indicating its potential role in managing conditions such as ulcerative colitis.

摘要

本研究探讨了紫苏油(PO)对溃疡性结肠炎小鼠模型的影响。将 5 周龄雄性 C57BL/6J 小鼠分为 HD(高脂肪饮食对照)、HDD(高脂肪饮食加葡聚糖硫酸钠[DSS]给药)、HDD+FO、HDD+PO 和 HDD+OO,其中 HDD+FO、HDD+PO 和 HDD+OO 组分别用鱼油(FO)、PO 和橄榄油(OO)处理。对血清进行生化分析、对结肠组织进行定量聚合酶链反应和蛋白质印迹分析,以测量炎症标志物水平。与 HD 组相比,DSS 给药导致结肠缩短和更高的疾病活动评分。这些症状在油处理组中得到显著逆转。与 HDD 和 HDD+FO 组相比,DSS 给药后 PO 和 OO 处理组的体重减轻明显减少。PO 显著降低了血清和结肠中肿瘤坏死因子-α、白细胞介素(IL)-6 和 IL-1 的水平。PO 处理降低了结肠中促炎标志物的 mRNA 表达水平,而增加了紧密连接蛋白和上皮防御屏障相关标志物的表达水平。与 HDD 组相比,PO 处理组的 p-p65 蛋白表达水平显著降低。综上所述,本研究表明 PO 改善了 DSS 诱导的小鼠模型中的结肠炎,表明其在管理溃疡性结肠炎等疾病方面具有潜在作用。

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