Chen Xing, Zheng Aijuan, Li Shuzhen, Wang Zedong, Chen Zhimin, Chen Jiang, Zou Zhiheng, Liang Haijun, Liu Guohua
Key Laboratory for Feed Biotechnology of the Ministry of Agriculture and Rural Affairs, Institute of Feed Research, Chinese Academy of Agriculture Sciences, Beijing 100081, China.
Jiangxi Province Key Laboratory of Animal Green and Healthy Breeding, Institute of Animal Husbandry and Veterinary Science, Jiangxi Academy of Agricultural Sciences, Nanchang 330200, China.
Antioxidants (Basel). 2024 Dec 17;13(12):1550. doi: 10.3390/antiox13121550.
This article aims to investigate the mechanism by which alleviates lipopolysaccharide (LPS)-induced intestinal oxidative stress. The study involved two experimental subjects: human colorectal adenocarcinoma (Caco-2) cells and Arbor Acres broiler chickens. The experiment involving two samples was designed with the same treatment groups, specifically the control (CK) group, lipopolysaccharide (LPS) group, (JF) group, and JF+LPS group. In the Caco-2 experiment, we administered 2 μg/mL of LPS and 1 × 10 CFU/mL of JF to the LPS and JF groups, respectively. In the broiler experiment, the LPS group (19-21 d) received an abdominal injection of 0.5 mg/kg BW of LPS, whereas the JF group was fed 1 × 10 CFU/g of JF throughout the entire duration of the experiment (1-21 d). The results indicated the following: (1) JF significantly decreased the DPPH free radical clearance rate and hydrogen peroxide levels ( < 0.05). (2) JF significantly enhanced the total antioxidant capacity (T-AOC), superoxide dismutase (SOD), and glutathione peroxidase (GSH Px) activity in Caco-2 cells ( < 0.05), while concurrently reducing malondialdehyde (MDA) content ( < 0.05). (3) Compared to the CK group, JF significantly increased the mRNA expression levels of (), (), SOD, (), GSH-Px, (), (), Claudin, Occludin1, (), and () in Caco-2 cells ( < 0.05), while concurrently reducing the mRNA expression of (), (), (), and () ( < 0.05). In comparison to the LPS group, the JF+LPS group demonstrated a significant increase in the mRNA expression of , , , and , as well as , , and in Caco-2 cells ( < 0.05), alongside a decrease in the mRNA expression of , , and ( < 0.05). (4) In broiler chickens, the JF group significantly elevated the levels of T-AOC, CAT, and GSH-Px in the jejunum while reducing MDA content ( < 0.05). Furthermore, the CAT level in the JF+LPS group was significantly higher than that observed in the LPS group, and the levels of MDA, TNF-α, and IL-1β were significantly decreased ( < 0.05). (5) In comparison to the CK group, the JF group exhibited a significant increase in levels in the jejunum of broiler chickens ( < 0.05). Notably, the mRNA expression levels of , , , , , and were reduced ( < 0.05), while the mRNA expression levels of , and also showed a decrease ( < 0.05). Furthermore, the mRNA expression levels of , , , and in the JF+LPS group were significantly elevated compared to those in the LPS group ( < 0.05), whereas the mRNA expression levels of and were significantly diminished ( < 0.05). In summary, JF can enhance the intestinal oxidative stress response, improve antioxidant capacity and intestinal barrier function, and decrease the expression of inflammatory factors by regulating the / signaling pathway.
本文旨在研究其减轻脂多糖(LPS)诱导的肠道氧化应激的机制。该研究涉及两个实验对象:人结肠腺癌(Caco-2)细胞和艾维茵肉鸡。涉及两个样本的实验设计了相同的处理组,具体为对照组(CK)、脂多糖(LPS)组、(JF)组和JF+LPS组。在Caco-2实验中,我们分别向LPS组和JF组给予2μg/mL的LPS和1×10 CFU/mL的JF。在肉鸡实验中,LPS组(19 - 21日龄)腹腔注射0.5mg/kg体重的LPS,而JF组在整个实验期间(1 - 21日龄)饲喂1×10 CFU/g的JF。结果表明:(1)JF显著降低了DPPH自由基清除率和过氧化氢水平(<0.05)。(2)JF显著增强了Caco-2细胞中的总抗氧化能力(T-AOC)、超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GSH Px)活性(<0.05),同时降低了丙二醛(MDA)含量(<0.05)。(3)与CK组相比,JF显著提高了Caco-2细胞中()、()、SOD、()、GSH-Px、()、()、Claudin、Occludin1、()和()的mRNA表达水平(<0.05),同时降低了()、()、()和()的mRNA表达(<0.05)。与LPS组相比,JF+LPS组在Caco-2细胞中、、、和以及、和的mRNA表达显著增加(<0.05),同时、和的mRNA表达降低(<0.05)。(4)在肉鸡中,JF组显著提高了空肠中T-AOC、CAT和GSH-Px的水平,同时降低了MDA含量(<0.05)。此外,JF+LPS组的CAT水平显著高于LPS组,MDA、TNF-α和IL-1β水平显著降低(<0.05)。(5)与CK组相比,JF组肉鸡空肠中的水平显著增加(<0.05)。值得注意的是,、、、、和的mRNA表达水平降低(<0.05),而和的mRNA表达水平也有所下降(<0.05)。此外,与LPS组相比,JF+LPS组中、、、和的mRNA表达水平显著升高(<0.05),而和的mRNA表达水平显著降低(<0.05)。综上所述,JF可通过调节/信号通路增强肠道氧化应激反应,提高抗氧化能力和肠道屏障功能,并降低炎症因子的表达。