Conjugated linoleic acid ameliorates necrotizing enterocolitis by suppressing inflammatory responses and maintaining intestinal barrier integrity via the PPARγ/NFxB signaling pathway

被引:0
作者
Jiang, Chengyao [1 ]
Zhang, Fan [1 ]
Zhang, Min [1 ]
Yan, Xiangyun [1 ]
Chen, Yanjie [1 ]
Yu, Qinlei [1 ]
Chen, Wenjuan [1 ]
Chen, Xiaohui [1 ]
Li, Shushu [1 ]
Han, Shuping [1 ]
机构
[1] Nanjing Med Univ, Nanjing Women & Childrens Healthcare Hosp, Womens Hosp, Dept Pediat, 123rd Tian Fei Xiang,Mo Chou Rd, Nanjing 210004, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Neonatal necrotizing enterocolitis; Conjugated linoleic acid; PPAR gamma; NFxB; Metabolomics; PARENTERAL-NUTRITION; PRETERM INFANTS; RECEPTOR; INJURY; CELLS; MICE;
D O I
10.1016/j.jff.2024.106581
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Necrotizing enterocolitis (NEC) is a severe inflammatory gastrointestinal disorder affecting preterm infants. Through fecal metabolomics, we found linoleic acid compounds (LAs) reduced in NEC and negatively correlated with C-reactive protein and NEC Bell stage. Conjugated linoleic acid (CLA) is a special kind of LAs with multiple functions. This study aims to investigate the role and mechanism of CLA in vivo and vitro. Experimental results in neonatal rats demonstrated that CLA significantly reduced mortality, weight loss, improved pathological scores, relieved inflammation and preserved intestinal cell homeostasis. In vitro, CLA promoted cell proliferation and reduced cell injury. RNA-sequencing analysis indicated that PPAR signaling pathway might be critical. Experiments showed that CLA facilitated PPAR gamma/NFxB signaling pathway by upregulating PPAR gamma expression, inactivating phosphorylated NFxB, and preventing translocation of NFxB P65. This study underscores the therapeutic potential of CLA and provides new insight and direction for developing NEC interventions.
引用
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页数:14
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