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营养脂质与黏膜炎症

Nutritional Lipids and Mucosal Inflammation.

机构信息

Division of Clinical Chemistry and Biochemistry, University Children's Hospital Zurich, Zurich, 8032, Switzerland.

Children's Research Center, University Children's Hospital Zurich, Zurich, 8032, Switzerland.

出版信息

Mol Nutr Food Res. 2021 Mar;65(5):e1901269. doi: 10.1002/mnfr.201901269. Epub 2020 Aug 26.

DOI:10.1002/mnfr.201901269
PMID:32780927
Abstract

Inflammatory bowel disease (IBD) is characterized by chronic relapsing inflammation in the intestine. Given their role in regulation of inflammation, long-chain n-3 polyunsaturated fatty acids (PUFAs) represent a potential supplementary therapeutic approach to current drug regimens used for IBD. Mechanistically, there is ample evidence for an anti-inflammatory and pro-resolution effect of long-chain n-3 PUFAs after they incorporate into cell membrane phospholipids. They disrupt membrane rafts and when released from the membrane suppress inflammatory signaling by activating PPAR-γ and free fatty acid receptor 4; furthermore, they shift the lipid mediator profile from pro-inflammatory eicosanoids to specialized pro-resolving mediators. The allocation of long-chain n-3 PUFAs also leads to a higher microbiome diversity in the gut, increases short-chain fatty acid-producing bacteria, and improves intestinal barrier function by sealing epithelial tight junctions. In line with these mechanistic studies, most epidemiological studies support a beneficial effect of long-chain n-3 PUFAs intake on reducing the incidence of IBD. However, the results from intervention trials on the prevention of relapse in IBD patients show no or only a marginal effect of long-chain n-3 PUFAs supplementation. In light of the current literature, international recommendations are supported that adequate diet-derived n-3 PUFAs might be beneficial in maintaining remission in IBD patients.

摘要

炎症性肠病(IBD)的特征是肠道慢性复发性炎症。鉴于长链 n-3 多不饱和脂肪酸(PUFA)在炎症调节中的作用,它们代表了一种潜在的补充治疗方法,可以补充目前用于 IBD 的药物治疗方案。从机制上讲,长链 n-3 PUFA 整合到细胞膜磷脂后,具有抗炎和促解决作用,这方面有充分的证据。它们破坏膜筏,从膜中释放出来后,通过激活 PPAR-γ 和游离脂肪酸受体 4 抑制炎症信号;此外,它们将脂质介质谱从促炎类二十烷酸转移到专门的促解决介质。长链 n-3 PUFAs 的分配也会导致肠道内的微生物组多样性增加,增加产生短链脂肪酸的细菌,并通过封闭上皮紧密连接来改善肠道屏障功能。与这些机制研究一致,大多数流行病学研究支持长链 n-3 PUFAs 摄入对降低 IBD 发病率的有益影响。然而,关于预防 IBD 患者复发的干预试验的结果表明,长链 n-3 PUFAs 补充没有或只有微小的作用。根据目前的文献,国际建议支持足够的饮食来源 n-3 PUFAs 可能有益于维持 IBD 患者的缓解。

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