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克罗恩病患者的黏膜和血浆多不饱和脂肪酸、氧化脂类和内源性大麻素谱发生改变。

Altered mucosal and plasma polyunsaturated fatty acids, oxylipins, and endocannabinoids profiles in Crohn's disease.

机构信息

University of Tunis El Manar, Faculty of Medicine of Tunis, 1007 Tunis, Tunisia; University of Tunis El Manar, Faculty of Sciences of Tunis, 2092 Tunis, Tunisia; Rabta Hospital, Laboratory of Biochemistry & LR99ES11, 1007 Tunis, Tunisia.

University of Tunis El Manar, Faculty of Medicine of Tunis, 1007 Tunis, Tunisia; Rabta Hospital, Laboratory of Biochemistry & LR99ES11, 1007 Tunis, Tunisia.

出版信息

Prostaglandins Other Lipid Mediat. 2023 Oct;168:106741. doi: 10.1016/j.prostaglandins.2023.106741. Epub 2023 May 4.

Abstract

Selected mucosal and plasma polyunsaturated fatty acids (PUFAs) and related oxylipins and endocannabinoids were determined in 28 Crohn's disease (CD) patients and 39 controls. Fasting blood and colonic biopsies were collected in all participants, during a disease flare for the patients. Thirty-two lipid mediators including PUFAs, oxylipins, and endocannabinoids were assessed by LC-MS/MS. The pattern of lipid mediators in CD patients is characterized by an increase in arachidonic acid-derived oxylipins and endocannabinoids and a decrease in n-3 PUFAs and related endocannabinoids. A model combining increased 6-epi-lipoxin A4 and 2-arachidonyl glycerol with decreased docoasapentaenoic acid in plasma fairly discriminates patients from controls and may represent a lipidomic signature for CD flare. The study findings suggest that lipid mediators are involved in CD pathophysiology and may serve as biomarkers for disease flare. Further research is required to confirm the role of these bioactive lipids and test their therapeutic potential in CD.

摘要

在 28 名克罗恩病 (CD) 患者和 39 名对照者中,测定了选定的黏膜和血浆多不饱和脂肪酸 (PUFAs) 及相关的氧化脂类和内源性大麻素。所有参与者均在疾病发作时采集空腹血和结肠活检。通过 LC-MS/MS 评估了 32 种脂质介质,包括 PUFAs、氧化脂类和内源性大麻素。CD 患者的脂质介质模式表现为花生四烯酸衍生的氧化脂类和内源性大麻素增加,n-3 PUFAs 和相关内源性大麻素减少。一个结合血浆中增加的 6-epi-脂氧素 A4 和 2-花生四烯酰甘油与减少的 docosahexaenoic 酸的模型,可相当好地区分患者和对照者,并且可能代表 CD 发作的脂质组学特征。研究结果表明,脂质介质参与 CD 的病理生理学,并且可以作为疾病发作的生物标志物。需要进一步的研究来确认这些生物活性脂质的作用,并测试它们在 CD 中的治疗潜力。

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