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消退素通过 HO-1 途径预防糖尿病诱导的结肠氧化应激、屏障功能障碍和相关腹泻。

Resolvins protect against diabetes-induced colonic oxidative stress, barrier dysfunction, and associated diarrhea via the HO-1 pathway.

机构信息

Department of Gastroenterology, The First Affiliated Hospital with Nanjing Medical University, Jiangsu Province, China.

出版信息

Biofactors. 2024 Sep-Oct;50(5):967-979. doi: 10.1002/biof.2049. Epub 2024 Mar 14.

Abstract

Diabetes is associated with increased oxidative stress, leading to altered tight junction formation and increased apoptosis in colonic epithelial cells. These changes may lead to intestinal barrier dysfunction and corresponding gastrointestinal symptoms in patients with diabetes, including diarrhea. The aim of this study was to characterize the effect and mechanism of Resolvin D1 (RvD1) on diabetes-induced oxidative stress and barrier disruption in the colon. Mice with streptozotocin-induced diabetes were treated with RvD1 for 2 weeks, then evaluated for stool frequency, stool water content, gut permeability, and colonic transepithelial electrical resistance as well as production of reactive oxygen species (ROS), apoptosis, and expression of tight junction proteins Zonula Occludens 1 (ZO-1) and occludin. The same parameters were assessed in human colonoid cultures subjected to elevated glucose. We found that RvD1 treatment did not affect blood glucose, but normalized stool water content and prevented intestinal barrier dysfunction, epithelial oxidative stress, and apoptosis. RvD1 also restored ZO-1 and occludin expression in diabetic mice. RvD1 treatment increased phosphorylation of Akt and was accompanied by a 3.5-fold increase in heme oxygenase-1 (HO-1) expression in the epithelial cells. The protective effects of RvD1 were blocked by ZnPP, a competitive inhibitor of HO-1. Similar findings were observed in RvD1-treated human colonoid cultures subjected to elevated glucose. In conclusion, Oxidative stress in diabetes results in mucosal barrier dysfunction, contributing to the development of diabetic diarrhea. Resolvins prevent ROS-mediated mucosal injury and protect gut barrier function by intracellular PI3K/Akt activation and subsequent HO-1 upregulation in intestinal epithelial cells. These actions result in normalizing stool frequency and stool water content in diabetic mice, suggesting that resolvins may be useful in the treatment of diabetic diarrhea.

摘要

糖尿病与氧化应激增加有关,导致结肠上皮细胞紧密连接形成改变和细胞凋亡增加。这些变化可能导致糖尿病患者肠道屏障功能障碍和相应的胃肠道症状,包括腹泻。本研究旨在探讨内源性消退素 D1(RvD1)对糖尿病诱导的结肠氧化应激和屏障破坏的作用及机制。链脲佐菌素诱导糖尿病小鼠给予 RvD1 治疗 2 周,然后评估粪便频率、粪便含水量、肠道通透性和结肠跨上皮电阻以及活性氧(ROS)产生、细胞凋亡和紧密连接蛋白 Zonula Occludens 1(ZO-1)和闭合蛋白的表达。在高糖培养的人结肠类器官中评估了相同的参数。我们发现 RvD1 治疗不影响血糖,但可使粪便含水量正常化,并预防肠道屏障功能障碍、上皮氧化应激和细胞凋亡。RvD1 还可恢复糖尿病小鼠中 ZO-1 和闭合蛋白的表达。RvD1 治疗可增加 Akt 的磷酸化,同时使上皮细胞中血红素加氧酶-1(HO-1)的表达增加 3.5 倍。HO-1 的竞争性抑制剂 ZnPP 阻断了 RvD1 的保护作用。在 RvD1 处理的高糖培养人结肠类器官中也观察到了类似的发现。总之,糖尿病中的氧化应激导致黏膜屏障功能障碍,导致糖尿病性腹泻的发生。消退素通过细胞内 PI3K/Akt 激活和随后的肠上皮细胞中 HO-1 的上调来防止 ROS 介导的黏膜损伤,从而保护肠道屏障功能。这些作用可使糖尿病小鼠的粪便频率和粪便含水量正常化,提示消退素可能对糖尿病性腹泻的治疗有用。

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