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褪黑素减轻白色大鼠聚乙烯微塑料引起的肠道屏障损伤作用。

Melatonin Alleviates Intestinal Barrier Damaging Effects Induced by Polyethylene Microplastics in Albino Rats.

机构信息

Department of Anatomy, Physiology and Biochemistry, Faculty of Medicine, The Hashemite University, P.O. Box 330127, Zarqa 13133, Jordan.

Department of Medical Biochemistry and Molecular Biology, Faculty of Medicine, Benha University, Benha 13518, Egypt.

出版信息

Int J Mol Sci. 2023 Sep 3;24(17):13619. doi: 10.3390/ijms241713619.

Abstract

There have been concerns about the potential health risks posed by microplastics (MP). The detection of MP in a variety of food products revealed that humans are ingesting MP. Nevertheless, there is a paucity of data about their impacts, as well as their uptake, on intestinal barrier integrity. This study examined the toxic effects of oral administration of two doses of polyethylene microplastics (PE-MP) (3.75 or 15 mg/kg/day for 5 weeks; mean particle size: 4.0-6.0 µm) on the intestinal barrier integrity in rats. Moreover, the effect of melatonin treatment with MP exposure was also assessed. The PE-MP particle uptake, histopathological changes, Alcian blue staining, Muc2 mRNA, proinflammatory cytokines (IL-1β and TNF-α), and cleaved caspase-3, as well as tight junction proteins (claudin-1, myosin light-chain kinase (MLCK), occludin, and zonula occludens-1 (ZO-1)) were assessed. Oral administration of PE-MP resulted in apparent jejunal histopathological alterations; significantly decreased mucin secretion, occludin, ZO-1, and claudin-1 expression; and significantly upregulated MLCK mRNA, IL-1β concentration, and cleaved caspase-3 expression. Melatonin reversed these altered parameters and improved the PE-MP-induced histopathological and ultrastructure changes. This study highlighted the PE-MP's toxic effect on intestinal barrier integrity and revealed the protective effect of melatonin.

摘要

人们一直担心微塑料 (MP) 可能带来的健康风险。在各种食品中检测到 MP 表明人类正在摄入 MP。然而,关于它们对肠道屏障完整性的影响及其摄取的数据仍然很少。本研究检查了口服两种剂量聚乙烯微塑料 (PE-MP) (3.75 或 15 mg/kg/天,持续 5 周;平均粒径:4.0-6.0 µm) 对大鼠肠道屏障完整性的毒性作用。此外,还评估了 MP 暴露时褪黑素治疗的效果。评估了 PE-MP 颗粒摄取、组织病理学变化、阿尔辛蓝染色、Muc2 mRNA、促炎细胞因子(IL-1β 和 TNF-α)和裂解的 caspase-3 以及紧密连接蛋白(闭合蛋白-1、肌球蛋白轻链激酶 (MLCK)、闭合蛋白和闭合蛋白-1 (ZO-1))。PE-MP 的口服给药导致明显的空肠组织病理学改变;显著降低粘蛋白分泌、闭合蛋白、ZO-1 和闭合蛋白-1 表达;并显著上调 MLCK mRNA、IL-1β 浓度和裂解的 caspase-3 表达。褪黑素逆转了这些改变的参数,并改善了 PE-MP 诱导的组织病理学和超微结构变化。本研究强调了 PE-MP 对肠道屏障完整性的毒性作用,并揭示了褪黑素的保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff15/10488227/0953e53e815d/ijms-24-13619-g001.jpg

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