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暴露于有害藻类水华(HAB)毒素微囊藻毒素-LR(MC-LR)会延长并加重葡聚糖硫酸钠(DSS)诱导的结肠炎的严重程度。

Exposure to the Harmful Algal Bloom (HAB) Toxin Microcystin-LR (MC-LR) Prolongs and Increases Severity of Dextran Sulfate Sodium (DSS)-Induced Colitis.

机构信息

Department of Medicine, The University of Toledo College of Medicine and Life Sciences, Toledo, OH 43614, USA.

Department of Pathology, The University of Toledo College of Medicine and Life Sciences, Toledo, OH 43614, USA.

出版信息

Toxins (Basel). 2019 Jun 25;11(6):371. doi: 10.3390/toxins11060371.

Abstract

Inflammatory Bowel Disease (IBD) represents a collection of gastrointestinal disorders resulting from genetic and environmental factors. Microcystin-leucine arginine (MC-LR) is a toxin produced by cyanobacteria during algal blooms and demonstrates bioaccumulation in the intestinal tract following ingestion. Little is known about the impact of MC-LR ingestion in individuals with IBD. In this study, we sought to investigate MC-LR's effects in a dextran sulfate sodium (DSS)-induced colitis model. Mice were separated into four groups: (a) water only (control), (b) DSS followed by water (DSS), (c) water followed by MC-LR (MC-LR), and (d) DSS followed by MC-LR (DSS + MC-LR). DSS resulted in weight loss, splenomegaly, and severe colitis marked by transmural acute inflammation, ulceration, shortened colon length, and bloody stools. DSS + MC-LR mice experienced prolonged weight loss and bloody stools, increased ulceration of colonic mucosa, and shorter colon length as compared with DSS mice. DSS + MC-LR also resulted in greater increases in pro-inflammatory transcripts within colonic tissue (TNF-α, IL-1β, CD40, MCP-1) and the pro-fibrotic marker, PAI-1, as compared to DSS-only ingestion. These findings demonstrate that MC-LR exposure not only prolongs, but also worsens the severity of pre-existing colitis, strengthening evidence of MC-LR as an under-recognized environmental toxin in vulnerable populations, such as those with IBD.

摘要

炎症性肠病(IBD)代表了一组由遗传和环境因素引起的胃肠道疾病。微囊藻毒素-亮氨酸-精氨酸(MC-LR)是藻类大量繁殖时蓝藻产生的一种毒素,摄入后会在肠道中生物积累。目前对于 IBD 患者摄入 MC-LR 的影响知之甚少。在这项研究中,我们试图在葡聚糖硫酸钠(DSS)诱导的结肠炎模型中研究 MC-LR 的作用。将小鼠分为四组:(a)仅饮水(对照),(b)DSS 后饮水(DSS),(c)先饮水后 MC-LR(MC-LR),和(d)DSS 后饮水 MC-LR(DSS + MC-LR)。DSS 导致体重减轻、脾肿大和严重结肠炎,表现为穿透性急性炎症、溃疡、结肠长度缩短和血便。与 DSS 组相比,DSS + MC-LR 组的小鼠经历了更长时间的体重减轻和血便、结肠黏膜溃疡增加以及结肠长度缩短。与仅摄入 DSS 相比,DSS + MC-LR 还导致结肠组织中促炎转录物(TNF-α、IL-1β、CD40、MCP-1)和促纤维化标志物 PAI-1 的增加更为显著。这些发现表明,MC-LR 暴露不仅延长了,而且还加重了原有结肠炎的严重程度,这进一步证明了 MC-LR 作为一种在易受影响的人群(如 IBD 患者)中被低估的环境毒素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9551/6628444/4998140c627e/toxins-11-00371-g001.jpg

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