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5-氟尿嘧啶通过改变肠道炎症细胞因子和水通道蛋白的表达诱导腹泻。

5-Fluorouracil induces diarrhea with changes in the expression of inflammatory cytokines and aquaporins in mouse intestines.

机构信息

Department of Pharmacology, Hoshi University, Tokyo, Japan.

出版信息

PLoS One. 2013;8(1):e54788. doi: 10.1371/journal.pone.0054788. Epub 2013 Jan 30.


DOI:10.1371/journal.pone.0054788
PMID:23382968
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3559799/
Abstract

Although the mechanisms of 5-fluorouracil (5-FU)-induced diarrhea remain unclear, accumulating evidence has indicated that changes in the mucosal immune system and aquaporins (AQPs) may play a role in its pathogenesis. Therefore, we investigated the possible changes in the gene expression of inflammatory cytokines and AQPs in the intestines of mice with 5-FU-induced diarrhea. In the present study, the expressions of mRNAs that encode inflammatory cytokines, TNF-α, IL-1β, IL-6, Il-17A and IL-22, were significantly increased throughout the entire colon of mice that exhibited diarrhea following 5-FU administration. In contrast, the gene expression of IFNγ was upregulated only in the distal colon. These increases were significantly reduced by the administration of etanercept. However, 5-FU-induced diarrhea was not recovered by etanercept. On the other hand, the genes for AQPs 4 and 8 were markedly present in the colon, and these expressions in the intestines were significantly decreased by treatment with 5-FU. These decreases were not reversed by etanercept. These findings suggest TNF-α neutralization had no effect on the acutely 5-FU-induced diarrhea and impaired AQPs but reduced dramatically several inflammatory cytokines.

摘要

虽然氟尿嘧啶(5-FU)引起腹泻的机制尚不清楚,但越来越多的证据表明,黏膜免疫系统和水通道蛋白(AQP)的变化可能在其发病机制中起作用。因此,我们研究了 5-FU 诱导腹泻小鼠肠道中炎症细胞因子和 AQP 基因表达的可能变化。在本研究中,在给予 5-FU 后出现腹泻的小鼠整个结肠中,编码炎症细胞因子 TNF-α、IL-1β、IL-6、IL-17A 和 IL-22 的 mRNAs 的表达显著增加。相比之下,IFNγ 的基因表达仅在上游结肠上调。这些增加通过给予依那西普显著减少。然而,依那西普并没有恢复 5-FU 诱导的腹泻。另一方面,AQP4 和 AQP8 基因在结肠中明显存在,5-FU 处理后肠道中的这些表达显著降低。依那西普不能逆转这些降低。这些发现表明 TNF-α 中和对急性 5-FU 诱导的腹泻和损害 AQP 没有影响,但显著降低了几种炎症细胞因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9085/3559799/1e3f40b7ad2a/pone.0054788.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9085/3559799/7208f26e571e/pone.0054788.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9085/3559799/91ec174f8540/pone.0054788.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9085/3559799/1790bf9ac9fd/pone.0054788.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9085/3559799/92042677b7c6/pone.0054788.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9085/3559799/bb0c8283ba93/pone.0054788.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9085/3559799/36989ff2ba5f/pone.0054788.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9085/3559799/1e3f40b7ad2a/pone.0054788.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9085/3559799/7208f26e571e/pone.0054788.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9085/3559799/91ec174f8540/pone.0054788.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9085/3559799/1790bf9ac9fd/pone.0054788.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9085/3559799/92042677b7c6/pone.0054788.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9085/3559799/bb0c8283ba93/pone.0054788.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9085/3559799/36989ff2ba5f/pone.0054788.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9085/3559799/1e3f40b7ad2a/pone.0054788.g007.jpg

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Is the pathobiology of chemotherapy-induced alimentary tract mucositis influenced by the type of mucotoxic drug administered?

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