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谷氨酰胺减轻肠道化疗诱导黏膜炎中氨甲喋呤对 TLR 信号的抑制作用。

Glutamine attenuates the inhibitory effect of methotrexate on TLR signaling during intestinal chemotherapy-induced mucositis in a rat.

机构信息

The Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Laboratory of intestinal adaptation and recovery, Haifa, Israel ; Department of Pediatric Surgery, Bnai Zion Medical Center, 47 Golomb St., P.O.B. 4940, Haifa 31048, Israel.

The Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Laboratory of intestinal adaptation and recovery, Haifa, Israel.

出版信息

Nutr Metab (Lond). 2014 Apr 17;11:17. doi: 10.1186/1743-7075-11-17. eCollection 2014.

Abstract

Toll-like receptor 4 (TLR-4) is crucial in maintaining intestinal epithelial homeostasis, participates in a vigorous signaling process and heightens inflammatory cytokine output. The objective of this study was to determine the effects of glutamine (GLN) on TLR-4 signaling in intestinal mucosa during methotrexate (MTX)-induced mucositis in a rat. Male Sprague-Dawley rats were randomly assigned to one of four experimental groups of 8 rats each: 1) control rats; 2) CONTR-GLN animals were treated with oral glutamine given in drinking water (2%) 48 hours before and 72 hours following vehicle injection; 3) MTX-rats were treated with a single IP injection of MTX (20 mg/kg); and 4) MTX-GLN rats were pre-treated with oral glutamine similar to group B, 48 hours before and 72 hours after MTX injection. Intestinal mucosal damage, mucosal structural changes, enterocyte proliferation and enterocyte apoptosis were determined 72 hours following MTX injection. The expression of TLR-4, MyD88 and TRAF6 in the intestinal mucosa was determined using real time PCR, Western blot and immunohistochemistry. MTX-GLN rats demonstrated a greater jejunal and ileal mucosal weight and mucosal DNA, greater villus height in ileum and crypt depth and index of proliferation in jejunum and ileum, compared to MTX animals. The expression of TLR-4 and MyD88 mRNA and protein in the mucosa was significantly lower in MTX rats versus controls animals. The administration of GLN increased significantly the expression of TLR-4 and MyD88 (vs the MTX group). In conclusion, treatment with glutamine was associated with up-regulation of TLR-4 and MyD88 expression and a concomitant decrease in intestinal mucosal injury caused by MTX-induced mucositis in a rat.

摘要

Toll 样受体 4(TLR-4)在维持肠道上皮细胞稳态方面起着至关重要的作用,它参与了剧烈的信号转导过程,并增强了炎症细胞因子的输出。本研究旨在确定谷氨酰胺(GLN)对 MTX 诱导的大鼠黏膜炎中肠黏膜 TLR-4 信号的影响。雄性 Sprague-Dawley 大鼠随机分为 4 个实验组,每组 8 只:1)对照组;2)CONTR-GLN 组在给予 MTX 前 48 小时和后 72 小时给予口服 GLN(2%);3)MTX 组给予单次腹腔注射 MTX(20mg/kg);4)MTX-GLN 组在给予 MTX 前 48 小时和后 72 小时给予口服 GLN 治疗,方法同 B 组。在给予 MTX 后 72 小时测定肠黏膜损伤、黏膜结构变化、肠上皮细胞增殖和肠上皮细胞凋亡。采用实时 PCR、Western blot 和免疫组织化学法测定肠黏膜 TLR-4、MyD88 和 TRAF6 的表达。与 MTX 组相比,MTX-GLN 组的空肠和回肠黏膜重量和黏膜 DNA 更高,回肠绒毛高度和隐窝深度以及空肠和回肠的增殖指数更高。MTX 组肠黏膜 TLR-4 和 MyD88 mRNA 和蛋白的表达明显低于对照组。给予 GLN 可显著增加 TLR-4 和 MyD88 的表达(与 MTX 组相比)。综上所述,谷氨酰胺治疗与 TLR-4 和 MyD88 表达上调有关,并可减轻 MTX 诱导的大鼠黏膜炎所致的肠黏膜损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e80/4005622/d5095f5f7ba3/1743-7075-11-17-1.jpg

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