Gong Zhen-Yu, Yuan Zhi-Qiang, Dong Zhi-Wei, Peng Yi-Zhi
State Key Laboratory of Trauma, Burns and Combined Injury, Institute of Burn Research, Southwest Hospital, The Third Military Medical UniversityChongqing 400038, China.
Am J Transl Res. 2017 May 15;9(5):2535-2547. eCollection 2017.
Severe burns may lead to intestinal inflammation and oxidative stress resulting in intestinal barrier damage and gut dysfunction. In the management of severe burns, therapies are needed to attenuate whole-body inflammatory responses and control the burden of oxidative stress. In this study, we evaluated the effects of oral glutamine (Gln) with probiotics on burn-induced intestinal inflammation and oxidative stress using a Wistar rat burn injury model. We then explored potential molecular mechanisms for the effects of glutamine and probiotics on intestinal tissue inflammation and oxidative stress. We found that glutamine and probiotics together significantly inhibited nitric oxide (NO) content; reduced levels of the inflammatory factors TNF-α, IL-6, and IL-8; and altered expression of oxidative stress factors including reactive oxygen species and superoxide dismutase. We found that the apoptotic proportion of intestinal epithelial cells in severely burned subjects was notably decreased following treatment with glutamine plus probiotics. We also found that glutamine and probiotics given together markedly reduced NO content by down-regulating the expression of iNOS in blood and intestinal tissue. These findings indicate that regulation of the iNOS gene plays a pivotal role in inflammation and oxidative stress in the response to severe burns in the Wistar rat. We then further investigated the mechanism by which combined therapy with glutamine and probiotics might reduce expression of iNOS and found that this treatment resulted in increased methylation of the iNOS gene. The methylation level of the iNOS gene was found to be regulated via differential expression of DNMT1 and Tet1. Collectively, our results suggest that combined therapy with glutamine and probiotics can markedly reduce the synthesis of NO, suppressing intestinal inflammation and oxidative stress in the Wistar rat burn injury model.
严重烧伤可能导致肠道炎症和氧化应激,进而造成肠道屏障损伤和肠道功能障碍。在严重烧伤的治疗中,需要采取措施减轻全身炎症反应并控制氧化应激负担。在本研究中,我们使用Wistar大鼠烧伤模型评估了口服谷氨酰胺(Gln)联合益生菌对烧伤诱导的肠道炎症和氧化应激的影响。然后,我们探讨了谷氨酰胺和益生菌对肠道组织炎症和氧化应激影响的潜在分子机制。我们发现,谷氨酰胺和益生菌联合使用可显著抑制一氧化氮(NO)含量;降低炎症因子TNF-α、IL-6和IL-8的水平;并改变包括活性氧和超氧化物歧化酶在内的氧化应激因子的表达。我们发现,谷氨酰胺加益生菌治疗后,严重烧伤受试者肠道上皮细胞的凋亡比例显著降低。我们还发现,谷氨酰胺和益生菌联合使用可通过下调血液和肠道组织中iNOS的表达显著降低NO含量。这些发现表明,iNOS基因的调控在Wistar大鼠严重烧伤反应中的炎症和氧化应激中起关键作用。然后,我们进一步研究了谷氨酰胺和益生菌联合治疗可能降低iNOS表达的机制,发现这种治疗导致iNOS基因甲基化增加。发现iNOS基因的甲基化水平通过DNMT1和Tet1的差异表达来调节。总的来说,我们的结果表明,谷氨酰胺和益生菌联合治疗可显著降低NO的合成,抑制Wistar大鼠烧伤模型中的肠道炎症和氧化应激。