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全胃肠外营养小鼠模型中急性肠内再喂养后小肠黏膜内的稳态改变

Homeostasis alteration within small intestinal mucosa after acute enteral refeeding in total parenteral nutrition mouse model.

作者信息

Feng Yongjia, Barrett Meredith, Hou Yue, Yoon Hong Keun, Ochi Takanori, Teitelbaum Daniel H

机构信息

Section of Pediatric Surgery, Department of Surgery, the University of Michigan Medical School and the C. S. Mott Children's Hospital, Ann Arbor, Michigan;

Section of Pediatric Surgery, Department of Surgery, the University of Michigan Medical School and the C. S. Mott Children's Hospital, Ann Arbor, Michigan; General Surgery, Department of Surgery, the University of Michigan Medical School, Ann Arbor, Michigan;

出版信息

Am J Physiol Gastrointest Liver Physiol. 2016 Feb 15;310(4):G273-84. doi: 10.1152/ajpgi.00335.2015. Epub 2015 Dec 3.

Abstract

Feeding strategies to care for patients who transition from enteral nutrient deprivation while on total parenteral nutrition (TPN) to enteral feedings generally proceed to full enteral nutrition once the gastrointestinal tract recovers; however, an increasing body of literature suggests that a subgroup of patients may actually develop an increased incidence of adverse events, including death. To examine this further, we studied the effects of acute refeeding in a mouse model of TPN. Interestingly, refeeding led to some beneficial effects, including prevention in the decline in intestinal epithelial cell (IEC) proliferation. However, refeeding led to a significant increase in mucosal expression of proinflammatory cytokines, including tumor necrosis factor-α (TNF-α), as well as an upregulation in Toll-like receptor 4 (TLR-4). Refeeding also failed to prevent TPN-associated increases in IEC apoptosis, loss of epithelial barrier function, and failure of the leucine-rich repeat-containing G protein-coupled receptor 5-positive stem cell expression. Transitioning from TPN to enteral feedings led to a partial restoration of the small bowel microbial population. In conclusion, while acute refeeding led to some restoration of normal gastrointestinal physiology, enteral refeeding led to a significant increase in mucosal inflammatory markers and may suggest alternative strategies to enteral refeeding should be considered.

摘要

对于从全胃肠外营养(TPN)期间肠内营养缺乏过渡到肠内喂养的患者,喂养策略通常是在胃肠道恢复后逐步过渡到完全肠内营养;然而,越来越多的文献表明,一部分患者实际上可能会出现不良事件发生率增加,包括死亡。为了进一步研究这一问题,我们在TPN小鼠模型中研究了急性再喂养的影响。有趣的是,再喂养产生了一些有益效果,包括防止肠上皮细胞(IEC)增殖下降。然而,再喂养导致促炎细胞因子黏膜表达显著增加,包括肿瘤坏死因子-α(TNF-α),以及Toll样受体4(TLR-4)上调。再喂养也未能预防TPN相关的IEC凋亡增加、上皮屏障功能丧失以及富含亮氨酸重复序列的G蛋白偶联受体5阳性干细胞表达失败。从TPN过渡到肠内喂养导致小肠微生物群部分恢复。总之,虽然急性再喂养导致胃肠道生理功能部分恢复正常,但肠内再喂养导致黏膜炎症标志物显著增加,这可能表明应考虑采用替代肠内再喂养的策略。

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