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谷氨酰胺对热打击下单层肠上皮Caco-2细胞屏障功能的影响

肖桂珍 李俊 易万华 罗家劲 苏磊

解放军医学杂志2017,Vol.42Issue(6):506-510,5.
解放军医学杂志2017,Vol.42Issue(6):506-510,5.DOI:10.11855/j.issn.0577-7402.2017.06.05

谷氨酰胺对热打击下单层肠上皮Caco-2细胞屏障功能的影响

Influence of glutamine on barrier function of heat-stressed intestinal epithelial Caco-2 cells

肖桂珍 1李俊 2易万华 3罗家劲 4苏磊5

作者信息

  • 1. 510515 广州 广州华博生物制药研究所博士后工作站
  • 2. 510010 广州 广州军区广州总医院 营养科
  • 3. 350001 福州 福建省立医院重症医学三科
  • 4. 510010 广州 广州军区广州总医院 重症医学科
  • 5. 523000 广东东莞 东莞市第五人民医院重症医学科
  • 折叠

摘要

Abstract

Objective To investigate the effect of Glutamine (Gln) on heat stress-induced dysfunction of intestinal epithelial barrier. Methods Human intestinal epithelial Caco-2 cells were pre-incubated with Gln for 24h and then exposed to heat 43℃ for 1h. Cell counting kit-8 (CCK-8) was used to detect the cellular proliferation with various concentrations of Gln and choose an optimum concentration for subsequent experiments. The barrier integrity was measured by transepithelial electrical resistance (TEER) and horseradish peroxidase (HRP) permeability. Levels of tight junction protein occludin and ZO-1 were analyzed by Western blotting. Cytoskeleton using Coomassie blue staining was observed by microscopy. Results At 0.7mmol/L concentration, Gln showed the most effective cell proliferation compared with other concentration groups (P<0.05). Therefore, 0.7mmol/L Gln was used as effective concentration in following experiments. Gln attenuated the TEER decrease and impairment of intestinal permeability induced by heat exposure compared with 43℃ group (P<0.01). The expressions of occludin and ZO-1 were significantly elevated by pretreatment with Gln. The distortion of cytoskeleton was also effectively prevented. Conclusion 0.7mmol/L Gln is potentially beneficial for protecting against heat stress-induced permeability dysfunction and epithelial barrier damage.

关键词

热打击/谷氨酰胺/肠黏膜

Key words

heat stress/glutamine/intestinal mucosa

分类

医药卫生

引用本文复制引用

肖桂珍,李俊,易万华,罗家劲,苏磊..谷氨酰胺对热打击下单层肠上皮Caco-2细胞屏障功能的影响[J].解放军医学杂志,2017,42(6):506-510,5.

基金项目

广东省自然科学基金(S2013030013217)This work was supported by the Natural Science Foundation of Guangdong Province (S2013030013217) (S2013030013217)

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