研究报告

谷氨酰胺肽对乙醇诱导的胃黏膜损伤的保护作用研究

  • 许润琦 ,
  • 王憬 ,
  • 孟德豪 ,
  • 张海欣 ,
  • 马永庆 ,
  • 毕园 ,
  • 徐国阳 ,
  • 陈亮 ,
  • 方磊
展开
  • 1(中国食品发酵工业研究院有限公司,北京,100015)
    2(浙江省农村实业发展有限公司,浙江 杭州,310005)
第一作者:硕士,工程师(方磊工程师和陈亮正高级工程师为共同通信作者,E-mail:wewe359@163.com;269462959@qq.com)

收稿日期: 2024-08-08

  修回日期: 2025-03-11

  网络出版日期: 2025-10-27

基金资助

宁夏回族自治区重点研发计划项目(2021BEG02027)

Study on the protective effect of glutamine peptides on ethanol-induced gastric mucosal injury

  • XU Runqi ,
  • WANG Jing ,
  • MENG Dehao ,
  • ZHANG Haixin ,
  • MA Yongqing ,
  • BI Yuan ,
  • XU Guoyang ,
  • CHEN Liang ,
  • FANG Lei
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  • 1(China National Research Institute of Food and Fermentation Industries Co.Ltd., Beijing 100015, China)
    2(Zhejiang Rural Industry Development Co.Ltd., Hangzhou 310005, China)

Received date: 2024-08-08

  Revised date: 2025-03-11

  Online published: 2025-10-27

摘要

该文探究谷氨酰胺肽对GES-1细胞在酒精损伤下的修复效应。首先,以分子质量分布为指标,研究了体外胃肠道模拟消化对谷氨酰胺肽稳定性的影响。随后,构建酒精损伤的GES-1细胞模型,通过检测细胞内部活性氧簇(reactive oxygen species,ROS)荧光强度、氧化损伤标志物、超氧化物歧化酶(superoxide dismutase,SOD)活力、谷胱甘肽(glutathione,GSH)和谷胱甘肽过氧化物酶(glutathione peroxidase,GSH-Px)含量,探究谷氨酰胺肽对氧化应激的抵抗能力和对细胞屏障的保护作用。结果表明,谷氨酰胺肽经消化后的分子质量比例变化均不超过1.5%,具备消化稳定性;谷氨酰胺肽和肽段pEQ、LQ均能减少活性氧的累积、减少丙二醛(malondialdehyde,MDA)含量,增强SOD活力,增加GSH和GSH-Px含量,且呈浓度依赖性,其中谷氨酰胺肽(800 μg/mL)减少活性氧累积和提高GSH、GSH-Px含量的效果最佳,LQ(60 μg/mL)降低MDA含量的效果最好,pEQ(60 μg/mL)提高SOD活力最佳,与模型组相比均有显著差异(P<0.05)。该研究证明谷氨酰胺肽能够显著提高GES-1细胞对酒精损伤的抵抗能力,为治疗或修复酒精性胃黏膜损伤以及保护胃黏膜屏障功能提供了支持。

本文引用格式

许润琦 , 王憬 , 孟德豪 , 张海欣 , 马永庆 , 毕园 , 徐国阳 , 陈亮 , 方磊 . 谷氨酰胺肽对乙醇诱导的胃黏膜损伤的保护作用研究[J]. 食品与发酵工业, 2025 , 51(20) : 239 -246 . DOI: 10.13995/j.cnki.11-1802/ts.040691

Abstract

This study investigated the protective effects of glutamine peptides (Gln-P) on ethanol-induced damage in GES-1 cells.Initially, to assess the stability of Gln-P throughout simulated gastrointestinal digestion, molecular weight distribution was utilized as a key evaluation criterion.Subsequently, an ethanol-damaged GES-1 cell model was established for evaluating resistance against oxidative stress of Gln-P and its effects on cellular barriers.The analysis encompassed key parameters such as the fluorescence intensity of intracellular reactive oxygen species (ROS), oxidative damage markers, superoxide dismutase (SOD) activity, glutathione (GSH) levels, and glutathione peroxidase (GSH-Px) levels.Results indicated that Gln-P maintained over 98.5% of its molecular weight after digestion, demonstrating robust digestive stability.Notably, Gln-P and its peptide fragments pEQ and LQ exhibited concentration-dependent reductions in ROS accumulation, malondialdehyde (MDA) content, and enhancements in SOD activity, GSH, and GSH-Px levels.Specifically, at a concentration of 800 μg/mL, Gln-P effectively mitigated ROS levels and enhanced GSH-Px activity.Additionally, LQ at 60 μg/mL demonstrated the most pronounced reduction in MDA, while pEQ at 60 μg/mL exhibited the highest increase in SOD activity.Notably, all these effects were statistically significant compared to the model group (P<0.05).This research highlights Gln-P’s considerable potential to strengthen GES-1 cells against ethanol damage.It also contributes to the advancement of therapeutic and reparative strategies aimed at addressing alcoholic gastric mucosal injury and protecting the gastric barrier.

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