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小肠缺血时间与GRP78表达的相关性研究及意义

Correlation between intestinal ischemia time and GRP78 expression in rats and its significance
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摘要 目的研究不同缺血时间下小肠组织细胞凋亡程度与GRP78表达量之间的关系。方法选用4周龄雌性SD大鼠,随机分为对照组,损伤组(缺血20、40、60、80和100 min),于再灌注6 h后处死,检测血清中DAO的表达水平,取小肠组织检测细胞凋亡情况以及GRP78表达情况,并观察大鼠两周内的存活情况。结果与对照组相比,损伤组GRP78的表达量随着缺血时间的延长逐渐升高,在80 min时达到峰值;与损伤组缺血80 min时相比,在100 min时GRP78 mRNA表达水平显著下降;与损伤组缺血80 min时相比,在100 min时GRP78蛋白表达水平略有下降;与对照组相比损伤组随着缺血时间的增加,细胞凋亡程度逐渐增加;与对照组相比,缺血时间越长大鼠的两周存活率越低。结论随着缺血时间的延长,大鼠小肠组织细胞绒毛层及粘膜层的细胞凋亡程度逐渐增加;在80 min之前随着大鼠小肠缺血时间的延长,GRP78表达水平逐渐升高,100 min时虽然小肠组织损伤程度较80 min时增大,但GRP78表达水平较80 min时降低,GRP78的表达水平与不同缺血时间小肠组织细胞凋亡程度密切相关。 Objective To study the relationship between the degree of apoptosis of small intestinal tissue cells and the expression of GRP78 under different ischemic times.Methods Four-week-old female SD rats were randomly divided into a control group and injury groups(20,40,60,80,and 100 minutes of ischemia).They were sacrificed 6 hours after reperfusion.The expression level of DAO in the serum was detected.Small intestine tissue was used to detect cell apoptosis and GRP78 expression,and the survival of rats within one week was observed.Results Compared with the control group,with the increasing of ischemia time,the expression of GRP78 in the injury group gradually increased,reached a peak at 80 min.Compared with the injury group at 80 min of ischemia,the expression level of GRP78 mRNA at 100 min decreased significantly.Compared with the injury group at 80 min of ischemia,the GRP78 protein expression level decreased slightly at 100 min.Compared with the control group,with the increasing of ischemia time,the degree of apoptosis in the injury group gradually increased.Compared with the control group,the longer the ischemic time,the lower the two-week survival rate of the rats.Conclusions With the increasing of ischemia time,the degree of apoptosis of rat small intestinal tissue cells in the villous layer and mucosal layer gradually increased.Before 80 min,with the prolongation of rat small intestine ischemia time,the expression level of GRP78 gradually increased.Although the injury degree of small intestine tissue increased at 100 min compared with that at 80 min,the expression level of GRP78 decreased than that at 80 min.The expression level of GRP78 was closely related to the degree of apoptosis of small intestine tissue cells at different ischemic times.
作者 臧成昊 杨金伟 马微 梁宇 刘矿嫔 刘伟 刘洁 王国栋 张丝嘉 吴红杰 朱科威 郭建辉 李力燕 Zang Chenghao;Yang Jinwei;Ma Wei;Liang Yu;Liu Kuangpin;Liu Wei;Liu Jie;Wang Guodong;Zhang Sijia;Wu Hongjie;Zhu Kewei;Guo Jianhui;Li Liyan(The Affiliated Hospital of Kunming University of Science and Technology,the First People's Hospital of Yunnan Province,Kunming 650032,China;Kunming Medical University,Institute of Neuroscience,Kunming 650500,China)
出处 《中国临床解剖学杂志》 CSCD 北大核心 2022年第4期418-424,共7页 Chinese Journal of Clinical Anatomy
基金 国家自然科学基金项目(31560295) 云南省创新团队(2019HC022) 云南省卫生科技计划项目(2018NS0270) 云南省科技厅科技计划项目[2019FE001(-175)] 云南省科技厅昆明医科大学联合专项面上项目[2018FE001(-016)] 云南省科技厅昆明医科大学联合专项重点项目[2018FE001(-163)] 昆明医科大学重大科技成果培育项目(CGPY201802) 云南省万人计划名医专项(YNWR-MY-2018-015)。
关键词 小肠缺血再灌注损伤 GRP78 细胞凋亡 Small intestine ischemia reperfusion injury GRP78 Cell apoptosis
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  • 1Schroder M ,Kaufman RJ.The mammalian unfolded protein response[J].Annu Rev Biochem, 2005,74:739-789.
  • 2Prachasilchai W,Sonoda H,Yokota-Ikeda,et al.A protective role of unfolded protein response in mouse ischemic acute kidney injury[J]. Eur J Pharmacol, 2008,592( 1-3): 138-145.
  • 3Pan YX,Ben AJ,Zheng J,et al.Delayed cytoprotection induced by hypoxic preconditioning in cultured neonatal rat cardiomyoeytes:role of GRP78[J].Life Sci,2007,81 (13) : 1042-1049.
  • 4Hayashi T,Saito A, Okuno S,et al.Induction of GRP78 by isehemic preconditioning reduces endoplasmie reticulum stress and prevents delayed neuronal cell death[J].J Cereb Blood Flow Metab, 2003,23 (8) : 949-961.
  • 5Li Y,Chen Y,Zhang J,et al.Proteetive effect of glutamine-enriched early enteral nutrition on intestinal mucosal barrier injury after liver transplantation in rats[J].Am J Surg, 2010,199( 1 ) :35-42.
  • 6Chiu CJ,McArdle AH,Brown R,et al.Intestinal mucosal lesion in low-flow states I and II A morphological,hemodynamic,and metabolic reappraisal[J].Arch Surg, 1970,101 (4) :478-483.
  • 7Wiseman RL, Haynes CM, Ron D.SnapShot : the unfolded protein response[J].Cell, 2010,140(4) : 590-590.
  • 8Morimoto N, Oida Y, Shimazawa M, et al.Involvement of endoplasmic reticulum stress after middle cerebral artery occlusion in mice[J]. Neuroscience, 2007,147 (4) : 957-967.
  • 9Sugawara S,Takeda K,Lee A,et al.Suppression of stress protein GRP78 induction in tumor B/CIOME eliminates resistance to cell mediated cytotoxicity[J].Cancer Res, 1993,53 (24) : 6001-6005.
  • 10Bilecova-Rabajdova M,Urban P,Maslankova J,et al.Analysis of changes in pro(Gadd153) and anti apoptotic(Grp78) gene expression after ischemic-reperfusion injury of the small intestine[J].Prague Med Rep,2010,111(4) :249-256.

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