Rhubarb Monomers Protect Intestinal Mucosal Barrier in Sepsis via Junction Proteins

被引:35
|
作者
Wang, Lyu [1 ]
Cui, Yun-Liang [2 ]
Zhang, Zhe [1 ]
Lin, Zhao-Fen [1 ]
Chen, De-Chang [3 ]
机构
[1] Second Mil Med Univ, Changzheng Hosp, Dept Emergency & Crit Care Med, Shanghai 200003, Peoples R China
[2] Jinan Mil Gen Hosp, Dept Crit Care Med, Jinan 250031, Shandong, Peoples R China
[3] Shanghai Jiao Tong Univ, Dept Crit Care Med, Ruijin Hosp, Shanghai 200025, Peoples R China
关键词
Junction Proteins; Mucosal Barrier; Rhubarb Monomers; Sepsis; TIGHT JUNCTIONS; LACTULOSE/MANNITOL TEST; CELLS; PERMEABILITY; EXPRESSION; ZO-2; DISRUPTION; APOPTOSIS; ZONULIN;
D O I
10.4103/0366-6999.205855
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Leakage of the intestinal mucosal barrier may cause translocation of bacteria, then leading to multiorgan failure. This study hypothesized that rhubarb monomers might protect the gut mucosal barrier in sepsis through junction proteins. Methods: Healthy male Sprague-Dawley rats (weighing 230-250 g) under anesthesia and sedation were subjected to cecal ligation and perforation (CLP). After surgical preparation, rats were randomly assigned to eight groups (n = 6 or 8 each group): sham group (GroupA: normal saline gavage); sepsis group (Group B: normal saline gavage); Group C (intraperitoneally, dexamethasone 0.5 mg/kg) immediately after CLP surgery; and rhubarb monomer (100 mg/kg in normal saline)-treated groups (Group D: rhein; Group E: emodin; Group F: 3,8-dihydroxy-1-methyl-anthraquinone-2-carboxylic acid; Group G: 1-O-caffeoyl-2-(4-hydroxy-O-cinnamoyl)-D-glucose; and Group H: daucosterol linoleate). Animals were sacrificed after 24 h. Intestinal histology, lactulose, mannitol concentrations were measured, and zonula occludens (ZO)-1, occludin and claudin-5 transcription (polymerase chain reaction), translation (by Western blot analysis), and expression (by immunohistochemistry) were also measured. Results: Intestinal histology revealed injury to intestinal mucosal villi induced by sepsis in Group B, compared with Group A. Compared with Group A (0.17 +/- 0.41), the pathological scores in Groups B (2.83 +/- 0.41, P < 0.001), C (1.83 +/- 0.41, P < 0.001), D (2.00 +/- 0.63, P < 0.001), E (1.83 +/- 0.41, P < 0.001), F (1.83 +/- 0.75, P < 0.001), G (2.17 +/- 0.41, P < 0.001), and H (1.83 +/- 0.41, P < 0.001) were significantly increased. Lactulose/mannitol (L/M) ratio in Group B (0.046 +/- 0.003) was significantly higher than in Group A (0.013 +/- 0.001, P < 0.001) while L/M ratios in Groups C (0.028 +/- 0.002, P < 0.001), D (0.029 +/- 0.003, P < 0.001), E (0.026 +/- 0.003, P < 0.001), F (0.027 + 0.003, P < 0.001), G (0.030 +/- 0.005, P < 0.001), and H (0.026 +/- 0.002, P < 0.001) were significantly lower than that in Group B. ZO-1, occludin and claudin-5 transcription, translation, and expression in Group B were significantly lower than that in Group A (P < 0.001), but they were significantly higher in Groups C, D, E, F, G, and H than those in Group B (P < 0.05). Conclusion: Rhubarb monomer treatment ameliorated mucosal damage in sepsis via enhanced transcription, translation, and expression of junction proteins.
引用
收藏
页码:1218 / 1225
页数:8
相关论文
共 50 条
  • [1] Rhubarb Monomers Protect Intestinal Mucosal Barrier in Sepsis via Junction Proteins
    Lyu Wang
    Yun?Liang Cui
    Zhe Zhang
    Zhao?Fen Lin
    De?Chang Chen
    中华医学杂志英文版, 2017, 130 (10) : 1218 - 1225
  • [2] Free total rhubarb anthraquinones protect intestinal mucosal barrier of SAP rats via inhibiting the NLRP3/caspase-1/GSDMD pyroptotic pathway
    Zeng, Yue
    Liu, Xingyu
    Yi, Qing
    Qiao, Gan
    Wang, Lulu
    Chen, Li
    Fan, Ling
    Li, Yao
    Duan, Lingjing
    Huang, Liqiang
    Zhuang, Qian
    Zhou, Yejiang
    Xiong, Yuxia
    JOURNAL OF ETHNOPHARMACOLOGY, 2024, 326
  • [3] Vitamin A supplementation improves the intestinal mucosal barrier and facilitates the expression of tight junction proteins in rats with diarrhea
    Xiao, Lu
    Cui, Ting
    Liu, Shu
    Chen, Baolin
    Wang, Yuting
    Yang, Ting
    Li, Tingyu
    Chen, Jie
    NUTRITION, 2019, 57 : 97 - 108
  • [4] PREVENTION OF INTESTINAL APOPTOSIS IN SEPSIS LEADS TO IMPROVED BARRIER FUNCTION VIA ALTERED TIGHT JUNCTION EXPRESSION
    Otani, Shunsuke
    Joseph, Benyam P.
    Klingensmith, Nathan J.
    Chen, Ching-wen
    Chihade, Deena B.
    Liang, Zhe
    Coopersmith, Craig M.
    SHOCK, 2018, 49 (06): : 106 - 106
  • [5] bFGF ameliorates intestinal mucosal permeability and barrier function through tight junction proteins in burn injury rats
    Jiang, Yan
    Zhang, Caifeng
    Wang, Tingli
    BURNS, 2021, 47 (05) : 1129 - 1136
  • [6] Berberine induces ZIP14 expression and modulates zinc redistribution to protect intestinal mucosal barrier during polymicrobial sepsis
    He, Yan
    Yuan, Xiaoming
    Zuo, Hao
    Li, Xiangwei
    Sun, Ying
    Feng, Aiwen
    LIFE SCIENCES, 2019, 233
  • [7] Protective effect of citrulline on the intestinal mucosal barrier of mice during sepsis
    Chen, Jianxin
    Xu, Rui
    Qiu, Lifang
    PAKISTAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2023, 36 (04) : 1079 - 1084
  • [8] Effect of Shenfu injection on intestinal mucosal barrier in a rat model of sepsis
    Wu, Wan
    Jiang, Rong-lin
    Wang, Ling-cong
    Lei, Shu
    Xing, Xi
    Zhi, Yi-hui
    Wu, Jian-nong
    Wu, Yan-chun
    Zhu, Mei-fei
    Huang, Li-quan
    AMERICAN JOURNAL OF EMERGENCY MEDICINE, 2015, 33 (09): : 1237 - 1243
  • [9] Tetrastigma hemsleyanum Diels et Gilg ameliorates lipopolysaccharide induced sepsis via repairing the intestinal mucosal barrier
    Zhan, Lianghui
    Pu, Jinbao
    Zheng, Jingru
    Hang, Suni
    Pang, Lisha
    Dai, Muhua
    Ji, Chunlian
    BIOMEDICINE & PHARMACOTHERAPY, 2022, 148
  • [10] Cryptosporidium parvum disrupts intestinal epithelial barrier function via altering expression of key tight junction and adherens junction proteins
    Kumar, Anoop
    Chatterjee, Ishita
    Anbazhagan, Arivarasu N.
    Jayawardena, Dulari
    Priyamvada, Shubha
    Alrefai, Waddah A.
    Sun, Jun
    Borthakur, Alip
    Dudeja, Pradeep K.
    CELLULAR MICROBIOLOGY, 2018, 20 (06)