Article Summary
段 凯,李小刚,黄国庆,易 峰,吴 磊.京尼平对脓毒血症小鼠T细胞的免疫调节作用及其潜在机制[J].现代生物医学进展英文版,2019,19(15):2818-2821.
京尼平对脓毒血症小鼠T细胞的免疫调节作用及其潜在机制
Immunomodulatory Effect of Genipin on T Cell in Sepsis Mice and Its Potential Mechanism
Received:February 11, 2019  Revised:February 28, 2019
DOI:10.13241/j.cnki.pmb.2019.15.004
中文关键词: 京尼平  脓毒血症  盲肠结扎穿孔手术  T细胞  凋亡蛋白  细胞因子
英文关键词: Genipin  Sepsis  Cecal ligation and puncture  T cell  Apoptotic proteins  Cytokines
基金项目:湖南省卫计委科研项目(B20160725)
Author NameAffiliationE-mail
DUAN Kai Department of Emergency, Xiangya Hospital, Central South University, Changsha, Hunan, 410008, China kaikai_vip@sina.com 
LI Xiao-gang Department of Emergency, Xiangya Hospital, Central South University, Changsha, Hunan, 410008, China  
HUANG Guo-qing Department of Emergency, Xiangya Hospital, Central South University, Changsha, Hunan, 410008, China  
YI Feng Department of Emergency, The First People's Hospital of Yueyang, Yueyang, Hunan, 414000, China  
WU Lei Department of Emergency, The First People's Hospital of Yueyang, Yueyang, Hunan, 414000, China  
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中文摘要:
      摘要 目的:探究京尼平对脓毒血症小鼠T细胞的免疫调节作用及其潜在机制。方法:小鼠盲肠结扎穿孔手术(CLP)后,分别在0h和24 h尾静脉注射1 mg/kg、2.5 mg/kg、5 mg/kg京尼平和磷酸盐缓冲液(PBS),连续7d观察和记录小鼠的死亡数。另取小鼠分为Sham组(n=8)、Genipin组(n=8)、CLP组(n=8)、Genipin+CLP组(n=14),Sham组注射PBS并实施假手术,Genipin组注射2.5 mg/kg京尼平并实施假手术,CLP组注射PBS并实施手术,Genipin+CLP组注射2.5 mg/kg京尼平并实施手术。CLP手术26 h后收集脾脏,检测脾脏淋巴细胞总数、CD4+、CD8+、细胞因子和凋亡蛋白FADD、caspase-3、caspase-8表达水平。结果:给药2.5 mg/kg的京尼平小鼠存活率高于其他小鼠。CLP组小鼠脾脏淋巴细胞总数、CD4+、CD8+、白介素(IL)-2、干扰素(IFN)-γ水平低于Sham组,CLP+Genipin组小鼠上述指标高于CLP组(P<0.05);CLP组小鼠凋亡蛋白FADD、caspase-3、caspase-8表达、IL-4、IL-10水平高于Sham组,CLP+Genipin组小鼠上述指标低于CLP组(P<0.05)。结论:京尼平能够通过抑制T细胞凋亡改善脓毒血症后期的免疫抑制,提高脓毒性小鼠的存活率。
英文摘要:
      ABSTRACT Objective: To explore the immunomodulatory effect of genipin on T cell in sepsis mice and its potential mechanism. Methods: After cecal ligation and puncture (CLP) in mice, 1 mg/kg, 2.5 mg/kg, 5 mg/kg genipin and phosphate buffer (PBS) were injected into tail vein at 0 h and 24 h, respectively. Mortality of mice was observed and recorded for 7 consecutive days. The mice were divided into Sham group (n=8), Genipin group (n=8), CLP group (n=8), CLP and Genipin group (n=14). Sham group was injected with PBS and Sham operation was performed. Genipin group was injected with 2.5 mg/kg genipin and sham operation was performed. CLP group was injected with PBS and operated. CLP and Genipin group was injected with 2.5 mg/kg Genipin and operated. The spleens were collected 26 hours after CLP. The total splenic lymphocyte count, CD4+, CD8+, cytokines and apoptotic proteins FADD, caspase-3 and caspase-8 were detected. Results: The survival rate of genipin mice treated with 2.5 mg/kg was higher than that of other mice. The total splenic lymphocyte count, CD4+, CD8+, interleukin (IL)-2, interferon (IFN) -γ levels in CLP group were lower than those in Sham group and Genipin group, the above indexes in CLP group were higher than those in CLP group(P<0.05). The expression of apoptotic proteins FADD, caspase-3, caspase-8, IL-4 and IL-10 levels in CLP group were higher than those in Sham group, Genipin group, the above indexes in CLP group were lower than those in CLP group (P<0.05). Conclusion: Genipin can improve the immune suppression in late sepsis by inhibiting T cell apoptosis, and it can improve the survival rate of septic mice.
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