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 Name | Affiliation | E-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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