[1]黄丽萍,乔博灵,颜雪珍,等.基于转录组测序及韦恩分析探寻补气中药制剂发挥补气作用的靶基因及其生物学功能[J].陕西中医,2022,(1):28-32.[doi:DOI:10.3969/j.issn.1000-7369.2022.01.006]
 HUANG Liping,QIAO Boling,YAN Xuezhen,et al.Target genes and biological functions related to tonifying Qi of Chinese medicine preparation based on transcriptome RNA sequencing and Venn analysis[J].,2022,(1):28-32.[doi:DOI:10.3969/j.issn.1000-7369.2022.01.006]
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基于转录组测序及韦恩分析探寻补气中药制剂发挥补气作用的靶基因及其生物学功能
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《陕西中医》[ISSN:1000-7369/CN:61-1281/TN]

卷:
期数:
2022年1期
页码:
28-32
栏目:
基础研究
出版日期:
2022-01-05

文章信息/Info

Title:
Target genes and biological functions related to tonifying Qi of Chinese medicine preparation based on transcriptome RNA sequencing and Venn analysis
作者:
黄丽萍1乔博灵2颜雪珍1赵 亭1纪昌春1杨 峥1张晓霞1郭正萍1罗苓芝1
(1.陕西省中医医院,陕西 西安 710003; 2.西北大学生命科学院,陕西 西安 710069)
Author(s):
HUANG Liping QIAO BolingYAN Xuezhen ZhAO TingJI ChangchunYANG ZhengZHANG XiaoxiaGUO ZhengpingLUO Lingzhi
(Shaanxi Provincial Hospital of Chinese Medicine,Xi'an 710003,China)
关键词:
补气 益气复脉 参芪扶正 高通量转录组测序 MAPK信号通路 FKBP5
Keywords:
Tonifying qi Yiqi Fumai Shenqi Fuzheng RNA-Seq MAPK signaling pathway FKBP5
分类号:
R 96
DOI:
DOI:10.3969/j.issn.1000-7369.2022.01.006
文献标志码:
A
摘要:
目的:探寻益气复脉/参芪扶正注射液发挥补气作用的潜在靶基因及其生物学功能。方法:利用高通量转录组测序技术,考察气虚患者经益气复脉/参芪扶正注射液治疗后,其外周血单核细胞的差异表达基因、GO(Gene Ontotology)分析及KEGG(Kyoto encyclopedia of genes and genomes)分析,并进一步进行韦恩分析,明确2个制剂治疗后共同的差异基因及生物学功能,最后利用一组临床队列样本,通过实时定量PCR,验证并明确与补气密切相关的基因。结果:两组共有的GO条目,包括生物过程的有32条,细胞组分的有2条,分子功能的有6条,生物通路有10条。共表达差异基因有6个,包括DUSP1、DUSP2、FKBP5、F8A2、C9orf129 EGR1。临床队列样本显示,FKBP5的下调有统计学差异(P=0.001)。结论:MAPK信号通路是益气复脉和参芪扶正发挥补气作用的核心通路,FKBP5基因水平下调是它们发挥补气作用的分子标志。
Abstract:
Objective:To identify the potential target genes and biological functions related to tonifying Qi of Yiqi Fumai and Shenqi Fuzheng injection.Methods:In this study,we performed RNA-seq experiments and comparative transcriptomic analysis on pre- and post- peripheral blood mononuclear cell samples collected from Qi-deficiency patients treated with Yiqi FuMai or Shenqi Fuzheng.The significant differentially expressed genes(DEGs)for each treatment were determined; GO(Gene ontology)and KEGG analysis were assigned.Subsequently,Venn analysis was performed to identify genes and biological functions involved in both treatments.Finally,the DEGs in common were investigated in a cohort study by using real time qPCR.Results:There were common items involved in both treatments including 32 of biological process,2 of cellular component,6 of molecular function and 10 of signaling pathway.Their consistent DEGs include DUSP1,DUSP2,FKBP5,F8A2,C9orf129 and EGR1.Down-regulation on FKBP5 showed significant differences in the cohort study(P=0.001).Conclusion:MAPK signaling pathway is an action core in both treatments.Down-regulation of FKBP5 is suggested as a response bio-marker for their function on tonifying Qi.

参考文献/References:

[1] 方金苗,杜武勋.中医气虚证实质研究概述[J].时珍国医国药,2016,27(2):430-432.
[2] Yang HP,Li L,Zhou KC,et al.Shengmai injection attenuates the cerebral ischemia/reperfusion induced autophagy via modulation of the AMPK,mTOR and JNK pathways [J].Pharm Biol,2016,54(10):2288-2297.
[3] 禹海文,董炎炎,党瑜华.益气复脉注射液对非ST抬高型急性心肌梗死内皮功能障碍及细胞凋亡因子影响的研究[J].陕西中医,2019,30(3):304-306.
[4] Cai YM,Zhang Y,Zhang PB,et al.Neuroprotective effect of Shenqi Fuzheng injection pretreatment in aged rats with cerebral ischemia/reperfusion injury[J].Neural Regen Res,2016,11(1):94-100.
[5] Chau SL,Huang ZB,Song YG,et al.Comprehensive quantitative analysis of sq injection using multiple chromatographic technologies [J].Molecules,2016,21(8):1092.
[6] 王俊萍,陈文璐.参芪扶正注射液治疗慢性心衰疗效及对患者BNP、CRP、MMP-9、TIMP-1水平的影响[J].陕西中医,2018,39(10):1366-1369.
[7] 夏博文,邢军超,艾秋池,等.基于转录组测序技术的椎间盘退变特异基因表达谱分析[J].南方医科大学学报,2021,41(6):883-890.
[8] 国家食品药品监督管理局.中药新药临床研究指导原则[M].北京:中国医药科技出版社,2002:361-390.
[9] 李泳浩.益气复脉注射液在化疗导致心脏损伤患者中的疗效研究[J].陕西中医,2017,38(4):432-433.
[10] 杨禹娟,张 勇,吕 军,等.益气复脉注射液治疗老年冠心病并发慢性心力衰竭30例[J].陕西中医,2016,37(10):1325-1326.
[11] 马建齐,郑 振,蒋 雷,等.参芪扶正注射液对脓毒症患者外周血淋巴细胞亚群及预后的影响研究[J].陕西中医,2018,39(3):365-367.
[12] 冯谢敏,胡海峰,胡云峰,等.参芪扶正注射液对胃癌根治术后化疗患者免疫功能及生活质量的影响[J].陕西中医,2017,38(10):1407-1408.
[13] 栗若兰,赵 峰,徐 岩,等.以FK506结合蛋白52为靶点的高通量药物筛选模型的建立及应用[J].中国抗生素杂志,2018,43(1):22-27.
[14] Fries GR,Gassen NC,Rein T.The FKBP51 glucocorticoid receptor co-chaperone:Regulation,function,and implications in health and disease[J].Int J Mol Sci,2017,18(12):e2614.
[15] Meijsing SH.Mechanisms of glucocorticoid-regulated gene transcription[J].Adv Exp Med Biol,2015,872:59-81.
[16] Touma C,Gassen NC,Herrmann L,et al.FK506 binding protein 5 shapes stress responsiveness:modulation of neuroendocrine reactivity and coping behavior[J].Biol Psychiatry,2011,70(10):928-936.
[17] 陈 娇,楚世峰,李 倩,等.FK506 bingding protein 51参与糖皮质激素介导的抑郁样行为的发生[J].中国药理学通报,2014,30(3):407-412.
[18] Hardie DG.AMP-activated protein kinase:An energy sensor that regulates all aspects of cell function[J].Genes Dev,2011,25:1895-1908.
[19] Li F,Cheng TF,Dong X,et al.Global analysis of chemical constituents in Shengmai injection using high performance liquid chromatography coupled with tandem mass spectrometry[J].J Pharm Biomed Anal,2016,117:61-72.
[20] Zhang YL,Dong C.MAP kinases in immune responses[J].Cell Mol Immunol,2005,2:20-27.
[21] Chen Z,Gibson TB,Robinson F,et al.MAP kinases[J].Chem Rev,2001,101:2449-2476.
[22] Huth TK,Staines D,Marshall-Gradisnik S.ERK1/2,MEK1/2 and p38 downstream signalling molecules impaired in CD56 dim CD16+ and CD56 bright CD16 dim natural killer cells in chronic fatigue syndrome/myalgic encephalomyelitis patients[J].J Transl Med,2016,14:97.

备注/Memo

备注/Memo:
基金项目:陕西省自然科学基金资助面上项目(2020JM-672)
更新日期/Last Update: 2022-01-09