1.中国人民解放军总医院第五医学中心,北京市丰台区西四环中路100号,100039
2.贵州中医药大学药学院
3.中国人民解放军总医院国家感染性疾病临床医学研究中心
郭玉明,guoyuming_0520@126.com
肖小河,pharmacy302xxh@126.com;
收稿:2022-08-06,
修回:2023-07-01,
纸质出版:2023-09-02
移动端阅览
母光頔,牛明,高云娟等.基于间接毒性认知的中药肝损伤风险预测模式的构建及应用[J].中医杂志,2023,64(17):1763-1770.
MU Guangdi,NIU Ming,GAO Yunjuan,et al.Construction and Application of Liver Injury Risk Prediction Model of Chinese Medicinals based on Indirect Toxicity[J].Journal of Traditional Chinese Medicine,2023,64(17):1763-1770.
母光頔,牛明,高云娟等.基于间接毒性认知的中药肝损伤风险预测模式的构建及应用[J].中医杂志,2023,64(17):1763-1770. DOI: 10.13288/j.11-2166/r.2023.17.008.
MU Guangdi,NIU Ming,GAO Yunjuan,et al.Construction and Application of Liver Injury Risk Prediction Model of Chinese Medicinals based on Indirect Toxicity[J].Journal of Traditional Chinese Medicine,2023,64(17):1763-1770. DOI: 10.13288/j.11-2166/r.2023.17.008.
目的
2
探索建立复方用药条件下中药间接毒性的肝损伤风险预测模式,为基于间接毒性认知的中药肝损伤评价研究提供新的思路及方法。
方法
2
以补骨脂制剂为模式药物,通过筛选补骨脂的高频配伍中药,运用TCMSP、TCMIP、PharmMapper数据库筛查高频配伍中药的成分及作用靶点,对作用于核因子κB(NF-κB)通路的中药进行关联强度值及风险值分析,同时大于关联强度值和风险值中位数的中药为筛选获得的间接肝损伤风险中药,从而构建基于免疫活化相关的间接肝损伤作用过程(以NF-κB通路为例)的肝损伤风险中药预测模式,在此基础上按照补骨脂研究方法采用何首乌制剂开展预测模式的验证。
结果
2
基于免疫活化的重要通路(NF-κB通路为例)的肝损伤风险药物预测模式筛选发现淫羊藿(关联强度值0.18、风险值0.25)为补骨脂制剂中具有间接肝损伤潜在风险的配伍中药,其可能通过正调控NF-κB通路上的布鲁顿酪氨酸激酶(Btk)和蛋白激酶C theta(PKCθ)增加肝损伤风险。进一步以何首乌制剂为对象,采用上述方法开展预测模式验证,发现补骨脂(关联强度值0.25、风险值0.33)、菟丝子(关联强度值0.34、风险值0.33)或可增加何首乌肝损伤的风险。
结论
2
构建了中药间接毒性肝损伤风险预测模式,可以为复方用药条件下中药间接肝损伤风险药物识别提供一定的方法学参考。
Objective
2
To explore and establish the liver injury risk prediction model of indirect toxicity of Chinese medicinals under the condition of compound formulas, and provide new ideas and methods for the study of evaluation of liver injury of Chinese medicinals based on indirect toxicity.
Methods
2
Taking Buguzhi (Fructus Psoraleae) pre-parations as model drug, the combined Chinese medicinals with Buguzhi (Fructus Psoraleae) of high frequency are screened out, and their components and action targets were obtained through TCMSP, TCMIP and PharmMapper databases. The association strength value and risk value of Chinese medicinals that acted on the nuclear factor κB (NF-κB) pathway were analyzed. For those having greater values than the median association strength value and risk value were regarded as indirect Chinese medicinals of liver injury risk. In this way, a prediction model of liver injury risk of Chinese medicinals was constructed based on immune activation-related indirect liver injury process (taking NF-κB pathway as an example). And verification of the prediction model was performed using Heshouwu (Radix Polygoni Multiflori) preparations.
Results
2
The prediction model of liver injury risk based on important immunoactivated pathway (taking NF-κB pathway as an example) found that Yinyanghuo (Herba Epimedii) (association strength value = 0.18, risk value = 0.25) was a Chinese medicinal with potential risk of indirect liver injury within Buguzhi (Fructus Psoraleae) prepartions, which may increase the risk of liver injury by positively regulating Bruton's tyrosine kinase (Btk) and protein kinase C theta (PKCθ) on NF-κB pathway. Further verification of prediction model by Heshouwu (Radix Polygoni Multiflori) preparations showed that Buguzhi (Fructus Psoraleae) (association strength value = 0.25, risk value = 0.33) and Tusizi (Semen Cuscutae) (Semen Cuscutae, association strength value = 0.34, risk value = 0.33) may increase the liver injury risk of Heshouzu.
Conclusion
2
The liver injury risk prediction model of indirect toxicity of Chinese medicinals has been constructed in this study, providing metho-dological reference for the identification of Chinese medicinals of indirect liver injury risk under the condition of compound formulas.
国家药品监督管理局 . 中药药源性肝损伤临床评价技术指导原则 [J]. 药学学报 , 2018 , 53 ( 11 ): 1931 - 1942 .
ZHANG P , YE YA , YANG XZ , et al . Systematic review on Chinese herbal medicine induced liver injury [J]. Evid Based Complement Alternat Med , 2016 : 3560812 . doi: 10.1155/2016/3560812 http://dx.doi.org/10.1155/2016/3560812 .
肖小河 . “健康中国”战略下的中药安全性研究与思考 [J]. 中国中药杂志 , 2018 , 43 ( 5 ): 857 - 860 .
HOOFNAGLE JH , BJÖRNSSON ES . Drug-induced liver injury; types and phenotypes [J]. N Engl J Med , 2019 , 381 ( 3 ): 264 - 273 .
GAO Y , WANG ZL , TANG JF , et al . New incompatible pair of TCM: Epimedii Folium combined with Psoraleae Fructus induces idiosyncratic hepatotoxicity under immunological stress conditions [J]. Front Med , 2020 , 14 ( 1 ): 68 - 80 .
肖小河 , 柏兆方 , 王伽伯 , 等 . 中药安全性评价与药物警戒 [J]. 科学通报 , 2021 , 66 ( Z1 ): 407 - 414 .
LI CP , TAI R , CHEN XP , et al . HLA-B*35:01 allele is a potential biomarker for predicting Polygonum multiflorum-induced liver injury in humans [J]. Hepatology , 2019 , 70 ( 1 ): 346 - 357 .
唐进法 , 王晓艳 , 杨伟 , 等 . 基于统计建模的壮骨关节丸诱发特异质肝损伤相关易感性细胞因子分析 [J]. 药学学报 , 2018 , 53 ( 4 ): 574 - 584 .
WANG ZL , XU G , WANG HB , et al . Icariside Ⅱ, a main compound in Epimedii Folium, induces idiosyncratic he-patotoxicity by enhancing NLRP3 inflammasome activation [J]. Acta Pharm Sin B , 2020 , 10 ( 9 ): 1619 - 1633 .
国家药典委员会 . 中华人民共和国药典 [M]. 北京 : 中国医药科技出版社 , 2020 .
柏兆方 , 王伽伯 , 肖小河 . 中药毒性认知创新与安全精准用药 [J]. 中国中药杂志 , 2022 , 47 ( 10 ): 2557 - 2564 .
KWAK A , LEE Y , KIM H , et al . Intracellular interleukin (IL)-1 family cytokine processing enzyme [J]. Arch Pharm Res , 2016 , 39 ( 11 ): 1556 - 1564 .
WARING JF , LIGUORI MJ , LUYENDYK JP , et al . Microarray analysis of lipopolysaccharide potentiation of trovafloxacin-induced liver injury in rats suggests a role for proinflammatory chemokines and neutrophils [J]. J Pharmacol Exp Ther , 2006 , 316 ( 3 ): 1080 - 1087 .
DENG XM , STACHLEWITZ RF , LIGUORI MJ , et al . Modest inflammation enhances diclofenac hepatotoxicity in rats: role of neutrophils and bacterial translocation [J]. J Pharmacol Exp Ther , 2006 , 319 ( 3 ): 1191 - 1199 .
李娜 , 曹书华 . NF-κB在机体炎症与免疫反应中作用的研究进展 [J]. 中华急诊医学杂志 , 2007 , 16 ( 4 ): 442 - 444 .
RU J , LI P , WANG J , et al . TCMSP: a database of systems pharmacology for drug discovery from herbal medicines [J]. J Cheminform , 2014 , 6 : 13 . doi: 10.1186/1758-2946-6-13 http://dx.doi.org/10.1186/1758-2946-6-13 .
XIA W , PAN CX , GONG JY , et al . Enhancing the enrichment of pharmacophore-based target prediction for the polypharmacological profiles of drugs [J]. J Chem Inf Model , 2016 , 56 ( 6 ): 1175 - 1183 .
XIA W , SHEN YH , WANG SW , et al . PharmMapper 2017 update: a web server for potential drug target identification with a comprehensive target pharmacophore database [J]. Nucleic Acids Res , 2017 , 45 ( W1 ): W356 - W360 .
XU HY , ZHANG YQ , LIU ZM , et al . ETCM: an encyclopaedia of traditional Chinese medicine [J]. Nucleic Acids Res , 2019 , 47 ( D1 ): D976 - D982 .
刘福梅 , 谢雁鸣 , 王志飞 , 等 . 含何首乌制剂致药物性肝损伤患者TCR免疫组库特征研究 [J]. 中国中药杂志 , 2019 , 44 ( 20 ): 4397 - 4404 .
李春雨 , 李晓菲 , 灿涂 , 等 . 基于内毒素模型的何首乌特异质肝损伤评价 [J]. 药学学报 , 2015 , 50 ( 1 ): 28 - 33 .
BARALDI E , DJINOVIC CARUGO K , HYVÖNEN M , et al . Structure of the PH domain from Bruton's tyrosine kinase in complex with inositol 1,3,4,5-tetrakisphosphate [J]. Structure , 1999 , 7 ( 4 ): 449 - 460 .
XU ZB , CHAUDHARY D , OLLAND S , et al . Catalytic domain crystal structure of protein kinase C-theta (PKCtheta) [J]. J Biol Chem , 2004 , 279 ( 48 ): 50401 - 50409 .
MINEEY KS , GONCHARUK SA , GONCHARUK MV , et al . Spatial structure of TLR4 transmembrane domain in bicelles provides the insight into the receptor activation mechanism [J]. Sci Rep , 2017 , 7 ( 1 ): 6864 .
中华中医药学会中成药分会 , 中华中医药学会肝胆病分会 , 中国药学会临床中药学专业委员会 , 等 . 何首乌安全用药指南 [J]. 中国中药杂志 , 2020 , 45 ( 5 ): 961 - 966 .
汪小莉 , 张雨婷 , 张影 , 等 . 菟丝子本草考证 [J]. 中药材 , 2022 , 45 ( 2 ): 476 - 484 .
夏卉芳 , 李啸红 . 菟丝子水提液对大鼠的急性毒性及微核试验 [J]. 中国实验方剂学杂志 , 2014 , 20 ( 13 ): 185 - 188 .
WANG Y , XU G , WANG ZL , et al . Psoralidin, a major component of Psoraleae Fructus, induces inflammasome activation and idiosyncratic liver injury [J]. Int Immunopharmacol , 2021 , 92 : 107352 . doi: 10.1016/j.intimp. 2020.107352 http://dx.doi.org/10.1016/j.intimp.2020.107352 .
0
浏览量
0
下载量
0
CSCD
关联资源
相关文章
相关作者
相关机构
京公网安备11010102007558号