• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

临床处方-蛋白质-小分子-疾病策略(CPSD):中医药发展的新策略——以心血管疾病为例

Clinical Prescription-Protein-Small Molecule-Disease Strategy (CPSD), A New Strategy for Chinese Medicine Development: A Case Study in Cardiovascular Diseases.

作者信息

Guo Yong-Zhi, Jiang Ying-Nan, Li Yi-Fang, Kurihara Hiroshi, Dai Yi, He Rong-Rong

机构信息

Guangdong Province Research and Development Center for Chinese Medicine in Disease Susceptibility, College of Pharmacy, Jinan University, Guangzhou, China.

International Cooperative Laboratory of Traditional Chinese Medicine Modernization and Innovative Drug Development of Chinese Ministry of Education (MOE), College of Pharmacy, Jinan University, Guangzhou, China.

出版信息

Front Pharmacol. 2020 Jan 22;10:1564. doi: 10.3389/fphar.2019.01564. eCollection 2019.

DOI:10.3389/fphar.2019.01564
PMID:32038243
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6987446/
Abstract

Chinese medicine is a national treasure that has been passed down for thousands of years in China. According to the statistics of the World Health Organization, there are currently four billion people in the world who use Chinese medicine to treat diseases, accounting for 80% of the world's total population. However, the obscurity of its theory, its unmanageable quality, its complex compositions, and the unknown effective substances and mechanisms are great obstacles to the internationalization of Chinese medicine. Here, we propose a new strategy for the development of Chinese medicine: the clinical prescription (C)-protein (P)-small-molecule (S)-disease (D) strategy, namely the CPSD strategy. The strategy uses clinical prescriptions as the source of medicine and uses computer simulation technology to find small-molecule drugs targeting therapeutic proteins for treating specific diseases so as to deepen awareness of the value of Chinese medicine. At the same time, this article takes cardiovascular drug development as an example to introduce the application of CPSD, which will be instrumental in the further development, modernization, and internationalization of Chinese medicine.

摘要

中医是中国传承了数千年的瑰宝。据世界卫生组织统计,目前全球有40亿人使用中医治病,占世界总人口的80%。然而,其理论晦涩、质量难以把控、成分复杂以及有效物质和作用机制不明,是中医国际化的巨大障碍。在此,我们提出一种中医发展的新策略:临床处方(C)-蛋白质(P)-小分子(S)-疾病(D)策略,即CPSD策略。该策略以临床处方为药物来源,利用计算机模拟技术寻找针对治疗特定疾病的治疗性蛋白质的小分子药物,以加深对中医价值的认识。同时,本文以心血管药物研发为例介绍CPSD的应用,这将有助于中医的进一步发展、现代化和国际化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfa4/6987446/ff4ffdb59a81/fphar-10-01564-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfa4/6987446/6767f3c2c453/fphar-10-01564-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfa4/6987446/ff4ffdb59a81/fphar-10-01564-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfa4/6987446/6767f3c2c453/fphar-10-01564-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfa4/6987446/ff4ffdb59a81/fphar-10-01564-g002.jpg

相似文献

1
Clinical Prescription-Protein-Small Molecule-Disease Strategy (CPSD), A New Strategy for Chinese Medicine Development: A Case Study in Cardiovascular Diseases.临床处方-蛋白质-小分子-疾病策略(CPSD):中医药发展的新策略——以心血管疾病为例
Front Pharmacol. 2020 Jan 22;10:1564. doi: 10.3389/fphar.2019.01564. eCollection 2019.
2
[Opportunities and challenges in development of compound preparations of traditional Chinese medicine: problems and countermeasures in research of ancient classical prescriptions].[中药复方制剂研发的机遇与挑战:古代经典名方研究中的问题与对策]
Zhongguo Zhong Yao Za Zhi. 2019 Oct;44(19):4300-4308. doi: 10.19540/j.cnki.cjcmm.20190630.305.
3
[Development and application of component-based Chinese medicine theory].[基于组件的中医理论的发展与应用]
Zhongguo Zhong Yao Za Zhi. 2017 Nov;42(21):4054-4058. doi: 10.19540/j.cnki.cjcmm.2017.0161.
4
[Study on function evaluation of health food containing Chinese materia medica based on data mining].基于数据挖掘的含中药保健食品功能评价研究
Zhongguo Zhong Yao Za Zhi. 2019 Mar;44(5):870-874. doi: 10.19540/j.cnki.cjcmm.20190115.005.
5
[Substance basis research on Chinese materia medica is one of key scientific problems of inheriting, development and innovation of Chinese materia medica].中药物质基础研究是中药传承、发展与创新的关键科学问题之一。
Zhongguo Zhong Yao Za Zhi. 2015 Sep;40(17):3429-34.
6
[Generalized science of Chinese material medica-from preventive treatment of disease to Chinese medicine health industry].[广义中药学——从治未病到中医药健康产业]
Zhongguo Zhong Yao Za Zhi. 2018 Nov;43(21):4177-4181. doi: 10.19540/j.cnki.cjcmm.2018.0109.
7
[Theory of toxic classification of traditional Chinese medicine and recommendations for revision of China pharmacopeia (volume 1)].[中药毒性分类理论及《中国药典》(一部)修订建议]
Zhongguo Zhong Yao Za Zhi. 2012 Aug;37(15):2193-8.
8
[Precise application of Traditional Chinese Medicine in minimally-invasive techniques].[中医在微创技术中的精准应用]
Zhongguo Gu Shang. 2018 Jun 25;31(6):493-496. doi: 10.3969/j.issn.1003-0034.2018.06.001.
9
The application of Chinese medicine to novel drug discovery.中药在新药发现中的应用。
Expert Opin Drug Discov. 2013 Jan;8(1):21-34. doi: 10.1517/17460441.2013.739602. Epub 2012 Nov 21.
10
Chinese Marine Materia Medica Resources: Status and Potential.中国海洋药物资源:现状与潜力
Mar Drugs. 2016 Mar 3;14(3):46. doi: 10.3390/md14030046.

引用本文的文献

1
Osteogenic Differentiation of Human Umbilical Cord Blood Mesenchymal Stem Cells Induced by Liu's Zhenggudan No. 2 Formula.刘氏正骨丹2号方诱导人脐带血间充质干细胞成骨分化
Evid Based Complement Alternat Med. 2022 Sep 6;2022:4718438. doi: 10.1155/2022/4718438. eCollection 2022.

本文引用的文献

1
Combination of HGF and IGF-1 promotes connexin 43 expression and improves ventricular arrhythmia after myocardial infarction through activating the MAPK/ERK and MAPK/p38 signaling pathways in a rat model.在大鼠模型中,肝细胞生长因子(HGF)和胰岛素样生长因子-1(IGF-1)联合通过激活丝裂原活化蛋白激酶/细胞外信号调节激酶(MAPK/ERK)和丝裂原活化蛋白激酶/p38(MAPK/p38)信号通路促进连接蛋白43表达并改善心肌梗死后的室性心律失常。
Cardiovasc Diagn Ther. 2019 Aug;9(4):346-354. doi: 10.21037/cdt.2019.07.12.
2
Cycloastragenol ameliorates experimental heart damage in rats by promoting myocardial autophagy via inhibition of AKT1-RPS6KB1 signaling.环黄芪醇通过抑制 AKT1-RPS6KB1 信号通路促进心肌自噬来改善大鼠实验性心脏损伤。
Biomed Pharmacother. 2018 Nov;107:1074-1081. doi: 10.1016/j.biopha.2018.08.016. Epub 2018 Aug 25.
3
Calycosin-7-O-β-D-glucoside reduces myocardial injury in heat stroke rats.毛蕊异黄酮-7-O-β-D-葡萄糖苷减轻热射病大鼠的心肌损伤。
J Formos Med Assoc. 2019 Mar;118(3):730-738. doi: 10.1016/j.jfma.2018.08.024. Epub 2018 Sep 21.
4
Baicalin attenuates myocardial ischemia-reperfusion injury through Akt/NF-κB pathway.黄芩苷通过 Akt/NF-κB 通路减轻心肌缺血再灌注损伤。
J Cell Biochem. 2019 Mar;120(3):3212-3219. doi: 10.1002/jcb.27587. Epub 2018 Sep 22.
5
Dragon's Blood exerts cardio-protection against myocardial injury through PI3K-AKT-mTOR signaling pathway in acute myocardial infarction mice model.龙血竭通过 PI3K-AKT-mTOR 信号通路对急性心肌梗死模型小鼠发挥心脏保护作用。
J Ethnopharmacol. 2018 Dec 5;227:279-289. doi: 10.1016/j.jep.2018.09.010. Epub 2018 Sep 6.
6
Wogonin Attenuates Isoprenaline-Induced Myocardial Hypertrophy in Mice by Suppressing the PI3K/Akt Pathway.汉黄芩素通过抑制PI3K/Akt信号通路减轻异丙肾上腺素诱导的小鼠心肌肥大。
Front Pharmacol. 2018 Aug 13;9:896. doi: 10.3389/fphar.2018.00896. eCollection 2018.
7
SMOC1 silencing suppresses the angiotensin II-induced myocardial fibrosis of mouse myocardial fibroblasts via affecting the BMP2/Smad pathway.SMOC1基因沉默通过影响骨形态发生蛋白2/ Smad信号通路抑制血管紧张素II诱导的小鼠心肌成纤维细胞心肌纤维化。
Oncol Lett. 2018 Sep;16(3):2903-2910. doi: 10.3892/ol.2018.8989. Epub 2018 Jun 19.
8
Honokiol Protects against Anti-1-Adrenergic Receptor Autoantibody-Induced Myocardial Dysfunction via Activation of Autophagy.霍诺酚醇通过激活自噬保护抗 1 肾上腺素能受体自身抗体诱导的心肌功能障碍。
Oxid Med Cell Longev. 2018 Jul 18;2018:1640804. doi: 10.1155/2018/1640804. eCollection 2018.
9
CD38 Deficiency Protects Heart from High Fat Diet-Induced Oxidative Stress Via Activating Sirt3/FOXO3 Pathway.CD38缺乏通过激活Sirt3/FOXO3信号通路保护心脏免受高脂饮食诱导的氧化应激。
Cell Physiol Biochem. 2018;48(6):2350-2363. doi: 10.1159/000492651. Epub 2018 Aug 16.
10
Sitagliptin attenuates myocardial apoptosis via activating LKB-1/AMPK/Akt pathway and suppressing the activity of GSK-3β and p38α/MAPK in a rat model of diabetic cardiomyopathy.西他列汀通过激活 LKB-1/AMPK/Akt 通路和抑制 GSK-3β 和 p38α/MAPK 的活性来减轻糖尿病心肌病大鼠模型中的心肌细胞凋亡。
Biomed Pharmacother. 2018 Nov;107:347-358. doi: 10.1016/j.biopha.2018.07.126. Epub 2018 Aug 9.