隐丹参酮的药理机制:在心血管、癌症和神经系统疾病应用中的最新进展。

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL Drug Design, Development and Therapy Pub Date : 2024-12-15 eCollection Date: 2024-01-01 DOI:10.2147/DDDT.S494555
Ziyao Zheng, Liyuan Ke, Shumin Ye, Peiying Shi, Hong Yao
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引用次数: 0

摘要

隐丹参酮(CTS)是丹参的重要活性成分。近年来,其显著的药理作用引发了广泛而深入的研究。本文旨在综述CTS的最新研究进展,并对今后的研究进行展望。讨论了纳入文献的选择、数据提取和方法学质量评价。研究包括(1)理化性质和ADME/Tox性质;(2)药理作用和机制;(3)结论和生物信息学分析。本综述共筛选了915篇题目和摘要,共收录184篇论文;CTS通过调节多种分子途径对多种疾病显示出治疗作用。例如,CTS主要靶向NF-κB通路和MAPK通路,在心血管疾病中发挥治疗作用;在癌症中,CTS通过PI3K/Akt/mTOR通路和JAK/STAT通路表现出优越的疗效;CTS通过Nrf2/HO-1通路来对抗神经系统疾病。此外,通过生物信息学分析预测CTS的关键靶点,参考疾病本体论(DO)、京都基因与基因组百科全书(KEGG)和基因本体论(GO)富集分析,使用R Studio;预计AKT1、MAPK1、STAT3、P53和EGFR是CTS治疗疾病的关键靶点。然后通过Autodock软件对关键蛋白进行对接,初步评估其结合活性。本文综述为CTS的研究和应用前景提供了新的思路,特别是CTS的靶点和直接结合模式有待进一步研究。
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Pharmacological Mechanisms of Cryptotanshinone: Recent Advances in Cardiovascular, Cancer, and Neurological Disease Applications.

Cryptotanshinone (CTS) is an important active ingredient of Salvia miltiorrhiza Bge. In recent years, its remarkable pharmacological effects have triggered extensive and in-depth studies. The aim of this study is to retrieve the latest research progress on CTS and provide prospects for future research. The selection of literature for inclusion, data extraction and methodological quality assessment were discussed. Studies included (1) physicochemical and ADME/Tox properties, (2) pharmacological effects and mechanism, (3) conclusion and bioinformatics analysis. A total of 915 titles and abstracts were screened, resulting in 184 papers used in this review; CTS has shown therapeutic effects on a variety of diseases by modulating multiple molecular pathways. For example, CTS primarily targets NF-κB pathway and MAPK pathway to have a therapeutic role in cardiovascular diseases; in cancer, CTS shows superior efficacy through the PI3K/Akt/mTOR pathway and the JAK/STAT pathway; CTS act on the Nrf2/HO-1 pathway to combat neurological diseases. In addition, key targets of CTS were predicted by bioinformatics analysis, referring to disease ontology (DO), Kyoto Encyclopedia of Genes and Genomes (KEGG) and gene ontology (GO) enrichment analysis, with R Studio; AKT1, MAPK1, STAT3, P53 and EGFR are predicted to be the key targets of CTS against diseases. The key proteins were then docked by Autodock software to preliminarily assess their binding activities. This review provided new insights into research of CTS and its potential applications in the future, and especially the targets and directly binding modes for CTS are waiting to be investigated.

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来源期刊
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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