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丹参酮IIA抗呼吸系统疾病的研究进展:治疗靶点及潜在机制

Progress of tanshinone IIA against respiratory diseases: therapeutic targets and potential mechanisms.

作者信息

Ding Zhaohui, Deng Youlin, Luo Huie, Liu Cuiwang, Yang Minjuan, Xue Hanrong, Chen Zhengtao

机构信息

Department of Clinical Medicine, Jiangxi University of Traditional Chinese Medicine, Nanchang, China.

Affiliated Hospital of Jiangxi University of Traditional Chinese Medicine, Nanchang, China.

出版信息

Front Pharmacol. 2025 Feb 24;16:1505672. doi: 10.3389/fphar.2025.1505672. eCollection 2025.

DOI:10.3389/fphar.2025.1505672
PMID:40066338
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11891354/
Abstract

The respiratory system stands as one of the eight pivotal systems within the human body, responsible for a range of essential functions. Primarily, it facilitates the absorption of oxygen from the external environment and the expulsion of carbon dioxide, thereby playing a crucial role in regulating the body's acid-base balance. Furthermore, it helps to maintain the stability of the internal environment, ensuring the smooth progression of normal metabolic processes and sustaining life activities. In the wake of the novel coronavirus pneumonia outbreak, respiratory diseases have continued to exhibit comparatively high morbidity and mortality rates, underscoring the urgent need for the discovery of novel therapeutic agents. Tanshinone IIA (Tan IIA), a bioactive chemical constituent derived from has emerged as a promising candidate. As a significant fat-soluble compound, Tan IIA has traditionally been utilized in the treatment of cardiovascular diseases. As research on Tan IIA has progressed, its multifaceted therapeutic potential has been unveiled. Specifically, Tan IIA has demonstrated anti-inflammatory, anti-oxidative stress, anti-fibrosis, and anti-cancer effects. In recent years, a wealth of studies has concentrated on elucidating its impact on various respiratory diseases, including asthma, chronic obstructive pulmonary disease, pulmonary hypertension, pulmonary fibrosis, acute lung injury/acute respiratory distress syndrome, and lung cancer. These findings collectively suggest that Tan IIA holds considerable promise in the realm of anti-respiratory disease therapies. The present article undertakes a comprehensive review of the targets and potential mechanisms of Tan IIA against respiratory diseases, offering valuable insights that can serve as a reference for future research endeavors and clinical applications of Tan IIA in the treatment of respiratory ailments.

摘要

呼吸系统是人体八大关键系统之一,负责一系列重要功能。它主要促进从外部环境中吸收氧气并排出二氧化碳,从而在调节人体酸碱平衡中发挥关键作用。此外,它有助于维持内环境的稳定,确保正常代谢过程的顺利进行并维持生命活动。在新型冠状病毒肺炎疫情爆发后,呼吸系统疾病的发病率和死亡率持续居高不下,凸显了发现新型治疗药物的迫切需求。丹参酮IIA(Tan IIA),一种从[具体来源未提及]中提取的生物活性化学成分,已成为一个有前景的候选药物。作为一种重要的脂溶性化合物,丹参酮IIA传统上一直用于治疗心血管疾病。随着对丹参酮IIA研究的进展,其多方面的治疗潜力已被揭示。具体而言,丹参酮IIA已显示出抗炎、抗氧化应激、抗纤维化和抗癌作用。近年来,大量研究集中于阐明其对各种呼吸系统疾病的影响,包括哮喘、慢性阻塞性肺疾病、肺动脉高压、肺纤维化、急性肺损伤/急性呼吸窘迫综合征和肺癌。这些发现共同表明,丹参酮IIA在抗呼吸系统疾病治疗领域具有相当大的潜力。本文对丹参酮IIA抗呼吸系统疾病的靶点和潜在机制进行了全面综述,提供了有价值的见解,可为丹参酮IIA治疗呼吸系统疾病的未来研究工作和临床应用提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9a8/11891354/9c36a374c8dc/fphar-16-1505672-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9a8/11891354/5a3e89289732/fphar-16-1505672-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9a8/11891354/1eaad61cd1b8/fphar-16-1505672-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9a8/11891354/9c36a374c8dc/fphar-16-1505672-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9a8/11891354/5a3e89289732/fphar-16-1505672-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9a8/11891354/1eaad61cd1b8/fphar-16-1505672-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9a8/11891354/9c36a374c8dc/fphar-16-1505672-g003.jpg

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本文引用的文献

1
Tanshinone IIA through the PGK1/PDHK1 Pathway Affecting Macrophage Reprogramming in the Repair Process of Myocardial Infarction.丹参酮IIA通过PGK1/PDHK1途径影响心肌梗死修复过程中的巨噬细胞重编程。
Cardiovasc Drugs Ther. 2024 Dec;38(6):1187-1188. doi: 10.1007/s10557-024-07607-8. Epub 2024 Jul 15.
2
Tanshinone IIA acts as a regulator of lipogenesis to overcome osimertinib acquired resistance in lung cancer.丹参酮 IIA 可作为脂生成调节剂克服肺癌奥希替尼获得性耐药。
Biochem Pharmacol. 2024 Jun;224:116207. doi: 10.1016/j.bcp.2024.116207. Epub 2024 Apr 25.
3
Research Progress on Regulation of Immune Response by Tanshinones and Salvianolic Acids of Danshen ( Bunge).
丹参(Bunge)中的丹参酮和丹酚酸调节免疫反应的研究进展。
Molecules. 2024 Mar 7;29(6):1201. doi: 10.3390/molecules29061201.
4
Tanshinone IIA induces ER stress and JNK activation to inhibit tumor growth and enhance anti-PD-1 immunotherapy in non-small cell lung cancer.丹参酮 IIA 通过诱导内质网应激和 JNK 激活抑制非小细胞肺癌肿瘤生长并增强抗 PD-1 免疫治疗。
Phytomedicine. 2024 Jun;128:155431. doi: 10.1016/j.phymed.2024.155431. Epub 2024 Feb 7.
5
Animals in Respiratory Research.动物在呼吸研究中的应用。
Int J Mol Sci. 2024 Mar 1;25(5):2903. doi: 10.3390/ijms25052903.
6
Tanshinone analog inhibits castration-resistant prostate cancer cell growth by inhibiting glycolysis in an AR-dependent manner.丹参酮类似物通过以雄激素受体(AR)依赖的方式抑制糖酵解来抑制去势抵抗性前列腺癌细胞的生长。
J Biol Chem. 2024 Apr;300(4):107139. doi: 10.1016/j.jbc.2024.107139. Epub 2024 Mar 5.
7
Recent Developments in Aerosol Pulmonary Drug Delivery: New Technologies, New Cargos, and New Targets.气溶胶肺部药物传递的新进展:新技术、新载体和新靶标。
Annu Rev Biomed Eng. 2024 Jul;26(1):307-330. doi: 10.1146/annurev-bioeng-110122-010848. Epub 2024 Jun 20.
8
Sodium tanshinone IIA sulfonate inhibits tumor growth via miR-138 upregulation in intermittent hypoxia-induced xenograft mice.丹参酮 IIA 磺酸钠通过上调 miR-138 抑制间歇性低氧诱导的异种移植瘤生长。
Aging (Albany NY). 2024 Feb 8;16(4):3231-3240. doi: 10.18632/aging.205531.
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Tanshinone IIA inhibits proliferation and migration by downregulation of the PI3K/Akt pathway in small cell lung cancer cells.丹参酮 IIA 通过下调小细胞肺癌细胞中的 PI3K/Akt 通路抑制增殖和迁移。
BMC Complement Med Ther. 2024 Jan 31;24(1):68. doi: 10.1186/s12906-024-04363-y.
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Tanshinone IIA reverses gefitinib resistance in EGFR-mutant lung cancer via inhibition of SREBP1-mediated lipogenesis.丹参酮 IIA 通过抑制 SREBP1 介导的脂生成逆转 EGFR 突变型肺癌中的吉非替尼耐药。
Phytother Res. 2024 Mar;38(3):1574-1588. doi: 10.1002/ptr.8130. Epub 2024 Jan 28.