Pulmonary fibrosis insights and therapy targets from disease models and administration of the lipophilic diterpene, sodium tanshinone IIA sulfonate: Review and meta-analysis.

IF 0.9 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Li-Ying Peng, Jun-Jun Shi, Yue Liang, Yang Li, Yan Tang, Tuo Kai, Andong Yang, Zi-Yue Xiong
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引用次数: 0

Abstract

Pulmonary fibrosis (PF) is a chronic and progressive pulmonary interstitial disease of unknown etiology and is also a sequela in severe patients with the Coronavirus Disease 2019 (COVID-19). Seven databases were systematically searched to evaluate the preclinical evidence of Tanshinone IIA (Tan IIA) on PF. The quality of the included studies was assessed using a 10-item risk of bias tool, and data were analyzed using RevMan 5.3 software. 22 experiments from 12 studies on a total of 248 animals were included. The results showed that PF phenotype, such as fibrotic score, collagen I (Col-I), collagen III (Col-III), hydroxyproline (Hyp), in the group treated with Tan IIA were significantly lower than those in the model group (p < 0.00001). The potential mechanisms of Tan IIA improvement of PF involve reducing inflammation, antioxidation, and suppressing activation of transforming growth factor beta 1 (TGF-β1). The subgroup analysis of different models, different rat species, and different dosage time showed significant reduction in fibrotic scores and Hyp levels with Tan IIA. The preclinical evidence indicated that Tan IIA might be a potent and promising agent for PF, but this conclusion should be further confirmed with more research.

从疾病模型和服用亲脂性二萜--丹参酮 IIA 磺酸钠中了解肺纤维化和治疗目标:综述和荟萃分析。
肺纤维化(PF)是一种病因不明的慢性进行性肺间质疾病,也是冠状病毒病2019(COVID-19)重症患者的后遗症。为了评估丹参酮 IIA(Tan IIA)对 PF 的临床前证据,我们系统地检索了七个数据库。使用10项偏倚风险工具评估了纳入研究的质量,并使用RevMan 5.3软件分析了数据。共纳入了 12 项研究的 22 项实验,共计 248 只动物。结果显示,使用 Tan IIA 治疗组的 PF 表型,如纤维化评分、胶原 I(Col-I)、胶原 III(Col-III)、羟脯氨酸(Hyp)等,均显著低于模型组(P<0.05)。
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来源期刊
CiteScore
1.70
自引率
12.50%
发文量
116
审稿时长
4-8 weeks
期刊介绍: The International Journal of Clinical Pharmacology and Therapeutics appears monthly and publishes manuscripts containing original material with emphasis on the following topics: Clinical trials, Pharmacoepidemiology - Pharmacovigilance, Pharmacodynamics, Drug disposition and Pharmacokinetics, Quality assurance, Pharmacogenetics, Biotechnological drugs such as cytokines and recombinant antibiotics. Case reports on adverse reactions are also of interest.
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