ZhuJiang Hospital, Southern Medical University, Guangzhou, China.
Research Center of Integrative Medicine, School of Basic Medical Sciences, Guangzhou University of Chinese Medicine, Guangzhou, China.
Pharm Biol. 2021 Dec;59(1):1607-1618. doi: 10.1080/13880209.2021.2001542.
Qingre Huoxue (QRHX) decoction, a traditional Chinese medicine, has been widely used to prevent and treat myocardial infarction (MI).
This study elucidates the possible mechanisms of QRHX in preventing or treating MI in a rat model.
The chemical constituents of QRHX were identified by UPLC-MS. Sprague-Dawley rats were randomly divided into the Sham (normal saline), Model (normal saline), QRHX-L, QRHX-M and QRHX-H group ( = 10 per group). QRHX decoction was administered by gavage to the rats for 14 days (5, 10 and 20 g/kg/day). The left anterior descending ligation method was performed to develop MI in Model and QRHX groups, and the same surgical procedures excluding ligation sutures were performed for the sham group. Finally, we evaluated cardiac function, myocardial fibrosis degree, serum inflammatory factors, autophagy levels and verified the signalling pathways .
A total of 68 active components of QRHX corresponding to 223 active targets were obtained and 2558 MI-related disease targets were collected. After integration, 123 QRHX anti-MI targets were obtained, and 70 signalling pathways, such as PI3K/Akt, were identified by enrichment analysis. experiments suggest that QRHX could reduce the degree of myocardial fibrosis, downregulate serum inflammatory factors, and promote autophagy in MI rats.
QRHX plays a protective role in the myocardium by mediating PI3K/Akt signalling pathway to activate autophagy and inhibiting inflammatory factor expression. These findings provide a scientific basis for further research and validation of QRHX as a potential therapeutic for MI.
清热活血(QRHX)汤是一种中药,已广泛用于预防和治疗心肌梗死(MI)。
本研究旨在阐明 QRHX 汤在大鼠模型中预防或治疗 MI 的可能机制。
采用 UPLC-MS 鉴定 QRHX 的化学成分。SD 大鼠随机分为假手术(生理盐水)、模型(生理盐水)、QRHX-L、QRHX-M 和 QRHX-H 组(每组 10 只)。QRHX 汤通过灌胃给予大鼠 14 天(5、10 和 20 g/kg/天)。在模型和 QRHX 组中采用左前降支结扎法制作 MI,假手术组仅进行相同的手术程序而不结扎缝线。最后,我们评估了心脏功能、心肌纤维化程度、血清炎症因子、自噬水平,并验证了信号通路。
获得了 68 种 QRHX 的活性成分,对应 223 种活性靶标,并收集了 2558 种 MI 相关疾病靶标。整合后,获得了 123 种 QRHX 抗 MI 靶标,并通过富集分析鉴定了 70 种信号通路,如 PI3K/Akt。实验表明,QRHX 可降低 MI 大鼠心肌纤维化程度,下调血清炎症因子,促进自噬。
QRHX 通过调节 PI3K/Akt 信号通路激活自噬,抑制炎症因子表达,在心肌中发挥保护作用。这些发现为进一步研究和验证 QRHX 作为 MI 潜在治疗药物提供了科学依据。