Department of Cardiology, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, Hangzhou 310006, China.
Translational Medicine Research Center, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, Hangzhou 310006, China.
Medicina (Kaunas). 2023 Sep 28;59(10):1740. doi: 10.3390/medicina59101740.
: With the growing incidence and disability associated with myocardial infarction (MI), there is an increasing focus on cardiac rehabilitation post-MI. Kuanxiongzhuyu decoction (KXZY), a traditional Chinese herbal formula, has been used in the rehabilitation of patients after MI. However, the chemical composition, protective effects, and underlying mechanism of KXZY remain unclear. : In this study, the compounds in KXZY were identified using a high-performance liquid chromatography-mass spectrometry (HPLC-MS) analytical method. Based on the compounds identified in the KXZY, we predictively selected the potential targets of MI and then constructed a protein-protein interaction (PPI) network to identify the key targets. Furthermore, the DAVID database was used for the GO and KEGG analyses, and molecular docking was used to verify the key targets. Finally, the cardioprotective effects and mechanism of KXZY were investigated in post-MI mice. : A total of 193 chemical compounds of KXZY were identified by HPLC-MS. In total, 228 potential targets were obtained by the prediction analysis. The functional enrichment studies and PPI network showed that the targets were largely associated with AKT-pathway-related apoptosis. The molecular docking verified that isoguanosine and adenosine exhibited excellent binding to the AKT. In vivo, KXZY significantly alleviated cardiac dysfunction and suppressed AKT phosphorylation. Furthermore, KXZY significantly increased the expression of the antiapoptotic proteins Bcl-2 and Bcl-xl and decreased the expression of the proapoptotic protein BAD. : In conclusion, the network pharmacological and experimental evidence suggests that KXZY manifests anti-cardiac dysfunction behavior by alleviating cardiomyocyte apoptosis via the AKT pathway in MI and, thus, holds promising therapeutic potential.
随着心肌梗死(MI)发病率和相关残疾的增加,对 MI 后心脏康复的关注度日益增加。宽胸逐瘀汤(KXZY)是一种传统的中药配方,已用于 MI 后患者的康复。然而,KXZY 的化学成分、保护作用和潜在机制尚不清楚。
在这项研究中,使用高效液相色谱-质谱(HPLC-MS)分析方法鉴定 KXZY 中的化合物。基于 KXZY 中鉴定的化合物,我们预测性地选择了 MI 的潜在靶点,然后构建了蛋白质-蛋白质相互作用(PPI)网络来识别关键靶点。此外,使用 DAVID 数据库进行 GO 和 KEGG 分析,并进行分子对接验证关键靶点。最后,在 MI 后小鼠中研究了 KXZY 的心脏保护作用和机制。
通过 HPLC-MS 鉴定了 KXZY 的 193 种化学成分。通过预测分析共获得 228 个潜在靶点。功能富集研究和 PPI 网络表明,这些靶点主要与 AKT 通路相关的细胞凋亡有关。分子对接验证了异鸟苷和腺苷与 AKT 具有良好的结合能力。在体内,KXZY 显著缓解了心脏功能障碍并抑制了 AKT 磷酸化。此外,KXZY 显著增加了抗凋亡蛋白 Bcl-2 和 Bcl-xl 的表达,并降低了促凋亡蛋白 BAD 的表达。
总之,网络药理学和实验证据表明,KXZY 通过 AKT 通路减轻 MI 中心肌细胞凋亡来表现出抗心脏功能障碍行为,因此具有有前途的治疗潜力。