Zhang Yu, Wang Shunshun, Wu Jiaqin, Du Qianqian, Yu Huiming, Yang Li, Liu Xianqiong, Xu Kang, Wang Chunli, Feng Fan
National Innovation and Attracting Talents "111" Base, Key Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Chongqing University, Chongqing, China.
Hubei Shizhen Laboratory, Wuhan, China.
Front Pharmacol. 2025 Jun 10;16:1547716. doi: 10.3389/fphar.2025.1547716. eCollection 2025.
Calcific aortic valve disease (CAVD) is the most common disease of the heart valves and is characterised by thickening, fibrosis and calcification of the aortic valve leaflets. Gastrodin, the active component of the traditional Chinese medicine , has antioxidant, anti-inflammatory, anti-apoptotic and antiviral activities and is widely used in the treatment of neurological and cardiovascular diseases. Here, we report that gastrodin attenuates calcification in CAVD, but the underlying mechanism is unclear. In the present study, we investigated the molecular targets and signaling mechanisms by which gastrodin inhibits CAVD calcification. experiments such as Alizarin Red staining and In-cell western were used to evaluated the anti-calcification effect of gastrodin in the treatment of aortic valves. Transcriptome sequencing and gas chromatography-mass spectrometry analyses showed that gastrodin inhibited the glycolysis level of valvular interstitial cells (VICs). Mechanistically, gastrodin reduces the glycolysis level and lactate production of VICs by inhibiting the enzymatic activity and protein expression of PKM2. Notably, gastrodin treatment inhibited the correlation between histone lactylation H3K9la, a novel lysine-modified modality using lactate as a substrate, and the CAVD marker BMP2. The beneficial effect of gastrodin in reducing aortic valve calcification was demonstrated in high-fat fed ApoE mice. In conclusion, our study shows that gastrodin exerts its anti-calcific effect by interfering with glycolysis and lactylation of VICs, demonstrating the potential of gastrodin as therapeutic agent for CAVD.
钙化性主动脉瓣疾病(CAVD)是最常见的心脏瓣膜疾病,其特征是主动脉瓣小叶增厚、纤维化和钙化。天麻素是中药的活性成分,具有抗氧化、抗炎、抗凋亡和抗病毒活性,广泛用于治疗神经和心血管疾病。在此,我们报告天麻素可减轻CAVD中的钙化,但潜在机制尚不清楚。在本研究中,我们研究了天麻素抑制CAVD钙化的分子靶点和信号传导机制。使用茜素红染色和细胞内western等实验来评估天麻素在治疗主动脉瓣中的抗钙化作用。转录组测序和气相色谱-质谱分析表明,天麻素抑制了瓣膜间质细胞(VICs)的糖酵解水平。从机制上讲,天麻素通过抑制PKM2的酶活性和蛋白表达来降低VICs的糖酵解水平和乳酸生成。值得注意的是,天麻素治疗抑制了组蛋白乳酸化H3K9la(一种以乳酸为底物的新型赖氨酸修饰方式)与CAVD标志物BMP2之间的相关性。在高脂喂养的ApoE小鼠中证实了天麻素在减少主动脉瓣钙化方面的有益作用。总之,我们的研究表明,天麻素通过干扰VICs的糖酵解和乳酸化发挥其抗钙化作用,证明了天麻素作为CAVD治疗药物的潜力。