Gao Yijie, Qin Gaofeng, Liang Shichao, Yin Jiajie, Wang Baofu, Jiang Hong, Liu Mengru, Luo Fangyuan, Li Xianlun
National Integrated Traditional and Western Medicine Center for Cardiovascular Disease, China-Japan Friendship Hospital, Beijing, People's Republic of China.
Department of Traditional Chinese Medicine, Binzhou Medical University Hospital, Shandong, People's Republic of China.
Drug Des Devel Ther. 2025 Feb 3;19:771-791. doi: 10.2147/DDDT.S504884. eCollection 2025.
Acute myocardial infarction (AMI) is a significant contributor to global morbidity and mortality. Allicin exhibits promising therapeutic potential in AMI as a primary bioactive component derived from garlic; however, its underlying mechanisms remain incompletely elucidated.
Our study induced AMI in mice by ligating the left coronary artery, and administered allicin orally for 28 days. The cardioprotective effects of allicin treatment were comprehensively assessed using echocardiography, histopathological examinations, intestinal barrier function, and serum inflammatory factors. The potential mechanisms of allicin were elucidated through analysis of metagenomics and serum metabolomics. Network pharmacology (NP) was used to further investigate and validate the possible molecular mechanisms of allicin.
Our findings revealed allicin's capacity to ameliorate cardiac impairments, improve intestinal barrier integrity, and reduce serum IL-18 and IL-1β levels after AMI. Further analysis demonstrated that the administration of allicin has the potential to ameliorate intestinal flora disorder following AMI by modulating the abundance of beneficial bacteria, such as _, and _, while reducing the abundance of harmful bacteria . Additionally, it exhibits the ability to enhance myocardial energy metabolism flexibility through modulating metabolites and key enzymes associated with the fatty acid metabolic pathway. Mechanistically, NP and in vivo experiments indicated that allicin might suppress pyroptosis and reduce inflammatory response via blocked activation of the NF-κB-mediated NLRP3/Caspase-1/GSDMD pathway. Moreover, Spearman correlation analysis suggested a significant association between the allicin-induced alterations in microbiota and metabolites with cardiac function and inflammatory cytokines.
Our study demonstrated that allicin alleviated myocardial injury and reduced inflammatory response by inhibiting the NF-κB-mediated NLRP3/Caspase-1/GSDMD pathway while remodeling microbiota disturbance, improving serum metabolic disorder, and enhancing the intestinal barrier. These research findings offer a novel perspective on the potential therapeutic value of allicin as an adjunctive dietary supplement to conventional treatments for AMI.
急性心肌梗死(AMI)是全球发病率和死亡率的重要原因。大蒜素作为大蒜中的一种主要生物活性成分,在急性心肌梗死中显示出有前景的治疗潜力;然而,其潜在机制仍未完全阐明。
我们的研究通过结扎左冠状动脉在小鼠中诱导急性心肌梗死,并口服大蒜素28天。使用超声心动图、组织病理学检查、肠道屏障功能和血清炎症因子全面评估大蒜素治疗的心脏保护作用。通过宏基因组学和血清代谢组学分析阐明大蒜素的潜在机制。使用网络药理学(NP)进一步研究和验证大蒜素可能的分子机制。
我们的研究结果显示,大蒜素能够改善急性心肌梗死后的心脏损伤、改善肠道屏障完整性并降低血清白细胞介素-18和白细胞介素-1β水平。进一步分析表明,给予大蒜素有可能通过调节有益细菌(如_和_)的丰度,同时降低有害细菌的丰度,来改善急性心肌梗死后的肠道菌群紊乱。此外,它还具有通过调节与脂肪酸代谢途径相关的代谢物和关键酶来增强心肌能量代谢灵活性的能力。从机制上讲,NP和体内实验表明,大蒜素可能通过阻断NF-κB介导的NLRP3/半胱天冬酶-1/ Gasdermin D途径的激活来抑制细胞焦亡并减少炎症反应。此外,Spearman相关性分析表明,大蒜素诱导的微生物群和代谢物变化与心脏功能和炎症细胞因子之间存在显著关联。
我们的研究表明,大蒜素通过抑制NF-κB介导的NLRP3/半胱天冬酶- caspase-1/Gasdermin D途径,同时重塑微生物群紊乱、改善血清代谢紊乱和增强肠道屏障,减轻心肌损伤并减少炎症反应。这些研究结果为大蒜素作为急性心肌梗死传统治疗辅助膳食补充剂的潜在治疗价值提供了新的视角。