南美超级胎牛血清999尝鲜特惠
转染试剂低至5折
基质胶阶梯特惠
积分商城,好礼送不停
南美超级胎牛血清999尝鲜特惠
转染试剂低至5折
基质胶阶梯特惠
积分商城,好礼送不停
分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

宽雄气雾剂通过HIF-1α-ITGAX轴路径促进血管生成,从而有效预防冠状动脉微血管功能障碍。

Kuanxiong aerosol protects against coronary microvascular dysfunction through improving angiogenesis via HIF-1α-ITGAX axis

Yuanqing Jiang, Kai Qian, Beibo Li, Mengmeng Xu, Pengfei OuYang, Yangyang Zhu, Jiaxu Wu, Xiaoying Shi, Yi Luo, Yao Xie, Meixiang Xiang

Journal:Frontiers in Pharmacology

IF:5.4

DOI:10.3389/fphar.2026.1881934

PMID:42661733

Published:2026-08-13

research field:神经药理学分子神经科学精神病学天然产物研究神经炎症

Abstract

Background Coronary microvascular dysfunction (CMVD) frequently complicates diabetes mellitus and serves as a major driver of cardiovascular morbidity, underscoring the urgent need for innovative therapeutic strategies. Kuanxiong aerosol (KX), a patented botanical formulation of four volatile oils widely used for angina, possesses established vasoprotective and hemodynamic benefits. However, its efficacy and mechanisms in CMVD remain uncharacterized. Methods To evaluate the therapeutic potential of KX, both preventive and therapeutic treatment regimens were administered to a db/db mouse model of diabetic CMVD. In vivo therapeutic effects were comprehensively assessed using echocardiography and histopathological analyses. Microvascular perfusion and endothelial barrier function were quantitatively evaluated via Lectin-FITC perfusion and permeability assays.These findings were further corroborated by bulk RNA sequencing, immunofluorescence, and cellular functional assays, while bioinformatics and biochemical analyses systematically revealed the molecular targets and pathways. Results KX restored coronary microvascular structure and function, promoting neovascularization and conferring both preventive and therapeutic benefits against CMVD in db/db mice. Mechanistically, RNA sequencing and biochemical analyses revealed that KX stabilizes HIF-1α against PHD2-mediated proteasomal degradation. This stabilization enhances HIF-1α transcriptional activity to upregulate ITGAX, which subsequently triggers the VEGF-FAK signaling pathway to drive endothelial proliferation, angiogenesis and tight junction formation. Consequently, the improved microvascular function and stabilized nascent vascular network restore myocardial blood supply, thereby rescuing CMVD. Conclusion KX exerts its therapeutic effects through modulation of the HIF-1α–ITGAX axis, thereby promoting angiogenesis and restoring microvascular integrity and perfusion. These findings establish KX as a promising the

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