Zheng Runxiu, Tan Junlan, Cao Xianya, Wang Shizhong, Dai Qing, Song Lan, Dai Aiguo
School of Integrated Chinses and Western Medicine, Hunan University of Chinese Medicine, Changsha, 410208, Hunan, China.
Hunan Provincial Key Laboratory of Vascular Biology and Translational Medicine, Changsha, 410208, Hunan, China.
J Mol Med (Berl). 2025 Sep 3. doi: 10.1007/s00109-025-02589-y.
Pulmonary hypertension (PH) is a life-threatening cardiovascular condition marked by the remodeling of pulmonary vasculature. Existing treatments provide limited efficacy, emphasizing the urgent need for deeper scientific exploration. This review investigates how vascular cell dysfunction and metabolic reprogramming contribute to PH pathology, with a focus on the interplay between epigenetic modifications and cellular metabolism. Epigenetic abnormalities are shown to influence the expression of key metabolic enzymes, shedding light on their potential as drivers of metabolic dysregulation in PH. By elucidating alterations in glucose, lipid, and amino acid metabolism in vascular cells, this study highlights epigenetic modifications as promising targets for therapeutic intervention. Additionally, it examines the feasibility of correcting these reversible epigenetic changes to mitigate disease progression. This review concludes with an assessment of the challenges and opportunities in leveraging epigenetic and metabolic insights to develop novel PH treatments.
肺动脉高压(PH)是一种危及生命的心血管疾病,其特征是肺血管重塑。现有治疗方法的疗效有限,这凸显了深入进行科学探索的迫切需求。本综述研究了血管细胞功能障碍和代谢重编程如何导致PH病理,重点关注表观遗传修饰与细胞代谢之间的相互作用。研究表明,表观遗传异常会影响关键代谢酶的表达,揭示了它们作为PH代谢失调驱动因素的潜力。通过阐明血管细胞中葡萄糖、脂质和氨基酸代谢的变化,本研究强调表观遗传修饰是有前景的治疗干预靶点。此外,还探讨了纠正这些可逆表观遗传变化以减轻疾病进展的可行性。本综述最后评估了利用表观遗传和代谢见解开发新型PH治疗方法所面临的挑战和机遇。