Liu Yundou, Wang Chunyi, Li Mengru, Zhu Yi, Liu Ke, Liu Yufei, Luo Maocai, Zhang Chuantao
Department of Respiratory Medicine, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Front Pharmacol. 2024 Dec 20;15:1507194. doi: 10.3389/fphar.2024.1507194. eCollection 2024.
Pulmonary diseases are a major category of diseases that pose a threat to human health. The most common drugs currently used to treat lung diseases are still chemical drugs, but this may lead to drug resistance and damage to healthy organs in the body. Therefore, developing new drugs is an urgent task. Lipid peroxidation is caused by the disruption of redox homeostasis, accumulation of reactive oxygen species (ROS), depletion of glutathione (GSH), and inactivation of glutathione peroxidase 4 (GPX4). Lipid peroxidation is closely related to the occurrence and progression of respiratory diseases, including acute lung injury, asthma, pulmonary fibrosis, pulmonary hypertension, chronic obstructive pulmonary disease, and lung cancer. Natural ingredients have high safety, high availability, and low cost, and can regulate lipid peroxidation through multiple pathways and targets, making them valuable new drugs. This article aims to summarize the pharmacology and mechanism of natural ingredients targeting lipid peroxidation in the treatment of lung diseases. The reviewed data indicate that natural ingredients are a promising anti-lipid peroxidation drug, mainly alleviating lipid peroxidation through the cystine/glutamate antiporter (System X )/GSH/GPX4 axis, Nrf2 pathway, and ROS pathway. In the future, it will still be necessary to further study the mechanisms of natural products in treating pulmonary diseases through lipid peroxidation and conduct multi-center, large-sample clinical trials to promote the development of new drugs.
肺部疾病是对人类健康构成威胁的一大类疾病。目前用于治疗肺部疾病的最常用药物仍然是化学药物,但这可能会导致耐药性并损害体内的健康器官。因此,开发新药是一项紧迫的任务。脂质过氧化是由氧化还原稳态破坏、活性氧(ROS)积累、谷胱甘肽(GSH)耗竭以及谷胱甘肽过氧化物酶4(GPX4)失活引起的。脂质过氧化与呼吸系统疾病的发生和发展密切相关,包括急性肺损伤、哮喘、肺纤维化、肺动脉高压、慢性阻塞性肺疾病和肺癌。天然成分具有高安全性、高可用性和低成本的特点,并且可以通过多种途径和靶点调节脂质过氧化,使其成为有价值的新药。本文旨在总结天然成分靶向脂质过氧化治疗肺部疾病的药理学和作用机制。综述数据表明,天然成分是一种有前景的抗脂质过氧化药物,主要通过胱氨酸/谷氨酸反向转运体(系统Xc-)/GSH/GPX4轴、Nrf2途径和ROS途径减轻脂质过氧化。未来,仍有必要进一步研究天然产物通过脂质过氧化治疗肺部疾病的机制,并开展多中心、大样本的临床试验,以促进新药的开发。