Tian Yuan, Sun JingMeng, Jiao DongMei, Zhang WeiYu
School of Pharmacy, Changchun University of Traditional Chinese Medicine, Changchun, China.
Department of Pharmacy, First Hospital of Jilin University, Changchun, China.
Front Immunol. 2024 Dec 10;15:1488570. doi: 10.3389/fimmu.2024.1488570. eCollection 2024.
Asthma, is a common, significant and diverse condition marked by persistent airway inflammation, with a major impact on human health worldwide. The predisposing factors for asthma are complex and widespread. The beneficial effects of omega-3 (n-3) polyunsaturated fatty acids (PUFAs) in asthma have increasingly attracted attention recently. In asthma therapy, n-3 PUFAs may reduce asthma risk by controlling on levels of inflammatory cytokines and regulating recruitment of inflammatory cells in asthma. The specialized pro-resolving mediators (SPMs) derived from n-3 PUFAs, including the E- and D-series resolvins, protectins, and maresins, were discovered in inflammatory exudates and their biosynthesis by lipoxygenase mediated pathways elucidated., SPMs alleviated T-helper (Th)1/Th17 and type 2 cytokine immune imbalance, and regulated macrophage polarization and recruitment of inflammatory cells in asthma via specific receptors such as formyl peptide receptor 2 (ALX/FPR2) and G protein-coupled receptor 32. In conclusion, the further study of n-3 PUFAs and their derived SPMs may lead to novel anti-inflammatory asthma treatments.
哮喘是一种常见、严重且多样的病症,其特征为持续性气道炎症,对全球人类健康有重大影响。哮喘的诱发因素复杂且广泛。近年来,ω-3(n-3)多不饱和脂肪酸(PUFAs)在哮喘中的有益作用越来越受到关注。在哮喘治疗中,n-3 PUFAs可通过控制炎症细胞因子水平和调节哮喘中炎症细胞的募集来降低哮喘风险。从n-3 PUFAs衍生而来的特异性促消退介质(SPMs),包括E-和D-系列消退素、保护素和maresin,在炎症渗出物中被发现,并且其通过脂氧合酶介导的途径进行生物合成也已阐明。SPMs减轻了辅助性T(Th)1/Th17和2型细胞因子免疫失衡,并通过甲酰肽受体2(ALX/FPR2)和G蛋白偶联受体32等特定受体调节哮喘中巨噬细胞极化和炎症细胞的募集。总之,对n-3 PUFAs及其衍生的SPMs的进一步研究可能会带来新的抗炎性哮喘治疗方法。