René Rachou Institute, Oswaldo Cruz Foundation, Belo Horizonte, MG, Brazil.
Department of Physiology and Biophysics, National Institute of Science and Technology in Nanobiopharmaceutics, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
Inflamm Res. 2024 Jun;73(6):1019-1031. doi: 10.1007/s00011-024-01880-x. Epub 2024 Apr 24.
Angiotensin-(1-7) [Ang-(1-7)] is a pro-resolving mediator. It is not known whether the pro-resolving effects of Ang-(1-7) are sustained and protect the lung from a subsequent inflammatory challenge. This study sought to investigate the impact of treatment in face of a second allergic or lipopolysaccharide (LPS) challenge.
Mice, sensitized and challenged with ovalbumin (OVA), received a single Ang-(1-7) dose at the peak of eosinophilic inflammation, 24 h after the final OVA challenge. Subsequently, mice were euthanized at 48, 72, 96, and 120 h following the OVA challenge, and cellular infiltrate, inflammatory mediators, lung histopathology, and macrophage-mediated efferocytic activity were evaluated. The secondary inflammatory stimulus (OVA or LPS) was administered 120 h after the last OVA challenge, and subsequent inflammatory analyses were performed.
Treatment with Ang-(1-7) resulted in elevated levels of IL-10, CD4Foxp3, Mres in the lungs and enhanced macrophage-mediated efferocytic capacity. Moreover, in allergic mice treated with Ang-(1-7) and then subjected to a secondary OVA challenge, inflammation was also reduced. Similarly, in mice exposed to LPS, Ang-(1-7) effectively prevented the lung inflammation.
A single dose of Ang-(1-7) resolves lung inflammation and protect the lung from a subsequent inflammatory challenge highlighting its potential therapeutic for individuals with asthma.
血管紧张素-(1-7)[Ang-(1-7)]是一种促解决介质。目前尚不清楚 Ang-(1-7) 的促解决作用是否持续存在,并能保护肺部免受随后的炎症挑战。本研究旨在探讨在第二次过敏或脂多糖(LPS)挑战时治疗的影响。
用卵清蛋白(OVA)致敏和攻击的小鼠,在嗜酸性粒细胞炎症高峰期后 24 小时给予单次 Ang-(1-7)剂量。随后,在 OVA 攻击后 48、72、96 和 120 小时处死小鼠,并评估细胞浸润、炎症介质、肺组织病理学和巨噬细胞介导的吞噬作用。在最后一次 OVA 攻击后 120 小时给予二次炎症刺激(OVA 或 LPS),并进行后续炎症分析。
用 Ang-(1-7)治疗可导致肺中 IL-10、CD4Foxp3 和 Mres 水平升高,并增强巨噬细胞介导的吞噬能力。此外,在接受 Ang-(1-7)治疗然后接受二次 OVA 攻击的过敏小鼠中,炎症也减少了。同样,在 LPS 暴露的小鼠中,Ang-(1-7)也能有效预防肺部炎症。
单次给予 Ang-(1-7)可解决肺部炎症,并保护肺部免受随后的炎症挑战,这突出了其在哮喘患者中的潜在治疗作用。