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哮喘马匹中性粒细胞中与肥胖相关的代谢组学和功能重编程

Obesity-Associated Metabolomic and Functional Reprogramming in Neutrophils from Horses with Asthma.

作者信息

Albornoz Alejandro, Morales Beatriz, Fernandez Valentina Bernal, Henriquez Claudio, Quiroga John, Alarcón Pablo, Moran Gabriel, Burgos Rafael A

机构信息

Institute of Pharmacology and Morphophysiology, Faculty of Veterinary Sciences, Universidad Austral de Chile, Valdivia 5090000, Chile.

Graduate School, Faculty of Veterinary Sciences, Universidad Austral de Chile, Valdivia 5090000, Chile.

出版信息

Animals (Basel). 2025 Jul 7;15(13):1992. doi: 10.3390/ani15131992.

DOI:10.3390/ani15131992
PMID:40646891
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12248518/
Abstract

Equine asthma is a chronic respiratory disease characterised by neutrophilic inflammation, airway hyperresponsiveness, and impaired pulmonary function. Obesity, increasingly prevalent among domestic horses, has been identified as a potential risk factor for exacerbating inflammatory conditions. This study aimed to explore whether obesity modifies neutrophil metabolism and inflammatory responses in horses affected by asthma. Six asthmatic horses in clinical remission were categorised into two groups: obese and non-obese, based on body condition score. Serum levels of interleukin-1β (IL-1β) and peripheral blood neutrophil counts were significantly higher in obese horses, indicating a heightened systemic inflammatory state. Neutrophils from obese horses displayed a stronger oxidative burst following zymosan stimulation and elevated IL-1β gene expression in response to lipopolysaccharide, suggesting a hyperinflammatory phenotype. Metabolomic profiling of neutrophils identified 139 metabolites, with notable differences in fatty acids, branched-chain amino acids, and tricarboxylic acid (TCA) cycle intermediates. Pathway enrichment analysis revealed significant alterations in fatty acid biosynthesis, amino acid metabolism, and glutathione-related pathways. Elevated levels of itaconate, citraconic acid, and citrate in obese horses indicate profound metabolic reprogramming within neutrophils. These results suggest that obesity promotes a distinct neutrophil phenotype marked by increased metabolic activity and heightened responsiveness to inflammatory stimuli. This altered profile may contribute to the persistence or worsening of airway inflammation in asthmatic horses. The findings underscore the importance of addressing obesity in the clinical management of equine asthma and open avenues for further research into metabolic-targeted therapies in veterinary medicine.

摘要

马哮喘是一种慢性呼吸道疾病,其特征为中性粒细胞炎症、气道高反应性和肺功能受损。肥胖在家庭饲养马匹中越来越普遍,已被确定为加剧炎症状况的潜在风险因素。本研究旨在探讨肥胖是否会改变受哮喘影响马匹的中性粒细胞代谢和炎症反应。根据身体状况评分,将6匹处于临床缓解期的哮喘马分为两组:肥胖组和非肥胖组。肥胖马的血清白细胞介素-1β(IL-1β)水平和外周血中性粒细胞计数显著更高,表明全身炎症状态加剧。肥胖马的中性粒细胞在经酵母聚糖刺激后表现出更强的氧化爆发,并且在对脂多糖的反应中IL-1β基因表达升高,提示存在高炎症表型。对中性粒细胞进行代谢组分析鉴定出139种代谢物,脂肪酸、支链氨基酸和三羧酸(TCA)循环中间体存在显著差异。通路富集分析显示脂肪酸生物合成、氨基酸代谢和谷胱甘肽相关通路有显著改变。肥胖马中衣康酸、柠康酸和柠檬酸水平升高表明中性粒细胞内存在深刻的代谢重编程。这些结果表明,肥胖促进了一种独特的中性粒细胞表型,其特征是代谢活性增加和对炎症刺激的反应性增强。这种改变的特征可能导致哮喘马气道炎症的持续或恶化。这些发现强调了在马哮喘临床管理中解决肥胖问题的重要性,并为兽医学中针对代谢的疗法的进一步研究开辟了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b4d/12248518/be11ef10c9a3/animals-15-01992-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b4d/12248518/9a5fc1815840/animals-15-01992-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b4d/12248518/365b023f13b6/animals-15-01992-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b4d/12248518/e1cc450a0714/animals-15-01992-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b4d/12248518/837e2438cdca/animals-15-01992-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b4d/12248518/c748c0d48417/animals-15-01992-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b4d/12248518/be11ef10c9a3/animals-15-01992-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b4d/12248518/9a5fc1815840/animals-15-01992-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b4d/12248518/365b023f13b6/animals-15-01992-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b4d/12248518/e1cc450a0714/animals-15-01992-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b4d/12248518/837e2438cdca/animals-15-01992-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b4d/12248518/c748c0d48417/animals-15-01992-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b4d/12248518/be11ef10c9a3/animals-15-01992-g006.jpg

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本文引用的文献

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High fat diet feeding impairs neutrophil phagocytosis, bacterial killing, and neutrophil-induced hematopoietic regeneration.高脂饮食会损害中性粒细胞的吞噬作用、细菌杀伤能力以及中性粒细胞诱导的造血再生。
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Suppressing neutrophil itaconate production attenuates Mycoplasma pneumoniae pneumonia.
抑制中性粒细胞衣康酸的产生可减轻肺炎支原体肺炎。
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