阿魏酸通过调节白细胞介素-17信号传导和组织重塑来减轻小鼠模型中白细胞介素- 17a诱导的肺部炎症

IF 3.7 Q1 CHEMISTRY, MEDICINAL
Anju K, , , Avtar Singh Gautam, , and , Rakesh Kumar Singh*, 
{"title":"阿魏酸通过调节白细胞介素-17信号传导和组织重塑来减轻小鼠模型中白细胞介素- 17a诱导的肺部炎症","authors":"Anju K,&nbsp;, ,&nbsp;Avtar Singh Gautam,&nbsp;, and ,&nbsp;Rakesh Kumar Singh*,&nbsp;","doi":"10.1021/acsptsci.5c00490","DOIUrl":null,"url":null,"abstract":"<p >Lung inflammation is a hallmark of several respiratory diseases and is frequently driven by proinflammatory cytokines such as interleukin-17A (IL-17A). IL-17A plays a critical role in amplifying inflammatory cascades, contributing to airway remodeling and tissue damage. This study investigated the therapeutic potential of ferulic acid (FA), a natural polyphenol with known antioxidant and anti-inflammatory properties, in mitigating recombinant IL-17A (rmIL-17A)-induced lung inflammation in BALB/c mice. Mice were intranasally exposed to rmIL-17A for seven consecutive days, while FA was administered orally from day 4 to day 7. FA treatment significantly downregulated IL-17A-mediated signaling pathways and restored the redox balance disrupted by rmIL-17A exposure. Additionally, FA markedly reduced proinflammatory cytokine levels, inflammatory cell infiltration, mast cell activity, mucus hypersecretion, and fibrosis in the lung tissue. Importantly, FA also decreased the expression of CD38 and restored CD206 expression, indicating a phenotypic shift toward anti-inflammatory macrophage polarization. Interestingly, FA also restored the expression level of occludin in the lungs of mice exposed to rmIL-17A. Overall, these findings demonstrate that FA effectively attenuates IL-17A-induced lung inflammation by modulating oxidative stress, cytokine production, and inflammatory cell responses. These outcomes show the potential of FA as a promising therapeutic option for regulating IL-17A-driven pulmonary inflammatory conditions.</p>","PeriodicalId":36426,"journal":{"name":"ACS Pharmacology and Translational Science","volume":"8 10","pages":"3641–3653"},"PeriodicalIF":3.7000,"publicationDate":"2025-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ferulic Acid Attenuated Interleukin-17A-Induced Lung Inflammation by Modulating Interleukin-17 Signaling and Tissue Remodeling in a Mouse Model\",\"authors\":\"Anju K,&nbsp;, ,&nbsp;Avtar Singh Gautam,&nbsp;, and ,&nbsp;Rakesh Kumar Singh*,&nbsp;\",\"doi\":\"10.1021/acsptsci.5c00490\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Lung inflammation is a hallmark of several respiratory diseases and is frequently driven by proinflammatory cytokines such as interleukin-17A (IL-17A). IL-17A plays a critical role in amplifying inflammatory cascades, contributing to airway remodeling and tissue damage. This study investigated the therapeutic potential of ferulic acid (FA), a natural polyphenol with known antioxidant and anti-inflammatory properties, in mitigating recombinant IL-17A (rmIL-17A)-induced lung inflammation in BALB/c mice. Mice were intranasally exposed to rmIL-17A for seven consecutive days, while FA was administered orally from day 4 to day 7. FA treatment significantly downregulated IL-17A-mediated signaling pathways and restored the redox balance disrupted by rmIL-17A exposure. Additionally, FA markedly reduced proinflammatory cytokine levels, inflammatory cell infiltration, mast cell activity, mucus hypersecretion, and fibrosis in the lung tissue. Importantly, FA also decreased the expression of CD38 and restored CD206 expression, indicating a phenotypic shift toward anti-inflammatory macrophage polarization. Interestingly, FA also restored the expression level of occludin in the lungs of mice exposed to rmIL-17A. Overall, these findings demonstrate that FA effectively attenuates IL-17A-induced lung inflammation by modulating oxidative stress, cytokine production, and inflammatory cell responses. These outcomes show the potential of FA as a promising therapeutic option for regulating IL-17A-driven pulmonary inflammatory conditions.</p>\",\"PeriodicalId\":36426,\"journal\":{\"name\":\"ACS Pharmacology and Translational Science\",\"volume\":\"8 10\",\"pages\":\"3641–3653\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-09-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Pharmacology and Translational Science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acsptsci.5c00490\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Pharmacology and Translational Science","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsptsci.5c00490","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

摘要

肺部炎症是几种呼吸系统疾病的标志,通常由促炎细胞因子如白细胞介素- 17a (IL-17A)驱动。IL-17A在放大炎症级联反应中起关键作用,促进气道重塑和组织损伤。本研究探讨了阿魏酸(FA)的治疗潜力,阿魏酸是一种已知具有抗氧化和抗炎特性的天然多酚,可减轻重组IL-17A (rmIL-17A)诱导的BALB/c小鼠肺部炎症。小鼠连续7天鼻内暴露于rmIL-17A,而FA从第4天到第7天口服。FA处理显著下调il - 17a介导的信号通路,恢复因暴露于rmIL-17A而中断的氧化还原平衡。此外,FA显著降低促炎细胞因子水平、炎症细胞浸润、肥大细胞活性、粘液分泌过多和肺组织纤维化。重要的是,FA还降低了CD38的表达,恢复了CD206的表达,表明表型向抗炎巨噬细胞极化转变。有趣的是,FA还恢复了暴露于rmIL-17A的小鼠肺部occludin的表达水平。总的来说,这些发现表明,FA通过调节氧化应激、细胞因子产生和炎症细胞反应,有效地减弱了il - 17a诱导的肺部炎症。这些结果表明,FA作为一种有希望的治疗选择,可以调节il - 17a驱动的肺部炎症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ferulic Acid Attenuated Interleukin-17A-Induced Lung Inflammation by Modulating Interleukin-17 Signaling and Tissue Remodeling in a Mouse Model

Ferulic Acid Attenuated Interleukin-17A-Induced Lung Inflammation by Modulating Interleukin-17 Signaling and Tissue Remodeling in a Mouse Model

Lung inflammation is a hallmark of several respiratory diseases and is frequently driven by proinflammatory cytokines such as interleukin-17A (IL-17A). IL-17A plays a critical role in amplifying inflammatory cascades, contributing to airway remodeling and tissue damage. This study investigated the therapeutic potential of ferulic acid (FA), a natural polyphenol with known antioxidant and anti-inflammatory properties, in mitigating recombinant IL-17A (rmIL-17A)-induced lung inflammation in BALB/c mice. Mice were intranasally exposed to rmIL-17A for seven consecutive days, while FA was administered orally from day 4 to day 7. FA treatment significantly downregulated IL-17A-mediated signaling pathways and restored the redox balance disrupted by rmIL-17A exposure. Additionally, FA markedly reduced proinflammatory cytokine levels, inflammatory cell infiltration, mast cell activity, mucus hypersecretion, and fibrosis in the lung tissue. Importantly, FA also decreased the expression of CD38 and restored CD206 expression, indicating a phenotypic shift toward anti-inflammatory macrophage polarization. Interestingly, FA also restored the expression level of occludin in the lungs of mice exposed to rmIL-17A. Overall, these findings demonstrate that FA effectively attenuates IL-17A-induced lung inflammation by modulating oxidative stress, cytokine production, and inflammatory cell responses. These outcomes show the potential of FA as a promising therapeutic option for regulating IL-17A-driven pulmonary inflammatory conditions.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
ACS Pharmacology and Translational Science
ACS Pharmacology and Translational Science Medicine-Pharmacology (medical)
CiteScore
10.00
自引率
3.30%
发文量
133
期刊介绍: ACS Pharmacology & Translational Science publishes high quality, innovative, and impactful research across the broad spectrum of biological sciences, covering basic and molecular sciences through to translational preclinical studies. Clinical studies that address novel mechanisms of action, and methodological papers that provide innovation, and advance translation, will also be considered. We give priority to studies that fully integrate basic pharmacological and/or biochemical findings into physiological processes that have translational potential in a broad range of biomedical disciplines. Therefore, studies that employ a complementary blend of in vitro and in vivo systems are of particular interest to the journal. Nonetheless, all innovative and impactful research that has an articulated translational relevance will be considered. ACS Pharmacology & Translational Science does not publish research on biological extracts that have unknown concentration or unknown chemical composition. Authors are encouraged to use the pre-submission inquiry mechanism to ensure relevance and appropriateness of research.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信