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GSK3179106 通过靶向 P38 MAPK 改善脂多糖诱导的炎症和急性肺损伤。

GSK3179106 ameliorates lipopolysaccharide-induced inflammation and acute lung injury by targeting P38 MAPK.

机构信息

Department of Pediatric Allergy and Immunology, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.

Affiliated Yueqing Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China.

出版信息

Respir Res. 2024 Oct 28;25(1):388. doi: 10.1186/s12931-024-03012-9.

DOI:10.1186/s12931-024-03012-9
PMID:39468539
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11520791/
Abstract

Acute lung injury (ALI) is a serious acute respiratory disease that can cause alveolar-capillary barrier disruption and pulmonary edema, respiratory failure and multiple organ dysfunction syndrome. However, there is no effective drugs in clinic until now. GSK3179106 has been reported can alleviate intestinal stress syndrome, but the protective effect of GSK3179106 on ALI has not been elucidated. The present study will evaluate the pharmacological activity of GSK3179106 on lipopolysaccharide (LPS)-induced inflammation and lung injury and clarify its underlying mechanism. We found that GSK3179106 significantly attenuated LPS-induced lung injury in vivo, accompanied by inhibited infiltration of inflammatory cells and reduced expression of inflammatory cytokines. Meanwhile, GSK3179106 dose-dependently reduced the LPS-induced IL-6 expression both in protein and gene levels in macrophages. Mechanistically, GSK3179106 could inhibited the phosphorylation of P38 MAPK induced by LPS. Importantly, results showed that there is a direct combination between GSK3179106 and P38 MAPK. Together, our findings not only clarified the anti-inflammatory activity of GSK3179106 but also discovered its new clinical indications. Therefore, compound GSK3179106 may be a potential candidate for the treatment of acute inflammatory diseases.

摘要

急性肺损伤(ALI)是一种严重的急性呼吸疾病,可导致肺泡毛细血管屏障破坏和肺水肿、呼吸衰竭和多器官功能障碍综合征。然而,目前临床上还没有有效的药物。据报道,GSK3179106 可减轻肠道应激综合征,但 GSK3179106 对 ALI 的保护作用尚未阐明。本研究将评估 GSK3179106 对脂多糖(LPS)诱导的炎症和肺损伤的药理活性,并阐明其潜在机制。我们发现,GSK3179106 显著减轻了 LPS 诱导的体内肺损伤,同时抑制了炎症细胞的浸润和炎症细胞因子的表达。同时,GSK3179106 可剂量依赖性地降低 LPS 诱导的巨噬细胞中 IL-6 的表达(蛋白和基因水平)。机制上,GSK3179106 可抑制 LPS 诱导的 P38 MAPK 磷酸化。重要的是,结果表明 GSK3179106 与 P38 MAPK 之间存在直接结合。总之,我们的研究结果不仅阐明了 GSK3179106 的抗炎活性,还发现了其新的临床适应证。因此,化合物 GSK3179106 可能是治疗急性炎症性疾病的潜在候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5fc/11520791/ac42d9860b6a/12931_2024_3012_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5fc/11520791/7f19231d2846/12931_2024_3012_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5fc/11520791/61712f8df8c0/12931_2024_3012_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5fc/11520791/a4afccdab9d7/12931_2024_3012_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5fc/11520791/96b8a00f6475/12931_2024_3012_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5fc/11520791/ac42d9860b6a/12931_2024_3012_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5fc/11520791/7f19231d2846/12931_2024_3012_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5fc/11520791/61712f8df8c0/12931_2024_3012_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5fc/11520791/a4afccdab9d7/12931_2024_3012_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5fc/11520791/96b8a00f6475/12931_2024_3012_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5fc/11520791/ac42d9860b6a/12931_2024_3012_Fig5_HTML.jpg

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本文引用的文献

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