Key Laboratory of Pharmacology of Traditional Chinese Medical Formulae, Ministry of Education, Tianjin University of Traditional Chinese Medicine, Tianjin, 301617, China; State Key Laboratory of Component-based Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, 301617, China; School of Traditional Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, 301617, China.
Key Laboratory of Pharmacology of Traditional Chinese Medical Formulae, Ministry of Education, Tianjin University of Traditional Chinese Medicine, Tianjin, 301617, China; State Key Laboratory of Component-based Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, 301617, China.
J Ethnopharmacol. 2025 Jan 10;336:118730. doi: 10.1016/j.jep.2024.118730. Epub 2024 Aug 23.
Acute lung injury (ALI) can lead to respiratory failure and even death. KAT2A is a key target to suppress the development of inflammation. A herb, perilla frutescens, is an effective treatment for pulmonary inflammatory diseases with anti-inflammatory effects; however, its mechanism of action remains unclear.
The purpose of this study was to investigate the therapeutic effect and underlying mechanism of perilla frutescens leaf extracts (PLE), in the treatment of ALI by focusing on its ability to treat inflammation.
In vivo and in vitro models of ALI induced by LPS. Respiratory function, histopathological changes of lung, and BEAS-2B cells damage were assessed upon PLE. This effect is also tested under conditions of KAT2A over expression and KAT2A silencing.
PLE significantly attenuated LPS-induced histopathological changes in the lungs, improved respiratory function, and increased survival rate from LPS stimuation background in mice. PLE remarkably suppressed the phosphorylation of STAT3, AKT, ERK (1/2) and the release of cytokines (IL-6, TNF-α, and IL-1β) induced by LPS via inhibiting the expression of KAT2A.
PLE has a dose-dependent anti-inflammatory effect by inhibiting KAT2A expression to suppress LPS-induced ALI n mice. Our study expands the clinical indications of the traditional medicine PLE and provide a theoretical basis for clinical use of acute lung injury.
急性肺损伤(ALI)可导致呼吸衰竭甚至死亡。KAT2A 是抑制炎症发展的关键靶标。一种草药,紫苏,是一种有效的治疗肺部炎症性疾病的药物,具有抗炎作用;然而,其作用机制尚不清楚。
本研究旨在通过研究紫苏叶提取物(PLE)对炎症的治疗作用,探讨其治疗 ALI 的疗效及其作用机制。
采用 LPS 诱导的体内和体外 ALI 模型。评估 PLE 对 LPS 诱导的肺组织呼吸功能、组织病理学改变和 BEAS-2B 细胞损伤的影响。在 KAT2A 过表达和 KAT2A 沉默的条件下,也测试了这种作用。
PLE 显著减轻 LPS 诱导的小鼠肺组织的组织病理学变化,改善呼吸功能,提高 LPS 刺激背景下的存活率。PLE 通过抑制 KAT2A 的表达,显著抑制 LPS 诱导的 STAT3、AKT、ERK(1/2)磷酸化和细胞因子(IL-6、TNF-α和 IL-1β)的释放。
PLE 通过抑制 KAT2A 的表达,具有剂量依赖性的抗炎作用,从而抑制 LPS 诱导的 ALI 小鼠模型的炎症反应。本研究扩展了传统医学 PLE 的临床应用范围,为急性肺损伤的临床应用提供了理论依据。