Suppr超能文献

瓦尔甲醇提取物通过抑制Src磷酸化改善急性肺损伤和胃炎。

Vahl Methanol Extract Ameliorates Acute Lung Injury and Gastritis by Suppressing Src Phosphorylation.

作者信息

Lee Dahae, Kim Ji Won, Lee Chae Young, Oh Jieun, Hwang So Hyun, Jo Minkyeong, Kim Seung A, Choi Wooram, Noh Jin Kyoung, Yi Dong-Keun, Song Minkyung, Kim Han Gyung, Cho Jae Youl

机构信息

Department of Integrative Biotechnology, Sungkyunkwan University, Suwon 16419, Republic of Korea.

Instituto de BioEconomia, Quito 170135, Ecuador.

出版信息

Plants (Basel). 2022 Dec 16;11(24):3560. doi: 10.3390/plants11243560.

Abstract

Many species in the genus are known to exert anti-inflammatory effects and are used as traditional medicinal plants to treat various inflammatory symptoms. However, no studies on the inflammatory activities of Vahl have been reported. The aim of the study was to investigate in vitro and in vivo the anti-inflammatory effects of a methanol extract of Vahl (Gc-ME). To determine the anti-inflammatory activity of Gc-ME, lipopolysaccharide (LPS)-, poly(I:C)-, or Pam3CSK4-treated RAW264.7 cells, HCl/EtOH- and LPS-treated mice were employed for in vitro and in vivo tests. LPS-induced nitric oxide production in RAW264.7 cells was determined by Griess assays and cytokine gene expression in LPS-activated RAW264.7 cells, confirmed by RT- and real-time PCR. Transcriptional activation was evaluated by luciferase reporter gene assay. Target protein validation was assessed by Western blot analysis and cellular thermal shift assays (CETSA) with LPS-treated RAW264.7 and gene-transfected HEK293 cells. Using both a HCl/EtOH-induced gastritis model and an LPS-induced lung injury model, inflammatory states were checked by scoring or evaluating gastric lesions, lung edema, and lung histology. Phytochemical fingerprinting of Gc-ME was observed by using liquid chromatography-mass spectrometry. Nitric oxide production induced by LPS and Pam3CSK4 in RAW264.7 cells was revealed to be reduced by Gc-ME. The LPS-induced upregulation of iNOS, COX-2, IL-6, and IL-1β was also suppressed by Gc-ME treatment. Gc-ME downregulated the promotor activities of AP-1 and NF-κB triggered by MyD88- and TRIF induction. Upstream signaling proteins for NF-κB activation, namely, p-p50, p-p65, p-IκBα, and p-Src were all downregulated by Ch-EE. Moreover, Src was revealed to be directly targeted by Gc-ME. This extract, orally treated strongly, attenuated the inflammatory symptoms in HCl/EtOH-treated stomachs and LPS-treated lungs. Therefore, these results strongly imply that can be developed as a promising anti-inflammatory remedy with Src-suppressive properties.

摘要

该属中的许多物种都具有抗炎作用,被用作传统药用植物来治疗各种炎症症状。然而,尚未有关于Vahl抗炎活性的研究报道。本研究的目的是在体外和体内研究Vahl甲醇提取物(Gc-ME)的抗炎作用。为了确定Gc-ME的抗炎活性,采用脂多糖(LPS)、聚肌苷酸-聚胞苷酸(poly(I:C))或Pam3CSK4处理的RAW264.7细胞,以及盐酸/乙醇和LPS处理的小鼠进行体外和体内试验。通过Griess法测定LPS诱导的RAW264.7细胞中一氧化氮的产生,并通过RT-PCR和实时PCR确认LPS激活的RAW264.7细胞中细胞因子基因的表达。通过荧光素酶报告基因测定评估转录激活。通过蛋白质印迹分析和细胞热位移分析(CETSA)对LPS处理的RAW264.7细胞和基因转染的HEK293细胞进行靶蛋白验证。使用盐酸/乙醇诱导的胃炎模型和LPS诱导的肺损伤模型,通过对胃损伤、肺水肿和肺组织学进行评分或评估来检查炎症状态。使用液相色谱-质谱法观察Gc-ME的植物化学指纹图谱。结果显示,Gc-ME可降低LPS和Pam3CSK4诱导的RAW264.7细胞中一氧化氮的产生。Gc-ME处理还可抑制LPS诱导的诱导型一氧化氮合酶(iNOS)、环氧化酶-2(COX-2)、白细胞介素-6(IL-6)和白细胞介素-1β(IL-1β)的上调。Gc-ME下调了由髓样分化因子88(MyD88)和TIR结构域衔接蛋白诱导的AP-1和核因子κB(NF-κB)的启动子活性。NF-κB激活的上游信号蛋白,即磷酸化的p50、磷酸化的p65、磷酸化的IκBα和磷酸化的Src均被Gc-ME下调。此外,Src被发现是Gc-ME的直接靶点。该提取物经口服强力给药后,可减轻盐酸/乙醇处理的胃和LPS处理的肺中的炎症症状。因此,这些结果强烈表明Vahl可被开发为一种具有Src抑制特性的有前景的抗炎药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/247f/9784507/326ee19f5eab/plants-11-03560-g001a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验