Anti-Gastritis and Anti-Lung Injury Effects of Pine Tree Ethanol Extract Targeting Both NF-κB and AP-1 Pathways.
Seung A KimJieun OhSe Rin ChoiChoong Hwan LeeByoung-Hee LeeMi-Nam LeeMohammad Amjad HossainJong-Hoon KimSarah LeeYoung-Jin SonPublished in: Molecules (Basel, Switzerland) (2021)
An ethanol extract (Pd-EE) of Pinus densiflora Siebold and Zucc was derived from the branches of pine trees. According to the Donguibogam, pine resin has the effects of lowering the fever, reducing pain, and killing worms. The purpose of this study is to investigate whether Pd-EE has anti-inflammatory effects. During in vitro trials, NO production, as well as changes in the mRNA levels of inflammation-related genes and the phosphorylation levels of related proteins, were confirmed in RAW264.7 cells activated with lipopolysaccharide depending on the presence or absence of Pd-EE treatment. The activities of transcription factors were checked in HEK293T cells transfected with adapter molecules in the inflammatory pathway. The anti-inflammatory efficacy of Pd-EE was also estimated in vivo with acute gastritis and acute lung injury models. LC-MS analysis was conducted to identify the components of Pd-EE. This extract reduced the production of NO and the mRNA expression levels of iNOS, COX-2, and IL-6 in RAW264.7 cells. In addition, protein expression levels of p50 and p65 and phosphorylation levels of FRA1 were decreased. In the luciferase assay, the activities of NF-κB and AP-1 were lowered. In acute gastritis and acute lung injury models, Pd-EE suppressed inflammation, resulting in alleviated damage.
Keyphrases
- oxidative stress
- lps induced
- induced apoptosis
- anti inflammatory
- transcription factor
- helicobacter pylori
- helicobacter pylori infection
- signaling pathway
- inflammatory response
- lipopolysaccharide induced
- liver failure
- cell cycle arrest
- drug induced
- chronic pain
- cell death
- protein kinase
- spinal cord injury
- neuropathic pain
- cell proliferation
- spinal cord
- combination therapy
- aortic dissection
- nitric oxide synthase