Anti-Inflammatory Effect of <i>Chamaecyparis obtusa</i> (Siebold & Zucc.) Endl. Leaf Essential Oil

<i>Chamaecyparis obtusa</i> (Siebold & Zucc.) Endl. (<i>C. obtusa</i>) belongs to the Cupressaceae family and is native to East Asian regions. Essential oils extracted from the leaves, bark, branches, and roots of <i>C. obtusa</i> have both aesthetic and medic...

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Bibliographic Details
Main Authors: Sung-Hee Kim, Young-Ah Jang, Yong-Jin Kwon
Format: Article
Language:English
Published: MDPI AG 2024-03-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/29/5/1117
Description
Summary:<i>Chamaecyparis obtusa</i> (Siebold & Zucc.) Endl. (<i>C. obtusa</i>) belongs to the Cupressaceae family and is native to East Asian regions. Essential oils extracted from the leaves, bark, branches, and roots of <i>C. obtusa</i> have both aesthetic and medicinal properties and are thus widely used. However, detailed analyses of the active ingredients of <i>C. obtusa</i> extract are lacking. In this study, the sabinene content in the hydro-distillation of <i>C. obtusa</i> leaf essential oil (COD) was analyzed using GC-MS, and the anti-inflammatory effect of COD was compared with that of pure sabinene. Cell viability was evaluated by MTT assay, and nitric oxide (NO) production was measured using Griess reagent. Relative mRNA and protein levels were analyzed using RT-qPCR and western blot, and secreted cytokines were analyzed using a cytokine array kit. The results showed that both COD and sabinene inhibited the expression of inducible nitric oxide synthase (iNOS) and the phosphorylation of c-Jun N-terminal kinase (JNK) and p38 in lipopolysaccharide (LPS)-induced RAW 264.7 cells. COD and sabinene also reduced the production of pro-inflammatory cytokines interleukin (IL)-1β, IL-6, IL-27, IL-1 receptor antagonist (IL-1ra), and granulocyte-macrophage colony-stimulating factor (GM-CSF). The anti-inflammatory mechanisms of COD and sabinene partially overlap, as COD was shown to inhibit MAPKs and the JAK/STAT axis, and sabinene inhibited MAPKs, thereby preventing LPS-induced macrophage activation.
ISSN:1420-3049