Mathematical Engineering Academy of Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
Guangdong Provincial Key Laboratory of New Drug Development and Research of Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
Mediators Inflamm. 2017;2017:1089028. doi: 10.1155/2017/1089028. Epub 2017 Jul 25.
According to the GC-MS analysis, compositional variation was observed between samples of patchouli oil, of which an unknown compound identified as patchoulene epoxide (PAO) was found only in the long-stored oil, whose biological activity still remains unknown. Therefore, the present study aimed to evaluate the potential anti-inflammatory activity with three in vivo inflammatory models: xylene-induced ear edema, acetic acid-induced vascular permeability, and carrageenan-induced paw edema. Further investigation into its underlying mechanism on carrageenan-induced paw edema was conducted. Results demonstrated that PAO significantly inhibited the ear edema induced by xylene, lowered vascular permeability induced by acetic acid and decreased the paw edema induced by carrageenan. Moreover, PAO markedly decreased levels of tumor necrosis factor- (TNF-), interleukin-1 (IL-1), interleukin-6 (IL-6), prostaglandin E2 (PGE), and nitric oxide (NO), but increased levels of interleukin-4 (IL-4) and interleukin-10 (IL-10). PAO was also shown to significantly downregulate the protein and mRNA expressions of cyclooxygenase-2 (COX-2) and inducible nitric-oxide synthase (iNOS). Western blot analysis revealed that PAO remarkably inhibited p50 and p65 translocation from the cytosol to the nucleus by suppressing IKK and IB phosphorylation. In conclusion, PAO exhibited potent anti-inflammatory activity probably by suppressing the activation of iNOS, COX-2 and NF-B signaling pathways.
根据 GC-MS 分析,广藿香油样品中观察到组成变化,其中一种未知化合物被鉴定为氧化石竹烯(PAO),仅存在于长期储存的油中,其生物活性尚不清楚。因此,本研究旨在评估三种体内炎症模型的潜在抗炎活性:二甲苯诱导的耳肿胀、醋酸诱导的血管通透性和角叉菜胶诱导的足肿胀。进一步研究了其对角叉菜胶诱导的足肿胀的潜在机制。结果表明,PAO 显著抑制二甲苯诱导的耳肿胀,降低醋酸诱导的血管通透性,并减少角叉菜胶诱导的足肿胀。此外,PAO 显著降低肿瘤坏死因子-(TNF-)、白细胞介素-1(IL-1)、白细胞介素-6(IL-6)、前列腺素 E2(PGE)和一氧化氮(NO)的水平,但增加白细胞介素-4(IL-4)和白细胞介素-10(IL-10)的水平。PAO 还显著下调环氧化酶-2(COX-2)和诱导型一氧化氮合酶(iNOS)的蛋白和 mRNA 表达。Western blot 分析表明,PAO 通过抑制 IKK 和 IB 磷酸化显著抑制 p50 和 p65 从细胞质向核内易位。综上所述,PAO 表现出强大的抗炎活性,可能是通过抑制 iNOS、COX-2 和 NF-B 信号通路的激活。