Jeong Se Yun, Yu Hyung-Seok, Ra Moon-Jin, Jung Sang-Mi, Yu Jeong-Nam, Kim Jin-Chul, Kim Ki Hyun
School of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Natural Product Research Institute, Korea Institute of Science and Technology, Gangneung 25451, Republic of Korea.
Pharmaceuticals (Basel). 2023 Oct 16;16(10):1478. doi: 10.3390/ph16101478.
L. (Equisetaceae), widely known as 'horsetail', is a perennial plant found extensively across Asia. Extracts of have been used in traditional medicine, particularly for the treatment of inflammatory disorders. This study aimed to determine the phytochemical compounds in ethanolic extract and their anti-inflammatory properties. Subsequently, we isolated and identified nine secondary metabolites, including kaempferol 3,7-di---D-glucopyranoside (), icariside B (), ()-3-hexenyl -D-glucopyranoside (), luteolin 5---D-glucopyranoside (), 4---D-glucopyranosyl caffeic acid (), clemastanin B (), 4--caffeoylshikimic acid (), (7,8)--7,9,9'-trihydroxy-3,3'-dimethoxy-8--4'-neolignan-4---D-glucopyranoside (), and 3--caffeoylshikimic acid (). The chemical structures of the isolated compounds () were elucidated using HR-ESI-MS data, NMR spectra, and ECD data. Next, the anti-inflammatory effects of the isolates were evaluated in tumor necrosis factor (TNF)α/interferon (IFN)γ-induced HaCaT, a human keratinocyte cell line. Among the isolates, compound showed the highest inhibitory effect on the expression of pro-inflammatory chemokines, followed by compounds and . Correspondingly, the preceding isolates inhibited TNFα/IFNγ-induced activation of pro-inflammatory transcription factors, signal transducer and activator of transcription 1, and nuclear factor-κB. Collectively, could be employed for the development of prophylactic or therapeutic agents for improving dermatitis.
木贼属(木贼科),广为人知的名称是“马尾草”,是一种多年生植物,在亚洲广泛分布。其提取物已被用于传统医学,特别是用于治疗炎症性疾病。本研究旨在确定木贼乙醇提取物中的植物化学化合物及其抗炎特性。随后,我们分离并鉴定了九种次生代谢产物,包括山奈酚3,7 - 二 - O - D - 吡喃葡萄糖苷(化合物1)、淫羊藿苷B(化合物2)、(Z)-3 - 己烯基 - O - D - 吡喃葡萄糖苷(化合物3)、木犀草素5 - O - D - 吡喃葡萄糖苷(化合物4)、4 - O - D - 吡喃葡萄糖基咖啡酸(化合物5)、淫羊藿素B(化合物6)、4 - O - 咖啡酰莽草酸(化合物7)、(7,8)-二氢-7,9,9'-三羟基-3,3'-二甲氧基-8 - O - 4'-新木脂素-4 - O - D - 吡喃葡萄糖苷(化合物8)和3 - O - 咖啡酰莽草酸(化合物9)。利用高分辨电喷雾电离质谱(HR - ESI - MS)数据、核磁共振(NMR)光谱和电子圆二色(ECD)数据阐明了所分离化合物(化合物1 - 9)的化学结构。接下来,在肿瘤坏死因子(TNF)α/干扰素(IFN)γ诱导的人角质形成细胞系HaCaT中评估了分离物的抗炎作用。在所分离的化合物中,化合物6对促炎趋化因子的表达显示出最高的抑制作用,其次是化合物2和化合物5。相应地,上述分离物抑制了TNFα/IFNγ诱导的促炎转录因子、信号转导和转录激活因子1以及核因子-κB的激活。总体而言,木贼可用于开发预防或治疗改善皮炎的药物。