Yoon Ju Young, Kim Ji Hye, Baek Kwang-Soo, Kim Geum Soog, Lee Seung Eun, Lee Dae Young, Choi Je Hun, Kim Seung Yu, Park Hyun Bong, Sung Gi-Ho, Lee Kang Ro, Cho Jae Youl, Noh Hyung Jun
Department of Genetic Engineering, Sungkyunkwan University, Suwon, Korea.
Department of Herbal Crop Research, National Institute of Horticultural and Herbal Science, RDA, Eumseoung 369 873, Korea.
Pharmacogn Mag. 2015 Jul-Sep;11(43):477-85. doi: 10.4103/0973-1296.160454.
Cordyceps militaris is one of well-known medicinal mushrooms with anti-inflammatory, anti-cancer, anti-diabetic, and anti-obesity activities.
The objective of the following study is to isolate chemical components from the ethanol extract (Cm-EE) from Cordyceps militaris and to evaluate their anti-inflammatory activities.
Column chromatographic separation was performed and anti-inflammatory roles of these compounds were also examined by using NO production and protein kinase B (AKT) activity assays.
From Cm-EE, 13 constituents, including trehalose (1), cordycepin (2), 6-hydroxyethyladenosine (3), nicotinic amide (4), butyric acid (5), β-dimorphecolic acid (6), α-dimorphecolic acid (7), palmitic acid (8), linoleic acid (9), cordycepeptide A (10), 4-(2-hydroxy-3-((9E,12E)-octadeca-9,12-dienoyloxy)propoxy)-2-(trimethylammonio)butanoate (11), 4-(2-hydroxy-3-(palmitoyloxy)propoxy)-2-(trimethylammonio)butanoate (12), and linoleic acid methyl ester (13) were isolated. Of these components, compound 2 displayed a significant inhibitory effect on NO production in lipopolysaccharide (LPS)-activated RAW264.7 cells. Furthermore, this compound strongly and directly suppressed the kinase activity of AKT, an essential signalling enzyme in LPS-induced NO production, by interacting with its ATP binding site.
C. militaris could have anti-inflammatory activity mediated by cordycepin-induced suppression of AKT.
蛹虫草是一种著名的药用真菌,具有抗炎、抗癌、抗糖尿病和抗肥胖活性。
以下研究的目的是从蛹虫草乙醇提取物(Cm-EE)中分离化学成分,并评估其抗炎活性。
进行柱色谱分离,并通过一氧化氮(NO)生成和蛋白激酶B(AKT)活性测定来检测这些化合物的抗炎作用。
从Cm-EE中分离出13种成分,包括海藻糖(1)、虫草素(2)、6-羟乙基腺苷(3)、烟酰胺(4)、丁酸(5)、β-二甲基吗啡酸(6)、α-二甲基吗啡酸(7)、棕榈酸(8)、亚油酸(9)、虫草肽A(10)、4-(2-羟基-3-((9E,12E)-十八碳-9,12-二烯酰氧基)丙氧基)-2-(三甲基铵)丁酸酯(11)、4-(2-羟基-3-(棕榈酰氧基)丙氧基)-2-(三甲基铵)丁酸酯(12)和亚油酸甲酯(13)。在这些成分中,化合物2对脂多糖(LPS)激活的RAW264.7细胞中NO的生成具有显著抑制作用。此外,该化合物通过与LPS诱导的NO生成中的关键信号酶AKT的ATP结合位点相互作用,强烈且直接地抑制了AKT的激酶活性。
蛹虫草可能具有由虫草素诱导的AKT抑制介导的抗炎活性。