Pharmacognosy Department, Faculty of Pharmacy, Cairo University, Kasr El-Ainy Street, Cairo 11562, Egypt; Department of Pharmacognosy, Faculty of Pharmacy, October University for Modern Science and Arts (MSA), 6th October, 12566, Egypt.
Pharmacognosy Department, Faculty of Pharmacy, Cairo University, Kasr El-Ainy Street, Cairo 11562, Egypt.
J Ethnopharmacol. 2018 Mar 25;214:113-123. doi: 10.1016/j.jep.2017.12.019. Epub 2017 Dec 16.
Ginger (Zingiber officinale Roscoe) is a well known anti-inflammatory drug in the Egyptian, Indian and Chinese folk medicines, yet its mechanism of action is unclear.
To explore its mechanism of action and to correlate it to its biophytochemicals.
Various extracts viz. water, 50%, 70%, 80%, and 90% ethanol were prepared from ginger rhizomes. Fractionation of the aqueous extract (AE) was accomplished using Diaion HP-20. In vitro anti-inflammatory activity of the different extracts and isolated compounds was evaluated using protein denaturation inhibition, membrane stabilization, protease inhibition, and anti-lipoxygenase assays. In vivo anti-inflammatory activity of AE was estimated using carrageenan-induced rat paw edema in rats at doses 25, 50, 100 and 200mg/kg b.wt.
All the tested extracts showed significant (p< 0.1) in vitro anti-inflammatory activities. The strongest anti-lipoxygenase activity was observed for AE that was more significant than that of diclofenac (58% and 52%, respectively) at the same concentration (125μg/ml). Purification of AE led to the isolation of 6-poradol (G1), 6-shogaol (G2); methyl 6- gingerol (G3), 5-gingerol (G4), 6-gingerol (G5), 8-gingerol (G6), 10-gingerol (G7), and 1-dehydro-6-gingerol (G8). G1, G2 and G8 exhibited potent activity in all the studied assays, while G4 and G5 exhibited moderate activity. In vivo administration of AE ameliorated rat paw edema in a dose-dependent manner. AE (at 200mg/kg) showed significant reduction in production of PGE2, TNF-α, IL-6, monocyte chemoattractant protein-1 (MCP-1), regulated upon activation, normal T-cell expressed and secreted (RANTES), myeloperoxidase (MPO) activity by 60%, 57%, 60%, 41%, 32% and 67%, respectively. AE at 100 and 200mg/kg was equipotent to indomethacin in reduction of NO level and in increasing the total antioxidant capacity (TAC). Histopathological examination revealed very few inflammatory cells infiltration and edema after administration of AE (200mg/kg) prior to carrageenan.
Ginger anti-inflammatory activity is mediated by inhibiting macrophage and neutrophils activation as well as negatively affecting monocyte and leukocyte migration. This was evidenced by the dose-dependent decrease in pro-inflammatory cytokines and chemokines and replenishment the total antioxidant capacity.
生姜(姜科姜属植物)是埃及、印度和中国民间医学中一种著名的抗炎药物,但它的作用机制尚不清楚。
探索其作用机制,并将其与生物植物化学物质相关联。
从生姜根茎中制备了各种提取物,如:水、50%、70%、80%和 90%乙醇。用水提取物(AE)进行了分级分离,使用 Diaion HP-20 进行。使用蛋白质变性抑制、膜稳定、蛋白酶抑制和抗脂氧合酶测定法评估不同提取物和分离化合物的体外抗炎活性。在大鼠角叉菜胶诱导的足肿胀模型中,以 25、50、100 和 200mg/kg 体重的剂量评估 AE 的体内抗炎活性。
所有测试的提取物均表现出显著的(p<0.1)体外抗炎活性。AE 的最强的抗脂氧合酶活性比双氯芬酸(分别为 58%和 52%)更显著,在相同浓度(125μg/ml)下。AE 的纯化导致分离出 6-poradol(G1)、6-shogaol(G2);甲基 6-姜酚(G3)、5-姜辣素(G4)、6-姜辣素(G5)、8-姜辣素(G6)、10-姜辣素(G7)和 1-去氢-6-姜辣素(G8)。G1、G2 和 G8 在所有研究的测定中表现出强烈的活性,而 G4 和 G5 则表现出中等活性。体内给予 AE 可改善大鼠足肿胀,呈剂量依赖性。AE(200mg/kg)可显著减少 PGE2、TNF-α、IL-6、单核细胞趋化蛋白-1(MCP-1)、调节正常 T 细胞表达和分泌(RANTES)、髓过氧化物酶(MPO)的产生,分别为 60%、57%、60%、41%、32%和 67%。AE 以 100 和 200mg/kg 的剂量与吲哚美辛等效,可降低 NO 水平并增加总抗氧化能力(TAC)。组织病理学检查显示,给予 AE(200mg/kg)后,在给予角叉菜胶之前,炎性细胞浸润和水肿非常少。
生姜的抗炎活性是通过抑制巨噬细胞和中性粒细胞的激活以及负性影响单核细胞和白细胞的迁移来介导的。这一点从依赖剂量的促炎细胞因子和趋化因子的减少和总抗氧化能力的补充中得到了证明。