Post-Graduate Research Center, Department of Pharmacology, K. L. E. S's College of Pharmacy, Belgaum, Karnataka, India.
Eur J Pharmacol. 2010 Sep 10;642(1-3):169-76. doi: 10.1016/j.ejphar.2010.05.062. Epub 2010 Jun 17.
Kaempferol has been reported to inhibit nitric oxide synthase and cyclooxygenase enzymes in animal models. The present study was designed to investigate whether kaempferol modulates the cyclooxygenase pathway via inhibition of nitric oxide production, which in turn contributes to its anti-inflammatory activity. Investigations were performed using carrageenan induced rat air pouch model. Inflammation was assessed by measurement of nitrites (nitrite, a breakdown product of nitric oxide), prostaglandin-E(2) levels and cellular infiltration in the pouch fluid exudates. To assess the anti-inflammatory effect of the extract, rat air pouch linings were examined histologically. The levels of nitrite and prostaglandin-E(2) in pouch fluid were measured by using Griess assay and ELISA respectively. Cell counts and differential counts were performed using a Coulter counter and Wright-Giemsa stain respectively. Kaempferol when administered orally at 50 and 100mg/kg dose showed significant inhibition of carrageenan induced production of nitrite (40.12 and 59.74%, respectively) and prostaglandin-E(2) generation (64.23 and 78.55%, respectively). Infiltration of the cells into the rat granuloma air pouch was also significantly inhibited by kaempferol. Modulation of cyclooxygenase pathway via inhibition of nitric oxide synthesis significantly contributes to kaempferol's anti-inflammatory activity. The present study characterizes the effects and mechanisms of naturally occurring phenolic flavonoid kaempferol, on inducible nitric oxide synthase expression and nitric oxide production. These results partially explain the pharmacological efficacy of flavonoids in general and kaempferol in particular as anti-inflammatory compounds.
山柰酚已被报道能抑制动物模型中的一氧化氮合酶和环氧化酶。本研究旨在探讨山柰酚是否通过抑制一氧化氮生成来调节环氧化酶途径,从而发挥其抗炎活性。该研究采用角叉菜胶诱导的大鼠气囊模型进行。通过测量囊液中亚硝酸盐(亚硝酸盐是一氧化氮的分解产物)、前列腺素 E2 水平和细胞浸润来评估炎症。为了评估提取物的抗炎作用,检查了大鼠气囊衬里的组织学变化。通过格里塞斯测定法和 ELISA 分别测定囊液中亚硝酸盐和前列腺素 E2 的水平。使用库尔特计数器和 Wright-Giemsa 染色分别进行细胞计数和分类计数。山柰酚口服 50 和 100mg/kg 剂量时,显著抑制角叉菜胶诱导的亚硝酸盐(分别为 40.12%和 59.74%)和前列腺素 E2 生成(分别为 64.23%和 78.55%)。山柰酚还显著抑制细胞浸润到大鼠肉芽肿气囊中。通过抑制一氧化氮合成来调节环氧化酶途径,显著促进了山柰酚的抗炎活性。本研究描述了天然存在的酚类类黄酮山柰酚对诱导型一氧化氮合酶表达和一氧化氮生成的影响和机制。这些结果部分解释了类黄酮作为抗炎化合物的一般药理学功效,特别是山柰酚的功效。