Department of Oral Biology, Medical University of Vienna, 1090 Vienna, Austria.
Key Laboratory of Modern Preparation of Traditional Chinese Medicine, Ministry of Education, Jiangxi University of Chinese Medicine, Nanchang 330004, China.
Molecules. 2022 Feb 15;27(4):1321. doi: 10.3390/molecules27041321.
has been widely used in traditional medicine because of its flavonoids; however, the impact of the flavonoids to modulate the inflammatory response to oral cells remains to be described. For this aim, we isolated 4,7,2'-trihydroxy-4'-methoxyisoflavanol (472T4MIF) and 6,4'-dihydroxy-7-methoxyflavane (64D7MF) from the heartwood of and confirmed the chemical structure by nuclear magnetic resonance. We show here that both flavonoids are inhibitors of an inflammatory response of murine RAW 264.7 inflammatory macrophages stimulated by LPS. This is indicated by interleukin (IL)1, IL6, and chemokine CCL2 production besides the phosphorylation of p65. Consistently, in primary murine macrophages, both flavonoids decreased the inflammatory response by lowering LPS-induced IL1 and IL6 expression. To introduce oral cells, we have used human gingival fibroblasts and provoked the inflammatory response by exposing them to IL1β and TNFα. Under these conditions, 472T4MIF, but not 64D7MF, reduced the expression of chemokines CXCL1 and CXCL2. Taken together, we identified two flavonoids that can reduce the expression of cytokines and chemokines in macrophages and fibroblastic cells.
因其类黄酮,它在传统医学中得到了广泛应用;然而,类黄酮调节口腔细胞炎症反应的影响仍有待描述。为此,我们从心材中分离出 4,7,2'-三羟基-4'-甲氧基异黄酮(472T4MIF)和 6,4'-二羟基-7-甲氧基黄烷(64D7MF),并通过核磁共振证实了其化学结构。我们在这里表明,这两种类黄酮均能抑制 LPS 刺激的鼠 RAW 264.7 炎性巨噬细胞的炎症反应。这表现在白细胞介素(IL)1、IL6 和趋化因子 CCL2 的产生以及 p65 的磷酸化上。一致地,在原代鼠巨噬细胞中,两种类黄酮均通过降低 LPS 诱导的 IL1 和 IL6 表达来降低炎症反应。为了引入口腔细胞,我们使用人牙龈成纤维细胞,并通过暴露于 IL1β 和 TNFα 来引发炎症反应。在这些条件下,472T4MIF 而非 64D7MF 可降低趋化因子 CXCL1 和 CXCL2 的表达。总之,我们鉴定出两种能够降低巨噬细胞和成纤维细胞中细胞因子和趋化因子表达的类黄酮。