Shin Hyun-Mo, Lee Yong Rok, Chang Yoon Sook, Lee Jun-Young, Kim Byung Hak, Min Kyung Rak, Kim Youngsoo
College of Pharmacy and Research Center for Bioresource and Health, Chungbuk National University, Cheongju 361-763, Republic of Korea.
Int Immunopharmacol. 2006 Jun;6(6):916-23. doi: 10.1016/j.intimp.2006.01.006. Epub 2006 Feb 3.
Furonaphthoquinone compounds have been reported to exhibit anticancer, antibacterial and antiviral properties. The molecular basis for these diverse properties is not known. 2-Methyl-2-(2-methylpropenyl)-2,3-dihydronaphthoquinone [2,3-b]furan-4,9-dione (NFD-37) is a synthetic furonaphthoquinone compound. In the present study, NFD-37 was found to inhibit interleukin (IL)-6 production in lipopolysaccharide (LPS)-stimulated murine macrophages RAW 264.7. Further, NFD-37 attenuated LPS-induced synthesis of IL-6 transcript but also inhibited LPS-induced IL-6 promoter activity. Since nuclear factor (NF)-kappaB activation has been shown to play a key role in LPS-induced IL-6 expression, the effect of NFD-37 on LPS-induced NF-kappaB activation was further analyzed. NFD-37 exhibited a dose-dependent inhibitory effect on LPS-induced phosphorylation of inhibitory kappaB alpha protein (IkappaB alpha), and subsequently inhibited LPS-induced IkappaB alpha degradation as well as NF-kappaB transcriptional activity. In another experiment, NFD-37 inhibited both IL-6 promoter activity and NF-kappaB transcriptional activity elicited by an expression vector encoding IkappaB kinase beta. Taken together, NFD-37 down-regulated LPS-induced IL-6 expression through NF-kappaB activation, which could provide a pharmacological basis for the anti-inflammatory properties of furonaphthoquinone analogs.
据报道,呋喃萘醌化合物具有抗癌、抗菌和抗病毒特性。这些多样特性的分子基础尚不清楚。2-甲基-2-(2-甲基丙烯基)-2,3-二氢萘醌[2,3-b]呋喃-4,9-二酮(NFD-37)是一种合成呋喃萘醌化合物。在本研究中,发现NFD-37可抑制脂多糖(LPS)刺激的小鼠巨噬细胞RAW 264.7中白细胞介素(IL)-6的产生。此外,NFD-37可减弱LPS诱导的IL-6转录物合成,但也抑制LPS诱导的IL-6启动子活性。由于已证明核因子(NF)-κB激活在LPS诱导的IL-6表达中起关键作用,因此进一步分析了NFD-37对LPS诱导的NF-κB激活的影响。NFD-37对LPS诱导的抑制性κBα蛋白(IkappaBα)磷酸化表现出剂量依赖性抑制作用,并随后抑制LPS诱导的IkappaBα降解以及NF-κB转录活性。在另一项实验中,NFD-37抑制了由编码IkappaB激酶β的表达载体引发的IL-6启动子活性和NF-κB转录活性。综上所述,NFD-37通过NF-κB激活下调LPS诱导的IL-6表达,这可为呋喃萘醌类似物的抗炎特性提供药理学依据。