Kim Seo-Yeon, Hassan Ahmed H E, Chung Kyung-Sook, Kim Su-Yeon, Han Hee-Soo, Lee Hwi-Ho, Jung Seang-Hwan, Lee Kwang-Young, Shin Ji-Sun, Jang Eungyeong, Yoon Seolmin, Lee Yong Sup, Lee Kyung-Tae
Department of Pharmaceutical Biochemistry, College of Pharmacy, Kyung Hee University, Seoul, South Korea.
Department of Life and Nanopharmaceutical Sciences, Graduate School, Kyung Hee University, Seoul, South Korea.
Front Pharmacol. 2022 Apr 21;13:857789. doi: 10.3389/fphar.2022.857789. eCollection 2022.
TMS-HDMF-5z is a hybrid of the natural products mosloflavone and resveratrol. It was discovered to show potent inhibitory effects against lipopolysaccharide (LPS)-induced production of inflammatory mediators in RAW 264.7 macrophages. However, its mechanism of action is unknown. Hence this study aimed to demonstrate and explore and anti-inflammatory effects of TMS-HDMF-5z and its mechanism of action employing RAW 264.7 macrophages and carrageenan-induced hind paw edema. This work revealed that TMS-HDMF-5z suppressed the LPS-induced inducible nitric-oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) at the protein, mRNA, and promoter binding levels and tumor necrosis factor-α (TNF-α), interleukin (IL)-1β, and IL-6, and interferon-β (IFN-β) at the mRNA expression in RAW 264.7 macrophages. The results showed that TMS-HDMF-5z reduced the transcription and DNA binding activities of nuclear factor-κB (NF-κB) through inhibiting nuclear translocation of p65 and phosphorylation of κB inhibitor α (IκBα), IκB kinase (IKK), and TGF-β activated kinase 1 (TAK1). Additionally, TMS-HDMF-5z attenuated the LPS-induced transcriptional and DNA binding activities of activator protein-1 (AP-1) by suppressing nuclear translocation of phosphorylated c-Fos, c-Jun, and activating transcription factor 2 (ATF2). TMS-HDMF-5z also reduced the LPS-induced phosphorylation of Janus kinase 1/2 (JAK1/2), signal transducers and activators of transcription 1/3 (STAT1/3), p38 mitogen-activated protein kinase (MAPK), and MAPK-activated protein kinase 2 (MK2). In rats, TMS-HDMF-5z alleviated carrageenan-induced hind paw edema through the suppressing iNOS and COX-2 NF-κB, AP-1, and STAT1/3 inactivation. Collectively, the TMS-HDMF-5z-mediated inhibition of NF-κB, AP-1, and STAT1/3 offer an opportunity for the development of a potential treatment for inflammatory diseases.
TMS-HDMF-5z是天然产物莫斯洛黄酮和白藜芦醇的一种混合物。已发现它对RAW 264.7巨噬细胞中脂多糖(LPS)诱导的炎症介质产生具有强大的抑制作用。然而,其作用机制尚不清楚。因此,本研究旨在利用RAW 264.7巨噬细胞和角叉菜胶诱导的后爪水肿来证明和探究TMS-HDMF-5z的抗炎作用及其作用机制。这项研究表明,TMS-HDMF-5z在蛋白质、mRNA和启动子结合水平上抑制LPS诱导的诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2),并在RAW 264.7巨噬细胞的mRNA表达水平上抑制肿瘤坏死因子-α(TNF-α)、白细胞介素(IL)-1β、IL-6和干扰素-β(IFN-β)。结果表明,TMS-HDMF-5z通过抑制p65的核转位以及κB抑制剂α(IκBα)、IκB激酶(IKK)和转化生长因子-β激活激酶1(TAK1)的磷酸化,降低核因子-κB(NF-κB)的转录和DNA结合活性。此外,TMS-HDMF-5z通过抑制磷酸化的c-Fos、c-Jun和激活转录因子2(ATF2)的核转位,减弱LPS诱导的激活蛋白-1(AP-1)的转录和DNA结合活性。TMS-HDMF-5z还降低了LPS诱导的Janus激酶1/2(JAK1/2)、信号转导子和转录激活子1/3(STAT1/3)、p38丝裂原活化蛋白激酶(MAPK)和MAPK激活的蛋白激酶2(MK2)的磷酸化。在大鼠中,TMS-HDMF-5z通过抑制iNOS和COX-2以及NF-κB、AP-1和STAT1/3的失活,减轻角叉菜胶诱导的后爪水肿。总体而言,TMS-HDMF-5z介导的对NF-κB、AP-1和STAT1/3的抑制为开发炎症性疾病的潜在治疗方法提供了机会。