Department of Pharmacy, College of Pharmacy, Pusan National University, Busan 46241, Republic of Korea.
Research Institute of Life Science and College of Veterinary Medicine, Gyeongsang National University, Jinju, Gyeongsang 52828, Republic of Korea.
Exp Gerontol. 2021 Jan;143:111153. doi: 10.1016/j.exger.2020.111153. Epub 2020 Nov 13.
We previously reported that 2,4-dihydroxyphenyl-benzo[d]thiazole (MHY553) is a PPARα agonist, which has been shown to inhibit tyrosinase activity in murine melanocyte and alleviate hepatic steatosis in aged rats. This study investigated the effects of MHY553 on the age-related occurrence of inflammatory responses via the molecular modulation of the nuclear factor-κB (NF-κB) signaling pathway in the skin of aged rats and skin fibroblast cells. Moreover, we investigated the antioxidant effect of MHY553 via in vitro assays of reactive oxygen species (ROS) and peroxynitrite (ONOO) scavenging activities. We also scrutinized the ability of MHY553 as a PPARα activator in aged rat skin and HO-induced Hs27 fibroblast cells. In vivo experiments were performed in young, aged, and MHY553-fed aged rats (3 mg or 5 mg∙kg ∙day for 4 weeks). MHY553 dose-dependently scavenged ROS and ONOO. Furthermore, we found that MHY553 suppressed the NF-κB transcription factor and downregulated mitogen-activated protein kinase (MAPK)/activator protein-1 (AP-1) signaling. MHY553 also inhibited the expression of pro-inflammatory cytokines including COX-2, iNOS, IL-1β, and IL-6. Our findings indicate the MHY553 scavenges ROS/reactive nitrogen species and inhibits inflammatory cytokines through PPARα activation in the skin. Thus, these results suggest that MHY553 may be of therapeutic interest for protecting skin from oxidative stress-induced damage and intrinsic aging.
我们之前报道过,2,4-二羟基二苯并[d]噻唑(MHY553)是一种过氧化物酶体增殖物激活受体α(PPARα)激动剂,已被证明可抑制小鼠黑素细胞中的酪氨酸酶活性并减轻老年大鼠的肝脂肪变性。本研究通过分子调节核因子-κB(NF-κB)信号通路,研究了 MHY553 对老年大鼠皮肤中与年龄相关的炎症反应发生的影响,以及皮肤成纤维细胞。此外,我们通过活性氧(ROS)和过氧亚硝酸盐(ONOO)清除活性的体外测定研究了 MHY553 的抗氧化作用。我们还研究了 MHY553 作为 PPARα 激活剂在老年大鼠皮肤和 HO 诱导的 Hs27 成纤维细胞中的作用。在体内实验中,我们使用了年轻、年老和用 MHY553 喂养的年老大鼠(3 或 5mg·kg·day,连续 4 周)。MHY553 可剂量依赖性地清除 ROS 和 ONOO。此外,我们发现 MHY553 抑制 NF-κB 转录因子并下调丝裂原活化蛋白激酶(MAPK)/激活蛋白-1(AP-1)信号。MHY553 还抑制了 COX-2、iNOS、IL-1β 和 IL-6 等促炎细胞因子的表达。我们的研究结果表明,MHY553 通过在皮肤中激活 PPARα 来清除 ROS/活性氮物种并抑制炎症细胞因子。因此,这些结果表明 MHY553 可能具有治疗潜力,可以保护皮肤免受氧化应激诱导的损伤和内在老化。