Department of Integrative Biotechnology, Sungkyunkwan University, Suwon 16419, Korea.
Department of Veterinary Physiology, College of Medicine, Chonbuk National University, Iksan 54596, Korea.
Int J Mol Sci. 2021 Dec 31;23(1):433. doi: 10.3390/ijms23010433.
Quercetin 3-O-β-D-glucuronide (Q-3-G), the glucuronide conjugate of quercetin, has been reported as having anti-inflammatory properties in the lipopolysaccharide-stimulated macrophages, as well as anticancer and antioxidant properties. Unlike quercetin, which has been extensively described to possess a wide range of pharmacological activities including skin protective effects, the pharmacological benefits and mechanisms Q-3-G in the skin remained to be elucidated. This study focused on characterizing the skin protective properties, including anti-inflammatory and antioxidant properties, of Q-3-G against UVB-induced or HO-induced oxidative stress, the hydration effects, and antimelanogenesis activities using human keratinocytes (HaCaT) and melanoma (B16F10) cells. Q-3-G down-regulated the expression of the pro-inflammatory gene and cytokine such as () and in HO or UVB-irradiated HaCaT cells. We also showed that Q-3-G exhibits an antioxidant effect using free radical scavenging assays, flow cytometry, and an increased expression of nuclear factor erythroid 2- related factor 2 (Nrf2). Q-3-G reduced melanin production in α-melanocyte-stimulating hormone (α-MSH)-induced B16F10 cells. The hydration effects and mechanisms of Q-3-G were examined by evaluating the moisturizing factor-related genes, such as , , and . In addition, Q-3-G increased the phosphorylation of c-Jun, Jun N-terminal kinase (JNK), Mitogen-activated protein kinase (MAPK) kinase 4 (MKK4), and TAK1, involved in the MAPKs/AP-1 pathway, and the phosphorylation of IκBα, IκB kinase (IKK)-α, Akt, and Src, involved in the NF-κB pathway. Taken together, we have demonstrated that Q-3-G exerts anti-inflammatory, antioxidant, moisturizing, and antimelanogenesis properties in human keratinocytes and melanoma cells through NF-κB and AP-1 pathways.
槲皮素 3-O-β-D-葡萄糖醛酸苷(Q-3-G)是槲皮素的葡萄糖醛酸缀合物,据报道具有抗炎特性,可在脂多糖刺激的巨噬细胞中发挥作用,同时还具有抗癌和抗氧化特性。与广泛描述具有广泛的药理活性(包括皮肤保护作用)的槲皮素不同,Q-3-G 在皮肤中的药理益处和机制仍有待阐明。本研究侧重于表征 Q-3-G 对 UVB 诱导或 HO 诱导的氧化应激、水合作用和黑素生成抑制活性的皮肤保护特性,包括抗炎和抗氧化特性,使用人角质形成细胞(HaCaT)和黑色素瘤(B16F10)细胞。Q-3-G 下调了 HO 或 UVB 照射的 HaCaT 细胞中促炎基因和细胞因子如()和()的表达。我们还表明,Q-3-G 通过自由基清除测定、流式细胞术和核因子红细胞 2 相关因子 2(Nrf2)的表达增加显示出抗氧化作用。Q-3-G 减少了α-黑色素细胞刺激激素(α-MSH)诱导的 B16F10 细胞中的黑色素生成。通过评估与保湿因子相关的基因,如()、()和(),研究了 Q-3-G 的水合作用及其机制。此外,Q-3-G 增加了丝裂原激活蛋白激酶(MAPK)/激活蛋白 1(AP-1)通路中涉及的 c-Jun、Jun N-末端激酶(JNK)、MAPK 激酶 4(MKK4)和 TAK1 的磷酸化,以及参与 NF-κB 通路的 IκBα、IκB 激酶(IKK)-α、Akt 和 Src 的磷酸化。综上所述,我们已经证明 Q-3-G 通过 NF-κB 和 AP-1 通路在人角质形成细胞和黑色素瘤细胞中发挥抗炎、抗氧化、保湿和抑制黑素生成的作用。