School of Food Science and Biotechnology, Kyungpook National University, Daegu 41566, Republic of Korea.
Department of Agricultural Biotechnology, Seoul National University, Seoul 08826, Republic of Korea.
J Microbiol Biotechnol. 2022 Aug 28;32(8):982-988. doi: 10.4014/jmb.2207.07043. Epub 2022 Aug 1.
Licorice () has been used as preventive and therapeutic material for hyperpigmentation disorders. Previously, we isolated noble compounds including dehydroglyasperin C (DGC), dehydroglyasperin D (DGD) and isoangustone A (IAA) from licorice hexane/ethanol extracts. However, their anti-melanogenic effects and underlying molecular mechanisms are unknown. The present study compared effects of DGC, DGD and IAA on pigmentation in melan-a melanocytes and human epidermal melanocytes (HEMn). DGD exerted the most excellent anti-melanogenic effect, followed by DGC and IAA at non-cytotoxic concentrations. In addition, DGD significantly inhibited tyrosinase activity in vitro cell-free system and cell system. Western blot result showed that DGD decreased expression of microphthalmia-associated transcription factor (MITF), tyrosinase and tyrosinase-related protein-1 (TRP-1) in melan-a cells and HEMn cells. DGD induced phosphorylation of MITF, ERK and Akt signal pathway promoting MITF degradation system. However, DGD did not influence p38 and cAMP-dependent protein kinase (PKA)/CREB signal pathway in melan-a cells. These result indicated that DGD inhibited melanogenesis not only direct regulation of tyrosinase but also modulating intracellular signaling related with MITF level. Collectively, these results suggested a protective role for DGD against melanogenesis.
甘草被用作预防和治疗色素沉着障碍的材料。以前,我们从甘草正己烷/乙醇提取物中分离出包括脱氢甘珀酸 C(DGC)、脱氢甘珀酸 D(DGD)和异角鲨酮 A(IAA)在内的多种贵重化合物。然而,它们的抗黑色素生成作用及其潜在的分子机制尚不清楚。本研究比较了 DGC、DGD 和 IAA 对黑素瘤细胞和人表皮黑素细胞(HEMn)中色素沉着的影响。在非细胞毒性浓度下,DGD 对黑色素生成的抑制作用最为显著,其次是 DGC 和 IAA。此外,DGD 显著抑制了体外无细胞体系和细胞体系中的酪氨酸酶活性。Western blot 结果表明,DGD 降低了黑素瘤细胞和 HEMn 细胞中小眼畸形相关转录因子(MITF)、酪氨酸酶和酪氨酸酶相关蛋白-1(TRP-1)的表达。DGD 诱导 MITF、ERK 和 Akt 信号通路磷酸化,促进 MITF 降解系统。然而,DGD 不影响 p38 和 cAMP 依赖性蛋白激酶(PKA)/CREB 信号通路在黑素瘤细胞中的作用。这些结果表明,DGD 抑制黑色素生成不仅直接调节酪氨酸酶,还调节与 MITF 水平相关的细胞内信号。总之,这些结果表明 DGD 对黑色素生成具有保护作用。