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去氢甘珀酸 D 通过降解黑素细胞中的 MITF 抑制黑色素合成。

Dehydroglyasperin D Suppresses Melanin Synthesis through MITF Degradation in Melanocytes.

机构信息

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.

出版信息

J Microbiol Biotechnol. 2022 Aug 28;32(8):982-988. doi: 10.4014/jmb.2207.07043. Epub 2022 Aug 1.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab12/9628959/162d28a5d7d5/jmb-32-8-982-f1.jpg

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