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L-茶氨酸对B16F10细胞和斑马鱼的抗黑色素生成作用

Anti-Melanogenic Effects of L-Theanine on B16F10 Cells and Zebrafish.

作者信息

Yu Chih-Li, Pang Haiyue, Run Zhao, Wang Guey-Horng

机构信息

Engineering Research Center of Natural Cosmeceuticals College of Fujian Province, Xiamen Medical College, Xiamen 361023, China.

出版信息

Molecules. 2025 Feb 19;30(4):956. doi: 10.3390/molecules30040956.

Abstract

L-Theanine, a natural amino acid found in green tea () leaves, is known for its diverse psychotropic effects. This study aimed to evaluate the inhibitory effect of L-theanine on melanin production and uncover its regulatory mechanism. We evaluated the anti-melanogenic activities of L-theanine in vitro and in vivo. In B16F10 murine melanoma cells induced by α-melanocyte-stimulating hormone, melanin content and intracellular tyrosinase activity were determined, and melanogenesis-related protein expression and signaling pathways were analyzed by Western blotting. Melanin reduction was further assessed using the zebrafish () test. L-Theanine reduced the intracellular tyrosinase activity and melanin content of B16F10 cells. It also attenuated the expression of melanogenesis-related proteins, such as microphthalmia- associated transcription factor, tyrosinase (TYR), TYR-related protein-1, and dopachrome tautomerase. L-Theanine modulated the protein kinase A (PKA), cAMP responder element binding protein (CREB), phosphorylation of/protein kinase B (Akt), glycogen synthase kinase-3β (GSK-3β), and β-catenin. The antimelanogenic activity of L-theanine (<2 mg/mL) was further confirmed using zebrafish larvae. L-Theanine inhibited melanogenesis by downregulating the PKA/CREB and Akt/GSK-3β/β-catenin signaling pathways. In summary, L-theanine shows potential as a skin-whitening compound, warranting further investigation for its possible applications in cosmetic and pharmaceutical products.

摘要

L-茶氨酸是一种存在于绿茶茶叶中的天然氨基酸,以其多样的精神药理作用而闻名。本研究旨在评估L-茶氨酸对黑色素生成的抑制作用,并揭示其调控机制。我们在体外和体内评估了L-茶氨酸的抗黑色素生成活性。在α-黑素细胞刺激激素诱导的B16F10小鼠黑色素瘤细胞中,测定黑色素含量和细胞内酪氨酸酶活性,并通过蛋白质印迹法分析黑色素生成相关蛋白的表达和信号通路。使用斑马鱼试验进一步评估黑色素减少情况。L-茶氨酸降低了B16F10细胞的细胞内酪氨酸酶活性和黑色素含量。它还减弱了小眼相关转录因子、酪氨酸酶(TYR)、TYR相关蛋白-1和多巴色素互变异构酶等黑色素生成相关蛋白的表达。L-茶氨酸调节蛋白激酶A(PKA)、环磷酸腺苷反应元件结合蛋白(CREB)、/蛋白激酶B(Akt)、糖原合酶激酶-3β(GSK-3β)和β-连环蛋白的磷酸化。使用斑马鱼幼虫进一步证实了L-茶氨酸(<2 mg/mL)的抗黑色素生成活性。L-茶氨酸通过下调PKA/CREB和Akt/GSK-3β/β-连环蛋白信号通路抑制黑色素生成。总之,L-茶氨酸显示出作为皮肤美白化合物的潜力,值得进一步研究其在化妆品和药品中的可能应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e72/11858779/ed40f8e7bea8/molecules-30-00956-g001.jpg

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