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在体、体内和计算机模拟分析泰国 rejuvenating 疗法和生物活性代谢物的分子抗色素沉着机制。

In Vitro, In Vivo, and In Silico Analyses of Molecular Anti-Pigmentation Mechanisms of Selected Thai Rejuvenating Remedy and Bioactive Metabolites.

机构信息

Department of Pharmacognosy and Pharmaceutical Botany, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat Yai 90112, Songkhla, Thailand.

Department of Oriental Medicinal Biotechnology, Graduate School of Biotechnology, College of Life Sciences, Kyung Hee University, Yongin-si 17104, Gyeonggi-do, Republic of Korea.

出版信息

Molecules. 2023 Jan 18;28(3):958. doi: 10.3390/molecules28030958.

DOI:10.3390/molecules28030958
PMID:36770624
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9920523/
Abstract

Thai rejuvenating remedies are mixed herbal formulas promoting longevity. Due to the complexity, the biological activities of these remedies are minimal. Therefore, in this study, the authors evaluated the anti-pigmentation effect at the molecular level of the selected Thai rejuvenating remedy to fulfill the knowledge gap. First, the authors found that the selected remedy showed promising activity against the tyrosinase enzyme with an IC value of 9.41 µg/mL. In the comparison, kojic acid (positive control) exhibited an IC value of 3.92 µg/mL against the same enzyme. Later, the authors identified glabridin as a bioactive molecule against tyrosinase with an IC value of 0.08 µg/mL. However, ethyl -methoxycinnamate was the most abundant metabolite found in the remedy. The authors also found that the selected remedy and glabridin reduced the melanin content in the cell-based assay (B16F1) but not in the zebrafish larvae experiment. Finally, the authors conducted a computational investigation through molecular docking proposing a theoretical molecular interplay between glabridin, ethyl -methoxycinnamate, and target proteins (tyrosinase and melanocortin-1 receptor, MC1R). Hence, in this study, the authors reported the molecular anti-pigmentation mechanism of the selected Thai rejuvenating remedy for the first time by combining the results from in silico, in vitro, and in vivo experiments.

摘要

泰国 rejuvenating 疗法是混合草药配方,可促进长寿。由于其复杂性,这些疗法的生物活性极小。因此,在这项研究中,作者从分子水平评估了所选泰国 rejuvenating 疗法的抗色素沉着作用,以填补知识空白。首先,作者发现所选疗法对酪氨酸酶表现出有希望的活性,IC 值为 9.41 µg/mL。相比之下,曲酸(阳性对照)对相同酶的 IC 值为 3.92 µg/mL。后来,作者鉴定出甘草素是一种针对酪氨酸酶的生物活性分子,IC 值为 0.08 µg/mL。然而,乙基 -甲氧基肉桂酸酯是该疗法中发现的最丰富的代谢物。作者还发现,所选疗法和甘草素降低了基于细胞的测定(B16F1)中的黑色素含量,但在斑马鱼幼虫实验中没有。最后,作者通过分子对接进行了计算研究,提出了甘草素、乙基 -甲氧基肉桂酸酯和靶蛋白(酪氨酸酶和黑素皮质素-1 受体,MC1R)之间的理论分子相互作用。因此,在这项研究中,作者首次通过结合体内、体外和体内实验的结果,报道了所选泰国 rejuvenating 疗法的分子抗色素沉着机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7179/9920523/fda9c90f6566/molecules-28-00958-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7179/9920523/4f8ac6b2b569/molecules-28-00958-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7179/9920523/b5eabc638362/molecules-28-00958-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7179/9920523/2adef3e0e309/molecules-28-00958-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7179/9920523/9787374d330b/molecules-28-00958-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7179/9920523/54b1fdfddb2f/molecules-28-00958-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7179/9920523/ccd5d960a35d/molecules-28-00958-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7179/9920523/160ef5b63467/molecules-28-00958-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7179/9920523/8fd4483a07f4/molecules-28-00958-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7179/9920523/66cc35164d09/molecules-28-00958-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7179/9920523/fda9c90f6566/molecules-28-00958-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7179/9920523/4f8ac6b2b569/molecules-28-00958-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7179/9920523/b5eabc638362/molecules-28-00958-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7179/9920523/2adef3e0e309/molecules-28-00958-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7179/9920523/9787374d330b/molecules-28-00958-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7179/9920523/54b1fdfddb2f/molecules-28-00958-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7179/9920523/ccd5d960a35d/molecules-28-00958-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7179/9920523/160ef5b63467/molecules-28-00958-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7179/9920523/8fd4483a07f4/molecules-28-00958-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7179/9920523/66cc35164d09/molecules-28-00958-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7179/9920523/fda9c90f6566/molecules-28-00958-sch001.jpg

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