Abdurrahman Syawal, Ruslin Ruslin, Hasanah Aliya Nur, Ifaya Mus, Mustarichie Resmi
Department of Pharmaceutical Analysis and Medicinal Chemistry, Faculty of Pharmacy, Universitas Padjadjaran, Sumedang 45363, Indonesia.
Department of Medical Laboratory Technology, Universitas Mandala Waluya, Kendari 93231, Indonesia.
Pharmaceuticals (Basel). 2023 Apr 28;16(5):669. doi: 10.3390/ph16050669.
Alopecia is a condition in which hair on the scalp or other areas of the body is lost or falls out excessively. Nutritional deficiency causes blood flow to the head to decrease causing the hormone testosterone to be changed by the enzyme 5-α-reductase to dihydrotestosterone, which inhibits the growth phase and accelerates the death phase. One of the methods developed to treat alopecia is through inhibition of the 5-α-reductase enzyme, which converts testosterone to its more potent metabolite, dihydrotestosterone (DHT). Ethnomedicinally, leaf is used by the people of Sulawesi as a remedy for baldness. Therefore, in this research, an in vivo study was conducted on rabbits to determine the anti-alopecia activity of leaf compounds. The structure of the compounds isolated from the leaf ethyl acetate fraction was determined by analysis of NMR and LC-MS data. An in silico study was then carried out using minoxidil as a comparison ligand; scopolin () and scopoletin () isolated from leaf were identified as anti-alopecia compounds by predicting docking, simulating molecular dynamics and predicting absorption, distribution, metabolism, excretion, and toxicology (ADME-Tox). Compounds and had a better effect on hair growth compared to positive controls, and NMR and LC-MS analysis showed that they had comparable binding energies to receptors in the molecular docking interaction study: -4.51 and -4.65 kcal/mol, respectively, compared to -4.8 kcal/mol for minoxidil. Molecular dynamics simulation analysis with the parameters binding free energy calculated using the MM-PBSA method and complex stability based on SASA, PCA, RMSD, and RMSF showed that scopolin () has a good affinity for androgens receptors. The ADME-Tox prediction for scopolin () showed good results for the parameters of skin permeability, absorption and distribution. Therefore, scopolin () is a potential antagonist to androgen receptors and could be useful in the treatment of alopecia.
脱发是一种头皮或身体其他部位的毛发脱落或过度掉落的病症。营养缺乏会导致流向头部的血液减少,致使激素睾酮被5-α-还原酶转化为二氢睾酮,而二氢睾酮会抑制毛发生长期并加速毛发死亡期。为治疗脱发所研发的方法之一是抑制5-α-还原酶,该酶可将睾酮转化为其活性更强的代谢产物二氢睾酮(DHT)。在民族医学中,苏拉威西岛的人们将[植物名称]叶用作治疗秃头的药物。因此,在本研究中,对兔子进行了一项体内研究,以确定[植物名称]叶化合物的抗脱发活性。通过对核磁共振(NMR)和液相色谱 - 质谱(LC-MS)数据的分析确定了从[植物名称]叶乙酸乙酯馏分中分离出的化合物结构。然后以米诺地尔作为对照配体进行了计算机模拟研究;通过预测对接、模拟分子动力学以及预测吸收、分布、代谢、排泄和毒理学(ADME-Tox),从[植物名称]叶中分离出的东莨菪苷(scopolin)和东莨菪素(scopoletin)被鉴定为抗脱发化合物。与阳性对照相比,化合物[scopolin]和[scopoletin]对毛发生长具有更好的效果,并且NMR和LC-MS分析表明,在分子对接相互作用研究中它们与受体具有相当的结合能:分别为-4.51和-4.65千卡/摩尔,而米诺地尔为-4.8千卡/摩尔。使用MM-PBSA方法计算结合自由能参数并基于溶剂可及表面积(SASA)、主成分分析(PCA)、均方根偏差(RMSD)和均方根波动(RMSF)进行的分子动力学模拟分析表明,东莨菪苷(scopolin)对雄激素受体具有良好的亲和力。对东莨菪苷(scopolin)的ADME-Tox预测在皮肤渗透性、吸收和分布参数方面显示出良好的结果。因此,东莨菪苷(scopolin)是一种潜在的雄激素受体拮抗剂,可能对脱发治疗有用。