Department of Pharmaceutical Analysis and Medicinal Chemistry, Faculty of Pharmacy, Universitas Padjadjaran, Andir 45363, Indonesia.
Department of Medical Laboratory Technology, Universitas Mandala Waluya, Kendari 93231, Indonesia.
ScientificWorldJournal. 2022 Aug 8;2022:1123047. doi: 10.1155/2022/1123047. eCollection 2022.
Alopecia is a health condition in which the hair loses its function in some or all of the body. Alopecia occurs due to various genetic, environmental, and nutritional factors. One of the methods developed to treat alopecia is through inhibition of the enzyme 5--reductase, which converts testosterone into its more potent metabolite, dihydrotestosterone (DHT). In ethnomedicine, the leaves of are used by the people of Sulawesi as a remedy for baldness. Therefore, in this study, an in vivo study was conducted on rabbits to investigate the antialopecia activity of the ethanolic extract of leaves. The purified leaf extract was fractionated using vacuum liquid chromatography with several solvents to produce fractions F1-F5. Each fraction was then retested in vivo in rabbits, and its content was then analyzed by LC-MS. An in silico study was then carried out using minoxidil as a comparison ligand; 17 compounds derived from leaves were identified as antialopecia compounds through prediction of molecular interactions and molecular dynamics simulation and prediction of absorption, distribution, metabolism, excretion, and toxicology (ADME-Tox). The assay results showed that fractions F2 and F3 had a better effect on hair growth compared to the positive control, and the test compound obtained from the LC-MS analysis, bufotalinin, had a strong binding energy to the receptor in the molecular docking interaction study: -5.99 kcal/mol compared to -4.8 kcal/mol for minoxidil. Molecular dynamics simulation analysis with complex stability parameters based on solvent-accessible surface area (SASA), principal component analysis (PCA), root mean square deviation (RMSD), and root mean square fluctuation (RMSF) showed that bufotalinin has good affinity for androgen receptors. ADME-Tox prediction for bufotalinin showed good results for the parameters of skin permeability, absorption, and distribution. Therefore, bufotalinin, a steroid compound, is a potential androgen receptor antagonist and could be useful in the treatment of alopecia.
脱发是一种毛发在身体的某些部位或全部失去功能的健康状况。脱发是由于各种遗传、环境和营养因素引起的。治疗脱发的方法之一是抑制 5--还原酶,该酶将睾酮转化为更有效的代谢物二氢睾酮(DHT)。在民族医学中,苏拉威西岛的人们使用 的叶子来治疗秃顶。因此,在这项研究中,对兔子进行了体内研究,以研究 的乙醇提取物的抗脱发活性。使用真空液相色谱法用几种溶剂对 叶的纯化提取物进行了馏分,得到了馏分 F1-F5。然后,将每个馏分在兔子体内进行重新测试,并通过 LC-MS 分析其含量。然后使用米诺地尔作为比较配体进行了计算机模拟研究;通过预测分子相互作用和分子动力学模拟以及吸收、分布、代谢、排泄和毒理学 (ADME-Tox) 的预测,从 叶中鉴定出 17 种化合物为抗脱发化合物。该测定结果表明,与阳性对照相比,馏分 F2 和 F3 对毛发生长的效果更好,并且从 LC-MS 分析获得的测试化合物,即布福他丁,与分子对接相互作用研究中的受体具有很强的结合能:-5.99 kcal/mol 与米诺地尔的-4.8 kcal/mol 相比。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) 的复杂稳定性参数的分子动力学模拟分析表明,布福他丁对雄激素受体具有良好的亲和力。对布福他丁的 ADME-Tox 预测显示,其皮肤渗透性、吸收和分布参数的结果良好。因此,布福他丁,一种甾体化合物,可能是一种潜在的雄激素受体拮抗剂,可用于治疗脱发。