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防晒霜成分奥克立林对维生素 D 合成的干扰能力。

Sunscreen Ingredient Octocrylene's Potency to Disrupt Vitamin D Synthesis.

机构信息

Department of Pharmacy, Al Baha University, Al Baha 1988, Saudi Arabia.

Department of Pharmaceutical Chemistry, College of Pharmacy, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia.

出版信息

Int J Mol Sci. 2022 Sep 5;23(17):10154. doi: 10.3390/ijms231710154.

DOI:10.3390/ijms231710154
PMID:36077552
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9456232/
Abstract

Octocrylene is a widely used ingredient in sunscreen products, and it has been observed that the use of sunscreen has been increasing over the last few decades. In this paper, we investigated the way in which sunscreen's ingredient octocrylene may disrupt normal vitamin D synthesis pathway, resulting in an imbalance in vitamin D levels in the body. The key techniques used for this insilico investigation were molecular docking, molecular dynamic (MD) simulation, and MMPBSA-based assessment. Vitamin D abnormalities have become very common in human health. Unknown exposure to chemicals may be one of the important risk factors. In molecular docking analysis, octocrylene exhibited a binding energy of -11.52 kcal/mol with vitamin D binding protein (1KXP) and -11.71 for the calcitriol native ligand. Octocrylene had a binding potency of -11.152 kcal/mol with the vitamin D receptor (1DB1), and calcitriol had a binding potency of -8.73 kcal/mol. In addition, octocrylene has shown binding energy of -8.96 kcal/mol with CYP2R1, and the calcitriol binding energy was -10.36 kcal/mol. Regarding stability, the root-mean-square deviation (RMSD), the root-mean-square fluctuation (RMSF), the radius of gyration, hydrogen bonding, and the solvent-accessible surface area (SASA) exhibited that octocrylene has a stable binding pattern similar to calcitriol. These findings revealed that incessant exposure to octocrylene may disrupt normal vitamin D synthesis.

摘要

辛氧烷醇是防晒霜中广泛使用的成分,人们发现过去几十年防晒霜的使用量一直在增加。在本文中,我们研究了防晒霜成分辛氧烷醇可能破坏正常维生素 D 合成途径的方式,导致体内维生素 D 水平失衡。这项计算机模拟研究使用的关键技术是分子对接、分子动力学(MD)模拟和基于 MMPBSA 的评估。维生素 D 异常在人类健康中已变得非常普遍。对化学品的未知暴露可能是一个重要的风险因素。在分子对接分析中,辛氧烷醇与维生素 D 结合蛋白(1KXP)的结合能为-11.52kcal/mol,与钙三醇天然配体的结合能为-11.71kcal/mol。辛氧烷醇与维生素 D 受体(1DB1)的结合能力为-11.152kcal/mol,钙三醇的结合能力为-8.73kcal/mol。此外,辛氧烷醇与 CYP2R1 的结合能为-8.96kcal/mol,钙三醇的结合能为-10.36kcal/mol。关于稳定性,均方根偏差(RMSD)、均方根波动(RMSF)、回转半径、氢键和溶剂可及表面积(SASA)表明,辛氧烷醇具有与钙三醇相似的稳定结合模式。这些发现表明,持续接触辛氧烷醇可能会破坏正常的维生素 D 合成。

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