从精选海洋生物碱中鉴定羟色胺转运体抑制剂:分子对接和 ADME 研究

Ummehani A Razvi, Laxmikant H Kamble
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摘要

抑郁症是影响全世界人们的常见精神疾病之一。它可以影响所有背景和年龄段的人。尽管有治疗抑郁症的药物,但只有极少数人能有效地对其做出反应。目前使用的抗抑郁药物会产生副作用,如尿潴留、恶心、体重增加、心血管疾病等。目前正在评估天然化合物的治疗潜力,以消除这些副作用。从海洋生物中提取的代谢物具有多种有益作用。各种海绵、珊瑚和海藻中的化合物具有治疗精神疾病的神奇功效。本研究展示了血清素转运体(SERT)与一些海洋生物碱的分子对接。PyRx 虚拟筛选软件生成的结果显示,在 13 种选定的生物碱中,只有 gelliusine A 的结合亲和力高于处方抗抑郁药帕罗西汀。根据 SwissADME,大多数入选生物碱都具有更好的吸收、分布、代谢和排泄(ADME)特性。但 gelliusine A 的胃肠道吸收率较低,而且不能穿过血脑屏障(BBB)。需要对这些化合物进行进一步的优化和实验研究,以提高它们的特性,使其成为更好的抗抑郁药,防止血清素的再摄取。
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Identification of Serotonin Transporter Inhibitors from Selected Marine Alkaloids: A Molecular Docking and ADME Study
One of the common mental illnesses that affect people worldwide is depression. It can impact people from all backgrounds and age groups. Despite having medications for depression, very few people respond to it in an efficient manner. Currently used anti-depressants show side effects like urine retention, nausea, weight gain, cardiovascular disorders, etc. Natural compounds are being evaluated for their therapeutic potential to eradicate these side effects. Metabolites obtained from marine organisms possess diverse beneficial effects. Various sponges, corals, and seaweeds contain compounds with magical properties to heal mental disorders. This study demonstrates the molecular docking of serotonin transporter (SERT) with some marine alkaloids. Results generated from PyRx virtual screening software shows that out of thirteen selected alkaloids, only gelliusine A have a higher binding affinity than the prescribed anti-depressant paroxetine. According to SwissADME, most of the selected alkaloids showed better absorption, distribution, metabolism and excretion (ADME) properties. But gelliusine A has low gastrointestinal absorption and does not cross blood-brain barrier (BBB). Further optimization and experimental investigations of these compounds are needed to enhance their properties to become better anti-depressants against reuptake of serotonin.
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