Will a glaucoma drug revolutionize the treatment of androgenetic alopecia? On drug repurposing, when the side effect becomes a desired therapeutic outcome.

Q3 Medicine
Postepy biochemii Pub Date : 2024-12-02 Print Date: 2024-12-31 DOI:10.18388/pb.2021_577
Kalina Spławska, Łukasz Zybaczyński, Maciej Wierzbicki, Katarzyna Koziak
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引用次数: 0

Abstract

Prostaglandins are hormones found in almost all mammalian tissues. As signaling molecules, they play a key role in the regulation of many physiological processes, including hair growth cycle. The article describes the history of the discovery of prostaglandins, including the work of Professor Ryszard Gryglewski – the discoverer of prostacyclin. Particular attention was paid to the synthetic analogue of prostaglandin F2α - latanoprost. Indicated for the treatment of glaucoma, the drug is known for inducing eyelash growth as a side effect. A prodrug, latanoprost is converted to its active metabolite, latanoprost acid. Recent research demonstrated that latanoprost acid has a chance to become an effective alternative to minoxidil and finasteride - the only drugs currently registered for the treatment of androgenetic alopecia. The development of anti-alopecia drugs containing prostaglandin derivatives, including latanoprost acid, will be a much faster process compared to the traditional path of product development based on a new chemical compound.

青光眼药物会给雄激素性脱发的治疗带来革命性的变化吗?当副作用成为期望的治疗结果时,重新利用药物。
前列腺素是一种几乎存在于所有哺乳动物组织中的激素。作为信号分子,它们在包括头发生长周期在内的许多生理过程的调节中起着关键作用。这篇文章描述了前列腺素的发现历史,包括前列腺素的发现者Ryszard Gryglewski教授的工作。重点研究了前列腺素F2α - latanoprost的合成类似物。该药用于治疗青光眼,其副作用是诱导睫毛生长。前药拉坦前列素转化为其活性代谢物拉坦前列酸最近的研究表明,拉坦前列酸有机会成为米诺地尔和非那雄胺的有效替代品,后者是目前唯一注册用于治疗雄激素性脱发的药物。与基于新化合物的传统产品开发路径相比,含有前列腺素衍生物(包括拉坦前列酸)的抗脱发药物的开发将是一个更快的过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Postepy biochemii
Postepy biochemii Medicine-Medicine (all)
CiteScore
0.80
自引率
0.00%
发文量
36
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