PCOS and Inositols - Advances and Lessons We are Learning. A Narrative Review.

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2025-05-21 eCollection Date: 2025-01-01 DOI:10.2147/DDDT.S524718
Guglielmo Lentini, Alessandro Querqui, Noemi Monti, Mariano Bizzarri
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引用次数: 0

Abstract

Introduction: This Expert Opinion covers recent updates in the use of Inositol in polycystic ovary syndrome (PCOS), highlighting the specific effects triggered upon ovarian steroidogenesis.

Areas covered: An impressive body of evidence, obtained from molecular, animal and clinical studies, demonstrated the striking association between PCOS and the metabolism of myo-Inositol (myo-Ins) and its isomer D-Chiro-Inositol (DCI). Early investigations focused primarily on the metabolic consequences of inositol in modulating insulin transduction. However, recent advances disclosed that Inositols trigger direct effects on steroidogenesis. High DCI levels exacerbate androgen synthesis, and downregulate aromatase expression. Myo-Ins modulates insulin effects too, but exerts opposite actions on steroidogenesis, by increasing aromatase and FSH receptor expression. Clinical studies demonstrated myo-Ins efficacy, suggesting that an appropriate ratio in between myo-Ins/DCI (40:1) improves the reproductive function in PCOS women, even in absence of insulin resistance.

Expert opinion: Inositol-based treatments in PCOS are gaining momentum, demonstrating safety and efficacy greater than those obtained with other pharmacological agents. The efficacy depends not only on the modulation of insulin sensitivity but also on the direct, steroidogenic effects upon the ovaries. Adequate adsorption of Inositol is a critical issue, and the association of α-Lactalbumin can significantly overcome this problem. However, if a treatment based on inositol could be equally effective on different phenotypes of PCOS needs a specific assessment.

多囊卵巢综合征和肌醇-我们正在学习的进展和教训。叙述性评论。
本专家意见涵盖了肌醇在多囊卵巢综合征(PCOS)中使用的最新进展,强调了卵巢类固醇生成引发的特定作用。涵盖领域:从分子、动物和临床研究中获得的大量令人印象深刻的证据表明,多囊卵巢综合征与肌醇(myo-Ins)及其异构体d -肌醇(DCI)的代谢之间存在显著关联。早期的研究主要集中在肌醇在调节胰岛素转导中的代谢后果。然而,最近的进展表明,肌醇触发类固醇生成的直接作用。高DCI水平加剧雄激素合成,下调芳香酶表达。Myo-Ins也调节胰岛素的作用,但通过增加芳香化酶和FSH受体的表达,对甾体生成产生相反的作用。临床研究证实了myo-Ins的有效性,表明myo-Ins/DCI的适当比例(40:1)可以改善PCOS女性的生殖功能,即使没有胰岛素抵抗。专家意见:肌醇为基础的多囊卵巢综合征治疗正在获得动力,证明安全性和有效性优于其他药物。其功效不仅取决于对胰岛素敏感性的调节,还取决于对卵巢的直接类固醇效应。肌醇的充分吸附是一个关键问题,α-乳清蛋白的结合可以显著克服这一问题。然而,如果基于肌醇的治疗对不同表型的多囊卵巢综合征同样有效,则需要进行特定的评估。
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
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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