Icariside II:自然发生、生物转化、药理活性、合成修饰、药代动力学和生物利用度。

IF 3.2 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Huynh Thi Ngoc Ni, Nguyen Ngoc Linh, Phi Thi Tuyet Nhung, Pham Thi Bich Dao, Vu Quoc Manh, Ninh The Son
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引用次数: 0

摘要

目的:Icariside II (ICS-II)是一种含有3-rhamnopyranosyl和8-prenyl基团的黄酮,是小檗科淫羊藿属植物中发现的主要天然化合物之一。本研究旨在对其天然存在、药理价值、合成修饰、药代动力学和生物利用度等方面进行系统综述。主要发现:使用谷歌Scholar、Web of Science、PubMed和期刊网站等来源收集有关ICS-II的参考文献。“Icariside II”是查找参考文献最有意义的关键字,参考文献更新至今。摘要:ICS-II是多种淫羊藿属植物的特征性代谢物,可通过酶解其他类黄酮得到。它是一种具有多种体外和体内药理潜力的有前途的化合物。所研究的黄酮通过细胞周期阻滞、增殖抑制、自噬和凋亡显示出与癌症相关的生物活性,并在抗炎作用中抑制细胞因子。值得注意的是,除了对健康有益外,它还具有抗糖尿病、有性生殖以及防止对心脏、大脑、骨骼、肺、肾脏、肝脏和眼睛有害的作用。从Akt/NOS/NF-κB、JAK/STAT3/MAPK、PI3K/Akt/mTOR等多种信号通路推断其作用的分子机制。药代动力学证据包括糖和甲基去除、羟基化、葡萄糖醛酸化和糖基化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Icariside II: natural occurrence, biotransformation, pharmacological activity, synthetic modification, pharmacokinetics, and bioavailability.

Objectives: Icariside II (ICS-II), a flavone containing 3-rhamnopyranosyl and 8-prenyl groups, is one of the main natural compounds found in Epimedum species (the family Berberidaceae). The current study aims to provide a systematic review of its natural occurrence, pharmacological value, synthetic modification, pharmacokinetics, and bioavailability.

Key findings: Sources such as Google Scholar, Web of Science, PubMed, and journal websites were used to gather references about ICS-II. 'Icariside II' is the most meaningful keyword to seek references, and references have been updated till now.

Summary: ICS-II is a characteristic metabolite of various Epimedum plants, and it can be obtained by enzymatic hydrolysis of other flavonoids. It is a promising compound with multiple in vitro and in vivo pharmacological potentials. The studied flavone showed cancer-related biological activity via cell cycle arrest, proliferation inhibition, autophagy, and apoptosis and inhibited cytokines in anti-inflammatory actions. Significantly, the health benefits were accompanied by its role in antidiabetics, sexual reproduction, and protection against harmful effects on the heart, brain, bones, lungs, kidneys, livers, and eyes. Molecular mechanisms of action were deduced from various signaling pathways, such as Akt/NOS/NF-κB, JAK/STAT3/MAPK, and PI3K/Akt/mTOR. Pharmacokinetic evidence involved sugar and methyl removals, hydroxylation, glucuronidation, and glycosylation.

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来源期刊
CiteScore
6.60
自引率
0.00%
发文量
91
审稿时长
3 months
期刊介绍: JPP keeps pace with new research on how drug action may be optimized by new technologies, and attention is given to understanding and improving drug interactions in the body. At the same time, the journal maintains its established and well-respected core strengths in areas such as pharmaceutics and drug delivery, experimental and clinical pharmacology, biopharmaceutics and drug disposition, and drugs from natural sources. JPP publishes at least one special issue on a topical theme each year.
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