关于黄芩苷药理作用和药代动力学的综述。

IF 4.3 3区 医学 Q2 CHEMISTRY, MEDICINAL
Jiang Lai, Chunxiao Li
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引用次数: 0

摘要

黄芩苷是从黄芩中提取的一种黄酮类化合物,已被证明具有多种药理活性。本综述旨在总结有关黄芩苷的药理学和药代动力学研究,为相关学者提供有用信息。药理研究表明,黄芩苷具有多种药理特性,包括但不限于抗炎、抗氧化、抗病毒、神经保护、降血糖、降血脂、抗癌和心血管保护作用。进一步研究发现,黄芩苷的药理作用由多种机制驱动。这些机制包括清除自由基、抑制炎症信号通路的激活和炎症介质的表达、抑制关键病毒蛋白的活性、抑制葡萄糖生成、改善胰岛素抵抗、改善脑缺血再灌注损伤、诱导癌细胞凋亡以及防止心肌肥大等。总之,这些药理研究表明,黄芩苷有望治疗各种疾病。当务之急是开展临床研究,进一步阐明黄芩苷的治疗效果。不过,值得注意的是,药代动力学研究显示,黄芩苷对尿苷-5'-二磷酸葡萄糖醛酸转移酶和细胞色素 P450 酶有抑制作用,可能会带来安全风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Review on the pharmacological effects and pharmacokinetics of scutellarein

Review on the pharmacological effects and pharmacokinetics of scutellarein

Review on the pharmacological effects and pharmacokinetics of scutellarein

Scutellarein is a flavonoid from Scutellaria baicalensis Georgi that has been shown to have a variety of pharmacological activities. This review aims to summarize the pharmacological and pharmacokinetic studies on scutellarein and provide useful information for relevant scholars. Pharmacological studies indicate that scutellarein possesses a diverse range of pharmacological properties, including but not limited to anti-inflammatory, antioxidant, antiviral, neuroprotective, hypoglycemic, hypolipidemic, anticancer, and cardiovascular protective effects. Further investigation reveals that the pharmacological effects of scutellarein are driven by multiple mechanisms. These mechanisms encompass the scavenging of free radicals, inhibition of the activation of inflammatory signaling pathways and expression of inflammatory mediators, inhibition of the activity of crucial viral proteins, suppression of gluconeogenesis, amelioration of insulin resistance, improvement of cerebral ischemia-reperfusion injury, induction of apoptosis in cancer cells, and prevention of myocardial hypertrophy, among others. In summary, these pharmacological studies suggest that scutellarein holds promise for the treatment of various diseases. It is imperative to conduct clinical studies to further elucidate the therapeutic effects of scutellarein. However, it is worth noting that studies on the pharmacokinetics reveal an inhibitory effect of scutellarein on uridine 5′-diphosphate glucuronide transferases and cytochrome P450 enzymes, potentially posing safety risks.

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来源期刊
Archiv der Pharmazie
Archiv der Pharmazie 医学-化学综合
CiteScore
7.90
自引率
5.90%
发文量
176
审稿时长
3.0 months
期刊介绍: Archiv der Pharmazie - Chemistry in Life Sciences is an international journal devoted to research and development in all fields of pharmaceutical and medicinal chemistry. Emphasis is put on papers combining synthetic organic chemistry, structural biology, molecular modelling, bioorganic chemistry, natural products chemistry, biochemistry or analytical methods with pharmaceutical or medicinal aspects such as biological activity. The focus of this journal is put on original research papers, but other scientifically valuable contributions (e.g. reviews, minireviews, highlights, symposia contributions, discussions, and essays) are also welcome.
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