β-Escin: An Updated Review of Its Analysis, Pharmacology, Pharmacokinetics, and Toxicity.

The American journal of Chinese medicine Pub Date : 2023-01-01 Epub Date: 2023-10-20 DOI:10.1142/S0192415X23500908
Yunyu Wang, Xiuwei Han, Xinhuan Wan, Fengjv Niu, Changzheng Zhou
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Abstract

[Formula: see text]-Escin is an oleanane-type pentacyclic triterpenoid saponin extracted from the seeds of Aesculus hippocastanum (AH), which is more widely distributed. [Formula: see text]-Escin sodium has been approved by the American FDA for clinical usage. This paper is intended to summarize an updated and comprehensive review of the pharmacological activities, pharmacokinetic properties, toxicity, and analytical methods of [Formula: see text]-escin. Studies have shown that [Formula: see text]-escin has significant antitumor, antiviral, anti-inflammatory, and other activities alongside less adverse effects and higher safety than other compounds. The review shows that the pharmacological effects of [Formula: see text]-escin involve mechanisms such as ATM/[Formula: see text]H2AX, RhoA/Rock, GSK-3[Formula: see text]/[Formula: see text]-Catenin, HER2/HER3/Akt, and PI3K/Akt signaling pathways, and Cyclin A, p21[Formula: see text], survivin, Bcl-2, Mcl-1, Caspases, TGF-[Formula: see text], MMPs, and TNF-[Formula: see text] among other inflammatory factors. [Formula: see text]-Escin has significant cytotoxicity; the use of the chitosan/xanthan gum-based polyelectrolyte complexes PA1 and PC-11 to modify it not only to reduces its toxicity, but also improves its drug efficacy. Because of this, these compounds may become a new research hotspot. [Formula: see text]-Escin in vivo metabolism can be converted by the CYP1A2 enzyme in the intestinal flora to produce [Formula: see text]-escin, deacylated, deglycosylated, and 21[Formula: see text]-[Formula: see text]-crotonoyl-protoescin, and the binding rate of the plasma proteins is higher than 90%. These are mainly metabolized by the liver, kidneys, and other organs, and excreted in the form of urine and feces. The number of reports on the specific mediators of the metabolism of [Formula: see text]-escin and their mechanisms and metabolites is relatively small; furthermore, the results are vague. Therefore, a complete and in-depth exploration of the pharmacokinetic characteristics of [Formula: see text]-escin is needed to provide a more complete and effective theoretical reference for the study of its pharmacodynamic activity.

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β-Escin:其分析、药理学、药代动力学和毒性的最新综述。
【配方:见正文】-七叶皂苷是从七叶树(AH)种子中提取的一种齐墩果烷型五环三萜皂苷,分布较为广泛。【配方:见正文】-Escin钠已被美国食品药品监督管理局批准用于临床。本文旨在对[配方:见正文]-七叶皂苷的药理活性、药代动力学特性、毒性和分析方法进行更新和全面的综述。研究表明,[配方:见正文]-七叶皂苷具有显著的抗肿瘤、抗病毒、抗炎和其他活性,与其他化合物相比,副作用更小,安全性更高。综述表明,[配方:见正文]-七叶皂苷的药理作用涉及ATM/[配方:参见正文]H2AX、RhoA/Rock、GSK-3[配方:见图正文]/[配方:详见正文]-儿茶素、HER2/HER3/Akt和PI3K/Akt信号通路,以及细胞周期蛋白A、p21[配方:参阅正文]、生存素、Bcl-2、Mcl-1、半胱氨酸蛋白酶、TGF-,和TNF-【公式:见正文】以及其他炎症因子。【配方:见正文】-Escin具有显著的细胞毒性;使用壳聚糖/黄原胶基聚电解质复合物PA1和PC-11对其进行修饰,不仅降低了其毒性,而且提高了其药效。正因为如此,这些化合物可能成为新的研究热点。【公式:见正文】-肠菌群中的CYP1A2酶可将Escin体内代谢转化为【公式:参见正文】-七叶皂苷、脱乙酰化、去糖基化和21【公式:详见正文】-【公式:请见正文】-巴豆酰基原七叶皂苷,血浆蛋白结合率高于90%。这些主要通过肝脏、肾脏和其他器官代谢,并以尿液和粪便的形式排出。关于【配方:见正文】-七叶皂苷代谢的特定介质及其机制和代谢产物的报道数量相对较少;此外,结果还很模糊。因此,需要对【配方:见正文】-七叶皂苷的药代动力学特征进行全面深入的探索,为其药效学活性的研究提供更完整有效的理论参考。
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