Therapeutic Potentials of Aconite-like Alkaloids: Bioinformatics and Experimental Approaches.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Catalina Mares, Ana-Maria Udrea, Catalin Buiu, Angela Staicu, Speranta Avram
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Abstract

Compounds from plants that are used in traditional medicine may have medicinal properties. It is well known that plants belonging to the genus Aconitum are highly poisonous. Utilizing substances derived from Aconitum sp. has been linked to negative effects. In addition to their toxicity, the natural substances derived from Aconitum species may have a range of biological effects on humans, such as analgesic, anti-inflammatory, and anti-cancer characteristics. Multiple in silico, in vitro, and in vivo studies have demonstrated the effectiveness of their therapeutic effects. In this review, the clinical effects of natural compounds extracted from Aconitum sp., focusing on aconitelike alkaloids, are investigated particularly by bioinformatics tools, such as the quantitative structure- activity relationship method, molecular docking, and predicted pharmacokinetic and pharmacodynamic profiles. The experimental and bioinformatics aspects of aconitine's pharmacogenomic profile are discussed. Our review could help shed light on the molecular mechanisms of Aconitum sp. compounds. The effects of several aconite-like alkaloids, such as aconitine, methyllycacintine, or hypaconitine, on specific molecular targets, including voltage-gated sodium channels, CAMK2A and CAMK2G during anesthesia, or BCL2, BCL-XP, and PARP-1 receptors during cancer therapy, are evaluated. According to the reviewed literature, aconite and aconite derivatives have a high affinity for the PARP-1 receptor. The toxicity estimations for aconitine indicate hepatotoxicity and hERG II inhibitor activity; however, this compound is not predicted to be AMES toxic or an hERG I inhibitor. The efficacy of aconitine and its derivatives in treating many illnesses has been proven experimentally. Toxicity occurs as a result of the high ingested dose; however, the usage of this drug in future research is based on the small quantity of an active compound that fulfills a therapeutic role.

乌头类生物碱的治疗潜力:生物信息学和实验方法。
传统医学中使用的植物化合物可能具有药用价值。众所周知,乌头属植物有剧毒。使用从乌头属植物中提取的物质会产生负面影响。除了毒性之外,从乌头属植物中提取的天然物质还可能对人体产生一系列生物效应,如镇痛、消炎和抗癌等。多项硅学、体外和体内研究都证明了其治疗效果的有效性。在这篇综述中,主要通过生物信息学工具,如定量结构-活性关系法、分子对接、预测药代动力学和药效学特征等,研究了从乌头中提取的天然化合物的临床效果,重点是乌头类生物碱。本文讨论了乌头碱药效基因组学的实验和生物信息学方面。我们的综述有助于阐明乌头类化合物的分子机制。我们评估了几种乌头类生物碱(如乌头碱、甲基乌头碱或次乌头碱)对特定分子靶点的影响,包括麻醉过程中的电压门控钠通道、CAMK2A 和 CAMK2G,或癌症治疗过程中的 BCL2、BCL-XP 和 PARP-1 受体。根据已查阅的文献,乌头和乌头衍生物对 PARP-1 受体具有很高的亲和力。乌头碱的毒性评估表明其具有肝毒性和 hERG II 抑制剂活性;但预计该化合物不具有 AMES 毒性或 hERG I 抑制剂活性。乌头碱及其衍生物治疗多种疾病的疗效已得到实验证明。高剂量摄入会产生毒性;然而,在未来的研究中使用这种药物的基础是少量的活性化合物能够发挥治疗作用。
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
CiteScore
7.20
自引率
4.30%
发文量
567
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