Corosolic acid and its structural analogs: A systematic review of their biological activities and underlying mechanism of action

熊果酸 白桦酸 齐墩果酸 化学 萜烯 药理学 立体化学 生物化学 传统医学 医学 生物 色谱法 遗传学 病理 替代医学
作者
Xu‐Ping Qian,Xuehui Zhang,Luning Sun,Wei-Fan Xing,Yu Wang,Shiyu Sun,Mengyuan Ma,Ziping Cheng,Zu-Dong Wu,Xing Chen,Beining Chen,Yongqing Wang
出处
期刊:Phytomedicine [Elsevier BV]
卷期号:91: 153696-153696 被引量:42
标识
DOI:10.1016/j.phymed.2021.153696
摘要

The corosolic acid (CA), also known as plant insulin, is a pentacyclic triterpenoid extracted from plants such as Lagerstroemia speciosa. It has been shown to have anti-diabetic, anti-inflammatory and anti-tumor effects. Its structural analogs ursolic acid (UA), oleanolic acid (OA), maslinic acid (MA), asiatic acid (AA) and betulinic acid (BA) display similar individual pharmacological activities to those of CA. However, there is no systematic review documenting pharmacological activities of CA and its structural analogues. This study aims to fill this gap in literature. This systematic review aims to summarize the medical applications of CA and its analogues. A systematic review summarizes and compares the extraction techniques, pharmacokinetic parameters, and pharmacological effects of CA and its structural analogs. Hypoglycemic effect is one of the key inclusion criteria for searching Web of Science, PubMed, Embase and Cochrane databases up to October 2020 without language restrictions. 'corosolic acid', 'ursolic acid', 'oleanolic acid', 'maslinic acid', 'asiatic acid', 'betulinic acid', 'extraction', 'pharmacokinetic', 'pharmacological' were used to extract relevant literature. The PRISMA guidelines were followed. At the end of the searching process, 140 articles were selected for the systematic review. Information of CA and five of its structural analogs including UA, OA, MA, AA and BA were included in this review. CA and its structural analogs are pentacyclic triterpenes extracted from plants and they have low solubilities in water due to their rigid scaffold and hydrophobic properties. The introduction of water-soluble groups such as sugar or amino groups could increase the solubility of CA and its structural analogs. Their biological activities and underlying mechanism of action are reviewed and compared. CA and its structural analogs UA, OA, MA, AA and BA are demonstrated to show activities in lowering blood sugar, anti-inflammation and anti-tumor. Their oral absorption and bioavailability can be improved through structural modification and formulation design. CA and its structural analogs are promising natural product-based lead compounds for further development and mechanistic studies.
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