Pharmacodynamic and pharmacokinetic aspects of combined use of glycyrrhizinic acid

V. A. Prikhodko, S. V. Okovityi
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引用次数: 0

Abstract

Glycyrrhizinic acid is a triterpenoid plant-derived compound with potent antisteatotic, anticytolitic, anti-inflammatory, antifibrotic, anticholestatic as well as antiapoptotic, antineoplastic and some other effects. Recent studies have demonstrated glycyrrhizinic acid to form supramolecular self-associates and micelles, which makes it a pharmacokinetic, and, hence, a pharmacodynamic enhancer. Thus, the prospects and possibilities of combined use of glycyrrhizinic acid in liver disease and other pathologies arise due to the pharmacological properties of the molecule itself as well as its function as drug carrier and delivery enhancer. The present review is focused on the pharmacodynamic and pharmacokinetic features of glycyrrhizinic acid combinations with essential phospholipids and ursodeoxycholic acid.
甘草酸联合使用的药效学和药代动力学方面
甘草酸是一种三萜类植物源化合物,具有有效的抗脂肪变性、抗血小板、抗炎、抗纤维化、抗胆固醇、抗细胞凋亡、抗肿瘤等作用。最近的研究表明,甘草酸可以形成超分子自结合物和胶束,这使其成为一种药代动力学,因此是一种药效学增强剂。因此,由于甘草酸分子本身的药理特性以及其作为药物载体和递送增强剂的功能,甘草酸在肝脏疾病和其他病理中联合使用的前景和可能性出现。本文综述了甘草酸与必需磷脂和熊去氧胆酸联合使用的药效学和药动学特点。
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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