Assessment of Herb-Drug Interaction Potential of Five Common Species of Licorice and Their Phytochemical Constituents.

IF 1.9 Q3 NUTRITION & DIETETICS
Journal of Dietary Supplements Pub Date : 2023-01-01 Epub Date: 2022-03-18 DOI:10.1080/19390211.2022.2050875
Mona H Haron, Bharathi Avula, Zulfiqar Ali, Amar G Chittiboyina, Ikhlas A Khan, Jing Li, Vivian Wang, Charles Wu, Shabana I Khan
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引用次数: 0

Abstract

The dried roots and rhizomes of Glycyrrhiza species (G. glabra, G. uralensis and G. inflata), commonly known as licorice, have long been used in traditional medicine. In addition, two other species, G. echinata and G. lepidota are also considered "licorice" in select markets. Currently, licorice is an integral part of several botanical drugs and dietary supplements. To probe the botanicals' safety, herb-drug interaction potential of the hydroethanolic extracts of five Glycyrrhiza species and their key constituents was investigated by determining their effects on pregnane X receptor, aryl hydrocarbon receptor, two major cytochrome P450 isoforms (CYP3A4 and CYP1A2), and the metabolic clearance of antiviral drugs. All extracts enhanced transcriptional activity of PXR and AhR (>2-fold) and increased the enzyme activity of CYP3A4 and CYP1A2. The highest increase in CYP3A4 was seen with G. echinata (4-fold), and the highest increase in CYP1A2 was seen with G. uralensis (18-fold) and G. inflata (16-fold). Among the constituents, glabridin, licoisoflavone A, glyasperin C, and glycycoumarin activated PXR and AhR, glabridin being the most effective (6- and 27-fold increase, respectively). Licoisoflavone A, glyasperin C, and glycycoumarin increased CYP3A4 activity while glabridin, glyasperin C, glycycoumarin, and formononetin increased CYP1A2 activity (>2-fold). The metabolism of antiretroviral drugs (rilpivirine and dolutegravir) was increased by G. uralensis (2.0 and 2.5-fold) and its marker compound glycycoumarin (2.3 and 1.6-fold). The metabolism of dolutegravir was also increased by G. glabra (2.8-fold) but not by its marker compound, glabridin. These results suggest that licorice and its phytochemicals could affect the metabolism and clearance of certain drugs that are substrates of CYP3A4 and CYP1A2.Supplemental data for this article is available online at https://doi.org/10.1080/19390211.2022.2050875 .

五种常见甘草及其植物化学成分的草药-药物相互作用潜力评估
甘草品种(Glycyrrhiza species)(G. glabra、G. uralensis 和 G. inflata)的干燥根茎和根状茎俗称甘草,长期以来一直被用于传统医药中。此外,另外两个品种,即 G. echinata 和 G. lepidota,在某些市场上也被视为 "甘草"。目前,甘草是多种植物药和膳食补充剂的组成部分。为了探究植物药的安全性,我们研究了五种甘草及其主要成分的水乙醇提取物的草药-药物相互作用潜力,确定了它们对孕烷 X 受体、芳香烃受体、两种主要细胞色素 P450 同工酶(CYP3A4 和 CYP1A2)以及抗病毒药物代谢清除率的影响。所有提取物都增强了 PXR 和 AhR 的转录活性(大于 2 倍),并提高了 CYP3A4 和 CYP1A2 的酶活性。G. uralensis(18 倍)和 G. inflata(16 倍)对 CYP3A4 的增幅最大。在这些成分中,苁蓉黄素、甘草异黄酮 A、甘草黄素 C 和甘草香豆素能激活 PXR 和 AhR,其中苁蓉黄素的效果最好(分别增加了 6 倍和 27 倍)。甘草异黄酮 A、甘草甜素 C 和甘草香豆素提高了 CYP3A4 活性,而苁蓉黄素、甘草甜素 C、甘草香豆素和福莫尼定提高了 CYP1A2 活性(>2 倍)。G. uralensis(2.0 倍和 2.5 倍)及其标记化合物甘氨酰香豆素(2.3 倍和 1.6 倍)增加了抗逆转录病毒药物(利匹韦林和多罗特拉韦)的代谢。甘草对多罗替拉韦的代谢也有促进作用(2.8 倍),但其标记化合物甘草次苷却没有促进作用。这些结果表明,甘草及其植物化学物质可能会影响作为 CYP3A4 和 CYP1A2 底物的某些药物的代谢和清除。本文的补充数据可在 https://doi.org/10.1080/19390211.2022.2050875 上在线获取。
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来源期刊
Journal of Dietary Supplements
Journal of Dietary Supplements Agricultural and Biological Sciences-Food Science
CiteScore
6.10
自引率
0.00%
发文量
34
期刊介绍: The Journal of Dietary Supplements (formerly the Journal of Nutraceuticals, Functional & Medical Foods) has been retitled to reflect the bold departure from a traditional scientific journal presentation to a leading voice for anyone with a stake in dietary supplements. The journal addresses important issues that meet the broad range of interests from researchers, regulators, marketers, educators, and health professionals from academic, governmental, industry, healthcare, public health, and consumer education sectors. This vital tool not only presents scientific information but interprets it - helping you more readily pass it on to your students, patients, clients, or company.
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