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Pharmacokinetics-based identification of pseudoaldosterogenic compounds originating from Glycyrrhiza uralensis roots (Gancao) after dosing LianhuaQingwen capsule.
- Source :
-
Acta pharmacologica Sinica [Acta Pharmacol Sin] 2021 Dec; Vol. 42 (12), pp. 2155-2172. Date of Electronic Publication: 2021 Apr 30. - Publication Year :
- 2021
-
Abstract
- LianhuaQingwen capsule, prepared from an herbal combination, is officially recommended as treatment for COVID-19 in China. Of the serial pharmacokinetic investigations we designed to facilitate identifying LianhuaQingwen compounds that are likely to be therapeutically important, the current investigation focused on the component Glycyrrhiza uralensis roots (Gancao). Besides its function in COVID-19 treatment, Gancao is able to induce pseudoaldosteronism by inhibiting renal 11β-HSD2. Systemic and colon-luminal exposure to Gancao compounds were characterized in volunteers receiving LianhuaQingwen and by in vitro metabolism studies. Access of Gancao compounds to 11β-HSD2 was characterized using human/rat, in vitro transport, and plasma protein binding studies, while 11β-HSD2 inhibition was assessed using human kidney microsomes. LianhuaQingwen contained a total of 41 Gancao constituents (0.01-8.56 μmol/day). Although glycyrrhizin (1), licorice saponin G2 (2), and liquiritin/liquiritin apioside (21/22) were the major Gancao constituents in LianhuaQingwen, their poor intestinal absorption and access to colonic microbiota resulted in significant levels of their respective deglycosylated metabolites glycyrrhetic acid (8), 24-hydroxyglycyrrhetic acid (M2 <subscript>D</subscript> ; a new Gancao metabolite), and liquiritigenin (27) in human plasma and feces after dosing. These circulating metabolites were glucuronized/sulfated in the liver and then excreted into bile. Hepatic oxidation of 8 also yielded M2 <subscript>D</subscript> . Circulating 8 and M2 <subscript>D</subscript> , having good membrane permeability, could access (via passive tubular reabsorption) and inhibit renal 11β-HSD2. Collectively, 1 and 2 were metabolically activated to the pseudoaldosterogenic compounds 8 and M2 <subscript>D</subscript> . This investigation, together with such investigations of other components, has implications for precisely defining therapeutic benefit of LianhuaQingwen and conditions for its safe use.<br /> (© 2021. The Author(s), under exclusive licence to CPS and SIMM.)
- Subjects :
- 11-beta-Hydroxysteroid Dehydrogenase Type 2 antagonists & inhibitors
11-beta-Hydroxysteroid Dehydrogenase Type 2 metabolism
Administration, Oral
Animals
Antiviral Agents administration & dosage
Antiviral Agents adverse effects
Biological Availability
Biotransformation
Capsules
Drugs, Chinese Herbal administration & dosage
Drugs, Chinese Herbal adverse effects
Female
Glycyrrhiza adverse effects
HEK293 Cells
Humans
Liddle Syndrome chemically induced
Liddle Syndrome enzymology
Male
Patient Safety
Phytochemicals administration & dosage
Phytochemicals adverse effects
Rats, Sprague-Dawley
Risk Assessment
Rats
Antiviral Agents pharmacokinetics
Drugs, Chinese Herbal pharmacokinetics
Phytochemicals pharmacokinetics
COVID-19 Drug Treatment
Subjects
Details
- Language :
- English
- ISSN :
- 1745-7254
- Volume :
- 42
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Acta pharmacologica Sinica
- Publication Type :
- Academic Journal
- Accession number :
- 33931765
- Full Text :
- https://doi.org/10.1038/s41401-021-00651-2