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Impact of Gut Microbiota on the Pharmacokinetics of Glycyrrhizic Acid in Yokukansan, a Kampo Medicine

Tomoaki IshidaDepartment of Pharmacy, Kochi Medical School HospitalKohei JobuDepartment of Pharmacy, Kochi Medical School HospitalKei KawadaDepartment of Pharmacy, Kochi Medical School HospitalShumpei MorisawaDepartment of Pharmacy, Kochi Medical School HospitalTetsushi KawazoeDepartment of Pharmacy, Kochi Medical School HospitalHisashi ShiraishiDepartment of Pharmacy, Kochi Medical School HospitalHiroko FujitaDepartment of Pharmacy, Kochi Medical School HospitalSatomi NishimuraDepartment of Pharmacy, Kochi Medical School HospitalHitomi KannoTsumura Advanced Technology Research Laboratories, Tsumura & CoMitsue NishiyamaTsumura Advanced Technology Research Laboratories, Tsumura & CoKazuo OgawaTsumura Advanced Technology Research Laboratories, Tsumura & CoYasuyo MoritaDepartment of Pharmacy, Kochi Medical School HospitalKazuhiro HanazakiDepartment of Surgery, Kochi Medical School HospitalMitsuhiko MiyamuraDepartment of Pharmacy, Kochi Medical School Hospital
2021en
ABI

Аннотация

Individual differences in gut microbiota can affect the pharmacokinetics of drugs. Yokukansan is a traditional Japanese kampo medicine used to treat peripheral symptoms of dementia and delirium. A study examining the pharmacokinetics of the components of yokukansan reported large individual differences in the pharmacokinetics of glycyrrhizic acid (GL). It is known that GL is metabolized by intestinal bacteria to glycyrrhetinic acid (GA), which is absorbed in the gastrointestinal tract. Thus, the gut microbiota may affect GL pharmacokinetics. We aimed to clarify the relationship between the gut microbiota composition and pharmacokinetics of GL in yokukansan. Mice were orally administered yokukansan, following the administration of various antibiotics, and the plasma concentration of GA and composition of gut microbiota were measured. The GA plasma concentration was low in mice treated with amoxicillin and vancomycin. The composition of gut microbiota revealed a different pattern from that of the control group. Mice with low plasma levels of GA had lower levels of the phylum Bacteroides and Firmicutes. Additionally, bacteria, such as those belonging to the genera Parabaceroides, Bacteroides, Ruminococcus and an unknown genus in families Lachnospiraceae and Ruminococcaceae, exerted positive correlations between the gene copies and plasma GA levels. These bacteria may contribute to the absorption of GA in the gastrointestinal tract, and multiple bacteria may be involved in GL pharmacokinetics. The pharmacokinetics of GL may be predicted by evaluating the composition of gut bacteria, rather than by evaluating the amount of a single bacterium.

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