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Liquiritigenin, a flavonoid aglycone from licorice, has a choleretic effect and the ability to induce hepatic transporters and phase-II enzymes

Authors
Kim, Young WooKang, Hee EunLee, Myung GullHwang, Se JinKim, Sang ChanLee, Chang HoKim, Sang Geon
Issue Date
Feb-2009
Publisher
AMER PHYSIOLOGICAL SOC
Keywords
choleresis; hepatocellular transporter; glucuronidation
Citation
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, v.296, no.2, pp.G372 - G381
Indexed
SCIE
SCOPUS
Journal Title
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY
Volume
296
Number
2
Start Page
G372
End Page
G381
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/177323
DOI
10.1152/ajpgi.90524.2008
ISSN
0193-1857
Abstract
Kim YW, Kang HE, Lee MG, Hwang SJ, Kim SC, Lee CH, Kim SG. Liquiritigenin, a flavonoid aglycone from licorice, has a choleretic effect and the ability to induce hepatic transporters and phase-II enzymes. Am J Physiol Gastrointest Liver Physiol 296: G372-G381, 2009. First published December 12, 2008; doi:10.1152/ajpgi.90524.2008.-Liquiritigenin (LQ), an active component of licorice, has an inhibitory effect on LPS-induced inhibitory nitric oxide synthase expression. This study investigated the effects of LQ on choleresis, the expression of hepatic transporters and phase-II enzymes, and fulminant hepatitis. The choleretic effect and the pharmacokinetics of LQ and its glucuronides were monitored in rats. After intravenous administration of LQ, the total area under the plasma concentration-time curve of glucuronyl metabolites was greater than that of LQ in plasma, which accompanied elevations in bile flow rate and biliary excretion of bile acid, glutathione, and bilirubin. The expressions of hepatocellular transporters and phase-II enzymes were assessed by immunoblots, real-time PCR, and immunohistochemistry. In the livers of rats treated with LQ, the protein and mRNA levels of multidrug resistance protein 2 and bile salt export pump were increased in the liver, which was verified by their increased localizations in canalicular membrane. In addition, LQ treatment enhanced the expression levels of major hepatic phase-II enzymes. Consistent with these results, LQ treatments attenuated galactosamine/LPS-induced hepatitis in rats, as supported by decreases in the plasma alanine aminotransferase, liver necrosis, and plasma TNF-alpha. These results demonstrate that LQ has a choleretic effect and the ability to induce transporters and phase-II enzymes in the liver, which may be associated with a hepatoprotective effect against galactosamine/LPS. Our findings may provide insight into understanding the action of LQ and its therapeutic use for liver disease.
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