Essential role of constitutive androstane receptor in Ginkgo biloba extract induced liver hypertrophy and hepatocarcinogenesis. (September 2015)

• Record Type: Journal Article
• Authors: Maeda, Jun; Inoue, Kaoru; Ichimura, Ryohei; Takahashi, Miwa; Kodama, Yukio; Saito, Naoaki; Yoshida, Midori
• Is Part Of: Food and chemical toxicology. Volume 83(2015)
• Page Start: 201
• Page End: 209
• Publication Date: 2015-09
• Subjects: Ginkgo biloba extract (GBE) -- Liver hypertrophy -- Hepatocarcinogenesis -- Constitutive androstane receptor (CAR); GBE Ginkgo biloba extract -- CAR Constitutive Androstane Receptor -- WT wild-type -- CARKO CAR knockout; Toxicology -- Periodicals; Food poisoning -- Periodicals; Food Poisoning -- Periodicals; Toxicology -- Periodicals; Toxicologie -- Périodiques; Intoxications alimentaires -- Périodiques; Food poisoning; Toxicology; Periodicals; Electronic journals; 615.9
• DOI: 10.1016/j.fct.2015.06.010
• Languages: English
• ISSNs: 0278-6915

Abstract

Abstract: Ginkgo biloba extract (GBE) is commonly used as a herbal supplement. The National Toxicology Program (NTP) study of GBE reported clear evidence of hepatocarcinogenicity in mice. To clarify the mode of action (MOA) for hepatocarcinogenesis by GBE, we investigated the involvement of the constitutive androstane receptor (CAR) in hepatocarcinogenesis induced by GBE using CAR-knockout (CARKO) and wild type (WT) mice. We used the same lot of GBE that was used for the NTP study. In 1-week GBE dietary treatment, hepatocellular DNA replication was increased in WT mice but not in CARKO mice. In 4- or 13-week treatment, greater hepatic Cyp2b10 induction and hepatocellular hypertrophy were observed in WT mice, whereas these effects of GBE were much smaller in CARKO mice. In a two-stage hepatocarcinogenesis model initiated by diethylnitrosamine, 27-week treatment with GBE resulted in an increase of eosinophilic altered foci and adenomas in WT mice. By contrast, foci and adenomas were clearly less evident in CARKO mice. These results indicate that GBE-induced hepatocarcinogenesis is mainly CAR-mediated. Since CAR-mediated MOA for hepatocarcinogenesis in rodents is considered to be qualitatively implausible for humans, our findings would be helpful to evaluate the carcinogenic characterization of GBE to humans. Highlights: NTP 2-year study: GBE induced hepatocarcinogenesis in mice. We investigated the mode of action for liver tumor by GBE using CAR knockout mice. CAR is mainly involved in liver hypertrophy induced by GBE. CAR plays a major role in the development of proliferative lesions induced by GBE. Hepatocarcinogenesis by GBE in mice is primary CAR-mediated.