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Cyclosporin A Affects the Bioavailability of Ginkgolic Acids via Inhibition of P-gp and BCRP

Cyclosporin A Affects the Bioavailability of Ginkgolic Acids via Inhibition of P-gp and BCRP

Li Li, Qing-Qing Yao, Si-Yun Xu, Hai-Hong Hu, Qi Shen, Ye Tian, Lan-Ying Pan, Hui Zhou, Hui-di Jiang, Chuang Lu, Lu-Shan Yu, Su Zeng

Eur J Pharm Biopharm. 2014 Nov;88(3):759-67.

PMID: 24980806

Abstract:

Ginkgolic acids (GAs) in natural product Ginkgobiloba L. are the pharmacological active but also toxic components. Two compounds, GA (C15:1) and GA (C17:1) are the most abundant GAs. In this study, several in vitro and in vivo models were applied to investigate transport mechanism of GAs. A rapid and sensitive LC-MS/MS method for the simultaneous determination of GA (C15:1) and GA (C17:1) was applied to analyze the biological specimens. The Papp(AP→BL) values of GA (C15:1) and GA (C17:1) were 1.66-2.13×10(-)(6)cm/s and 1.34-1.85×10(-)(6)cm/s determined using MDCK and MDCK-MDR1 cell monolayers, respectively. The Papp(BL→AP) were remarkably greater in the MDCK-MDR1 cell line, which were 6.77-11.2×10(-)(6)cm/s for GA (C15:1) and 4.73-5.15×10(-)(6)cm/s for GA (C17:1). Similar results were obtained in LLC-PK1 and LLC-PK1-BCRP cell monolayers. The net efflux ratio of GA (C15:1) and GA (C17:1) in both cell models was greater than 2 and markedly reduced by the presence of Cyclosporin A (CsA) or GF120918, inhibitors of P-gp and BCRP, suggesting that GAs are P-gp and BCRP substrates. The results from a rat bioavailability study also showed that co-administrating CsA intravenously (20mg/kg) could significantly increase GA (C15:1) and GA (C17:1) AUC0-t by 1.46-fold and 1.53-fold and brain concentration levels of 1.43-fold and 1.51-fold, respectively, due to the inhibition of P-gp and BCRP efflux transporters by CsA.

Chemicals Related in the Paper:

Catalog Number	Product Name	Structure	CAS Number	Price
AP111047304	Ginkgolic acid C17:1		111047-30-4	Price

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