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- W4386002854 abstract "Phalloidin, a bicyclic heptapeptide found in Amanita mushroom, specifically binds to F-actin in the liver causing cholestatic hepatotoxicity. However, the toxicokinetics and tissue distribution properties of phalloidin as well as their underlying mechanisms have to be studied further. The area under the plasma concentration curve (AUC) of phalloidin increased in proportion to the doses (0.2, 0.4, and 0.8 mg/kg for intravenous injection and 2, 5, and 10 mg/kg for oral administration). Phalloidin exhibited dose-independent low volume of distribution (395.6–456.9 mL/kg) and clearance (21.4–25.5 mL/min/kg) and low oral bioavailability (2.4%–3.3%). This could be supported with its low absorptive permeability (0.23 ± 0.05 × 10−6 cm/s) in Caco-2 cells. The tissue-to-plasma AUC ratios of intravenously injected and orally administered phalloidin were the highest in the liver and intestines, respectively, and also high in the kidneys, suggesting that the liver, kidneys, and intestines could be susceptible to phalloidin exposure and that active transport via the hepatic and renal organic anion transporters (OATP1B1, OATP1B3, and OAT3) may contribute to the higher distribution of phalloidin in the liver and kidneys." @default.
- W4386002854 created "2023-08-20" @default.
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- W4386002854 date "2023-09-01" @default.
- W4386002854 modified "2023-10-17" @default.
- W4386002854 title "Toxicokinetics and tissue distribution of phalloidin in mice" @default.
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- W4386002854 doi "https://doi.org/10.1016/j.fct.2023.113994" @default.
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