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Inhibition of carrier‐mediated uptake of epirubicin reduces cytotoxicity in primary culture of rat hepatocytes
Author(s) -
Iwakiri Tomomi,
Okumura Manabu,
Hidaka Muneaki,
Kumagai Yuki,
Ichihara Emi,
Kawano Yohei,
Arimori Kazuhiko
Publication year - 2008
Publication title -
journal of applied toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.784
H-Index - 87
eISSN - 1099-1263
pISSN - 0260-437X
DOI - 10.1002/jat.1283
Subject(s) - epirubicin , chemistry , tetraethylammonium , organic cation transport proteins , sodium azide , pharmacology , dids , biochemistry , verapamil , transporter , medicine , biology , chemotherapy , calcium , potassium , organic chemistry , membrane , gene , cyclophosphamide
Epirubicin, an antineoplastic drug, is considered to be taken up by tumor cells via a common carrier by facilitated diffusion and is then pumped out in an energy‐dependent manner because epirubicin is a substrate for P‐glycoprotein (P‐gp). However, this study investigated the details of the influx mechanism of epirubicin and demonstrated that epirubicin uptake was mediated by active carrier systems in addition to facilitated diffusion in the primary culture of rat hepatocytes. The uptake of epirubicin gradually increased in a saturated manner when the concentrations were between 1 × 10 −7 m and 1 × 10 −6 m . In contrast, the uptake increased progressively in a linear manner when the concentration was high (greater than 1 × 10 −6 m ). The uptake of epirubicin at a clinical concentration (7.5 × 10 −7 m ) was significantly reduced at 4 °C and significantly inhibited when pretreated with metabolic inhibitors (carbonyl cyanide p‐trifluoromethoxyphenylhydrazone (FCCP), rotenone and sodium azide) by nearly 25%. Furthermore, an organic anion transporter inhibitor, namely, 4,4′‐diisothiocyanato‐stilbene‐2,2′‐disulfonic acid (DIDS); organic anion transport substrates, namely, para‐aminohippurate (PAH), taurocholic acid and estradiol 17‐ β ‐ d ‐glucuronide; and organic cation transporter inhibitors, namely, verapamil and tetraethylammonium significantly reduced the uptake of epirubicin. Furthermore, pretreatment with verapamil and PAH significantly prevented epirubicin‐induced reduction of proliferative activity in rat hepatocytes. These results indicated that the uptake of epirubicin was induced, at least in part, by the active transport protein in rat hepatocytes; the inhibition of the probable transport protein protected the intact normal cells from the injury induced by the cytotoxicity of epirubicin. Copyright © 2007 John Wiley & Sons, Ltd.