ABCB1 c.2677G>T/c.3435C>T diplotype increases the early-phase oral absorption of losartan
Losartan has been shown to be a substrate of the drug-efflux transporter MDR1, encoded by the ABCB1 gene. ABCB1 c.2677G>T and c.3435C>T variants are known to be associated with reduced expression and function of P-glycoprotein (P-gp). We investigated the effects of ABCB1 diplotype on the pharm...
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Veröffentlicht in: | Archives of pharmacal research 2020, 43(11), , pp.1187-1196 |
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Sprache: | eng |
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Zusammenfassung: | Losartan has been shown to be a substrate of the drug-efflux transporter MDR1, encoded by the
ABCB1
gene.
ABCB1
c.2677G>T and c.3435C>T variants are known to be associated with reduced expression and function of P-glycoprotein (P-gp). We investigated the effects of
ABCB1
diplotype on the pharmacokinetics of losartan. Thirty-eight healthy Korean volunteers with different
ABCB1
diplotypes [c.2677G> T and c.3435C>T; carriers of GG/CC (n = 13), GT/CT (n = 12) and TT/TT (n = 13) diplotype] were recruited and administered a single 50 mg oral dose of losartan potassium. Losartan and its active metabolite E-3174 samples in plasma and urine were collected up to 10 and 8 h after drug administration, respectively, and the concentrations of both samples were determined by HPLC method. Significant differences were observed in
C
max
of losartan and losartan plus E-3174 (Lo + E) among the three diplotype groups (both
P
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ISSN: | 0253-6269 1976-3786 |
DOI: | 10.1007/s12272-020-01294-3 |