SLC22A1 transports Cipro into hepatic cell

Stable Identifier
R-HSA-9795207
Type
Reaction [transition]
Species
Homo sapiens
Compartment
ReviewStatus
5/5
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General
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Facilitated transport of Cipro through the basolateral parts of the hepatocyte membrane is the most probable mechanism by which Cipro enters hepatic cells (reviewed by Jetter & Kullak-Ublick, 2019). Transport of drugs by solute carrier family 22 member 1 (SLC22A1, OCT1), highly expressed in liver, is inhibited by most fluoroquinolones including Cipro (Mulgaonkar et al, 2013). Direct binding of Cipro to SLC22A1 or its role as substrate has not been shown, however.
Literature References
PubMed ID Title Journal Year
23545524 Human organic cation transporters 1 (SLC22A1), 2 (SLC22A2), and 3 (SLC22A3) as disposition pathways for fluoroquinolone antimicrobials

Mulgaonkar, A, Venitz, J, GrĂ¼ndemann, D, Sweet, DH

Antimicrob Agents Chemother 2013
31004787 Drugs and hepatic transporters: A review

Jetter, A, Kullak-Ublick, GA

Pharmacol Res 2020
Participants
Participates
Catalyst Activity

transmembrane transporter activity of SLC22A1 [basolateral plasma membrane]

Orthologous Events
Authored
Reviewed
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