Results 11 to 20 of about 24,839 (187)
Identification of dequalinium as a potent inhibitor of human organic cation transporter 2 by machine learning based QSAR model [PDF]
Human organic cation transporter 2 (hOCT2/SLC22A2) is a key drug transporter that facilitates the transport of endogenous and exogenous organic cations.
Fumihiro Yamane +4 more
doaj +4 more sources
Mechanism of Electrogenic Cation Transport by the Cloned Organic Cation Transporter 2 from Rat [PDF]
The organic cation transporter 2 (OCT2) is expressed in plasma membranes of kidney and brain. Its transport mechanism and substrates are debated. We studied substrate-induced changes of electrical current with the patch clamp technique after expression of rat OCT2 in oocytes.
Budiman, T. +3 more
openaire +4 more sources
Interaction of Cisplatin with the Human Organic Cation Transporter 2 [PDF]
AbstractPurpose: Cisplatin is predominantly eliminated in the urine through active secretion. As the solute carrier organic cation transporter 2 (OCT2) is highly expressed in the basolateral membrane of proximal tubules, we determined its contribution to cisplatin transport and assessed the relation of variation in the gene encoding OCT2 (SLC22A2) with
Filipski, KK +3 more
openaire +5 more sources
Colistin is Substrate of the Carnitine/Organic Cation Transporter 2 (OCTN2, SLC22A5) [PDF]
Colistin is a polycation antibiotic used for the treatment of multidrug-resistance (MDR) gram-negative infections; nevertheless, its use is often limited by the high incidence of renal damage. The mechanism underlying colistin-induced nephrotoxicity is not known, but perhaps related to its accumulation in the renal cortex upon extensive reabsorption ...
Visentin, Michele +4 more
openaire +5 more sources
Contribution of Organic Cation Transporter 2 (OCT2) to Cisplatin-Induced Nephrotoxicity [PDF]
Cisplatin is one of the most widely used anticancer agents for the treatment of solid tumors. The clinical use of cisplatin is associated with dose-limiting nephrotoxicity, which occurs in one-third of patients despite intensive prophylactic measures. Organic cation transporter 2 (OCT2) has been implicated in the cellular uptake of cisplatin, but its ...
Filipski, K K +4 more
openaire +5 more sources
The membrane impermeability of a drug poses a significant challenge in drug research and development, preventing effective drug delivery to the target site.
Toshihiko Tashima
doaj +2 more sources
.: Histamine is inactivated by the histamine-metabolizing enzyme histamine N-methyl-transferase (HNMT) in bronchus, kidney, and the central nervous system.
Ogasawara Masahito +7 more
doaj +2 more sources
Identification of functional amino acid residues involved in polyamine and agmatine transport by human organic cation transporter 2. [PDF]
Polyamine (putrescine, spermidine and spermine) and agmatine uptake by the human organic cation transporter 2 (hOCT2) was studied using HEK293 cells transfected with pCMV6-XL4/hOCT2.
Kyohei Higashi +8 more
doaj +2 more sources
Functional significance of conserved cysteines in the human organic cation transporter 2.
The significance of conserved cysteines in the human organic cation transporter 2 (hOCT2), namely the six cysteines in the long extracellular loop (loop cysteines) and C474 in transmembrane helix 11, was examined. Uptake of tetraethylammonium (TEA) and 1-methyl-4-phenypyridinium (MPP) into Chinese hamster ovary cells was stimulated >20-fold by hOCT2
Pelis RM +5 more
europepmc +4 more sources
Disease-mediated alterations to drug disposition constitute a significant source of adverse drug reactions. Cisplatin (CDDP) elicits nephrotoxicity due to exposure in proximal tubule cells during renal secretion.
Joseph L. Jilek +6 more
doaj +1 more source

