نتایج جستجو برای: oct1

تعداد نتایج: 439  

Journal: :Diabetes 2008
Iouri Bachmakov Hartmut Glaeser Martin F Fromm Jörg König

OBJECTIVE The uptake of drugs into hepatocytes is a key determinant for hepatic metabolism, intrahepatic action, their subsequent systemic plasma concentrations, and extrahepatic actions. In vitro and in vivo studies indicate that many drugs used for treatment of cardiovascular diseases (e.g., oral antidiabetic drugs, statins) are taken up into hepatocytes by distinct organic anion transporters...

Journal: :Molecular cancer therapeutics 2011
Tsuyoshi Minematsu Kathleen M Giacomini

The drug-drug interaction (DDI) potential of tyrosine kinase inhibitors (TKI) as interacting drugs via transporter inhibition has not been fully assessed. Here, we estimated the half maximal inhibitory concentration (IC(50)) values for 8 small-molecule TKIs (imatinib, dasatinib, nilotinib, gefitinib, erlotinib, sunitinib, lapatinib, and sorafenib) on [(14)C]metformin transport by human organic ...

2016
Xiao He Denisse Garza Sanjay K. Nigam Geoffrey Chang

Organic cation transporter 1 (OCT1, SLC22A1), like many solute carrier 22 (SLC22) family members, is important for the disposition of clinically important drugs, metabolites and signaling molecules. Several studies suggest that SLC22 family (eg. organic anion transporters or OATs and OCTs) bind and possibly transport prostaglandins with relatively high affinity (submicromolar). The affinities o...

2015
Dan C. Li Darian Wigfall Simonne Francis

5 GENERAL INTRODUCTION 7 MATERIALS AND METHODS 13 PART I: POLYAMINE TRANSPORT BY POLYSPECIFIC OCT1, OCT2, AND OCT3

Journal: :American journal of physiology. Renal physiology 2009
Wing-Kee Lee Markus Reichold Bayram Edemir Giuliano Ciarimboli Richard Warth Hermann Koepsell Frank Thévenod

The positively charged fluorescent dyes ethidium (Et(+)) and propidium (Pr(2+)) are widely used as DNA and necrosis markers. Et(+) is cytotoxic and mutagenic. The polyspecific organic cation transporters OCT1 (SLC22A1), OCT2 (SLC22A2), and OCT3 (SLC22A3) mediate electrogenic facilitated diffusion of small (< or =500 Da) organic cations with broad specificities. In humans, OCT2 mediates basolate...

2017
Gayathri N Sekhar Ana R Georgian Lisa Sanderson Gema Vizcay-Barrena Rachel C Brown Paula Muresan Roland A Fleck Sarah A Thomas

Pentamidine is an effective trypanocidal drug used against stage 1 Human African Trypanosomiasis (HAT). At the blood-brain barrier (BBB), it accumulates inside the endothelial cells but has limited entry into the brain. This study examined transporters involved in pentamidine transport at the human and mouse BBB using hCMEC/D3 and bEnd.3 cell lines, respectively. Results revealed that both cell...

Journal: :International journal of oncology 2013
Anja Lautem Michael Heise Andreas Gräsel Maria Hoppe-Lotichius Nina Weiler Daniel Foltys Johanna Knapstein Jörn M Schattenberg Arno Schad Anca Zimmermann Gerd Otto Hauke Lang Peter R Galle Marcus Schuchmann Tim Zimmermann

Cholangiocellular carcinoma (CCA) is a primary hepatic malignancy derived from cholangiocytes. The prognosis for CCA patients is very poor and conventional chemotherapy has been proven ineffective in improving long‑term patient survival rates. Organic cation transporters (OCTs) mediate the transport of a broad spectrum of endogenous substrates and the detoxification of xenobiotics. Moreover, OC...

Journal: :Human molecular genetics 1999
S S Branda Z Y Yang A Chew G Isaya

Friedreich's ataxia (FRDA) is a neurodegenerative disease typically caused by a deficiency of frataxin, a mitochondrial protein of unknown function. In Saccharomyces cerevisiae, lack of the yeast frataxin homolog ( YFH1 gene, Yfh1p polypeptide) results in mitochondrial iron accumulation, suggesting that frataxin is required for mitochondrial iron homeostasis and that FRDA results from oxidative...

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