Literature DB >> 27964953

Blood-to-retina transport of riboflavin via RFVTs at the inner blood-retinal barrier.

Yoshiyuki Kubo1, Shizuka Yahata2, Satoshi Miki2, Shin-Ichi Akanuma2, Ken-Ichi Hosoya2.   

Abstract

Riboflavin (vitamin B2) supply to the retina across the inner blood-retinal barrier (BRB) was investigated. In rats, the apparent influx permeability clearance of [3H]riboflavin (62.8 μL/(min·g retina)) was much higher than that of a non-permeable paracellular marker, suggesting the facilitative influx transport of riboflavin across the BRB. The retinal uptake index (RUI) of [3H]riboflavin was 59.0%, and significantly reduced by flavin adenine dinucleotide (FAD), but not by l-ascorbic acid, suggesting the substrate specificity of riboflavin transport. TR-iBRB2 cells, an in vitro model of the inner BRB, showed a temperature- and concentration-dependent [3H]riboflavin uptake with a Km of 113 nM, suggesting that the influx transport of riboflavin across the inner BRB involves a carrier-mediated process. [3H]Riboflavin uptake by TR-iBRB2 cells was slightly altered by Na+- and Cl--free buffers, suggesting that riboflavin transport at the inner BRB is preferentially Na+- and Cl--independent. [3H]Riboflavin uptake by TR-iBRB2 cells was significantly reduced by riboflavin analogues while the uptake remained unchanged by other vitamins. The function and inhibition profile suggested the involvement of riboflavin transporters (SLC52A/RFVT) in riboflavin transport at the inner BRB, and this is supported by expression and knockdown analysis of rRFVT2 (Slc52a2) and rRFVT3 (Slc52a3) in TR-iBRB2 cells.
Copyright © 2016. Published by Elsevier Ltd.

Entities:  

Keywords:  Inner blood-retinal barrier; RFVT; Riboflavin; Riboflavin transporter; Vitamin B(2)

Mesh:

Substances:

Year:  2016        PMID: 27964953     DOI: 10.1016/j.dmpk.2016.09.006

Source DB:  PubMed          Journal:  Drug Metab Pharmacokinet        ISSN: 1347-4367            Impact factor:   3.614


  7 in total

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6.  Elimination of a Retinal Riboflavin Binding Protein Exacerbates Degeneration in a Model of Cone-Rod Dystrophy.

Authors:  Ayse M Genc; Mustafa S Makia; Tirthankar Sinha; Shannon M Conley; Muayyad R Al-Ubaidi; Muna I Naash
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  7 in total

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