Functional expression of the glycine transporter 1 on bullfrog retinal cones.
Xin-Jun Zhang, Li-Hao Ge, Jian Liu, Xiong-Li Yang
Index: Neuroreport 19(17) , 1667-71, (2008)
Full Text: HTML
Abstract
Using patch clamp techniques, we characterized glycine-induced currents from cones in bullfrog retinal slices. Application of glycine to cone terminals induced an inward current, which was in part suppressed by strychnine. The remaining strychnine-resistant current component, which did not show polarity reversion in a range of -120 mV to +40 mV, was blocked by N[3-(4'-fluorophenyl)-3-(4'-phenylphenoxy)propyl] sarcosine, an antagonist of glycine transporter 1 (GlyT1), but not affected by amoxapine, an inhibitor of glycine transporter 2. Application of sarcosine, an agonist of GlyT1, to cone terminals induced an inward current that was completely suppressed by N[3-(4'-fluorophenyl)-3-(4'-phenylphenoxy)propyl] sarcosine or when external Na in Ringer's was replaced by choline. All these results show for the first time the functional expression of GlyT1 on bullfrog cones.
Related Compounds
Related Articles:
2011-01-01
[PLoS ONE 6(12) , e28208, (2011)]
2012-01-01
[J. Pharm. Biomed. Anal. 58 , 83-93, (2012)]
2010-12-01
[Bioanalysis 2(12) , 1989-2000, (2010)]
2012-08-01
[J. Biomol. Screen. 17(7) , 957-65, (2012)]
2008-01-01
[Respirology 13(1) , 149-51, (2008)]