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Characterization of [125I]RTI-121 binding to dopamine transporter in vitro

  
@article{APS6549,
	author = {Nian-Hang Chen and Jian-Hua Ding and You-Lin Wang and Maarten E A Peith},
	title = {Characterization of [125I]RTI-121 binding to dopamine transporter in vitro},
	journal = {Acta Pharmacologica Sinica},
	volume = {18},
	number = {2},
	year = {2016},
	keywords = {},
	abstract = {AIM: To characterize the binding of [125I]3 beta-(4-iodophenyl) tropane-2
beta-carboxylic acid isopropyl ester (RTI-121) to the dopamine transporter (DAT) 
under physiologically relevant conditions.
METHODS: [125I]RTI-121 was used to label the DAT on fresh rat striatum
synaptosomal membranes in artificial cerebrospinal fluid (ACSF) at 37 degrees C.
RESULTS: [125I]RTI-121 binding reached equilibrium within 3 min and remained at
its plateau value for at least 9 min. The data from kinetic, saturation, and
competition studies supported a one-site model for the binding of [125I]RTI-121
to the DAT. Various DAT blockers (oocaine, GBR12935, and BTCP) and substrates
(dopamine and d-amphetamine) competitively inhibited the binding of
[125I]RTI-121. Compared with NaPhos-KCl-NaCl assay buffer, ACSF containing Ca2+
and Mg2+ markedly increased the IC50 of DAT blockers for inhibiting [125I]RTI-121
binding with less effect on that of substrates. Various D2 receptor ligands
(pergolide, quinirole, sulpiride, and l-stepholidine) had no direct effect on the
binding of [125I]RTI-121.
CONCLUSION: [125I]RTI-121 binding under physiologically relevant conditions
fulfills the basic criteria for DAT binding assay.},
	issn = {1745-7254},	url = {http://www.chinaphar.com/article/view/6549}
}