[Differential regulation of dopamine receptors on pre- and postsynaptic Na+, K(+)-ATPase in rat striatum]
Related Experiment Video
Updated: Oct 5, 2026

Modeling Fast-scan Cyclic Voltammetry Data from Electrically Stimulated Dopamine Neurotransmission Data Using QNsim1.0
Published on: June 5, 2017
Abstract:
The pre- and postsynaptic membranes isolated from rat striatum were used to investigate the regulation of dopamine receptors on striatal Na+, K(+)-ATPase in these membranes. The activity of Na+, K(+)-ATPase was determined by colorimetric method. Dopamine (DA) was found to inhibit the Na+, K(+)-ATPase activity on postsynaptic membranes in a concentration-dependent manner with a IC50 value of 4.6 mumol.L-1. This inhibitory effect was reversed by either selective D1 receptor antagonist SCH23390 or selective D2 receptor antagonist spipernone. The inhibitory effect similar to DA was produced by combination with selective D1 receptor agonist SKF38393 and selective D2 receptor agonist LY171555. In contrast, under the same experimental conditions, DA (10(-8)-10(-5) mol.L-1) was shown to activate the activity of Na+, K(+)-ATPase on presynaptic membranes in a concentration-dependent manner. Meanwhile, the stimulatory effect was reversed by spiperone alone rather than by SCH23390. These results show the differential regulation of presytnaptic and postsynaptic DA receptors on Na+, K(+)-ATPase in rat striatum.
Related Concept Videos
Adrenergic Neurons: Neurotransmission
Synthesis: Catecholamine synthesis requires tyrosine, which is taken...
Adrenergic Receptors: β Subtype
Isoprenaline > Adrenaline > Noradrenaline
Neurotransmitter binding to these receptors causes activation of adenylyl cyclase resulting in increased concentrations of cAMP and modulation of calcium ion channels within the cell. They are further classified into β1, β2, and β3 subtypes.
β1-adrenoceptors: β1-adrenoceptors have equal affinities for...
Drugs Affecting Neurotransmitter Synthesis
Neurochemical Transmission: Sites of Drug Action
Adrenergic Receptors: ɑ Subtype
Adrenaline ≥ Noradrenaline >> Isoprenaline
α-adrenoceptors are further divided into α1 and α2-adrenoceptors.
α1-Adrenoceptors: These receptors are located postsynaptically on the effector organs and cause constriction of smooth muscle mediated by activation of phospholipase C—inositol-1,4,5-trisphosphate...
Drugs Affecting Neurotransmitter Release or Uptake

