Kinetic features of the dopamine release and uptake in the dorsal and ventral striatum of rats

Valery N. Mukhin , Ivan R. Borovets , Vadim V. Sizov , Konstantin I. Pavlov , Victor M. Klimenko

Medical academic journal ›› 2019, Vol. 19 ›› Issue (4) : 47 -54.

PDF
Medical academic journal ›› 2019, Vol. 19 ›› Issue (4) : 47 -54. DOI: 10.17816/MAJ17532
Original research
research-article

Kinetic features of the dopamine release and uptake in the dorsal and ventral striatum of rats

Author information +
History +
PDF

Abstract

Kinetics of the evoked dopamine release and subsequent uptake in the parts of the rat striatum has not been studied sufficiently.

The aim of this study is to fill this gap and to investigate kinetics of dopamine release and uptake in vivo so that comparison can be made between the dorsal and the parts of the ventral striatum and with taking into account the overlapping electrochemical factors during the subsequent analysis of voltammetry recordings.

Materials and methods. The evoked wave of dopamine release and uptake in the dorsal striatum, core, and shell of the nucleus accumbens in the different groups of rats was recorded by the fast-scan cyclic voltammetry. Voltammetry recordings were subjected to principal component analysis and only the components associated with dopamine were taken for further analysis. The values of the parameters of the curves of dopamine release and uptake were defined. Then factor and variance analyses of the parameters were carried out.

Results. Factor analysis showed that the set of parameters of the dopamine wave can be reduced to the 4 factors that are comparable with the variables of the known from the literature mathematical model that describes the dopamine wave based on the Michaelis–Menten equation. Two of the factors and the corresponding parameters of the dopamine curve differ within the dorsal and ventral striatum. Factor 1 is associated with the parameters HL, T80_20, T20_0, slope_T20T0, which are significantly larger in the core of the nucleus accumbens. Factor 3 is associated with the parameters T50_2, AUC, FWHH, T100_80 which are significantly less in the dorsal striatum.

Conclusions. The parameters of the curve of dopamine release and uptake are determined by 4 factors. Among the dopamine curve parameters, the best measures of the factors are T50_1, DAC, T100_80 и T20_0. The kinetics of stimulated dopamine release and uptake varies within the dorsal and ventral striatum. The final phase of dopamine uptake is slowed in the core of the nucleus accumbens in comparison to the shell, and the dorsal striatum. The slope of initial phase of dopamine uptake in the dorsal striatum is steeper.

Keywords

kinetics / dopamine / fast-scan cyclic voltammetry / nucleus accumbens / dorsal striatum

Cite this article

Download citation ▾
Valery N. Mukhin, Ivan R. Borovets, Vadim V. Sizov, Konstantin I. Pavlov, Victor M. Klimenko. Kinetic features of the dopamine release and uptake in the dorsal and ventral striatum of rats. Medical academic journal, 2019, 19(4): 47-54 DOI:10.17816/MAJ17532

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Yorgason JT, Espana RA, Jones SR. Demon voltammetry and analysis software: analysis of cocaine-induced alterations in dopamine signaling using multiple kinetic measures. J Neurosci Methods. 2011;202(2):158-164. https://doi.org/10.1016/j.jneumeth.2011.03.001.

[2]

Jones SR, O’Dell SJ, Marshall JF, Wightman RM. Functional and anatomical evidence for different dopamine dynamics in the core and shell of the nucleus accumbens in slices of rat brain. Synapse. 1996;23(3):224-231. https://doi.org/10.1002/(SICI)1098-2396(199607)23:3<224::AID-SYN12>3.0.CO;2-Z.

[3]

Jones SR, Mathews TA, Budygin EA. Effect of moderate ethanol dose on dopamine uptake in rat nucleus accumbens in vivo. Synapse. 2006;60(3):251-255. https://doi.org/10.1002/syn.20294.

[4]

Мухин В.Н., Сизов В.В., Павлов К.И., Клименко В.М. β-Амилоид 25-35 подавляет секреторную активность дофаминергических систем мозга крыс // Российский физиологический журнал им И.М. Сеченова. – 2017. – Т. 103. – № 12. – С. 1350–1360. [Mukhin VN, Sizov VV, Pavlov KI, Klimenko VM. Amyloid β 25-35 downregulates phasic secretory activity of the brain dopaminergic systems in rats. Russian journal of physiology. 2017;103(12):1350-1360. (In Russ.)]

[5]

González-Mora JL, Salazar P, Martín M, Mas M. Monitoring extracellular molecules in neuroscience by in vivo electrochemistry: methodological considerations and biological applications. In: In Vivo Neuropharmacology and Neurophysiology. Ed. by A. Philippu. New York: Springer New York; 2017. P. 181-206.

[6]

Saddoris MP. Terminal dopamine release kinetics in the accumbens core and shell are distinctly altered after withdrawal from cocaine self-administration. eNeuro. 2016;3(5). https://doi.org/10.1523/ENEURO.0274-16.2016.

[7]

Wightman RM, Amatorh C, Engstrom RC, et al. Real-time characterization of dopamine overflow and uptake in the rat striatum. Neuroscience. 1988;25(2):513-523. https://doi.org/10.1016/0306-4522(88)90255-2.

[8]

Wightman RM, Zimmerman JB. Control of dopamine extracellular concentration in rat striatum by impulse flow and uptake. Brain Res Rev. 1990;15(2):135-144. https://doi.org/10.1016/0165-0173(90)90015-g.

[9]

Harun R, Grassi CM, Munoz MJ, et al. Neurobiological model of stimulated dopamine neurotransmission to interpret fast-scan cyclic voltammetry data. Brain Res. 2015;1599:67-84. https://doi.org/10.1016/j.brainres.2014.12.020.

RIGHTS & PERMISSIONS

Mukhin V.N., Borovets I.R., Sizov V.V., Pavlov K.I., Klimenko V.M.

AI Summary AI Mindmap
PDF

80

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/