Cortico-accumbens fiber stimulation does not induce dopamine release in the nucleus accumbens in vitro.

作者: Marianne Benoit-Marand , Patricio O’Donnell

DOI: 10.1007/S00429-008-0187-Z

关键词: AMPA receptorGlutamate receptorBiophysicsChemistryPostsynaptic potentialNucleus accumbensCNQXDopamineNeuroscienceSlice preparationMedium spiny neuron

摘要: Interactions between dopamine (DA) and glutamate in the nucleus accumbens (NA) are important for a variety of cognitive limbic functions. Although, there is strong evidence that DA controls responses, converse (glutamate affecting release) controversial. To determine whether endogenous released from corticostriatal terminals can evoke release by local interactions NA, we measured with amperometry simultaneously whole cell recordings NA medium spiny neurons (MSNs) slice preparation preserving (but not bodies) cortico-accumbens fibers. MSNs responded to cortical stimulation postsynaptic potential was blocked AMPA antagonist CNQX, but no overflow detected carbon fiber electrode. This absence cannot be accounted deterioration this since evoked caudal same slices. The signal modulated as expected bath application transporter blocker. data show cortico-striatal activation does induce interactions, suggesting observations glutamate-evoked previously reported vivo may taking place via an extra-NA circuit.

参考文章(34)
J F Bowyer, G W Lipe, S F Ali, R R Holson, A C Scallet, W Slikker, Interactions of MK-801 with glutamate-, glutamine- and methamphetamine-evoked release of [3H]dopamine from striatal slices. Journal of Pharmacology and Experimental Therapeutics. ,vol. 257, pp. 262- 270 ,(1991)
Tsuyoshi Yamaguchi, Whitney Sheen, Marisela Morales, Glutamatergic neurons are present in the rat ventral tegmental area European Journal of Neuroscience. ,vol. 25, pp. 106- 118 ,(2007) , 10.1111/J.1460-9568.2006.05263.X
Stan B. Floresco, Charles R. Yang, Anthony G. Phillips, Charles D. Blaha, Basolateral amygdala stimulation evokes glutamate receptor-dependent dopamine efflux in the nucleus accumbens of the anaesthetized rat. European Journal of Neuroscience. ,vol. 10, pp. 1241- 1251 ,(1998) , 10.1046/J.1460-9568.1998.00133.X
K Jhamandas, D W Clow, Characterization of L-glutamate action on the release of endogenous dopamine from the rat caudate-putamen. Journal of Pharmacology and Experimental Therapeutics. ,vol. 248, pp. 722- 728 ,(1989)
Yvonne Schmitz, Claudia Schmauss, David Sulzer, Altered Dopamine Release and Uptake Kinetics in Mice Lacking D2 Receptors The Journal of Neuroscience. ,vol. 22, pp. 8002- 8009 ,(2002) , 10.1523/JNEUROSCI.22-18-08002.2002
Sara R. Jones, Raul R. Gainetdinov, R. Mark Wightman, Marc G. Caron, Mechanisms of Amphetamine Action Revealed in Mice Lacking the Dopamine Transporter The Journal of Neuroscience. ,vol. 18, pp. 1979- 1986 ,(1998) , 10.1523/JNEUROSCI.18-06-01979.1998
H.T. Chang, S.T. Kitai, Intracellular recordings from rat nucleus accumbens neurons in vitro Brain Research. ,vol. 366, pp. 392- 396 ,(1986) , 10.1016/0006-8993(86)91326-0
Marc Marien, James Brien, Khem Jhamandas, Regional release of [3H]dopamine from rat brain in vitro: effects of opioids on release induced by potassium, nicotine, and L-glutamic acid Canadian Journal of Physiology and Pharmacology. ,vol. 61, pp. 43- 60 ,(1983) , 10.1139/Y83-005
Matthew T. Taber, Sheela Das, Hans C. Fibiger, Cortical Regulation of Subcortical Dopamine Release: Mediation via the Ventral Tegmental Area Journal of Neurochemistry. ,vol. 65, pp. 1407- 1410 ,(2002) , 10.1046/J.1471-4159.1995.65031407.X