In vivo modulation of ventral tegmental area dopamine and glutamate efflux by local GABAB receptors is altered after repeated amphetamine treatment

Neuroscience ◽  
2002 ◽  
Vol 109 (3) ◽  
pp. 585-595 ◽  
Author(s):  
M Giorgetti ◽  
G Hotsenpiller ◽  
W Froestl ◽  
M.E Wolf
Keyword(s):  
Ventral Tegmental Area ◽  
Gabab Receptors ◽  
Amphetamine Treatment ◽  
Ventral Tegmental ◽  
Glutamate Efflux

scholarly journals Glucocorticoid receptors in the prefrontal cortex regulate dopamine efflux to stress via descending glutamatergic feedback to the ventral tegmental area

2013 ◽  
Vol 16 (8) ◽  
pp. 1799-1807 ◽  
Author(s):  
Kelly A. Butts ◽  
Anthony G. Phillips
Keyword(s):  
Prefrontal Cortex ◽  
Ventral Tegmental Area ◽  
Glucocorticoid Receptors ◽  
Acute Stress ◽  
Pyramidal Cells ◽  
Gaba Release ◽  
Underlying Mechanism ◽  
Ventral Tegmental ◽  
Glutamate Efflux

Abstract Enhanced dopamine (DA) efflux in the medial prefrontal cortex (mPFC) is a well-documented response to acute stress. We have previously shown that glucocorticoid receptors in the mPFC regulate stress-evoked DA efflux but the underlying mechanism is unknown. DA neurons in the ventral tegmental area (VTA) receive excitatory input from and send reciprocal projections to the mPFC. We hypothesize that blockade of prefrontal glucocorticoid receptors can reduce activity of descending glutamatergic input to the VTA, thereby attenuating stress-evoked DA efflux in the mPFC. Using in vivo microdialysis, we demonstrate that acute tail-pinch stress leads to a significant increase in glutamate efflux in the VTA. Blockade of prefrontal glucocorticoid receptors with the selective antagonist CORT 108297 attenuates stress-evoked glutamate efflux in the VTA together with DA efflux in the mPFC. Furthermore, blockade of ionotrophic glutamate receptors in the VTA attenuates stress-evoked DA efflux in the mPFC. We also examine the possible role of glucocorticoid-induced synthesis and release of endocannabinoids acting presynaptically via cannabinoid CB1 receptors to inhibit GABA release onto prefrontal pyramidal cells, thus enhancing descending glutamatergic input to the VTA leading to an increase in mPFC DA efflux during stress. However, administration of the cannabinoid CB1 receptor antagonist into the mPFC does not attenuate stress-evoked DA efflux in the mPFC. Taken together, our data indicate that glucocorticoids act locally within the mPFC to modulate mesocortical DA efflux by potentiation of glutamatergic drive onto DA neurons in the VTA.

scholarly journals A probabilistic atlas of the human ventral tegmental area (VTA) based on 7 Tesla MRI data

2021 ◽  
Vol 226 (4) ◽  
pp. 1155-1167 ◽  
Author(s):  
Anne C. Trutti ◽  
Laura Fontanesi ◽  
Martijn J. Mulder ◽  
Pierre-Louis Bazin ◽  
Bernhard Hommel ◽  
...  
Keyword(s):  
Ventral Tegmental Area ◽  
Region Of Interest ◽  
Reward Processing ◽  
7 Tesla ◽  
Subcortical Structures ◽  
7 Tesla Mri ◽  
Subcortical Nuclei ◽  
Ventral Tegmental ◽  
The Brain

AbstractFunctional magnetic resonance imaging (fMRI) BOLD signal is commonly localized by using neuroanatomical atlases, which can also serve for region of interest analyses. Yet, the available MRI atlases have serious limitations when it comes to imaging subcortical structures: only 7% of the 455 subcortical nuclei are captured by current atlases. This highlights the general difficulty in mapping smaller nuclei deep in the brain, which can be addressed using ultra-high field 7 Tesla (T) MRI. The ventral tegmental area (VTA) is a subcortical structure that plays a pivotal role in reward processing, learning and memory. Despite the significant interest in this nucleus in cognitive neuroscience, there are currently no available, anatomically precise VTA atlases derived from 7 T MRI data that cover the full region of the VTA. Here, we first provide a protocol for multimodal VTA imaging and delineation. We then provide a data description of a probabilistic VTA atlas based on in vivo 7 T MRI data.

scholarly journals Insulin in the ventral tegmental area reduces cocaine‐evoked dopamine in the nucleus accumbens in vivo

2018 ◽  
Vol 50 (3) ◽  
pp. 2146-2155 ◽  
Author(s):  
Lindsay Naef ◽  
Lauren Seabrook ◽  
Jeff Hsiao ◽  
Calvin Li ◽  
Stephanie L. Borgland
Keyword(s):  
Nucleus Accumbens ◽  
Ventral Tegmental Area ◽  
Ventral Tegmental

Slow Oscillatory Firing: A Major Firing Pattern of Dopamine Neurons in the Ventral Tegmental Area

2005 ◽  
Vol 94 (5) ◽  
pp. 3516-3522 ◽  
Author(s):  
Wei-Xing Shi
Keyword(s):  
Ventral Tegmental Area ◽  
Single Unit ◽  
Firing Pattern ◽  
Receptor Activation ◽  
Dopamine Neurons ◽  
Interspike Intervals ◽  
Firing Activity ◽  
Unit Recording ◽  
Ventral Tegmental

Using spectral analysis and in vivo single-unit recording in rats, the present study revealed a pronounced slow oscillation (SO) in the firing activity of about half the dopamine (DA) neurons recorded in the ventral tegmental area. DA neurons in this group tended to fire repetitive spike clusters, making them appear to be rhythmic bursting cells. However, only some of these burst-like events met the traditional “80/160 ms” burst criteria entirely. The observation that the SO could be found in nonbursting DA cells, occurred at frequencies different from those of bursts, and persisted after bursts were digitally removed from spike trains further supports the suggestion that the SO is different from the traditionally defined bursting. Interspike intervals (ISIs) had been thought to be bimodally distributed in bursting DA neurons. This study found that some nonbursting DA cells also had a bimodal ISI distribution and a significant number of bursting cells did not. In the majority of cells where less than half the spikes occurred in bursts, a bimodal ISI distribution was highly predictive of the presence of the SO. Results further showed that the generation of the SO required forebrain inputs to DA neurons but not the adrenergic α1 receptor activation responsible for psychostimulant-induced increases in the SO. Taken together, these results suggest that the SO is distinct from the traditionally defined bursting and represents a major firing pattern of DA neurons in the ventral tegmental area.

Long-lasting synaptic regulation of dopamine neurons by astrocytes in the Ventral Tegmental Area

2021 ◽  
Author(s):  
Linda Requie ◽  
Marta Gómez-Gonzalo ◽  
Francesca Managò ◽  
Mauro Congiu ◽  
Marcello Melone ◽  
...  
Keyword(s):  
Ventral Tegmental Area ◽  
Metabotropic Glutamate Receptor ◽  
Receptor Activation ◽  
Dopamine Neuron ◽  
Dopamine Neurons ◽  
Neuron Activity ◽  
Astrocytic Process ◽  
Metabotropic Glutamate ◽  
Ventral Tegmental

Abstract The plasticity of glutamatergic transmission in the Ventral Tegmental Area (VTA) represents a fundamental mechanism in the modulation of dopamine neuron burst firing and the phasic dopamine release at VTA target regions. These processes encode basic behavioral responses, including locomotor activity, learning and motivated-behaviors. Here we describe a hitherto unidentified mechanism of long-lasting potentiation of glutamatergic synapses on DA neurons. We found that VTA astrocytes respond to dopamine neuron bursts with Ca2+ elevations that require activation of endocannabinoid CB1 and dopamine D2 receptors colocalized at the same astrocytic process. Astrocytes, in turn, release glutamate that, through presynaptic metabotropic glutamate receptor activation coupled with neuronal nitric oxide production, induces long-lasting potentiation of excitatory synapses on adjacent dopamine neurons. Consistent with this finding, selective activation of VTA astrocytes increases dopamine neuron bursts in vivo and induces locomotor hyperactivity. Astrocytes play, therefore, a key role in the modulation of VTA dopamine neuron activity.

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