Medial prefrontal cortex inversely regulates toluene-induced changes in markers of synaptic plasticity of mesolimbic dopamine neurons

• Published in: The Journal of neuroscience 2013-01, Vol.33 (2), p.804-813
• Main Authors: Beckley, Jacob T, Evins, Caitlin E, Fedarovich, Hleb, Gilstrap, Meghin J, Woodward, John J
• Format: Article
• Language: English
• Subjects: Animals; Biomarkers; Data Interpretation, Statistical; Dopaminergic Neurons - drug effects; Dopaminergic Neurons - physiology; Electric Stimulation; Electrophysiological Phenomena; Limbic System - cytology; Limbic System - drug effects; Limbic System - physiology; Male; Microinjections; Neuronal Plasticity - drug effects; Neuronal Plasticity - physiology; Prefrontal Cortex - cytology; Prefrontal Cortex - drug effects; Prefrontal Cortex - physiology; Rats; Rats, Sprague-Dawley; Reference Standards; Stereotaxic Techniques; Synapses - drug effects; Synapses - physiology; Toluene - pharmacology; Tyrosine 3-Monooxygenase - metabolism; Ventral Tegmental Area - cytology; Ventral Tegmental Area - drug effects; Ventral Tegmental Area - physiology
• ISSN: 0270-6474; 1529-2401; 1529-2401
• DOI: 10.1523/jneurosci.3729-12.2013

Toluene is a volatile solvent that is intentionally inhaled by children, adolescents, and adults for its intoxicating effects. Although voluntary use of toluene suggests that it possesses rewarding properties and abuse potential, it is unknown whether toluene alters excitatory synaptic transmission in reward-sensitive dopamine neurons like other drugs of abuse. Here, using a combination of retrograde labeling and slice electrophysiology, we show that a brief in vivo exposure of rats to a behaviorally relevant concentration of toluene vapor enhances glutamatergic synaptic strength of dopamine (DA) neurons projecting to nucleus accumbens core and medial shell neurons. This effect persisted for up to 3 d in mesoaccumbens core DA neurons and for at least 21 d in those projecting to the medial shell. In contrast, toluene vapor exposure had no effect on synaptic strength of DA neurons that project to the medial prefrontal cortex (mPFC). Furthermore, infusion of GABAergic modulators into the mPFC before vapor exposure to pharmacologically manipulate output, inhibited, or potentiated toluene's action on mesoaccumbens DA neurons. Together, the results of these studies indicate that toluene induces a target-selective increase in mesolimbic DA neuron synaptic transmission and strongly implicates the mPFC as an important regulator of drug-induced plasticity of mesolimbic dopamine neurons.