Background: DAT regulates dopamine neurotransmission in the brain. Results: ␣-Synuclein influences DA efflux and membrane microdomain distribution of DAT. Conclusion: DAT activation recruits ␣-synuclein to the membrane, which in turn influences dopamine neurotransmission. Significance: Understanding the mechanisms associated with ␣-synuclein regulation of DAT may reveal disease-modifying targets for the treatment of pathologies associated with DA dysregulation.

Background: Behavioral and neurophysiological correlates of methamphetamine and amphetamine differ via unknown mechanisms. Results: Although extracellular amphetamine produces a higher increase in neuronal firing and inward DAT current, only intracellular methamphetamine prevents dopamine-induced neuronal firing and inward current. Conclusion: Methamphetamine differently regulates the DAT-mediated conductances and thus the excitability of dopaminergic neuron. Significance: Results reveal a new mechanism for methamphetamine-induced dysregulation of dopaminergic neurons.

Alpha-synuclein is a small, highly charged protein encoded by the synuclein or SNCA gene that is predominantly expressed in central nervous system neurons. Although its physiological function remains enigmatic, alpha-synuclein is implicated in movement disorders such as Parkinson’s disease, multiple system atrophy, and in neurodegenerative diseases such as Dementia with Lewy bodies. Here we have focused on reviewing the existing literature pertaining to wild-type alpha-synuclein structure, its properties, and its potential involvement in regulation of dopamine neurotransmission.

Methamphetamine (METH) is a highly addictive and neurotoxic psychostimulant. Its use in humans is often associated with neurocognitive impairment. Whether this is due to long-term deficits in short-term memory and/or hippocampal plasticity remains unclear. Recently, we reported that METH increases baseline synaptic transmission and reduces LTP in an ex vivo preparation of the hippocampal CA1 region from young mice. In the current study, we tested the hypothesis that a repeated neurotoxic regimen of METH exposure in adolescent mice decreases hippocampal synaptic plasticity and produces a deficit in short-term memory. Contrary to our prediction, there was no change in the hippocampal plasticity or short-term memory when measured after 14 days of METH exposure. However, we found that at 7, 14, and 21 days of drug abstinence, METH-exposed mice exhibited a deficit in spatial memory, which was accompanied by a decrease in hippocampal plasticity. Our results support the interpretation that the deleterious cognitive consequences of neurotoxic levels of METH exposure may manifest and persist after drug abstinence. Therefore, therapeutic strategies should consider short-term as well as long-term consequences of methamphetamine exposure.