Abstract
Aberrant dopamine transmission is a hallmark of several psychiatric disorders. Dopamine neurons in the ventral tegmental area (VTA) display distinct activity states that are regulated by discrete afferent inputs. For example, burst firing requires excitatory input from the mesopontine-tegmentum, while dopamine neuron population activity, defined as the number of spontaneously active dopamine neurons, is thought to be dependent on inhibitory drive from the ventral pallidum (VP). Rodent models used to study psychiatric disorders, such as psychosis, consistently exhibit elevated dopamine neuron population activity, due to decreased tonic inhibition from the VP. However, it remains unclear whether the VP can modulate all dopamine neurons, or if only a specific subset of VTA dopamine neurons receive innervation from the VP to be recruited as required. This knowledge is critical for understanding dopamine regulation in normal and pathological conditions. Here, we used in vivo electrophysiology in male and female rats to record VTA dopamine neurons inhibited by electrical stimulation of the VP. Specifically, VP stimulation inhibited ∼22% of spontaneously active dopamine neurons; however, activation of the ventral hippocampus, a modulator of VTA population activity, increased the proportion to ∼48%. This increase suggests that VP selectively modulates a subset of dopamine neurons that can be recruited by afferent activation. Anterograde monosynaptic tracing revealed that approximately half of the VTA dopamine neurons receive input from the VP. Taken together, we demonstrate that a subset of VTA dopamine neurons receive monosynaptic input from the VP, which provides valuable information regarding the regulation of VTA neuron activity.
Significance statement Dysregulated dopamine signaling has been linked to many psychiatric disorders. Therefore, understanding how dopamine neuron activity is regulated is essential for identifying mechanisms contributing to normal and pathologic states. Dopamine neuron population activity refers to a dynamic collection of neurons that can be recruited to assign salience to stimuli. This activity state is known to be regulated by afferent inputs to the ventral pallidum, which provides a tonic inhibition to dopamine neurons. This study demonstrates that the VP provides flexible, targeted control of dopamine signaling. These findings improve our understanding of how dopamine activity is regulated and may help guide future treatments for psychiatric disorders involving dopamine dysfunction.
Footnotes
We would like to thank Dr. David Morilak for thoughtful discussions on the topic that inspired the conceptualization of this work.
This work was supported by Merit Awards #BX004693 and #BX004646 from the United States Department of Veterans Affairs, Biomedical Laboratory Research and Development Service (to D.J.L.), the National Institutes of Health R01-AG076030, T32-NS082145 (to O.J.Y., H.B.E., K.L., and A.M.M.), and F31-MH127890-01A1 to H.B.E.
Animal Statement: All experiments were performed in accordance with guidelines outlined in the USPH Guide for the Care and Use of Laboratory animals and were approved by the Institutional Animal Care and the Use Committees of UT Health San Antonio and the US Department of Veterans Affairs
This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.






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