Impairments in laterodorsal tegmentum to VTA projections underlie glucocorticoid-triggered reward deficits.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 28837419.
- Also identified by DOI 10.7554/eLife.25843 and PMC identifier 5576484.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Ventral tegmental area (VTA) activity is critical for reward/reinforcement and is tightly modulated by the laterodorsal tegmentum (LDT). <i>In utero</i> exposure to glucocorticoids (iuGC) triggers prominent motivation deficits but nothing is known about the impact of this exposure in the LDT-VTA circuit. We show that iuGC-rats have long-lasting changes in cholinergic markers in the LDT, together with a decrease in LDT basal neuronal activity. Interestingly, upon LDT stimulation, iuGC animals present a decrease in the magnitude of excitation and an increase in VTA inhibition, as a result of a shift in the type of cells that respond to the stimulus. In agreement with LDT-VTA dysfunction, we show that iuGC animals present motivational deficits that are rescued by selective optogenetic activation of this pathway. Importantly, we also show that LDT-VTA optogenetic stimulation is reinforcing, and that iuGC animals are more susceptible to the reinforcing properties of LDT-VTA stimulation.
Medical subject headings
- Cognitive Dysfunction
- Glucocorticoids
- Prenatal Exposure Delayed Effects
- Raphe Nuclei
- Reward
- Ventral Tegmental Area