FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Citation
Argue, K.J., Neckameyer, W.S. (2013). Temporally dimorphic recruitment of dopamine neurons into stress response circuitry in Drosophila.  Behav. Neurosci. 127(5): 725--733.
FlyBase ID
FBrf0223056
Publication Type
Research paper
Abstract
Many studies have pointed to vulnerability to stress and stress-related pathologies at different timepoints during an individual's life span. These sensitive windows are usually during periods of neural development, such as embryogenesis, infancy, and adolescence. It is critical to understand how neural circuitry may change as an individual ages in ways that could affect susceptibility to stress. Here we compare two stages in Drosophila melanogaster: sexual immaturity and sexual maturity. We used the genetic resources available in Drosophila to manipulate pre- and postsynaptic dopamine signaling in sexually immature and mature animals that were then assayed for heart rate and locomotor behavior in response to starvation and oxidative stress. Our results show significant differences in the stress response for sexually immature and mature animals for heart rate, periods of high mobility, mean velocity, and several other parameters of locomotor behavior. Our data show that dopamine neurons are differentially recruited into the stress response circuitry for sexually immature and mature individuals. By observing behaviors that have been previously shown in mammalian models to be affected by stress and altered in models of affective disorders, we provide a genetically tractable model for development and maintenance of the stress response circuitry during sexual maturation.
PubMed ID
PubMed Central ID
PMC4212825 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Behav. Neurosci.
    Title
    Behavioral Neuroscience
    Publication Year
    1983-
    ISBN/ISSN
    0735-7044
    Data From Reference
    Genes (3)