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1.
Peer Community J ; 42024 Apr 24.
Article in English | MEDLINE | ID: mdl-38827787

ABSTRACT

Animals need to switch between motivated behaviours, like drinking, feeding or social interaction, to meet environmental availability, internal needs and more complex ethological needs such as hiding future actions from competitors. Inflexible, repetitive behaviours are a hallmark of many neuropsychiatric disorders. However, how the brain orchestrates switching between the neural mechanisms controlling motivated behaviours, or drives, is unknown. This is partly due to a lack of appropriate measurement systems. We designed an automated extended home-cage, the Switchmaze, using open-source hardware and software. In this study, we use it to establish a behavioural assay of motivational switching in mice. Individual animals access the Switchmaze from the home-cage and choose between entering one of two chambers containing different goal objects or returning to the home-cage. Motivational switching is measured as a ratio of switching between chambers and continuous exploitation of one chamber. Behavioural transition analysis is used to further dissect altered motivational switching. As proof-of-concept, we show environmental manipulation, and targeted brain manipulation experiments which altered motivational switching without effect on traditional behavioural parameters. Chemogenetic inhibition of the prefrontal-hypothalamic axis increased the rate of motivation switching, highlighting the involvement of this pathway in drive switching. This work demonstrates the utility of open-design in understanding animal behaviour and its neural correlates.

2.
J Insect Physiol ; 118: 103943, 2019 10.
Article in English | MEDLINE | ID: mdl-31518554

ABSTRACT

Social insects are emerging models for studying aging and the longevity/fecundity trade-off. Research on the demography of colonies and populations are hampered by the lack of reliable age markers. Here we investigate the suitability of cuticular pigmentation and pteridine fluorescence for age grading individuals of the clonal ant Platythyrea punctata. We found that both traits varied with age. Cuticular color darkened with individual's age until 25-30 days after hatching. For pteridine fluorescence, we found that P. punctata workers show a decrease in head pteridine levels over time until 70-80 days of age. Together with other markers, such as age-based behavior, cuticular coloration and pteridine fluorescence may help to estimate the age structure of colonies.


Subject(s)
Aging , Ants/physiology , Pteridines/analysis , Animals , Color , Fluorescence
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