Conditioning learning in an attentional task relates to age and ventricular expansion in a nonhuman primate

Jennifer Wittkowski1, Rebecca G Fritz1, Martin Meier2

  • 1Institute of Zoology, University of Veterinary Medicine Hannover, Hannover, Germany.

Insights

Grey mouse lemurs show age-related learning deficits in a visuo-spatial attention task (5CSRTT). Performance correlated with age and occipital lobe changes, suggesting visual processing deficits contribute to cognitive decline.

Area of Science:

  • Neuroscience
  • Primate Cognition
  • Aging Research

Background:

  • The grey mouse lemur (Microcebus murinus) is a valuable nonhuman primate model for studying brain aging and neurodegenerative diseases.
  • While age-related cognitive decline is documented, specific attention-age relationships are not well understood in this species.

Purpose of the Study:

  • To investigate visuo-spatial attention in grey mouse lemurs using a touchscreen-based 5-choice-serial-reaction-time-task (5CSRTT).
  • To explore the relationship between age, cognitive performance, and structural brain changes (ventricular expansion) in this primate model.

Main Methods:

  • Ten grey mouse lemurs were trained on a touchscreen 5CSRTT, assessing performance at varying stimulus presentation durations (SPD).
  • Structural magnetic resonance imaging (MRI) was used to measure ventricular expansion.
  • Correlation analyses examined relationships between task acquisition, performance, age, and ventricular size.

Main Results:

  • Learning acquisition (reaching 80% performance at 4s SPD) significantly correlated with age and occipital lobe ventricular expansion.
  • Performance during a 2s SPD challenge was independent of age once criterion was met.
  • Further challenges revealed a linear decline in performance with decreasing SPD, indicating increased attentional demand.

Conclusions:

  • The 5CSRTT is applicable for assessing visuo-spatial attention in grey mouse lemurs.
  • Age-related deficits in learning the 5CSRTT were observed.
  • These deficits may be linked to age-related occipital structure atrophy and impaired central visual processing.

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