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Physiological and Behavioral Capabilities

The Behavioral Phenotyping Core at IU School of Medicine offers the following in vivo physiological and behavioral capabilities. 

  • Frailty index, grip strength, & negative geotaxis reflex
  • Motor function (rotarod / wheel running coordination)
  • Acoustic and tactile startle reactivity
  • 24-hr home-cage core body temperature + activity (circadian rhythm integrity). Capabilities to measure HR/BP and EEG.
  • 24-hr food / liquid intake patterns; taste preferences

  • Startle responsivity (dark vs enhanced light conditions)
  • Social approach / withdrawal
  • Stress-induced hyperthermia
  • Open-field activity w/ light:dark preference
  • Novelty neophobia
  • Social dominance behavior
  • Resident intruder aggression
  • Forced swim / Tail suspension (‘behavioral despair’)
  • Elevated plus maze

  • Reward-seeking / compulsive drinking:
    • 2-bottle access
    • Schedule-induced polydipsia
  • Dependence:
    • Autonomic measurement of withdrawl
    • Somatic endpoints [e.g. activity / circadian changes]
    • Dysphoria / anhedonia [e.g. sucrose preference, immobility in forced swim / tail suspension]

  • Habituation / dishabituation of startle / open-field activity (nonassociative learning)
  • Prepulse inhibition (sensorimotor gating)
  • Spontaneous & food-reinforced Y-maze alternation (working memory)
  • Novel object recognition (short-term memory)
  • Social recognition / learning (ethological memory processes)
  • One-trial inhibitory avoidance (memory consolidation/retrieval)
  • Active avoidance acquisition / Go, No-Go discrimination (mesolimbic DA, executive function)
  • 8-arm radial (dry) maze (spatial learning & memory)
  • Morris water maze (spatial learning & memory)
  • Active Place Avoidance (spatial learning & memory)
  • Classical fear (tone/context) conditioning (associative learning; amygdala/hippocampal circuits)
  • Conditioned taste aversion (long-term memory; attentional processes)

  • Volitional wheel running (motivational processes)
  • Standard acute nociception assays (e.g. mechanical allodynia via Von Frey or algometer)
  • Volitional 2-plate thermal place preference (hot-cold allodynia)
  • Automated shock sensitivity thresholds using flinch response