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Good things come to those who wait: attenuated discounting of delayed rewards in aged Fischer 344 rats.

Nicholas W Simon | Candi L LaSarge | Karienn S Montgomery | Matthew T Williams | Ian A Mendez | Barry Setlow | Jennifer L Bizon
Neurobiology of aging | 2010

The ability to make advantageous choices among outcomes that differ in magnitude, probability, and delay until their arrival is critical for optimal survival and well-being across the lifespan. Aged individuals are often characterized as less impulsive in their choices than their young adult counterparts, demonstrating an increased ability to forgo immediate in favor of delayed (and often more beneficial) rewards. Such "wisdom" is usually characterized as a consequence of learning and life experience. However, aging is also associated with prefrontal cortical dysfunction and concomitant impairments in advantageous choice behavior. Animal models afford the opportunity to isolate the effects of biological aging on decision-making from experiential factors. To model one critical component of decision-making, young adult and aged Fischer 344 rats were trained on a two-choice delay discounting task in which one choice provided immediate delivery of a small reward and the other provided a large reward delivered after a variable delay period. Whereas young adult rats showed a characteristic pattern of choice behavior (choosing the large reward at short delays and shifting preference to the small reward as delays increased), aged rats maintained a preference for the large reward at all delays (i.e., attenuated "discounting" of delayed rewards). This increased preference for the large reward in aged rats was not due to perceptual, motor, or motivational factors. The data strongly suggest that, independent of life experience, there are underlying neurobiological factors that contribute to age-related changes in decision-making, and particularly the ability to delay gratification.

Pubmed ID: 18657883

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Associated grants

  • Agency: NIA NIH HHS, United States
    Id: R01 AG029421
  • Agency: NIMH NIH HHS, United States
    Id: MH65728
  • Agency: NINDS NIH HHS, United States
    Id: NS059324
  • Agency: NIMH NIH HHS, United States
    Id: T32 MH065728
  • Agency: NIDA NIH HHS, United States
    Id: F31 DA023331-01A1
  • Agency: NINDS NIH HHS, United States
    Id: F31 NS059324
  • Agency: NIDA NIH HHS, United States
    Id: DA023331
  • Agency: NIA NIH HHS, United States
    Id: AG029421
  • Agency: NIA NIH HHS, United States
    Id: R01 AG029421-01A1
  • Agency: NIDA NIH HHS, United States
    Id: F31 DA023331

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