Abstract
Motor sequence learning, planning and execution of goal-directed behaviors, and decision making rely on accurate time estimation and production of durations in the seconds-to-minutes range. The pathways involved in planning and execution of goal-directed behaviors include cortico-striato-thalamo-cortical circuitry modulated by dopaminergic inputs. A critical feature of interval timing is its scalar property, by which the precision of timing is proportional to the timed duration. We examined the role of medial prefrontal cortex (mPFC) in timing by evaluating the effect of its reversible inactivation on timing accuracy, timing precision and scalar timing. Rats were trained to time two durations in a peak-interval (PI) procedure. Reversible mPFC inactivation using GABA agonist muscimol resulted in decreased timing precision, with no effect on timing accuracy and scalar timing. These results are partly at odds with studies suggesting that ramping prefrontal activity is crucial to timing but closely match simulations with the Striatal Beat Frequency (SBF) model proposing that timing is coded by the coincidental activation of striatal neurons by cortical inputs. Computer simulations indicate that in SBF, gradual inactivation of cortical inputs results in a gradual decrease in timing precision with preservation of timing accuracy and scalar timing. Further studies are needed to differentiate between timing models based on coincidence detection and timing models based on ramping mPFC activity, and clarify whether mPFC is specifically involved in timing, or more generally involved in attention, working memory, or response selection/inhibition.
Highlights
IntroductionAnimal and human studies have revealed critical roles of the medial prefrontal cortex (mPFC; and its human counterpart, dorso-lateral prefrontal cortex) in a variety of cognitive processes from attention (Arnsten, 2009; Paneri and Gregoriou, 2017), working memory (Funahashi, 2017; Murray et al, 2017; Spaak et al, 2017), inhibitory control (Jonkman et al, 2009) or habit mPFC and Interval Timing formation (Yin and Knowlton, 2006; Limpens et al, 2015) to more complex functions such as planning and decision making (Dixon and Christoff, 2014; Padoa-Schioppa and Conen, 2017) and action selection (Matsumoto et al, 2003; Ridderinkhof et al, 2004) or cognitive flexibility (Robbins, 2007; Kehagia et al, 2010)
The role of the medial prefrontal cortex (mPFC) in timing behavior was evaluated by its reversible inactivation with GABA agonist muscimol (MUSC)
Rather than globally inactivating mPFC with large muscimol doses, here our doses were rather small, which allowed us to evaluate the effect of mPFC inactivation on timing accuracy, scalar timing, timing precision and response rate in a PI procedure
Summary
Animal and human studies have revealed critical roles of the medial prefrontal cortex (mPFC; and its human counterpart, dorso-lateral prefrontal cortex) in a variety of cognitive processes from attention (Arnsten, 2009; Paneri and Gregoriou, 2017), working memory (Funahashi, 2017; Murray et al, 2017; Spaak et al, 2017), inhibitory control (Jonkman et al, 2009) or habit mPFC and Interval Timing formation (Yin and Knowlton, 2006; Limpens et al, 2015) to more complex functions such as planning and decision making (Dixon and Christoff, 2014; Padoa-Schioppa and Conen, 2017) and action selection (Matsumoto et al, 2003; Ridderinkhof et al, 2004) or cognitive flexibility (Robbins, 2007; Kehagia et al, 2010) These functions are based on the extensive interconnectivity of the mPFC with other cortical (Crowe et al, 2013; Phillips et al, 2014) and subcortical regions, such as the thalamus, amygdala, hippocampus and striatum (Kesner and Churchwell, 2011). Introducing extraneous response requirements (e.g., remaining in the port for the duration followed by exit in Xu et al, 2014) is likely to introduce artifacts related to response inhibition followed by action (for a similar argument see Namboodiri and Hussain Shuler, 2014)
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