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Simpson, E. H.

Publications and source records attributed to Simpson, E. H..

2 recordsLinked to original sources

Impact of Temporal Uncertainty on Sign-tracking Behavior

Sign-tracking behavior, also known as "autoshaping", is defined as approach and interaction with reward-predictive cues. It is associated with addiction-related phenotypes and compulsive behavior. Several previous studies have demonstrated that when there is uncertainty about reward properties (e.g. probability, size), sign-tracking is increased. However, the effect of cue-uncertainty on sign-tracking behavior is not known. Here, using a Pavlovian conditioning paradigm, we manipulated the temporal uncertainty about the appearance of cues by implementing either fixed or variable inter-trial intervals (ITIs) of different durations across groups of mice. We found that temporal uncertainty during acquisition significantly enhances sign-tracking, which persists during extinction, even when ITI variability was different in the extinction session than in the acquisition session. This suggests that the effects of temporal uncertainty are learned and retained, rather than performance-based. Our results demonstrate that sign-tracking behavior is not only modified by the characteristic of the reward, but it can also be modified by the uncertainty regarding cues. These findings highlight how temporal predictability shapes cue-directed behaviors and has implications for understanding reward-related behavioral responses including sign-tracking behaviors.

animal behavior and cognition↗

Robust Methods For Quantifying Neuronal Morphology And Molecular Signaling Reveal That Psychedelics Do Not Induce Neuroplasticity

Induction of neuroplasticity has become the dominant explanatory framework for the rapid and sustained therapeutic effects of classic psychedelics. Within this broad concept, examination of morphological neuronal plasticity, such as dendritic arbor growth, is widely used to assess the neuroplasticity effects of classic and novel psychedelics. At the molecular level, it has been reported that serotonergic psychedelic compounds mediate dendritogenesis via the master molecular regulator of plasticity, TrkB, either directly via BDNF/TrkB signaling potentiation or indirectly through 5-HT2A receptor. To examine these hypotheses in detail, we developed a robust multimodal screening platform for unbiased, semi-automated quantification of cellular morphology and multiplex molecular signaling in the same cortical neurons. We found that in widely used primary neuronal cultures psychedelics do not directly modulate TrkB receptor or BDNF-TrkB signaling. We also found 5HT2a receptor gene expression and functional receptor levels are low, and psychedelics do not induce morphological growth, in contrast to significant dendritogenesis elicited by BDNF. Our results challenge recently published results in the field and indicate a need for rigorous experimental methods to study morphological manifestations of neuroplasticity effects induced by clinically used and experimental therapeutics.

neuroscience↗