Lost in translation: no effect of repeated optogenetic cortico-striatal stimulation on compulsivity in rats
Abstract The orbitofrontal cortex–ventromedial striatum (OFC–VMS) circuitry is widely believed to drive compulsive behavior. Hyperactivating this pathway in inbred mice produces excessive and persistent self-grooming, which has been considered a model for human compulsivity. We aimed to replicate th...
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doaj-811f3a9517ea44bbaaaa39ebad2210a72021-05-30T11:50:26ZengNature Publishing GroupTranslational Psychiatry2158-31882021-05-0111111610.1038/s41398-021-01448-xLost in translation: no effect of repeated optogenetic cortico-striatal stimulation on compulsivity in ratsAmanda R. de Oliveira0Adriano E. Reimer1Gregory J. Simandl2Sumedh S. Nagrale3Alik S. Widge4Department of Psychology, Federal University of São Carlos (UFSCar)Department of Psychiatry, University of MinnesotaDepartment of Psychiatry, University of MinnesotaDepartment of Psychiatry, University of MinnesotaDepartment of Psychiatry, University of MinnesotaAbstract The orbitofrontal cortex–ventromedial striatum (OFC–VMS) circuitry is widely believed to drive compulsive behavior. Hyperactivating this pathway in inbred mice produces excessive and persistent self-grooming, which has been considered a model for human compulsivity. We aimed to replicate these findings in outbred rats, where there are few reliable compulsivity models. Male Long-Evans rats implanted with optical fibers into VMS and with opsins delivered into OFC received optical stimulation at parameters that produce OFC–VMS plasticity and compulsive grooming in mice. We then evaluated rats for compulsive self-grooming at six timepoints: before, during, immediately after, and 1 h after each stimulation, 1 and 2 weeks after the ending of a 6-day stimulation protocol. To further test for effects of OFC–VMS hyperstimulation, we ran animals in three standard compulsivity assays: marble burying, nestlet shredding, and operant attentional set-shifting. OFC–VMS stimulation did not increase self-grooming or induce significant changes in nestlet shredding, marble burying, or set-shifting in rats. Follow-on evoked potential studies verified that the stimulation protocol altered OFC–VMS synaptic weighting. In sum, although we induced physiological changes in the OFC–VMS circuitry, we could not reproduce in a strongly powered study in rats a model of compulsive behavior previously reported in mice. This suggests possible limitations to translation of mouse findings to species higher on the phylogenetic chain.https://doi.org/10.1038/s41398-021-01448-x |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Amanda R. de Oliveira Adriano E. Reimer Gregory J. Simandl Sumedh S. Nagrale Alik S. Widge |
spellingShingle |
Amanda R. de Oliveira Adriano E. Reimer Gregory J. Simandl Sumedh S. Nagrale Alik S. Widge Lost in translation: no effect of repeated optogenetic cortico-striatal stimulation on compulsivity in rats Translational Psychiatry |
author_facet |
Amanda R. de Oliveira Adriano E. Reimer Gregory J. Simandl Sumedh S. Nagrale Alik S. Widge |
author_sort |
Amanda R. de Oliveira |
title |
Lost in translation: no effect of repeated optogenetic cortico-striatal stimulation on compulsivity in rats |
title_short |
Lost in translation: no effect of repeated optogenetic cortico-striatal stimulation on compulsivity in rats |
title_full |
Lost in translation: no effect of repeated optogenetic cortico-striatal stimulation on compulsivity in rats |
title_fullStr |
Lost in translation: no effect of repeated optogenetic cortico-striatal stimulation on compulsivity in rats |
title_full_unstemmed |
Lost in translation: no effect of repeated optogenetic cortico-striatal stimulation on compulsivity in rats |
title_sort |
lost in translation: no effect of repeated optogenetic cortico-striatal stimulation on compulsivity in rats |
publisher |
Nature Publishing Group |
series |
Translational Psychiatry |
issn |
2158-3188 |
publishDate |
2021-05-01 |
description |
Abstract The orbitofrontal cortex–ventromedial striatum (OFC–VMS) circuitry is widely believed to drive compulsive behavior. Hyperactivating this pathway in inbred mice produces excessive and persistent self-grooming, which has been considered a model for human compulsivity. We aimed to replicate these findings in outbred rats, where there are few reliable compulsivity models. Male Long-Evans rats implanted with optical fibers into VMS and with opsins delivered into OFC received optical stimulation at parameters that produce OFC–VMS plasticity and compulsive grooming in mice. We then evaluated rats for compulsive self-grooming at six timepoints: before, during, immediately after, and 1 h after each stimulation, 1 and 2 weeks after the ending of a 6-day stimulation protocol. To further test for effects of OFC–VMS hyperstimulation, we ran animals in three standard compulsivity assays: marble burying, nestlet shredding, and operant attentional set-shifting. OFC–VMS stimulation did not increase self-grooming or induce significant changes in nestlet shredding, marble burying, or set-shifting in rats. Follow-on evoked potential studies verified that the stimulation protocol altered OFC–VMS synaptic weighting. In sum, although we induced physiological changes in the OFC–VMS circuitry, we could not reproduce in a strongly powered study in rats a model of compulsive behavior previously reported in mice. This suggests possible limitations to translation of mouse findings to species higher on the phylogenetic chain. |
url |
https://doi.org/10.1038/s41398-021-01448-x |
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