Abnormal Whisker-Dependent Behaviors and Altered Cortico-Hippocampal Connectivity in Shank3b−/− Mice

  • Luigi Balasco
  • , Marco Pagani
  • , Luca Pangrazzi
  • , Gabriele Chelini
  • , Alessandra Georgette Ciancone Chama
  • , Evgenia Shlosman
  • , Lorenzo Mattioni
  • , Alberto Galbusera
  • , Giuliano Iurilli
  • , Giovanni Provenzano
  • , Alessandro Gozzi
  • , Yuri Bozzi

Risultato della ricerca: Contributo in rivistaArticolo

Abstract

Abnormal tactile response is an integral feature of Autism Spectrum Disorders (ASDs), and hypo-responsiveness to tactile stimuli is often associated with the severity of ASDs core symptoms. Patients with Phelan-McDermid syndrome (PMS), caused by mutations in the SHANK3 gene,show ASD-like symptoms associated with aberrant tactile responses. The neural underpinnings of these abnormalities are still poorly understood. Here we investigated, in Shank3b−/− adult mice, the neural substrates of whisker-guided behaviors, a key component of rodents’ interaction with the surrounding environment. We assessed whisker-dependent behaviors in Shank3b−/− adult mice and age-matched controls, using the textured novel object recognition (tNORT) and whisker nuisance (WN) test. Shank3b−/−mice showed deficits in whisker-dependent texture discrimination in tNORT and behavioral hypo-responsiveness to repetitive whisker stimulation in WN. Sensory hypo-responsiveness was accompanied by a significantly reduced activation of the primary somatosensory cortex (S1) and hippocampus, as measured by c-fos mRNA induction, a proxy of neuronal activity following whisker stimulation. Moreover,resting-state fMRI showed a significantly reduced S1-hippocampal connectivity in Shank3b mutants, in the absence of altered connectivity between S1 and other somatosensory areas. Impaired crosstalk between hippocampus and S1 might underlie Shank3b−/−hypo-reactivity to whisker dependent cues, highlighting a potentially generalizable somatosensory dysfunction in ASD.
Lingua originaleInglese
pagine (da-a)3042-3056
Numero di pagine15
RivistaCerebral Cortex
Volume32
DOI
Stato di pubblicazionePubblicato - 2022

Keywords

  • autism spectrum disorder

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