Nature Communications (Nov 2017)

NitroSynapsin therapy for a mouse MEF2C haploinsufficiency model of human autism

  • Shichun Tu,
  • Mohd Waseem Akhtar,
  • Rosa Maria Escorihuela,
  • Alejandro Amador-Arjona,
  • Vivek Swarup,
  • James Parker,
  • Jeffrey D. Zaremba,
  • Timothy Holland,
  • Neha Bansal,
  • Daniel R. Holohan,
  • Kevin Lopez,
  • Scott D. Ryan,
  • Shing Fai Chan,
  • Li Yan,
  • Xiaofei Zhang,
  • Xiayu Huang,
  • Abdullah Sultan,
  • Scott R. McKercher,
  • Rajesh Ambasudhan,
  • Huaxi Xu,
  • Yuqiang Wang,
  • Daniel H. Geschwind,
  • Amanda J. Roberts,
  • Alexey V. Terskikh,
  • Robert A. Rissman,
  • Eliezer Masliah,
  • Stuart A. Lipton,
  • Nobuki Nakanishi

DOI
https://doi.org/10.1038/s41467-017-01563-8
Journal volume & issue
Vol. 8, no. 1
pp. 1 – 12

Abstract

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Human MEF2C haploinsufficiency results in Autism Spectrum Disorder (ASD), but it is unclear if the same is true in mice. Here, the authors show that Mef2c +/− mice have behavioral defects and neuronal abnormalities similar to ASD, and symptoms can be ameliorated with the new drug, NitroSynapsin.