PLoS ONE (Jan 2015)

PE859, a novel tau aggregation inhibitor, reduces aggregated tau and prevents onset and progression of neural dysfunction in vivo.

  • Michiaki Okuda,
  • Ichiro Hijikuro,
  • Yuki Fujita,
  • Xiaofeng Wu,
  • Shinichi Nakayama,
  • Yoko Sakata,
  • Yuji Noguchi,
  • Makoto Ogo,
  • Shigeru Akasofu,
  • Yoshimasa Ito,
  • Yoshiyuki Soeda,
  • Nobuhiko Tsuchiya,
  • Naoki Tanaka,
  • Takashi Takahashi,
  • Hachiro Sugimoto

DOI
https://doi.org/10.1371/journal.pone.0117511
Journal volume & issue
Vol. 10, no. 2
p. e0117511

Abstract

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In tauopathies, a neural microtubule-associated protein tau (MAPT) is abnormally aggregated and forms neurofibrillary tangle. Therefore, inhibition of the tau aggregation is one of the key approaches for the treatment of these diseases. Here, we have identified a novel tau aggregation inhibitor, PE859. An oral administration of PE859 resulted in the significant reduction of sarkosyl-insoluble aggregated tau along with the prevention of onset and progression of the motor dysfunction in JNPL3 P301L-mutated human tau transgenic mice. These results suggest that PE859 is useful for the treatment of tauopathies.