Effects of histone acetyltransferase inhibitors on l-DOPA-induced dyskinesia in a murine model of Parkinson’s disease

Young Kyoung Ryu, Hye Yeon Park, Jun Go, Yong Hoon Kim, Jung Hwan Hwang, Dong Hee Choi, Jung Ran Noh, Myungchull Rhee, Pyung Lim Han, Chul Ho Lee, Kyoung Shim Kim

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

Histone acetylation is a key regulatory factor for gene expression in cells. Modulation of histone acetylation by targeting of histone acetyltransferases (HATs) effectively alters many gene expression profiles and synaptic plasticity in the brain. However, the role of HATs on l-DOPA-induced dyskinesia of Parkinson’s disease (PD) has not been reported. Our aim was to determine whether HAT inhibitors such as anacardic acid, garcinol, and curcumin from natural plants reduce severity of l-DOPA-induced dyskinesia using a unilaterally 6-hydroxydopamine (6-OHDA)-lesioned PD mouse model. Anacardic acid 2 mg/kg, garcinol 5 mg/kg, or curcumin 100 mg/kg co-treatment with l-DOPA significantly reduced the axial, limb, and orofacial (ALO) score indicating less dyskinesia with administration of HAT inhibitors in 6-OHDA-lesioned mice. Additionally, l-DOPA’s efficacy was not altered by the compounds in the early stage of treatment. The expression levels of c-Fos, Fra-2, and Arc were effectively decreased by administration of HAT inhibitors in the ipsilateral striatum. Our findings indicate that HAT inhibitor co-treatment with l-DOPA may have therapeutic potential for management of l-DOPA-induced dyskinesia in patients with PD.

Original languageEnglish
Pages (from-to)1319-1331
Number of pages13
JournalJournal of Neural Transmission
Volume125
Issue number9
DOIs
StatePublished - 1 Sep 2018

Keywords

  • 6-Hydroxydopamine
  • Anacardic acid
  • Curcumin
  • Garcinol
  • HAT inhibitor
  • l-DOPA-induced dyskinesia

Fingerprint

Dive into the research topics of 'Effects of histone acetyltransferase inhibitors on l-DOPA-induced dyskinesia in a murine model of Parkinson’s disease'. Together they form a unique fingerprint.

Cite this