Gadd45β ameliorates L-DOPA-induced dyskinesia in a Parkinson's disease mouse model

Neurobiol Dis. 2016 May:89:169-79. doi: 10.1016/j.nbd.2016.02.013. Epub 2016 Feb 10.

Abstract

The dopamine precursor 3,4-dihydroxyphenyl-l-alanine (L-DOPA) is currently the most efficacious pharmacotherapy for Parkinson's disease (PD). However, long-term L-DOPA treatment leads to the development of abnormal involuntary movements (AIMs) in patients and animal models of PD. Recently, involvement of growth arrest and DNA damage-inducible 45β (Gadd45β) was reported in neurological and neurobehavioral dysfunctions. However, little is known about the role of Gadd45β in the dopaminergic nigrostriatal pathway or L-DOPA-induced dyskinesia (LID). To address this issue, we prepared an animal model of PD using unilateral 6-hydroxydopamine (6-OHDA) lesions in the substantia nigra of Gadd45β(+/+) and Gadd45β(-/-) mice. Dyskinetic symptoms were triggered by repetitive administration of L-DOPA in these 6-OHDA-lesioned mice. Whereas dopamine denervation in the dorsal striatum decreased Gadd45β mRNA, chronic L-DOPA treatment significantly increased Gadd45β mRNA expression in the 6-OHDA-lesioned striatum of wild-type mice. Using unilaterally 6-OHDA-lesioned Gadd45β(+/+) and Gadd45β(-/-) mice, we found that mice lacking Gadd45β exhibited long-lasting increases in AIMs following repeated administration of L-DOPA. By contrast, adeno-associated virus-mediated expression of Gadd45β in the striatum reduced AIMs in Gadd45β knockout mice. The deficiency of Gadd45β in LID increased expression of ΔFosB and c-Fos in the lesioned striatum 90 min after the last administration of L-DOPA following 11days of daily L-DOPA treatments. These data suggest that the increased expression of Gadd45β induced by repeated administration of L-DOPA may be beneficial in patients with PD.

Keywords: Dyskinesia; GADD45β; L-DOPA; Parkinson's disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Differentiation / genetics
  • Antigens, Differentiation / metabolism*
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Disease Models, Animal
  • Dyskinesia, Drug-Induced / metabolism*
  • Dyskinesia, Drug-Induced / pathology
  • Levodopa / toxicity*
  • MAP Kinase Signaling System / drug effects
  • Male
  • Mice
  • Mice, Knockout
  • Motor Activity / drug effects
  • Oxidopamine
  • Parkinsonian Disorders / metabolism*
  • Parkinsonian Disorders / pathology
  • RNA, Messenger / metabolism
  • Receptors, Dopamine D1 / metabolism
  • Substantia Nigra / metabolism
  • Substantia Nigra / pathology

Substances

  • Antigens, Differentiation
  • Gadd45b protein, mouse
  • RNA, Messenger
  • Receptors, Dopamine D1
  • Levodopa
  • Oxidopamine
  • Cyclic AMP-Dependent Protein Kinases