Dopamine-dependent CB1 receptor dysfunction at corticostriatal synapses in homozygous PINK1 knockout mice

G. Madeo, T. Schirinzi, M. Maltese, G. Martella, C. Rapino, F. Fezza, N. Mastrangelo, P. Bonsi, M. MacCarrone, A. Pisani

Research output: Contribution to journalArticle

Abstract

Recessive mutations in the PTEN-induced putative kinase 1 (PINK1) gene cause early-onset Parkinson's disease (PD). We investigated the interaction between endocannabinoid (eCB) and dopaminergic transmission at corticostriatal synapses in PINK1 deficient mice. Whole-cell patch-clamp and conventional recordings of striatal medium spiny neurons (MSNs) were made from slices of PINK1-/-, heterozygous PINK1+/- mice and wild-type littermates (PINK1+/+). In PINK1+/+ mice, CB1 receptor (CB1R) activation reduced spontaneous excitatory postsynaptic currents (sEPSCs). Likewise, CB1R agonists (ACEA, WIN55,212-3 and HU210) induced a dose-dependent reduction of cortically-evoked excitatory postsynaptic potential (eEPSP) amplitude. While CB1R agonists retained their inhibitory effect in heterozygous PINK1+/- mice, conversely, in PINK1-/- mice they failed to modulate sEPSC amplitude. Similarly, CB1R activation failed to reduce eEPSP amplitude in PINK1-/- mice. Parallel biochemical measurements revealed no significant difference in the levels of the two main eCBs, 2-arachidonoylglycerol (2-AG) and anandamide (AEA) in PINK1-/- striata. Similarly, no change was observed in the enzymatic activity of both fatty acid amide hydrolase (FAAH) and monoacylglycerol lipase (MAGL), responsible for eCB hydrolysis. Instead, a significant reduction of binding ability of CB1R agonists was found in PINK1-/- mice. Notably, the CB1R-dependent inhibition of synaptic activity was restored either by amphetamine or after chronic treatment with the D2 dopamine receptor agonist quinpirole. Additionally, CB1R binding activity returned to control levels after chronic pretreatment with quinpirole. Consistent with the hypothesis of a close interplay with dopaminergic neurotransmission, our findings show a CB1R dysfunction at corticostriatal synapses in PINK1-/-, but not in PINK1+/- mice, and provide a mechanistic link to the distinct plasticity deficits observed in both genotypes.

Original languageEnglish
Pages (from-to)460-470
Number of pages11
JournalNeuropharmacology
Volume101
DOIs
Publication statusE-pub ahead of print - Oct 20 2015

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Keywords

  • Dopamine
  • Electrophysiology
  • Endocannabinoid
  • Parkinson's disease
  • PINK1
  • Striatum

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience
  • Pharmacology

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