Acoustic startle response, prepulse inhibition, and spontaneous locomotor activity in MPTP-treated mice

Andreas Leng, Kay Yan Benjamin Yee, Joram Feldon, Boris Ferger

Research output: Journal article publicationJournal articleAcademic researchpeer-review

11 Citations (Scopus)


Parkinson's disease (PD) is marked by characterised motor deficits and is accompanied by a severe degeneration of the nigrostriatal dopamine (DA) pathway. It has also been reported that PD patients exhibited additional behavioural deficits, including a deficiency in sensorimotor gating mechanisms. We therefore examined whether the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) model of PD in mice could lead to a sensorimotor gating deficit in the prepulse inhibition (PPI) of the acoustic startle response (ASR) paradigm. Two MPTP treatment schedules were separately examined here in male C57BL/6 mice. Post-mortem HPLC analysis confirmed that they were effective in depleting DA in the dorsal striatum (75-88%). PPI was evaluated on days 2, 9 and 16 after the last MPTP treatment; spontaneous locomotor activity was assessed 24 h before each PPI test. No significant change in the expression of PPI was detected across the three time points. On the other hand, the MPTP treatment reduced activity on post-treatment day 1. This effect subsided on post-treatment day 8, and was reversed on day 15. The possibility remains therefore that the reported sensorimotor gating deficits in PD patients might stem from structural or neurochemical aberrations beyond those induced by MPTP treatment.
Original languageEnglish
Pages (from-to)449-456
Number of pages8
JournalBehavioural Brain Research
Issue number2
Publication statusPublished - 5 Oct 2004
Externally publishedYes


  • 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine
  • Behaviour
  • Open field
  • Parkinson's disease
  • PPI

ASJC Scopus subject areas

  • Behavioral Neuroscience


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