Acute morphine treatments alleviate tremor in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-treated monkeys

PLoS One. 2014 Feb 10;9(2):e88404. doi: 10.1371/journal.pone.0088404. eCollection 2014.

Abstract

Parkinson's disease (PD) is a chronic and progressive neurodegenerative disorder associated with decreased striatal dopamine levels. Morphine has been found to elevate dopamine levels, which indicates a potential therapeutic effect in PD treatment that has not been investigated previously. To evaluate this hypothesis, an investigation of the acute effects of morphine on PD symptoms was carried out in male rhesus PD monkeys that had been induced with MPTP. All MPTP induced monkeys displayed progressive and irreversible PD motor symptoms. The behavioral response of these animals to morphine and L-Dopa were quantified with the Kurlan scale. It was found that L-Dopa alleviated bradykinesia, but did not significantly improve tremor. In contrast, acute morphine alleviated tremor significantly. These results suggested that, compared to L-Dopa, morphine has different therapeutic effects in PD therapy and may act through different biological mechanisms to alleviate PD symptoms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine
  • Animals
  • Behavior, Animal / drug effects
  • Hypokinesia / drug therapy
  • Hypokinesia / physiopathology
  • Levodopa / administration & dosage
  • Levodopa / pharmacology
  • Levodopa / therapeutic use
  • Macaca mulatta / physiology*
  • Male
  • Morphine / administration & dosage
  • Morphine / pharmacology
  • Morphine / therapeutic use*
  • Motor Activity / drug effects
  • Parkinson Disease / drug therapy
  • Parkinson Disease / physiopathology
  • Postural Balance / drug effects
  • Tremor / drug therapy*
  • Tremor / physiopathology

Substances

  • Levodopa
  • Morphine
  • 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine

Grants and funding

This research was supported by the Strategic Priority Research Program of the Chinese Academy of Science XDB02020000, 973 program 2012CB825500, 2012CBA01304 and 2011CB707800, the 863 program 2012AA020701, KSCX2-EW-J-23 and KSCX2-EW-R-11, the National Science Foundation of China NSFC 91332120, 31271167, 31070963, 31271168, 81271495 and 31070965. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.