Pharmacological effects of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) on striatal dopamine receptor system

Brain Res. 1986 Mar 26;369(1-2):311-5. doi: 10.1016/0006-8993(86)90541-x.


In mice, chronic administration of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) produces an increase in the maximum number of [3H]spiperone binding sites in the striatum. The sensitivity of striatal protein phosphorylation to calcium plus calmodulin is also potentiated in MPTP-treated mice. These observations are associated with an enhancement of apomorphine-induced climbing behavior in the drug-treated animals. The results of this study suggest that in an animal model for Parkinson's disease, MPTP interrupts the dopamine (DA) transmission by chemically denervating the nigrostriatal neurons and through a compensatory mechanism, it increases the number of DA receptors as well as the sensitivity of protein phosphorylation to calcium plus calmodulin in mouse striatum. The latter two events may contribute to the development of DA receptor supersensitivity.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine
  • Animals
  • Apomorphine / pharmacology
  • Calmodulin / physiology
  • Corpus Striatum / drug effects*
  • Male
  • Mice
  • Motor Activity / drug effects
  • Nerve Tissue Proteins / metabolism
  • Phosphorylation
  • Pyridines / pharmacology*
  • Rats
  • Rats, Inbred Strains
  • Receptors, Dopamine / drug effects*
  • Species Specificity


  • Calmodulin
  • Nerve Tissue Proteins
  • Pyridines
  • Receptors, Dopamine
  • 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine
  • Apomorphine