Connecting Parkinson's disease and drug addiction: common players reveal unexpected disease connections and novel therapeutic approaches

Curr Pharm Des. 2011;17(5):449-61. doi: 10.2174/138161211795164103.

Abstract

Parkinson´s disease (PD) is generally a sporadic disease, and only a small proportion of cases have a clear genetic component. During the last few years, a possible specific cause triggering death of dopaminergic neurons in the substantia nigra, drug of abuse-induced neurotoxicity, is being considered as a potential mechanism to develop PD, especially in the case of abuse of amphetamine and its derivatives. Recent evidences have shown pleiotrophin, a growth factor with important functions in remodeling and repair of injured neural tissue, as an important factor involved in the pathogenesis of both diseases by preventing neurodegeneration in Parkinson's disease, neurotoxicity induced by drug abuse and by its ability to modulate drugs addictive effects. This review discusses targeting growth factors such as glial-derived neurotrophic factor (GDNF) and brain-derived neurotrophic factor (BDNF) to treat Parkinson's disease and/or drug addiction and compiles recent evidences to propose the pleiotrophin/receptor protein tyrosine phosphatase β/ζ signaling pathway as a new therapeutic target to treat Parkinson's disease and to prevent drug of abuse-induced neurotoxicity and addictive effects.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Carrier Proteins / biosynthesis
  • Carrier Proteins / physiology
  • Cytokines / biosynthesis
  • Cytokines / physiology
  • Disease Models, Animal
  • Drug Discovery / methods*
  • Humans
  • Nerve Degeneration / chemically induced
  • Nerve Degeneration / complications
  • Nerve Degeneration / drug therapy*
  • Nerve Degeneration / physiopathology
  • Nerve Growth Factors / pharmacology
  • Nerve Growth Factors / therapeutic use*
  • Parkinson Disease / complications
  • Parkinson Disease / drug therapy*
  • Parkinson Disease / physiopathology
  • Receptor-Like Protein Tyrosine Phosphatases, Class 5 / antagonists & inhibitors*
  • Signal Transduction / drug effects
  • Signal Transduction / physiology
  • Substance-Related Disorders / complications
  • Substance-Related Disorders / drug therapy*
  • Substance-Related Disorders / physiopathology

Substances

  • Carrier Proteins
  • Cytokines
  • Nerve Growth Factors
  • pleiotrophin
  • Receptor-Like Protein Tyrosine Phosphatases, Class 5