Is there neuroprotection in Parkinson syndrome?

J Neurol. 2000 Sep:247 Suppl 4:IV/8-11. doi: 10.1007/pl00007777.

Abstract

Parkinson's disease (PD) is a neurodegenerative disorder of the aging population with unknown etiopathogenesis. It is assumed that the underlying pathobiochemical processes comprise multifactorial and multigenetic disturbances leading to a progressive and devastating disorder without remission. Subtypes exist suggesting that "PD" is a spectrum disorder with variations in the cascade of pathobiochemical and genetic events. Neuroprotective endogenous processes are lost at the very beginning of PD. Supplementation of substances with neuroprotective and/or neurorescue capacity is eminent for future therapeutic strategies. MAO-B inhibitors, NMDA-receptor antagonists and dopamine receptor agonists fulfill such a criterion in preclinical studies while there is no clear evidence for clinical neuroprotection. However, PET-controlled studies comparing L-DOPA-treated and ropinirol-treated PD patients give evidence for the "concept of neuroprotective treatment strategies".

Publication types

  • Review

MeSH terms

  • Dopamine Agonists / therapeutic use
  • Drug Therapy, Combination
  • Humans
  • Monoamine Oxidase Inhibitors / therapeutic use
  • Neuroprotective Agents / therapeutic use*
  • Parkinsonian Disorders / drug therapy*
  • Parkinsonian Disorders / etiology
  • Parkinsonian Disorders / physiopathology
  • Receptors, N-Methyl-D-Aspartate / antagonists & inhibitors
  • Selegiline / therapeutic use
  • Vitamin E / therapeutic use

Substances

  • Dopamine Agonists
  • Monoamine Oxidase Inhibitors
  • Neuroprotective Agents
  • Receptors, N-Methyl-D-Aspartate
  • Vitamin E
  • Selegiline