Metformin, besides exhibiting strong in vivo anti-inflammatory properties, increases mptp-induced damage to the nigrostriatal dopaminergic system

Toxicol Appl Pharmacol. 2016 May 1:298:19-30. doi: 10.1016/j.taap.2016.03.004. Epub 2016 Mar 10.

Abstract

Metformin is a widely used oral antidiabetic drug with known anti-inflammatory properties due to its action on AMPK protein. This drug has shown a protective effect on various tissues, including cortical neurons. The aim of this study was to determine the effect of metformin on the dopaminergic neurons of the substantia nigra of mice using the animal model of Parkinson's disease based on the injection of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine, an inhibitor of the mitochondrial complex I. In vivo and in vitro experiments were used to study the activation of microglia and the damage of the dopaminergic neurons. Our results show that metformin reduced microglial activation measured both at cellular and molecular levels. Rather than protecting, metformin exacerbated dopaminergic damage in response to MPTP. Our data suggest that, contrary to other brain structures, metformin treatment could be deleterious for the dopaminergic system. Hence, metformin treatment may be considered as a risk factor for the development of Parkinson's disease.

Keywords: Diabetes mellitus; Dopaminergic system; MPTP; Metformin; Parkinson's disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology
  • Anti-Inflammatory Agents / toxicity*
  • Apoptosis / drug effects
  • Apoptosis / immunology
  • Cell Culture Techniques
  • Cell Line
  • Corpus Striatum / drug effects*
  • Corpus Striatum / metabolism
  • Corpus Striatum / pathology
  • Dopamine / metabolism
  • Dopaminergic Neurons / drug effects*
  • Dopaminergic Neurons / metabolism
  • Dopaminergic Neurons / pathology
  • Immunohistochemistry
  • Male
  • Metformin / pharmacology
  • Metformin / toxicity*
  • Mice, Inbred C57BL
  • Microglia / drug effects
  • Microglia / immunology
  • Oxidative Stress / drug effects
  • Oxidative Stress / immunology
  • Parkinsonian Disorders* / chemically induced
  • Parkinsonian Disorders* / pathology
  • Reactive Oxygen Species / metabolism
  • Real-Time Polymerase Chain Reaction
  • Substantia Nigra / drug effects*
  • Substantia Nigra / metabolism
  • Substantia Nigra / pathology

Substances

  • Anti-Inflammatory Agents
  • Reactive Oxygen Species
  • Metformin
  • Dopamine