Striatal 6-OHDA lesion in mice: Investigating early neurochemical changes underlying Parkinson's disease

Behav Brain Res. 2010 Mar 17;208(1):137-43. doi: 10.1016/j.bbr.2009.11.020. Epub 2009 Nov 13.

Abstract

Early phases of Parkinson's disease (PD) are characterized by a mild reduction of dopamine (DA) in striatum and by emergence of psychiatric disturbances that precede overt motor symptoms. In order to characterize the neurochemical re-arrangements induced by such striatal impairment, we used a mouse model in which a low dose of 6-hydroxydopamine (6-OHDA) was bilaterally injected into the dorsal striatum. These mice showed a DA reduction of about 40% that remained stable up to 12 weeks after injection. This reduction was accompanied by changes in DA metabolite levels, such as HVA, transiently reduced at 4 weeks, and DOPAC, decreased at 12 weeks. No change in the 5-hydroxytryptamine (5-HT) levels was found but the 5-hydroxyindoleacetic acid (5-HIAA)/5-HT ratio was increased at 4 weeks. In addition, at the same time-point, the levels of 15-F(2t)-IsoP, an index of oxidative stress, and of PGE(2), a major product of cyclooxygenase-2, were decreased in different brain areas while BDNF levels were increased. These neurochemical changes were accompanied by altered behavioral responses concerning the emotional reactivity. Overall, the present findings suggest that a change of 5-HT metabolism and a modification of oxidative stress levels may play a role in the early PD degeneration phases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic Agents / toxicity*
  • Animals
  • Behavior, Animal / drug effects
  • Biogenic Monoamines / metabolism
  • Brain Chemistry / drug effects*
  • Brain-Derived Neurotrophic Factor / metabolism
  • Corpus Striatum / drug effects*
  • Corpus Striatum / metabolism
  • Dinoprost / analogs & derivatives
  • Dinoprost / metabolism
  • Dinoprostone / metabolism
  • Disease Models, Animal
  • Exploratory Behavior / drug effects
  • Locomotion / drug effects
  • Male
  • Maze Learning / drug effects
  • Mice
  • Mice, Inbred C57BL
  • Oxidopamine / toxicity*
  • Parkinson Disease* / etiology
  • Parkinson Disease* / metabolism
  • Parkinson Disease* / pathology
  • Swimming

Substances

  • Adrenergic Agents
  • Biogenic Monoamines
  • Brain-Derived Neurotrophic Factor
  • 8-epi-prostaglandin F2alpha
  • Oxidopamine
  • Dinoprost
  • Dinoprostone