Quercetin improves behavioral deficiencies, restores astrocytes and microglia, and reduces serotonin metabolism in 3-nitropropionic acid-induced rat model of Huntington's Disease

CNS Neurosci Ther. 2014 Jan;20(1):10-9. doi: 10.1111/cns.12189. Epub 2013 Nov 4.

Abstract

Aim: Huntington's disease (HD) is an autosomal dominant disorder, for which clinically available drugs offer only symptomatic relief. These prescription drugs are not free of side effects, and the patients usually suffer from anxiety and depression. We investigated quercetin, a dietary flavonoid with free radical scavenging properties, for its beneficial potential if any, in 3-nitropropionic acid (3-NP)-induced HD in rats where both drugs were administered simultaneously.

Methods: Performance of rats on beam balancing, elevated plus maze and gait traits were investigated following 3-NP and/or quercetin treatments for 4 days. Striatal biogenic amine levels and monoamine oxidase activity were assayed. Striatal sections were examined for Cd11B and glial fibrillary acidic protein immunoreactivity, and for evidences of neuronal lesion.

Results: Quercetin significantly attenuated 3-NP-induced anxiety, motor coordination deficits, and gait despair. While the dopaminergic hyper-metabolism was unaffected, quercetin provided a significant reduction of 3-NP mediated increase in serotonin metabolism. Quercetin failed to affect 3-NP-induced striatal neuronal lesion, but decreased microglial proliferation, and increased astrocyte numbers in the lesion core.

Conclusion: These results taken together suggest that quercetin could be of potential use not only for correcting movement disturbances and anxiety in HD, but also for addressing inflammatory damages.

Keywords: Depression; Gait disturbances; Glial fibrillary acidic protein; Inflammatory mediators; Serotonin metabolism; Striatal dopamine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / therapeutic use*
  • Astrocytes / drug effects*
  • Astrocytes / pathology
  • Astrocytes / physiology
  • Cell Proliferation / drug effects
  • Cerebral Cortex / drug effects
  • Cerebral Cortex / pathology
  • Cerebral Cortex / physiopathology
  • Corpus Striatum / pathology
  • Corpus Striatum / physiopathology
  • Disease Models, Animal
  • Dopamine / metabolism
  • Huntington Disease / chemically induced
  • Huntington Disease / drug therapy*
  • Huntington Disease / pathology
  • Huntington Disease / physiopathology
  • Male
  • Maze Learning / drug effects
  • Microglia / drug effects*
  • Microglia / pathology
  • Microglia / physiology
  • Monoamine Oxidase / metabolism
  • Motor Activity / drug effects
  • Neurons / drug effects
  • Neurons / pathology
  • Neurons / physiology
  • Nitro Compounds
  • Propionates
  • Quercetin / therapeutic use*
  • Rats
  • Rats, Sprague-Dawley
  • Serotonin / metabolism*
  • Weight Loss / drug effects

Substances

  • Antioxidants
  • Nitro Compounds
  • Propionates
  • Serotonin
  • Quercetin
  • Monoamine Oxidase
  • 3-nitropropionic acid
  • Dopamine