Swimming training prevents pentylenetetrazol-induced inhibition of Na+, K+-ATPase activity, seizures, and oxidative stress

Epilepsia. 2009 Apr;50(4):811-23. doi: 10.1111/j.1528-1167.2008.01908.x. Epub 2008 Dec 4.

Abstract

Purpose: In the present study we decided to investigate whether physical exercise protects against the electrographic, oxidative, and neurochemical alterations induced by subthreshold to severe convulsive doses of pentyltetrazole (PTZ).

Methods: The effect of swimming training (6 weeks) on convulsive behavior induced by PTZ (30, 45, and 60 mg/kg, i.p.) was measured and different electrographic electroencephalography (EEG) frequencies obtained from freely moving rats. After EEG recordings, reactive oxygen species (ROS) generation, nonprotein sulfhydryl (NPS), protein carbonyl, thiobarbituric acid-reactive substances (TBARS), superoxide dismutase (SOD), catalase (CAT), Na(+), K(+)-ATPase activity, and glutamate uptake were measured in the cerebral cortex of rats.

Results: We showed that physical training increased latency and attenuated the duration of generalized seizures induced by administration of PTZ (45 mg/kg). EEG recordings showed that physical exercise decreased the spike amplitude after PTZ administration (all doses). Pearson's correlation analysis revealed that protection of physical training against PTZ-induced seizures strongly correlated with NPS content, Na(+), K(+)-ATPase activity, and glutamate-uptake maintenance. Physical training also increased SOD activity, NPS content, attenuated ROS generation per se, and was effective against inhibition of Na(+), K(+)-ATPase activity induced by a subthreshold convulsive dose of PTZ (30 mg/kg). In addition, physical training protected against 2',7'-dichlorofluorescein diacetate (DCFH-DA) oxidation, TBARS and protein carbonyl increase, decrease of NPS content, inhibition of SOD and catalase, and inhibition glutamate uptake induced by PTZ.

Conclusions: These data suggest that effective protection of selected targets for free radical damage, such as Na(+), K(+)-ATPase, elicited by physical training protects against the increase of neuronal excitability and oxidative damage induced by PTZ.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Behavior, Animal
  • Body Weight / drug effects
  • Body Weight / physiology
  • Catalase / metabolism
  • Disease Models, Animal
  • Electroencephalography
  • Exercise Therapy / methods*
  • Fluoresceins
  • Glutamic Acid / metabolism
  • Male
  • Oxidative Stress / drug effects
  • Oxidative Stress / physiology*
  • Pentylenetetrazole
  • Protein Carbonylation / drug effects
  • Rats
  • Rats, Wistar
  • Reaction Time / drug effects
  • Reaction Time / physiology
  • Reactive Oxygen Species / metabolism
  • Seizures / chemically induced
  • Seizures / enzymology*
  • Seizures / prevention & control*
  • Sodium-Potassium-Exchanging ATPase / metabolism*
  • Statistics as Topic
  • Superoxide Dismutase / metabolism
  • Swimming*
  • Thiobarbituric Acid Reactive Substances / metabolism

Substances

  • Fluoresceins
  • Reactive Oxygen Species
  • Thiobarbituric Acid Reactive Substances
  • Glutamic Acid
  • 2',7'-dichlorofluorescein
  • Catalase
  • Superoxide Dismutase
  • Sodium-Potassium-Exchanging ATPase
  • Pentylenetetrazole