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Running wheel exercise before a binge regimen of methamphetamine does not protect against striatal dopaminergic
Steven J O'dell1, John F Marshall
1Department of Neurobiology and Behavior, University of California, Irvine, California, 92697.
Abstract:
Repeated administration of methamphetamine (mAMPH) to rodents in a single-day "binge" dosing regimen produces long-lasting damage to forebrain dopaminergic nerve terminals as measured by decreases in tissue dopamine (DA) content and levels of the plasmalemmal DA transporter (DAT). However, the midbrain cell bodies from which the DA terminals arise survive, and previous reports show that striatal DA markers return to control levels by 12 months post-mAMPH, suggesting long-term repair or regrowth of damaged DA terminals. We previously showed that when rats engaged in voluntary aerobic exercise for 3 weeks before and 3 weeks after a binge regimen of mAMPH, exercise significantly ameliorated mAMPH-induced decreases in striatal DAT. However, these data left unresolved the question of whether exercise protected against the initial neurotoxicity from the mAMPH binge or accelerated the repair of the damaged DA terminals. The present experiments were designed to test whether exercise protects against the mAMPH-induced injury. Adult male Sprague-Dawley rats were allowed to run in wheels for 3 weeks before an acute binge regimen of mAMPH or saline, then placed into nonwheel cages for an additional week before autoradiographic determination of striatal DAT binding. The autoradiographic findings showed that prior exercise provided no protection against mAMPH-induced damage to striatal DA terminals. These results, together with analyses from our previous experiments, suggest that voluntary exercise may accelerate the repair of mAMPH-damaged DA terminals and that voluntary exercise may be useful as therapeutic adjunct in the treatment mAMPH addicts.
Insights
Voluntary exercise does not protect against methamphetamine (mAMPH) neurotoxicity. However, exercise may accelerate the repair of damaged dopamine terminals, suggesting a therapeutic role for addicts.
Area of Science:
- Neuroscience
- Pharmacology
- Exercise Science
Background:
- Methamphetamine (mAMPH) binge use causes long-lasting damage to dopaminergic nerve terminals.
- Dopamine transporter (DAT) levels are decreased after mAMPH exposure.
- Previous studies suggest potential for dopamine terminal repair over time.
Purpose of the Study:
- To investigate whether voluntary exercise protects against acute methamphetamine-induced neurotoxicity.
- To differentiate between exercise's protective effects and its potential to accelerate repair.
Main Methods:
- Rats underwent 3 weeks of voluntary wheel running before mAMPH or saline administration.
- Following drug exposure, rats were housed without wheels for 1 week.
- Striatal DAT binding was assessed using autoradiography.
Main Results:
- Prior voluntary exercise offered no protection against mAMPH-induced damage to striatal DAT.
- These findings indicate exercise does not prevent initial neurotoxicity.
Conclusions:
- Voluntary exercise does not protect against methamphetamine neurotoxicity.
- Exercise may accelerate the repair of damaged dopamine terminals, suggesting potential as a therapeutic adjunct for methamphetamine addiction.