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A General Method for Evaluating Deep Brain Stimulation Effects on Intravenous Methamphetamine Self-Administration
Published on: January 22, 2016
The antibiotic minocycline prevents methamphetamine-induced rewarding effects in mice
Yuko Fujita1, Shinsui Kunitachi, Masaomi Iyo
1Division of Clinical Neuroscience, Chiba University Center for Forensic Mental Health, Chiba, Japan.
Abstract:
Repeated use of methamphetamine (METH) causes dependence in humans, and to date, there are no effective medication treatments for METH addiction. We previously reported that the antibiotic minocycline attenuated behavioral abnormalities (hyperactivity and behavioral sensitization) and dopaminergic neurotoxicity in mice and monkeys, after the administration of METH. In this study, we examined the effect of minocycline on METH-induced rewarding effects in mice using the conditioned place preference (CPP) paradigm. Minocycline (40 mg/kg, IP) significantly attenuated METH (1.0 mg/kg, SC)-induced place preference in mice. In vivo microdialysis experiments using free-moving mice, showed that minocycline (40 mg/kg, IP) significantly attenuated the increased extracellular dopamine (DA) levels within the nucleus accumbens, typically seen after the administration of METH (1.0 mg/kg, SC). These findings suggest that minocycline may block METH-induced rewarding effects by down regulating extracellular DA levels in the nucleus accumbens of mice. This would make minocycline a potential therapeutic drug for the treatment of METH induced disorders.
Insights
The antibiotic minocycline reduced methamphetamine (METH) addiction's rewarding effects in mice. This suggests minocycline could be a potential treatment for METH addiction by lowering dopamine levels.
Area of Science:
- Neuroscience
- Pharmacology
- Addiction Research
Background:
- Methamphetamine (METH) dependence is a significant human health issue with no current effective medication treatments.
- Previous research indicated minocycline's potential to mitigate METH-induced behavioral and neurotoxic effects in animal models.
Purpose of the Study:
- To investigate the efficacy of minocycline in blocking the rewarding effects of METH in mice.
- To explore the neurochemical mechanisms underlying minocycline's potential anti-addiction properties.
Main Methods:
- Utilized the conditioned place preference (CPP) paradigm to assess METH-induced reward.
- Employed in vivo microdialysis in free-moving mice to measure extracellular dopamine (DA) levels in the nucleus accumbens.
Main Results:
- Minocycline (40 mg/kg) significantly attenuated METH (1.0 mg/kg)-induced place preference.
- Minocycline administration markedly reduced the METH-induced increase in extracellular DA levels within the nucleus accumbens.
Conclusions:
- Minocycline effectively blocks METH-induced rewarding effects in mice.
- The observed effects are likely mediated by the down-regulation of extracellular dopamine in the nucleus accumbens.
- Minocycline shows promise as a therapeutic agent for treating METH-induced disorders.
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