Synergistic interaction between mazindol, an anorectic drug, and swim-stress on analgesic responses in the formalin test in mice
Autor: | Reinaldo N. Takahashi, Leandro F. Vendruscolo |
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Rok vydání: | 2004 |
Předmět: |
Male
medicine.medical_specialty Dopamine Narcotic Antagonists Analgesic Pain (+)-Naloxone Pharmacology Receptors N-Methyl-D-Aspartate Receptors Dopamine chemistry.chemical_compound Mice Dopamine Uptake Inhibitors Stress Physiological Dopamine receptor D2 Internal medicine Neural Pathways medicine Animals Drug Interactions Neurotransmitter Pain Measurement Mazindol Dose-Response Relationship Drug Chemistry General Neuroscience Brain Endocrinology Opioid Opioid Peptides Receptors Opioid Dopamine Antagonists Sulpiride Excitatory Amino Acid Antagonists medicine.drug |
Zdroj: | Neuroscience letters. 355(1-2) |
ISSN: | 0304-3940 |
Popis: | The present study examined the interaction between mazindol (MZ), an anorectic drug extensively used in Brazil and opioid/non-opioid endogenous analgesic systems activated by swim-stress. Further, the role of opioid, dopamine and N-methyl-D-aspartate (NMDA) receptors in mediating the analgesic effect was evaluated. The stress-induced analgesia of a 3-min swimming at 32 degrees C (opioid/non-opioid) and 20 degrees C (non-opioid) were assessed using the formalin test. Male Swiss mice were intraperitoneally injected with naloxone (1.0 mg/kg), sulpiride (3.0 mg/kg), MK-801 (0.075 mg/kg) or saline/vehicle 15 min prior, and with MZ (0.5 mg/kg) or saline/vehicle 5 min prior to swimming. The dose of MZ (0.5 mg/kg) did not cause analgesic effect, however, the association of MZ and swim-stress at both temperatures displayed synergistic interaction on analgesia that was blocked by sulpiride and MK-801 but not by naloxone. The present results suggest that MZ and swim-stress acted synergistically on analgesic responses, involving mainly the non-opioid component and possibly mediated by dopamine D2 receptors and NMDA receptors. |
Databáze: | OpenAIRE |
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