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Additive and sub-additive antiallodynic interactions between mu-opioid agonists and N-Methyl D-Aspartate antagonists in male rhesus monkeys
Mu-opioid agonists are clinically effective analgesics, but also produce undesirable effects such as sedation and abuse potential that limit their clinical utility. Glutamatergic systems also modulate nociception, and N-Methyl D-Aspartate (NMDA) receptor antagonists have been proposed as one useful...
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| 發表在: | Behav Pharmacol |
|---|---|
| Main Authors: | , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2018
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5760441/ https://ncbi.nlm.nih.gov/pubmed/29239974 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/FBP.0000000000000336 |
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