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. 2014 Jul 14;9(7):e102027. doi: 10.1371/journal.pone.0102027

Table 1. Pharmacological treatments tested for potential anti-allodynic effects in spinal cord-transected rats.

Drugs Pharmacological effect Dose Efficacy on biting behavior
Morphine Opioid receptor agonist 1, 3, 10 mg/kg s.c. +++
Tapentadol Opioid receptor agonist and noradrenaline reuptake inhibitor 10, 20 mg/kg i.p. +++
Ketamine NMDA receptor antagonist 50 mg/kg i.p. ++
Baclofen GABA B receptor agonist 10 mg/kg i.p. +
Clonazepam Benzodiazepine (agonist) 0.25, 2 mg/kg i.p. -
Gabapentin Blockade of calcium channel α2δ subunit 30, 100, 300 mg/kg i.p. -
Pregabalin Blockade of calcium channel α2δ subunit 30 mg/kg i.p. -
Amitriptyline Tricyclic antidepressant 10 mg/kg i.p. -
Amitriptyline + Gabapentin Tricyclic antidepressant + Blockade of calcium channel α2δ subunit 10 mg/kg i.p. +100 mg/kg i.p. -
Cyclotraxin B TrkB receptor blocker 20 mg/kg i.p. -
Naratriptan 5-HT1B/D receptor agonist 0.1 mg/kg i.p. -
Ondansetron 5-HT3 receptor antagonist 20 µg i.t. -
8-OH-DPAT 5-HT1A/7 receptor agonist 0.25 mg/kg i.p. -

+++: potent anti-allodynic effect (complete recovery of control mechanical sensitivity);

++: potent but short lasting anti-allodynic effect;

+: modest but significant anti-allodynic effect; -: inactive treatment.