Antiallodynic activity in STZ-induced diabetic neuropathy pain Albino Swiss mouse model assessed as reduced tactile allodynia at 5 mg/kg, ip administered after 3 weeks of STZ stimulation and measured after 1 hr by von Frey test
Antiallodynic activity in STZ-induced diabetic neuropathy pain Albino Swiss mouse model assessed as reduced tactile allodynia at 10 mg/kg, ip administered after 3 weeks of STZ stimulation and measured after 1 hr by von Frey test
Antiallodynic activity in STZ-induced diabetic neuropathy pain Albino Swiss mouse model assessed as reduced tactile allodynia at 30 mg/kg, ip administered after 3 weeks of STZ stimulation and measured after 1 hr by von Frey test
Antihyperalgesic activity in STZ-induced diabetic neuropathy pain Albino Swiss mouse model assessed as reduced heat nociceptive threshold at 10 mg/kg, ip administered after 3 weeks of STZ stimulation and measured after 1 hr by hot plate method
Antihyperalgesic activity in STZ-induced diabetic neuropathy pain Albino Swiss mouse model assessed as reduced heat nociceptive threshold at 30 mg/kg, ip administered after 3 weeks of STZ stimulation and measured after 1 hr by hot plate method
Antiallodynic activity in oxaliplatin-induced diabetic neuropathy pain Albino Swiss mouse model assessed as reduced acute-phase tactile allodynia at 10 mg/kg, ip administered after 3 hrs of oxaliplatin stimulation and measured after 1 hr by von Frey test
Antiallodynic activity in oxaliplatin-induced diabetic neuropathy pain Albino Swiss mouse model assessed as reduced acute-phase tactile allodynia at 30 mg/kg, ip administered after 3 hrs of oxaliplatin stimulation and measured after 1 hr by von Frey test
Antiallodynic activity in oxaliplatin-induced diabetic neuropathy pain Albino Swiss mouse model assessed as reduced late-phase tactile allodynia at 30 mg/kg, ip administered after 7 days of oxaliplatin stimulation by van Frey test
Antihyperalgesic activity in oxaliplatin-induced diabetic acute neuropathy pain Albino Swiss mouse model assessed as reduction in cold allodynia at 10 mg/kg, ip administered after 3 hrs of oxaliplatin stimulation by cold plate method
Antihyperalgesic activity in oxaliplatin-induced diabetic acute neuropathy pain Albino Swiss mouse model assessed as reduction in cold allodynia at 30 mg/kg, ip administered after 3 hrs of oxaliplatin stimulation by cold plate method
Antihyperalgesic activity in oxaliplatin-induced diabetic late neuropathy pain Albino Swiss mouse model assessed as reduction in cold allodynia at 10 mg/kg, ip administered after 7 days of oxaliplatin stimulation by cold plate method
Antihyperalgesic activity in oxaliplatin-induced diabetic late neuropathy pain Albino Swiss mouse model assessed as reduction in cold allodynia at 30 mg/kg, ip administered after 7 days of oxaliplatin stimulation by cold plate method
Antiallodynic activity in oxaliplatin-induced diabetic neuropathy pain Albino Swiss mouse model assessed as reduced late-phase tactile allodynia at 30 mg/kg, ip administered after 3 hrs of oxaliplatin stimulation and measured after 1 hr by van Frey test