Evaluation of antinociceptive effect of methanolic extract of leaves of Crataeva nurvala Buch.-Ham

• Published in: BMC complementary and alternative medicine 2014-09, Vol.14 (1), p.354-354, Article 354
• Main Authors: Moniruzzaman, Md, Imam, Mohammad Zafar
• Format: Article
• Language: English
• Subjects: acetic acid; analgesic effect; Analgesics; Analgesics - chemistry; Analgesics - pharmacology; Analgesics - toxicity; Analysis; Animals; antagonists; antipyretics; Behavior, Animal - drug effects; Capparaceae - chemistry; complement; contraceptives; Crateva magna; diclofenac; dose response; Drug dosages; Experiments; formalin; glibenclamide; glutamic acid; hot plate test; Laboratories; Medicinal plants; Metabolic disorders; Methanol - chemistry; Mice; morphine; naloxone; Naloxone - pharmacology; nociception; pain; Pain - drug therapy; Pain - physiopathology; Pain Management; Pharmacy; Physiological aspects; Plant Extracts - chemistry; Plant Extracts - pharmacology; Plant Extracts - toxicity; Plant Leaves - chemistry; Plants, Medicinal - chemistry; Rodents; Studies; tail immersion test; traditional medicine
• ISSN: 1472-6882; 1472-6882
• DOI: 10.1186/1472-6882-14-354

Crataeva nurvala Buch.-Ham. (Family: Capparidaceae) is widely used as anti-inflammatory, contraceptive, laxative, lithotropic, febrifuge and as tonic in traditional medicine. This study evaluated the antinociceptive effect of the methanolic extract of the leaves of Crataeva nurvala (MECN). The antinociceptive activity was investigated using heat-induced (hot-plate and tail-immersion test) and chemical-induced (acetic acid, formalin and glutamic acid) nociception models in mice at different doses (50, 100, and 200 mg/kg, p.o.) of MECN. Morphine sulphate (5 mg/kg, i.p.) and diclofenac sodium (10 mg/kg, i. p.) were used as reference analgesic drugs. MECN produced significant dose-dependent antinociception when assessed using hot plate test, tail immersion test and acetic acid-induced abdominal writhing test (65.55%). Likewise, MECN at similar doses produced significant dose-dependent inhibition in both neurogenic (50.82%) and inflammatory pain (73.53%) induced by intraplantar injection of formalin (2.5% formalin, 20 μl/paw). Besides, MECN also significantly inhibited the glutamate-induced (10 μM/paw) pain in mice (74.68%). It was demonstrated that pretreatment with naloxone (2 mg/kg, i.p.) significantly reversed antinociception produced by MECN in hot plate and tail immersion test suggesting the involvement of opioid receptor. In addition, administration of glibenclamide (10 mg/kg, i.p.), an ATP-sensitive K+ channel antagonist could not reverse antinociceptive activity induced by MECN. The results suggest that MECN possesses antinociceptive activity involving inhibition of opioid system as well as the glutamatergic system supporting its traditional uses.