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Journal of Pharmacy and Pharmacology 2012-Dec

Antinociceptive activity of carvacrol (5-isopropyl-2-methylphenol) in mice.

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Francisca Helvira Cavalcante Melo
Emiliano Ricardo Vasconcelos Rios
Nayrton Flávio Moura Rocha
Maria do Carmo de Oliveira Citó
Mariana Lima Fernandes
Damião Pergentino de Sousa
Silvânia Maria Mendes de Vasconcelos
Francisca Cléa Florenço de Sousa

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Abstrak

OBJECTIVE

Carvacrol (5-isopropyl-2-methylphenol) is a monoterpenic phenol which is present in the essential oil of oregano and thyme. We have investigated the behavioural effects of carvacrol in animal models of pain, such as acetic acid-induced abdominal constriction, formalin and hot-plate tests in mice. The spontaneous motor activity of animals treated with carvacrol was investigated using open-field and rotarod tests.

METHODS

Carvacrol was administered orally, at single doses of 50 and 100 mg/kg while indometacin (5 mg/kg), morphine (7.5 mg/kg) and diazepam (2 mg/kg) were used as standard drugs. Naloxone (1 mg/kg) and l-arginine (150 mg/kg) were used to elucidate the possible antinociceptive mechanism of carvacrol on acetic acid-induced abdominal constriction and formalin tests.

RESULTS

The results showed that carvacrol produced significant inhibitions on nociception in the acetic acid-induced abdominal constriction, formalin and hot-plate tests. In the open-field and rotarod tests carvacrol did not significantly impair the motor performance. The effect of the highest dose of carvacrol in mice in the acetic acid-induced abdominal constriction and formalin tests were not reversed by naloxone or l-arginine.

CONCLUSIONS

Based on these results, it has been suggested that carvacrol presents antinociceptive activity that may not act through the opioid system nor through inhibition of the nitric oxide pathway.

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