The antinociceptive activity of Malva sylvestris (Malvaceae) aqueous extract (10 mg/kg, i.p.) was evaluated against classical models of pain in mice, indicating promising results. It showed significant antinociceptive activity in writhing test (76.4% of inhibition) and also inhibited the neurogenic (61.8%)
and inflammatory (46.6%) phases of the formalin model. When analysed against capsaicin-induced pain model, the aqueous extract was also effective with inhibition of 62.9%, but it did not cause significant activity against hot-plate model. The results suggest that the antinociception caused by aqueous extract is related to the inhibition of prostaglandins synthesis pathway cyclooxygenase and unrelated to the stimulation
of the opioid receptors.