Abstract
Context: Linalool oxide (OXL) (a monoterpene) is found in the essential oils of certain aromatic plants, or it is derived from linalool. The motivation for this work is the lack of psychopharmacological studies on this substance. Objective: To evaluate OXL’s acute toxicity, along with its anticonvulsant and antinociceptive activities in male Swiss mice. Material and methods: OXL (50, 100 and 150 mg/kg, i.p.) was investigated for acute toxicity and in the Rota-rod test. Antinociceptive activity was evaluated by the acetic acid-induced writhing test, and by formalin testing. Anticonvulsant effects were demonstrated by testing for pentylenetetrazol (PTZ)-induced seizures and by Maximum Electroshock headset (MES) test. OXL was administered to the animals intraperitoneally 30 min before for pharmacological tests. Results: OXL showed an LD50 of ~721 (681-765) mg/kg. In the Rota-rod test, it was observed that OXL caused no damage to the animal’s motor coordination. OXL significantly reduced (p
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Souto-Maior, F. N., Da Fonsêca, D. V., Salgado, P. R. R., Monte, L. de O., De Sousa, D. P., & De Almeida, R. N. (2017). Antinociceptive and anticonvulsant effects of the monoterpene linalool oxide. Pharmaceutical Biology, 55(1), 63–67. https://doi.org/10.1080/13880209.2016.1228682
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