The reaction of painful stimulation was studied in rats by means of three different techniques. Lesions of the midbrain raphe in rats, which reduced the levels of brain 5-hydroxytryptamine (5-HT) and 5-hydroxyindoleacetic acid (5-HIAA) decreased the analgesic activity of morphine. In some tests, an increase in sensitivity to painful stimulation was noted in lesioned animals. The results obtained support the view that a decrease of brain 5-HT concentration antagonizes morphine analgesia. The possible role of the other brain monoamines in the analgesic activity of morphine is also discussed. |