Mapping of Brain Activity in the Analgesia Induced by Phα1β and Morphine

Preclinical evidence suggests the potential of Ph α 1 β , a toxin obtained from the venom of spider Phoneutria nigriventer , as a new analgesic drug. Molecular brain imaging techniques have afforded exciting opportunities to examine brain processes in clinical pain conditions. This paper aims to study the brain regions involved in the analgesic effects of Ph α 1 β compared with Morphine, in a model of acute pain induced by formalin in Sprague Dawley rats. We used 18 F-fluorodeoxyglucose as a metabolic radiotracer to perform brain imaging of rats pretreated with Ph α 1 β or Morphine in a model of acute inflammatory pain caused by intraplantar injection of formalin. The rats’ hind paw’s formalin stimulation resulted in a brain metabolic increase at the bilateral motor cortex, visual cortex, somatosensory cortex, thalamus, and cingulate cortex.In rats treated with Ph α 1 β , selective inhibition of unilateral motor cortex and cingulate cortex was observed. Morphine treatment leads to small and selective inhibition at the bilateral amygdala striatum and accumbens. Our results indicate that the analgesic effect of Ph α 1 β and Morphine possesses a differential profile of central processing in the pain state.