Spinal cords were obtained from 3- to 5-week-old male Sprague–Dawley rats by dorsal laminectomy. The rats were anesthetized with 3% isoflurane in an induction box and kept under isoflurane anesthesia during the extraction of the spinal cord, which took < 2 min and included euthanasia by bilateral thoracotomy. Coronal slices (400 μm) were cut with a vibratome (Integraslice 7550PSDS; Campden Instruments USA, Lafayette, IN, USA) from a lumbar click here spinal cord segment (L2–L4), as described (Marvizon et al., 2003a; Lao & Marvizon, 2005; Adelson et al., 2009). The spinal cord segment was glued vertically

to a block of agar on the stage of the vibratome and immersed in ice-cold sucrose-aCSF. Slices were cut using minimum forward speed and maximum vibration while BKM120 cell line under observation with a stereo microscope mounted over the vibratome. Slices were prepared either without roots or with

one dorsal root, which was used for electrical stimulation. In the later case, fiber continuity between the dorsal root and the dorsal horn was assessed by examining the dorsal root and the dorsal surface of the slice with the stereo microscope. Slices were discarded if they did not meet the following criteria: (i) at least 80% of the dorsal funiculus had to be continuous with the dorsal root, and (ii) the dorsal root had no cuts or compression damage. Slices were kept for 1 h in K+-aCSF at 35°C, and then in regular aCSF at 35°C. The dorsal root attached to the slice was electrically stimulated using a custom-made chamber, as previously described (Marvizon et al., 2003b; Adelson et al., 2009). The root was placed on a bipolar stimulation electrode (platinum wire of 0.5 mm diameter, 1 mm pole separation) in a compartment separated from the superfusion chamber by a grease bridge. The root and the electrodes were covered with mineral oil, and

any excess aCSF was suctioned away. This ensured that electrical current circulated through the root and that the stimulus was consistent between preparations. Electrical stimulation was provided by a Master-8 stimulator and SIU5A stimulus isolating unit (A.M.P. Progesterone Instruments, Jerusalem, Israel), and consisted of 1000 square pulses of 20 V and 0.4 ms (C-fiber intensity) delivered at 1 Hz or 100 Hz. In some experiments, the root was chemically stimulated by incubating it for 10 min with 1 μm capsaicin in aCSF in the side compartment of the chamber, as described (Lao et al., 2003). Slices were superfused at 3–6 mL/min with aCSF at 35°C. Drugs were present in the superfusate continuously starting 5 or 10 min before root stimulation. Ten minutes after the stimulus slices were fixed by immersion in ice-cold fixative (4% paraformaldehyde and 0.18% picric acid in 0.1 m sodium phosphate buffer). A round hole was punched in the ventral horn of the slice ipsilateral to the stimulus in order to identify it in the histological sections after immunohistochemistry.