Abstract
Responses of single lumbar spinal neurons to noxious skin heating (50°C, 10 s) were electrophysiologically recorded in barbiturate-anesthetized rats. Responses of all neurons were suppressed by electrical stimulation in the midbrain periaqueductal gray (PAG) or lateral reticular formation (LRF). Microinjection of glutamate (GLU, 0.1–0.3 μl, 0.5 M) into the PAG rapidly (within 15 s) suppressed (to 13–55% of control) the responses of 6 16 neurons with recovery within 8 min. The remainder were affected less at even higher doses (0.5–1 μl). Responses of 4 10 neurons were suppressed following GLU microinjected into the LRF. We also tested effects of microinjection of morphine (MOR, 5 μg/0.5 μl) into GLU-sensitive and insensitive PAG sites. Responses of 4 neurons were unaffected, 4 were enhanced (to 130–155%), and 2 suppressed (to 43 and 57%) following MOR in PAG, with enhancement or suppression beginning within 12–20 min and lasting 40 to over 70 min. The differing effects of GLU and MOR may reflect different mechanisms for the descending modulation of spinal nociceptive transmission.
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