Anatomical distribution and sensory properties of brain stem and posterior diencephalic neurons responding to genital, somatosensory, and nociceptive stimulation in the squirrel monkey

Abstract

In chloralose-urethane-anesthetized female squirrel monkeys, 325 single units sampled from a region extending from the caudal medulla to the posterior diencephalon were examined for responsiveness to genital, rectal, innocuous somatosensory, and various forms of nociceptive stimulation. The units were highly responsive, with 84% responding to at least one stimulus type. The responsive units were widely distributed in the brain stem tegmentum, deep tectum, and posterior diencephalon. Very few neurons responded to only one type of stimulation. The patterns of convergent responsiveness to the various stimulus types were not, however, a simple random function of unit responsiveness to each type of stimulus per se. Unit responses to vaginal stimulation consisted of simple increases or decreases in firing which outlasted the duration of the probing stimulus in most cases. Some units responded more strongly to cervical than to vaginal tract stimuli. The somatic receptive fields of units responding to touch-pressure stimuli were typically bilateral and quite extensive. A forceps pinch of nociceptive intensity elicited a response from 64% of the cells, and of these, 11% showed significant linear correlations between their firing rates and increasing pinch pressure in the nociceptive intensity range. Brief, localized nociceptive thermal stimuli and needle pricks failed to elicit responses from the neurons tested. Based on a comparison between the response properties of monkey brain stem neurons and the previous findings for rat and cat neurons, it was concluded that brain stem cells display species-typical sensory characteristics which have parallels in the properties of behavioral responses of these three species to genital and other sensory stimuli. Properties of unit responses to nociceptive stimuli have implications in relation to the neural mechanisms of first and second pain.