Hr. Weng et J. Schouenborg, ON THE CUTANEOUS RECEPTORS CONTRIBUTING TO WITHDRAWAL REFLEX PATHWAYSIN THE DECEREBRATE SPINAL RAT, Experimental Brain Research, 118(1), 1998, pp. 71-77
Previous studies indicate that the withdrawal reflex system in the rat
has a ''modular'' organization, each reflex pathway performing a spec
ific sensorimotor transformation. Here, we wished to clarify which cut
aneous receptors contribute to this system and to determine whether th
ere are differences in this respect between reflex pathways of differe
nt muscles. Withdrawal reflexes of the peroneus longus, extensor digit
orum longus, and semitendinosus muscles were recorded with EMG techniq
ues during high reflex excitability in decerebrate spinal rats (n=26).
While maintained innocuous pressure on glabrous skin could elicit a s
ustained reflex activity in all muscles studied, vibration of glabrous
skin (10-300 Hz) always failed to evoke a reflex response, suggesting
that slowly adapting, but not rapidly adapting, low-threshold mechano
receptive fibers from this type of skin contribute to withdrawal refle
x pathways. Thermal stimulation in the innocuous range, i.e., cooling
from 32 to 17 degrees C, or warming the skin from 32 to 41 degrees C,
always failed to produce reflex responses, indicating that neither col
d nor warm receptors contribute to withdrawal reflex pathways. When ei
ther cooling or warming the skin to the noxious temperatures of 1 degr
ees C or above 45 degrees C, respectively, a reflex discharge was ofte
n evoked in the muscles studied. Intradermal administration of histami
ne, a potent pruritogenic substance, produced very weak, or no, reflex
response. In contrast, mustard oil produced vigorous reflex responses
in all muscles studied. These findings suggest that some chemonocicep
tors contribute only weakly, or not at all, to withdrawal reflex pathw
ays. The present data suggest that a selective set of cutaneous recept
ors contribute to withdrawal reflex pathways and that different withdr
awal reflex pathways receive input from essentially the same cutaneous
receptor types.