Clinical pain syndromes, and experimental assays of nociception, are differ
entially affected by manipulations such as drug administration and exposure
to environmental stress. This suggests that there are different 'types' of
pain, We exploited genetic differences among inbred strains of mice in an
attempt to define these primary 'types'; that is, to identify the fundament
al parameters of pain processing. Eleven randomly-chosen inbred mouse strai
ns were tested for their basal sensitivity on I? common measures of nocicep
tion, These measures provided for a range of different nociceptive dimensio
ns including noxious stimulus modality, location, duration and etiology, am
ong others. Since individual members of inbred strains are identical at all
genetic loci, the observation of correlated strain means in any given pair
of nociceptive assays is an index of genetic correlation between these ass
ays, and hence an indication of common physiological mediation, Obtained co
rrelation matrices were subjected to multivariate analyses to identify cons
tellations of nociceptive assays with common genetic mediation. This analys
is revealed three major clusters of nociception: (1) baseline thermal nocic
eption, (2) spontaneously emitted responses to chemical stimuli, and (3) ba
seline mechanical sensitivity and cutaneous hypersensitivity. Many other no
ciceptive parameters that might a priori have been considered closely relat
ed proved to bt:genetically divergent. (C) 1999 International Association f
or the Study of Pain. Published by Elsevier Science B.V.