The current study, for which ethical approval was obtained, was designed to
assess the extent to which the tenderness or mechanical allodynia observed
in delayed onset muscle soreness (DOMS) might be mediated by large diamete
r myelinated nerve fibres. Healthy human volunteers were recruited and rand
omly allocated to one of three groups: Normal-Control, Ischaemic-Control, a
nd Test-DOMS (total n = 21; n = 7 in each group). In the Normal-Control gro
up, subjects attended on a single occasion for assessment of mechanical pai
n threshold (MPT) at standardized sites over the biceps brachii using a pre
ssure algometer for a period of 20 min. In both remaining groups, ischaemia
was induced in subjects' non-dominant upper limbs by elevation of the limb
, followed by application of a sphygmomanometer cuff at a pressure of 250 m
mHg. Throughout the period of the block (20-40 min), sharp/blunt sensation
was assessed at regular intervals. MPT was assessed upon inflation of the c
uff and reassessed at 10 min intervals until deflation. In the two ischaemi
c block groups, current level of pain was also monitored using a computeriz
ed visual analogue scale (VAS) at the beginning and end of the procedure. S
ubjects in the Test-DOMS group attended 48 h prior to ischaemic block for i
nduction of DOMS using a standardized regime of eccentric exercise, but the
reafter were treated in exactly the same manner as the Ischaemic-Control gr
oup. Results showed a significant (P < 0.05; ANOVA) increase in MPT in the
Test-DOMS group by the 20 min point, corresponding to a 'normalization' of
MPT; loss of the ability to distinguish between sharp/blunt sensation accom
panied such changes. Parallel increases in reported pain were seen in both
groups undergoing ischaemic block, indicating that the procedure did not al
ter nociception. While not definitive, these results suggest that altered p
rocessing of activity in large diameter (myelinated) afferents might underl
ie the mechanical allodynia observed in DOMS; thus, this is an area which w
arrants further investigation. (C) 2000 International Association for the S
tudy of Pain. Published by Elsevier Science B.V. All rights reserved.