Functional neuromuscular connections are critical for appropriate behaviour
al responses, but can be negatively affected by increases in temperature. W
e investigated the effects of heat shock on the thermosensitivity of a neur
omuscular pathway to the hindleg tibial extensor muscle of Locusta migrator
ia. We found that exposure to heat shock induced thermoprotection of both n
euromuscular transmission and extensor muscle contraction by (i) increasing
the upper temperature limit for failure, (ii) improving recovery following
heat-induced failure and (iii) stabilizing excitatory junction potential a
mplitude and duration rind extensor muscle contraction force at high temper
atures, Furthermore, the heat-shock-induced thermoprotection of extensor mu
scle contraction was not attributable to a protective effect on intrinsic c
omponents of muscle contraction. Finally, the use of jumping as a locomotor
strategy to avoid capture, a behavioural response dependent upon functiona
lly competent neuromuscular connections at the hindleg tibial extensor musc
le, became less sensitive to temperature following heat shock. We conclude
that the natural stress response of the locust stabilizes neuromuscular sig
nalling during temperature stress, and that this can underlie a thermoprote
ction of muscle contraction force and thus alter the thermosensitivity of a
n escape behaviour critical for survival.