Even though homeothermic animals regulate the body temperature, fluctu
ations up to 2-3 degrees C may occur during physiological conditions.
In many species, including the rat, a similar variation can be measure
d in the brain temperature. Such changes are expressed throughout the
brain with a preserved gradient between the warmer basal and cooler do
rsal parts. In spite of these recordable physiological changes, spatia
l learning is quite robust, in that it occurs at brain temperatures be
tween 30 and 39 degrees C. Even drastic cooling (to below 15 degrees C
) fails to affect consolidation or storage of information when the ani
mal is tested after rewarming. The physiological temperature fluctuati
ons have significant consequences for electrophysiological responses i
n the brain. Various bioelectrical signals are more sensitive during w
arming, axonal conduction is speeded up, and stimulus-elicited transmi
tter release becomes faster and more synchronized. Action potentials h
ave shorter rise and decay times in warm conditions, and the amplitude
becomes slightly smaller. Population responses are differently affect
ed by these changes. Dentate field potentials in response to stimulati
on of perforant-path fibers appear with shorter latency in warm condit
ions, and the rate of rise in the field EPSP is increased. Paradoxical
ly, the amplitude of the population spike is reduced. This is due to a
combination of reduced amplitude of individual action potentials and
reduced efficiency of the summation of groups of action potentials. Du
e to the large effects of temperature on hippocampal field potentials,
it is mandatory that brain temperature changes are monitored and/or c
ontrolled whenever such responses are recorded in freely moving and an
esthetized animals. (C) 1995 Wiley-Liss, Inc.