Ne. Farber et al., THE EFFECTS OF HALOTHANE, ISOFLURANE, AND ENFLURANE ON THERMOREGULATORY RESPONSES IN THE NEURAXIS OF CATS, Anesthesiology, 80(4), 1994, pp. 879-891
Background: Normal thermoregulatory function is believed to be modulat
ed by thermosensitive neurons in the preoptic region of the anterior h
ypothalamus and other sites within the central nervous system includin
g the spinal cord. Previous evidence has demonstrated modulation of se
gmental spinal cord thermoregulatory mechanisms from more rostral cent
ral nervous system sites. The ability of the volatile anesthetics to d
isrupt normal thermoregulatory function and produce shivering-like act
ivity during emergence is well documented. The purpose of the current
investigation was to examine the action of the volatile anesthetics ha
lothane, isoflurane, and enflurane on thermoregulatory responses produ
ced at the preoptic region and spinal cord. Methods: Cats were chronic
ally instrumented with bilateral cannulas allowing selective heating a
nd cooling of the preoptic region. Electrodes were implanted in hindli
mb and forelimb muscles for electromyographic (EMG) analysis. Animals
underwent selective heating and cooling of the preoptic region in the
awake state, during volatile agent anesthesia and during emergence. In
a separate series of animals, pontine-transected cats with epidural t
hermodes and a thermocouple underwent alternate heating and cooling of
the spinal cord. Heating and cooling was performed in the nonanesthet
ized state, at graded concentrations of halothane, and during emergenc
e. In all animals, deep core peritoneal temperature, epidural spinal c
ord temperature, forelimb and hindlimb EMG activity were continuously
recorded and digitally processed. EMG responses in both experiments we
re quantitated and analyzed for power spectral density. Results: In th
e chronically prepared animals, heating and cooling of the preoptic re
gion in the conscious state resulted in appropriate thermoregulatory r
esponses, including shivering-like activity and increased EMG power wi
th preoptic region cooling. Halothane, isoflurane, and enflurane each
abolished these thermoregulatory responses. During emergence from anes
thesia, however, the typical spontaneous increases in EMG power observ
ed at normothermia were significantly attenuated by heating of the pre
optic region and augmented by cooling of the preoptic region. In the a
cutely prepared animals, cooling of the spinal cord produced graded in
creases in EMG activity. Increased concentrations of halothane dose-de
pendently diminished this response to cooling of the spinal cord. Duri
ng emergence, cooling of the spinal cord resulted in a shivering respo
nse similar to those observed during control conditions. Conclusions:
The ability of preoptic region heating and cooling to modulate postane
sthetic shivering implies that while thermoregulatory pathways remain
intact, volatile anesthetics produce an imprecision in the control of
thermoregulatory responses at the level of the anterior hypothalamus.
Attenuation of shivering-like responses generated at spinal cord level
s in pontine-transected cats implies a significant blunting action of
thermoregulatory response mechanisms at the level of the spinal cord o
r lower brain stem.