As. Pickoff et al., TEMPERATURE DEPENDENCY OF THE VAGAL CHRONOTROPIC RESPONSE IN THE YOUNG PUPPY - AN ENVIRONMENTAL-AUTONOMIC INTERACTION, Journal of the autonomic nervous system, 64(2-3), 1997, pp. 107-114
We investigated the effects of mild hypothermia (34.3 +/- 0.2 degrees
C [mean +/- SD]), hyperthermia (40.8 +/- 0.2 degrees C) and hypoxia (P
a-O2 = 43 +/- 4 mmHg) on the response of heart rate to continuous righ
t vagus nerve stimulation (the 'vagal chronotropic response') in young
puppies, aged 5-22 days. Puppies were anesthetized with a-chloralose,
vagotomized and pre-treated with propranolol (1 mg/kg i.v.) and phent
olamine(1 mg/kg, 1-2 mg/kg/h i.v.). Hypoxia (n = 9) did not significan
tly alter the resting sinus cycle length and did not alter the respons
e of sinus cycle length to a 30 s train of 8 Hz right vagal stimulatio
n. Mild hypothermia tn = 8) increased the resting sinus cycle length b
y 16 +/- 4% and greatly augmented the vagal chronotropic response (fro
m 76 +/- 27% change in the sinus cycle length (normothermia) to 155 +/
- 38% (hypothermia)). Both the sinus cycle length and the vagal chrono
tropic response returned towards pre-hypothermia values with rewarming
. Mild hypothermia also increased the negative chronotropic response t
o 20 mu g/kg/min i.v. of methacholine (12 +/- 2% change in the sinus c
ycle length (normothermia) versus 24 +/- 14% (hypothermia)), suggestin
g that a postsynaptic mechanism is involved in the hypothermia-induced
augmentation of the cardiac vagal chronotropic response. In contrast
to hypothermia, mild hyperthermia (n = 8) decreased the resting sinus
cycle length slightly (-5 +/- 5% change) and significantly attenuated
the cardiac vagal chronotropic response (from 88 +/- 28% change in sin
us cycle length (normothermia) to 50 +/- 26% (hyperthermia)). These ch
anges were also reversible with the re-establishment of normothermia.
This demonstrates that clinically relevant, environmentally-induced ch
anges in body temperature can directly and reversibly modify parasympa
thetic efferent responses.