Thermoregulatory effects of methoxamine and isoprenaline following injections into the cerebral ventricles of conscious rabbits

1977 ◽  
Vol 55 (4) ◽  
pp. 821-827 ◽  
Author(s):  
D. L. Jones ◽  
W. L. Veale ◽  
K. E. Cooper

There is evidence to suggest that within the hypothalamus noradrenaline (NA) is an inhibitory neurotransmitter acting on both the heat production and heat loss pathways in the rabbit. Further, it has been proposed that the inhibition of the heat loss pathway which results in hyperthermia is mediated primarily through α-adrenergic receptors within the anterior hypothalamic–preoptic area. We have investigated the effects of the α-receptor agonist methoxamine, administered directly into the cerebral ventricles, on body temperature at various ambient temperatures in both the shorn and unshorn rabbit. At all ambient temperatures tested, administration of methoxamine into a lateral cerebral ventricle produced a gradual dose-dependent hyperthermia. The magnitude of the hyperthermic response diminished with decreasing ambient temperatures. It is already known that the β-adrenergic agonist isoprenaline produces little or no effect on body temperature following intracranial application at ambient temperatures above 18 °C. In our experiments conducted at the lower ambient temperature, it produced a pronounced dose-dependent fall in body temperature in the shorn rabbit. The results of this work support the suggestion that NA can act as an inhibitory substance on the heat production or heat loss pathway in the rabbit. Which pathway is inhibited at any one time is dependent on the ambient temperature. Further, it would appear that inhibition of the heat loss pathway is largely mediated through α-adrenergic receptors, whilst the inhibition of the heat production pathway is mediated to a large extent through β-adrenergic receptors.

1965 ◽  
Vol 20 (3) ◽  
pp. 405-410 ◽  
Author(s):  
Hermann Pohl

Characteristics of cold acclimation in the golden hamster, Mesocricetus auratus, were 1) higher metabolic rate at -30 C, 2) less shivering when related to ambient temperature or oxygen consumption, and 3) higher differences in body temperature between cardiac area and thoracic subcutaneous tissues at all ambient temperatures tested, indicating changes in tissue insulation. Cold-acclimated hamsters also showed a rise in temperature of the cardiac area when ambient temperature was below 15 C. Changes in heat distribution in cold-acclimated hamsters suggest higher blood flow and heat production in the thoracic part of the body in the cold. The thermal conductance through the thoracic and lumbar muscle areas, however, did not change notably with lowering ambient temperature. Marked differences in thermoregulatory response to cold after cold acclimation were found between two species, the golden hamster and the thirteen-lined ground squirrel, showing greater ability to regulate body temperature in the cold in hamsters. hibernator; oxygen consumption— heat production; body temperature — heat conductance; muscular activity — shivering; thermoregulation Submitted on July 6, 1964


1961 ◽  
Vol 12 (6) ◽  
pp. 1152 ◽  
Author(s):  
G Alexander

Studies were made on temperature regulation of lambs in a closed circuit indirect calorimeter. Dry new-born lambs were able to maintain normal body temperature in ambient temperatures as low as -5°C. This was accomplished by increasing heat production to 2–3 times "basal" levels, apparently by increased oxidation of fats, and by reducing heat loss through the extremities by vasoconstriction. The lower limit of the zone of thermal neutrality was about 29°C. In unsuckled lambs within 24 hr of birth, the heat produced in response to cold appeared to be independent of pre-natal nutrition and age. It was considerably lower in lambs with hairy coats than in lambs with fine coats. Milk intake increased heat production, and this increase was abolished after 12 hr of fasting in lambs up to 3 days old, but the increase persisted in older lambs. The increase was accompanied by, and was apparently due to, elevated heat loss from the extremities, which persisted even at low temperatures. The maximal thermal insulation of the tissues, calculated from these results, was about 1 Clo; that of the fleece plus air was only 1 to 2 Clo.


1979 ◽  
Vol 57 (11) ◽  
pp. 1205-1212 ◽  
Author(s):  
M. T. Lin ◽  
F. F. Chen ◽  
Y. F. Chern ◽  
T. C. Fung

Systemic and central administration of methacholine (a synthetic choline derivative) both produced dose-dependent decreases in rectal temperature in rats at all the ambient temperatures studied. Both at room temperature (22 °C) and in the cold (8 °C), the hypothermia in response to methacholine application was brought about by both a decrease in metabolic heat production and an increase in cutaneous circulation. In the heat (29 °C), the hypothermia was due solely to an increase in respiratory evaporative heat loss. Furthermore, the methacholine-induced hypothermia was antagonized by central pretreatment of atropine (a selective blocker of cholinergic receptors), but not by the central administration of either 6-hydroxy-dopamine (a relative depletor of catecholaminergic nerve fibers) or 5,6-dihydroxytryptamine (predominately a serotonin depletor). The data indicate that activation of the cholinergic receptors within brain with methacholine decreases heat production and (or) increases heat loss which leads to hypothermia in rats.


2021 ◽  
Vol 7 ◽  
Author(s):  
Yoshimitsu Ouchi ◽  
Vishwajit S. Chowdhury ◽  
John F. Cockrem ◽  
Takashi Bungo

Effects of increased summer temperatures on poultry production are becoming more pronounced due to global warming, so it is important to consider approaches that might reduce heat stress in chickens. Thermal conditioning in chickens in the neonatal period can improve thermotolerance and reduce body temperature increases when birds are exposed to high ambient temperature later in life. The objective of this study was to investigate physiological and molecular changes associated with heat production and hence body temperature regulation under high ambient temperatures in thermally conditioned chicks. Three-day-old broiler chicks (Chunky) were thermally conditioned by exposure to a high ambient temperature (40°C) for 12 h while control chicks were kept at 30°C. Four days after the treatment, both groups were exposed to 40°C for 15 or 90 min. The increase in rectal temperature during 90 min of exposure to a high ambient temperature was less in thermally conditioned than control chicks. At 15-min of re-exposure treatment, gene expression for uncoupling protein and carnitine palmitoyletransferase 1, key molecules in thermogenesis and fatty acid oxidation, were significantly higher in pectoral muscle of control chicks but not conditioned chicks. Hepatic argininosuccinate synthase (ASS) decreased and hepatic argininosuccinate lyase (ASL) increased after reexposure to a high temperature. The concentrations of hepatic arginosuccinic acid, and ASS and ASL expression, were upregulated in conditioned chicks compared with the control chicks, indicating activity of the urea cycle could be enhanced to trap more energy to reduce heat production in conditioned chicks. These results suggest thermal conditioning can reduce the increase in heat production in muscles of chickens that occurs in high ambient temperatures to promote sensible heat loss. Conditioning may also promote energy trapping process in the liver by altering the heat production system, resulting in an alleviation of the excessive rise of body temperature.


1980 ◽  
Vol 58 (8) ◽  
pp. 909-914 ◽  
Author(s):  
M. T. Lin ◽  
A. Chandra ◽  
J. J. Jou

The effects of intracerebroventricular injections of angiotensin II on thermoregulatory responses of conscious rats to ambient temperatures (Ta) of 8, 22, and 30 °C were assessed. Administration of angiotensin II produced dose-dependent hypothermia in rats at both Ta 8 and 22 °C. The hypothermia in response to angiotensin II was due to decreased metabolic heat production. In addition, angiotensin II produced cutaneous vasoconstriction at Ta 8–22 °C. However, at Ta 30 °C angiotensin II produced no change in rectal temperature or other thermoregulatory responses. Furthermore, the hypothermia induced by angiotensin II was antagonized by pretreatment with 6-hydroxydopamine (a selective catecholamine neurotoxin) and propranolol (a selective β-adrenergic antagonist) but not by either 5,6-dihydroxytryptamine (a selective serotonin neurotoxin), atropine (a cholinergic antagonist), or phentolamine (a selective α-adrenergic antagonist). The data indicate that angiotensin II inhibits both heat production and heat loss mechanisms which lead to an alteration in body temperature, probably via the activation of central adrenergic receptors.


1975 ◽  
Vol 53 (6) ◽  
pp. 679-685 ◽  
Author(s):  
J. B. Holter ◽  
W. E. Urban Jr. ◽  
H. H. Hayes ◽  
H. Silver ◽  
H. R. Skutt

Six adult white-tailed deer (Odocoileus virginianus borealis) were exposed to 165 periods of 12 consecutive hours of controlled constant ambient temperature in an indirect respiration calorimeter. Temperatures among periods varied from 38 to 0 (summer) or to −20C (fall, winter, spring). Traits measured were energy expenditure (metabolic rate), proportion of time spent standing, heart rate, and body temperature, the latter two using telemetry. The deer used body posture extensively as a means of maintaining body energy equilibrium. Energy expenditure was increased at low ambient temperature to combat cold and to maintain relatively constant body temperature. Changes in heart rate paralleled changes in energy expenditure. In a limited number of comparisons, slight wind chill was combatted through behavioral means with no effect on energy expenditure. The reaction of deer to varying ambient temperatures was not the same in all seasons of the year.


1962 ◽  
Vol 15 (2) ◽  
pp. 386 ◽  
Author(s):  
PR Morrison

Body temperature measurements on the short-nosed bandicoot (Thylacis obeaulus) have shown a nocturnal cycle with a range of 1� 2�C and a short active phase at 2200-0400 hr. The bilby or rabbit bandicoot (Macrotis lagoti8) had a sharply defined temperature cycle, with a range of almost 3�C after several months of captivity, during which the day-time resting temperature was progressively lowered from 36� 4 to 34� 2�C. Forced activity raised the diurnal temperature substantially but not to the nocturnal level. Forced activity did not raise the nocturnal level which was similar in the two species (37' O�C). Both species could regulate effectively at an ambient temperature of 5�C, but only Thylaci8 showed regulation at ambient temperatures of between 30 and 40�C.


1979 ◽  
Vol 80 (1) ◽  
pp. 217-229 ◽  
Author(s):  
HEINRICH BERND

1. While foraging, attacking, or leaving or returning to their hives, both the African and European honeybees maintained their thoracic temperature at 30 °C or above, independent of ambient temperature from 7 to 23 °C (in shade). 2. Thoracic temperatures were not significantly different between African and European bees. 3. Thoracic temperatures were significantly different during different activities. Average thoracic temperatures (at ambient temperatures of 8–23 °C) were lowest (30 °C) in bees turning to the hive. They were 31–32 °C during foraging, and 36–38 °C in bees leaving the hive, and in those attacking. The bees thus warm up above their temperature in the hive (32 °C) before leaving the colony. 4. In the laboratory the bees (European) did not maintain the minimum thoracic temperature for continuous flight (27 °C) at 10 °C. When forced to remain in continuous flight for at least 2 min, thoracic temperature averaged 15 °C above ambient temperature from 15 to 25 °C, and was regulated only at high ambient temperatures (30–40 °C). 5. At ambient temperatures > 25 °C, the bees heated up during return to the hive, attack and foraging above the thoracic temperatures they regulated at low ambient temperatures to near the temperatures they regulated during continuous flight. 6. In both African and European bees, attack behaviour and high thoracic temperature are correlated. 7. The data suggest that the bees regulate thoracic temperature by both behavioural and physiological means. It can be inferred that the African bees have a higher metabolic rate than the European, but their smaller size, which facilitates more rapid heat loss, results in similar thoracic temperatures.


1984 ◽  
Vol 246 (6) ◽  
pp. R994-R999 ◽  
Author(s):  
J. M. Krueger ◽  
J. Walter ◽  
C. A. Dinarello ◽  
S. M. Wolff ◽  
L. Chedid

When infused into the lateral cerebral ventricles of rabbits, human endogenous pyrogen (EP) preparations induced dose-dependent increases in slow-wave sleep concomitant with increasing body temperature. Heating EP to 70 degrees C destroyed its sleep-promoting and pyrogenic activity. Anisomycin (an antipyretic) prevented EP from increasing body temperature without affecting its sleep-promoting activity. Intravenous injection of EP induced fever and transient increases in slow-wave sleep but failed to induce prolonged increases in slow-wave sleep. We conclude that the somnogenic activity of EP is not secondary to its pyrogenic activity.


1999 ◽  
Vol 276 (2) ◽  
pp. R298-R307 ◽  
Author(s):  
Edward L. Robinson ◽  
Charles A. Fuller

Whole body heat production (HP) and heat loss (HL) were examined to determine their relative contributions to light masking of the circadian rhythm in body temperature (Tb). Squirrel monkey metabolism ( n = 6) was monitored by both indirect and direct calorimetry, with telemetered measurement of body temperature and activity. Feeding was also measured. Responses to an entraining light-dark (LD) cycle (LD 12:12) and a masking LD cycle (LD 2:2) were compared. HP and HL contributed to both the daily rhythm and the masking changes in Tb. All variables showed phase-dependent masking responses. Masking transients at L or D transitions were generally greater during subjective day; however, L masking resulted in sustained elevation of Tb, HP, and HL during subjective night. Parallel, apparently compensatory, changes of HL and HP suggest action by both the circadian timing system and light masking on Tb set point. Furthermore, transient HL increases during subjective night suggest that gain change may supplement set point regulation of Tb.


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