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At least 199 records · Page 11Linked to original sources
PubMed1984

Deficits in locomotor behaviour and thermoregulation produced by intrahypothalamic dopamine injections.

When nigrostriatal dopamine neurones degenerate, a loss of functional dopamine in the striatum occurs and is accompanied by increased dopamine in the degenerating axons which traverse the hypothalamus. While the behavioural deficits which occur after nigrostriatal degeneration have been attributed to the loss of functional dopamine neurotransmission, evidence produced by us suggests that the increased levels of amines in the degenerating axons may be neuroactive and participate in the production of these behavioural deficits. To test this hypothesis further, albino rats were injected bilaterally with 200 nmol of dopamine in a location just rostral to the diencephalon/mesencephalon border, where amine accumulation is commonly observed following lateral hypothalamic damage. The effect of these injections upon open field performance, thermoregulation and motor reflex control was determined 40 min after dopamine injection. In a second study, pargyline (15 mg/kg. i.p.) was administered 30 min before intracerebral dopamine to determine whether this treatment would increase the severity of motor and thermoregulatory deficits which occurred after dopamine injections alone. Deficits in locomotion, rearing and the ability to regulate body temperature were seen after the dopamine injections while motor reflex control in these animals was similar to that seen in vehicle-injected controls. The behavioural deficits displayed by pargyline pretreated, dopamine injected animals were slightly but not significantly more severe than those displayed by animals receiving dopamine injections alone. Fluorescent histochemical assessment of injection sites revealed that dopamine injection produced an increase in fluorescence or "amine accumulation" at the site of injection but this was considerably less than that seen after catecholamine degeneration.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1992

Thermoregulation and evaporative cooling in the cicada Okanagodes gracilis (Homoptera: Cicadidae).

1. Okanagodes gracilis uses a combination of physiological and behavioral mechanisms to regulate body temperature (Tb) to a prescribed range. 2. High thermal tolerances (48.6 degrees C Tb) and evaporative cooling permit the species to remain active during the hottest parts of the day. 3. The regression of Tb on ambient temperature (Ta) (Y = 0.142X + 34.63) intersects the isothermal line at 40.4 degrees C, below the shade-seeking value of 41.2 degrees C. 4. In the laboratory, weight (water) loss is faster at higher (46 degrees C) than at lower (43 degrees C) temperatures; the cicadas were able to survive mass losses of 25% in the laboratory. 5. Pores in the dorsal thorax and abdomen are the probable sites of water loss. 6. O. gracilis is the first cicada reported that is able to continue activity while simultaneously feeding and evaporatively cooling. 7. Behavioral mechanisms of thermoregulation and the possible thermoregulatory value of the species' coloration are discussed.

Animals↗
PubMed2004

Hysteresis of heart rate and heat exchange of fasting and postprandial savannah monitor lizards (Varanus exanthematicus).

Reptiles are ectothermic, but regulate body temperatures (T(b)) by behavioural and physiological means. Body temperature has profound effects on virtually all physiological functions. It is well known that heating occurs faster than cooling, which seems to correlate with changes in cutaneous perfusion. Increased cutaneous perfusion, and hence elevated cardiac output, during heating is reflected in an increased heart rate (f(H)), and f(H), at a given T(b), is normally higher during heating compared to cooling ('hysteresis of heart rate'). Digestion is associated with an increased metabolic rate. This is associated with an elevated f(H) and many species of reptiles also exhibited a behavioural selection of higher T(b) during digestion. Here, we examine whether digestion affects the rate of heating and cooling as well as the hysteresis of heart rate in savannah monitor lizards (Varanus exanthematicus). Fasting lizards were studied after 5 days of food deprivation while digesting lizards were studied approximately 24 h after ingesting dead mice that equalled 10% of their body mass. Heart rate was measured while T(b) increased from 28 to 38 degrees C under a heat lamp and while T(b) decreased during a subsequent cooling phase. The lizards exhibited hysteresis of heart rate, and heating occurred faster than cooling. Feeding led to an increased f(H) (approximately 20 min(-1) irrespective of T(b)), but did not affect the rate of temperature change during heating or cooling. Therefore, it is likely that the increased blood flows during digestion are distributed exclusively to visceral organs and that the thermal conductance remains unaffected by the elevated metabolic rate during digestion.

Animals↗
PubMed2001

Characterization of mouse GBP28 and its induction by exposure to cold.

OBJECTIVE: To investigate whether the expression of the novel adipose tissue-specific protein GBP28 in adipose tissue and serum are altered in mice under a variety of conditions. DESIGN: Mice were fed a high-fat diet for 4 weeks, fasted for 48 h or exposed at 4 degrees C. SUBJECTS: C57BL/6J mouse, male, 4--6 weeks old. MEASUREMENTS: GBP28 mRNA, GBP28 protein, blood glucose, insulin and fad pad weight of the mice. RESULTS: We first confirmed that the mouse has GBP28 and its characteristics are the same as human GBP28. Serum concentration and mRNA levels of GBP28 significantly increased in the mice exposed to cold. CONCLUSION: GBP28 may play a role in homeostasis, regulating body temperature and basal metabolic rate in response to changing environmental conditions. International Journal of Obesity (2001) 25, 75-83

Adiponectin↗
PubMed1998

Poikilothermia syndrome.

Poikilothermia syndrome is a rare cause of intrinsic thermoregulatory failure. Patients with this syndrome regulate body temperature poorly, if at all. Recently, a patient was referred to us who had clinical evidence of poikilothermia syndrome, as well as long-standing multiple sclerosis. Computerized tomography and magnetic resonance scanning failed to identify a hypothalamic lesion. The patient was gradually warmed to sweating, and then cooled to vasoconstriction and shivering. The core-temperature thresholds triggering each defence were calculated, after compensating for the changes in skin temperature. The calculated sweating threshold was 38.3 degrees C (normal: 37.0 +/- 0.3 degrees C). The vasoconstriction threshold was 34.4 degrees C (normal: 36.4 +/- 0.3 degrees C). The sweating-to-vasoconstriction interthreshold range was thus approximately 4 degrees C, which is between 10 and 20 times the normal value. The shivering threshold was 31.8 degrees C (normal: 35.6 +/- 0.3 degrees C). The vasoconstriction-to-shivering range was thus approximately 2.5 degrees C which is more than twice the normal value. The pattern of thermoregulatory failure in this patient resembled that resulting from general anaesthesia.

Body Temperature↗
PubMedDate not supplied

Heat waves: their impact on the health of elders.

A trend toward more hot and humid summers in the United States raises concern for the health of our elderly population. Older adults are more vulnerable to heat illness than younger people because of dysfunctional thermoregulatory mechanisms, chronic dehydration, medications, and diseases involving the systems that regulate body temperature. Heat exhaustion, if untreated, will lead to heat stroke, which is fatal if body temperature is not quickly lowered, and research shows that survivors may suffer long-term disabilities. Prevention requires strong knowledge and application of measures necessary to keep elders healthy in extreme heat. Should illness occur, careful monitoring and assessment will ensure early detection and prompt treatment. This article provides information for caregivers that will enable them to protect their patients from heat illness. It also discusses age-related changes in the thermoregulatory system's response to heat, risk factors, assessment criteria, preventive measures, and first aid for victims of heat exhaustion and heat stroke.

Aged↗
PubMed2003

The role of arginine vasopressin in thermoregulation during fever.

Fever is common in postoperative neurosurgical patients. When fever is present, thermoregulatory responses regulate body temperature within a range that appears to have an upper limit. Endogenous substances, such as arginine vasopressin (AVP), modulate the thermoregulatory response during fever and are referred to as endogenous antipyretics. Endogenous antipyretics attenuate fever by influencing the thermoregulatory neurons in the preoptic region and anterior hypothalamus and in adjacent septal areas. Well known for its antidiuretic and vasopressive properties, AVP plays an important role in antipyresis via the ventral septal area of the limbic system. Evidence suggests that there may be a synergistic relationship between AVP receptors and cyclo-oxygenase enzyme during antipyresis, and the presence of AVP may enhance the efficacy of nonsteroidal antipyretic drugs. On the other hand, there is evidence that increased levels of AVP released during fever may play a role in febrile seizures. Although the antipyretic effect of AVP release during fever is beneficial, excessively high levels of AVP may be detrimental.

Anti-Inflammatory Agents, Non-Steroidal↗
PubMed1989

Effect of high pressure on metabolic response to cold in rats.

The ability of rats to regulate body temperature in a cool helium-oxygen (heliox) atmosphere at high pressure was studied. Thermoregulatory ability in seven awake rats was assessed in a pressure chamber at 1.5, 21 and 41 ATA by monitoring body temperature and oxygen consumption during a gradual reduction of ambient temperature. Body temperature was measured by a radiotelemetry transmitter implanted into the intraperitoneal cavity. The thermal conductance of the rats increased from 0.37 to 0.75 W kg-1 degrees C-1 as air was substituted by heliox and increased further to 1.47 and 1.81 W kg-1 degrees C-1 as the pressure was increased to 21 and 41 ATA, respectively. At high pressure the rats were able to maintain body temperature until the metabolic rate reached a value of 21.9 +/- 2.0 W kg-1, which corresponds to peak metabolic rate. This occurred at an ambient temperature of approximately 21 degrees C. Below this ambient temperature the rats did not manage to maintain body temperature. The results show that the thermal effector mechanisms of rats respond adequately to a slowly decreasing ambient temperature in hyperbaric heliox environments.

Animals↗
PubMed1974

Behavioral thermoregulation in lizards: importance of associated costs.

The Puerto Rican lizard Anolis cristatellus behaviorally regulates body temperature in an open habitat but passively tolerates lower and more variable temperatures in an adjacent forest where basking sites are few and distant. Thermoregulation may be adaptive only when costs resulting from associated losses of time and energy are low.

Adaptation, Physiological↗
PubMed1994

Heat strain in the Canadian Forces chemical defence clothing: problems and solutions.

The Canadian Forces chemical defence protective clothing can induce an overwhelming strain on one's ability to regulate body temperature. Recently a number of investigations have been completed at the Defence and Civil Institute of Environmental Medicine that focused initially on understanding the interaction of metabolic rate, ambient temperature, and ambient vapour pressure on the severity of heat strain associated with wearing the protective clothing. This paper presents a summary of these initial studies together with an overview of different attempts to reduce heat strain during exercise in a hot environment. Factors such as improved aerobic fitness or a period of dry heat acclimation have little if any benefit on tolerance time while wearing the clothing during light or moderate exercise. The best solution to the problem of heat strain remains the use of microclimate conditioning (personal cooling), and these techniques have been successful for Naval and Air Force personnel. For our Land Forces, however, microclimate conditioning is not feasible until a lightweight high-energy power source is developed.

Acclimatization↗
PubMed1981

Regulation of energy balance.

The past 10-15 years have produced a significant increase in knowledge and theories concerning the regulation of energy balance, but the precision of this regulation is still uncertain. However, the fact that investigators have had to resort to a variety of techniques and ploys (some of them bizarre) to produce marked pertubations in body weight is in itself an indication that the regulatory system can be very robust. Although control of food intake obviously plays a major role in this system, control of energy expenditure (i.e. DIT) also has to be considered as an important factor in the maintenance of energy balance. In this review most of the evidence for DIT and its biochemical origins has been derived from studies on experimental animals. Many of the overfeeding studies carried out on man are consistent with the animal work, but because of differences in interpretation and some equivocal results, the role of DIT in human metabolism is still a contentious issue. This problem may not be fully resolved to everyone's satisfaction until complete, continuous, and very precise energy balance measurements are made on chronically overfed lean subjects. Before this expensive and arduous experiment is undertaken, evidence for thermogenesis in man will continue to depend on acute measurements of the metabolic response to various stimuli. An increasing number of studies (e.g. 35, 80) have demonstrated the existence of NST in man, and the possibility that this could originate from BAT is supported by histological (62, 148) and thermographic data (130). Conversely, reductions in cold tolerance (2, 18) and thermogenic responses to noradrenaline (82) with increasing adiposity are similar to the blunted responses seen in genetically obese animals, which suggests that human obesity may also involve an impairment in thermogenesis. At the present time these ideas concerning the important of DIT in man and its role in obesity remain somewhat speculative, but no doubt this area will now be the subject of further research. Similarly, the impact of early nutritional influences on subsequent energy balance regulation and resistance to obesity will receive more attention following the report (144) that hyperphagia in rats during early life results in a reduced body fat content and leanness in adulthood. The relative contributions and interactions between intake and output in energy balance need clarifying, and in terms of central organization, the mechanisms of appetite control should now be considered for their relevance to the control of thermogenesis.(ABSTRACT TRUNCATED AT 400 WORDS)

Adipose Tissue↗
PubMed1992

Thermogenesis and mitochondrial GDP binding with age in response to the novel agonist CGP-12177A.

The ability to regulate body temperature diminishes with age in both humans and rodents. To investigate whether attenuation of sympathetically activated thermogenesis in brown adipose tissue (BAT) may account for the loss of thermoregulation with age, we assessed O2 consumption and body temperature in response to norepinephrine and the specific BAT beta-adrenergic agonist CGP-12177A in 6-, 18-, and 24-mo-old rats. In addition, the effects of this agonist on interscapular BAT mitochondrial GDP binding in young and senescent rats were determined. CGP-12177A rapidly induced an elevation in O2 consumption, which peaked at 25 min, followed by a decline over 4 h. The peak increase in O2 consumption over baseline and the cumulative 4-h response were decreased with age [P less than 0.02, analysis of variance (ANOVA)]. CGP-12177A induced an increase in body temperature that paralleled but appropriately lagged behind the increase in O2 consumption and that was decreased with age (P less than 0.02, ANOVA). The norepinephrine-induced increase in O2 consumption was also reduced with age but was not paralleled by a change in body temperature and was associated with a four- to fivefold increase in physical activity. In young rats CGP-12177A increased the number of available BAT mitochondrial GDP binding sites at 20 and 60 min post-injection, but in senescent rats GCP-12177A was unable to increase GDP binding. These data indicate that CGP-12177A is a novel agonist for BAT thermogenesis. With age there is a reduced capacity for thermogenesis that involves a failure to increase GDP binding, either due to a diminished amount of uncoupling protein with age or a failure to unmask reserve GDP binding sites.

Adipose Tissue, Brown↗
PubMed1988

Dopaminergic modulation of some central actions of angiotensin II in vivo.

Studies were performed in 12 conscious sheep of both sexes to determine if a brain dopaminergic pathway is involved in modulating the central actions of angiotensin II (Ang II) in regulating body temperature and plasma renin activity (PRA). Previous data showed that intracerebroventricular (ICV) infusion of Ang II significantly decreased PRA and body temperature. In contrast, converting enzyme inhibitor SQ 20881 (SQ) or dopamine (DA) significantly increased PRA and body temperature of sheep. In the present study, ICV infusion of the DA antagonist metoclopramide (MCP) (20 micrograms/min) significantly decreased PRA to 68 +/- 5% of the basal level. When sheep were pretreated with ICV MCP (20 micrograms/min) for 2 hr and then infused ICV with MCP (20 micrograms/min) plus DA (20 micrograms/min), Ang II (25 ng/min), or SQ (1 microgram/min), the PRA and temperature responses to DA, Ang II, or SQ were all abolished or attenuated significantly. The converse did not hold. Sheep pretreated with SQ (1 microgram/min) still showed a significant increase in body temperature (0.43 +/- 0.05 degree C) when infused with DA (20 micrograms/min). These results support the hypothesis that a central DA pathway is involved in the modulation of the actions of centrally administered Ang II on temperature and PRA.

Angiotensin II↗