Biomedical subjects

M Caputa

Publications and source records attributed to M Caputa.

At least 19 recordsLinked to original sources

PubMed2001

Effect of temperature on postanoxic, potentially neurotoxic changes of plasma pH and free iron level in newborn rats.

In asphyxiated newborns, iron, released from heme and ferritin and deposited in the brain, contributes to neurodegeneration. Because hypothermia provides neuroprotection, newborn mammals, showing reduced body temperature, might avoid iron-mediated neurotoxicity. However, hypothermia leads to acidosis, which induces hyperferremia. Therefore, we decided to study the effects of body temperature on plasma pH and iron levels in newborn rats exposed to a critical anoxia. Rectal temperature was kept at 33 degrees C (typical of neonates), reduced by 2 degrees C, or elevated to a level typical of healthy (37 degrees C) or febrile (39 degrees C) adults. Arterial blood samples were collected at 0, 10, 20, 30, and 120 min postanoxia. Control samples were obtained from normoxic, temperature-matched neonates. Anoxia tolerance time decreased progressively at rectal temperatures exceeding 33 degrees C. Neither pH nor plasma iron were significantly affected by anoxia at 33 degrees C. Although hypothermia (31 degrees C) resulted in acidosis in normoxic rats, both pH and iron levels were hardly influenced by anoxia. However, acidosis and hyperferremia, proportional to body temperature, developed at 37 and 39 degrees C. In conclusion, reduced body temperature is likely to protect asphyxiated newborns against iron-mediated brain injury.

Acidosis↗

PubMed2000

Endotoxaemia does not limit heat tolerance in rats: the role of plasma lipoproteins.

Severe hyperthermia disrupts the intestinal barrier, allowing bacterial lipopolysaccharides (LPS) to enter the bloodstream. Since the symptoms of heat stroke resemble those of endotoxic shock, there is a common belief that endotoxaemia induces heat stroke. Therefore, we studied the effects of different doses, from moderate to sublethal, of Escherichia coli LPS and an antipyretic (indomethacin) upon the temperature equilibrium of the brain and body of rats exposed to a constant ambient temperature of 38 degrees C. The animals were then heated until they developed heat stroke, which was identified using a critical thermal maximum (CTM) behavioural test. In separate experiments on defence against endotoxaemia, we compared plasma lipid composition in rats exposed to a sublethal dose of LPS, hyperthermia and heat stroke. Neither LPS nor indomethacin, injected into rats while they were in a hyperthermic steady-state condition of 40-41 degrees C, influenced their thermal equilibrium. Unexpectedly, moderate doses of LPS significantly elevated the thermal tolerance of rats, such that the mean (SEM) CTM value of body temperature was raised from 42.7 (0.3) degrees C to 43.1 (0.1) degrees C (P < 0.05). Indomethacin and huge doses of LPS failed to induce any change in this parameter. The sublethal dose of LPS did not induce mortality in rats subjected to heat stroke. Hyperthermic steady-state conditions and heat stroke alone significantly decreased plasma concentrations of cholesterol, triglyceride and high-density lipoproteins, while the concentrations of low-density lipoproteins increased. A similar pattern of changes was recorded in normothermic rats injected with a sublethal dose of LPS. In conclusion, endotoxaemia in heat-stressed rats induces neither a secondary increase in their core temperature nor a decrease in their ultimate thermal tolerance. Low-density lipoproteins are likely to protect heat-stressed animals against endotoxin-induced death.

Animals↗

PubMed1999

Brain cooling in diving seals.

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Animals↗

PubMed1998

Behavioral approach to the study of the upper limit of temperature tolerance in rats.

A simple test of critical thermal maximum (CTM) to assess a break-down of heat-escape behavior in rats is described. Experiments were performed on 18 unrestrained adult Wistar rats of both sexes. Hypothalamic and intraperitoneal (i.p.) temperatures as well as motor activity were simultaneously and continuously recorded in the rats exposed to heat. When animals were growing restless, as evidenced by an increase in their motor activity, which was usually recorded at hypothalamic temperatures well above 41 degrees C, we started testing CTM. To assess heat-escape behavior we used a precooled cooling bar (a part of a camp-cooler) which was placed at intervals in a climatic chamber. The hyperthermic rats, given the bar for 30 s, mounted it vigorously until they failed at particular levels of brain and body temperatures which were recognized as respective CTM values. Rapid external cooling of rats prevented lethal effects of the heat exposure. We were able to show effects of timing of heat exposure on heat tolerance. We also managed to detect small but significant differences in heat tolerance of warm-reared (an increase), cold-reared (a decrease), and bacterial-endotoxin-treated (an increase) rats. The heat-escape behavior was less heat-resistant than selective brain cooling response which was still present at CTM point. In conclusion, our CTM test is a safe and reliable way to study heat tolerance in rats.

Animals↗

PubMed1998

Rapid brain cooling in diving ducks.

Hypothermia may limit asphyxic damages to the brain, and many small homeotherms have been shown to use anapyrexic strategies when exposed to asphyxic conditions. Larger homeotherms do not seem to use the same strategy, but could save oxygen and prevent hypoxic brain damage by employing selective brain cooling (SBC) in connection with asphyxia. To test the hypothesis that selective brain cooling may take place in connection with asphyxia, we have recorded brain [hypothalamic (THyp)] and body [colonic (TC)] temperatures and heart rates in four Pekin ducks during 5-min simulated (head submersion) diving in cold water (10 degrees C). Diving resulted in a drop in THyp (3.1 +/- 1.4 degrees C) that continued into the recovery period (P < 0.001). Restricting heat loss from the buccal cavity and eyes during diving compromised brain cooling in an additive manner. TC was not influenced by diving. Control cooling of the head with crushed ice during a 5-min period of undisturbed breathing had no effect on THyp. Warm water (35 degrees C) markedly reduced brain cooling, and dive capacity was reduced by approximately 14% (P < 0.05) compared with diving in water at 10 degrees C. The data suggest that SBC is used in ducks during diving, and we propose that this mechanism may enable the bird to save oxygen for prolonged aerobic submergence and to protect the brain from asphyxic damages.

Animals↗

PubMed1997

A comparison of febrile responses induced by LPS from E. coli and S. abortus in unrestrained rats placed in a thermal gradient.

The purpose of our study was a comparison of pyrogenic and behavioural effects of Escherichia coli (E.coli) and Salmonella abortus (S.abortus) endotoxins in unrestrained, freely moving Wistar rats, placed in a thermal gradient and having an easy access to ambient temperatures within a range 5-40 degrees C. Hypothalamic and chosen by the rats ambient temperatures as well as locomotor activity were recorded before and after intraperitoneal injection of 1 mg/kg lipopolysaccharide from E. coli or from S. abortus. Control animals were injected with pyrogen-free saline. Both endotoxins induced warm-seeking behaviour which was accompanied by biphasic fever. Locomotor activity of LPS-injected rats was reduced. S. abortus-induced fever peaked at 100th minute (reaching 37.5 +/- 0.2 degrees C) and at 250th minute (reaching 38.1 +/- 0.1 degrees C). Respective data for E. coli fever were: 170th minute (when hypothalamic temperature reached 37.6 +/- 0.3 degrees C) and 430th minute (with hypothalamic temperature of 38.6 +/- 0.1 degrees C). Comparing to S. abortus-generated fever both peaks of E. coli LPS-induced fever were significantly delayed (p < 0.05). A limited structural variability of lipid A from both bacteria is likely to be responsible for the difference in fever timing recorded in this study.

Animals↗

PubMed1995

Warm rearing modifies temperature regulation in rats.

The effects of early (postnatal), long-term warm exposure on thermoregulatory system of rats were compared with those resulting from warm acclimation induced in adult animals. To obtain warm-reared (wr) rats pregnant females 7 days before term were permanently exposed to a constant ambient temperature of 35 degrees C and their offsprings were housed under these conditions for at least 6 months. Wr rats differed from both control and warm acclimated (wa) animals morphologically as well as functionally. They were leaner and lighter but their tails and feet grew relatively bigger. Moreover, warm rearing led to a marked and highly significant elevation in mass of salivary gland (the main source of water for evaporative cooling). Core temperature in wr rats was regulated at a significantly higher level during the day and at night. Moreover, hyperthermia reduced the exercise performance less in wr than in wa rats. In conclusion, early exposure to high environmental temperature modifies the development of temperature regulation in a way different from that occurring during thermal acclimation in the adult. Changes occurring in wr rats might mimic genetical adaptations of a population to variety of thermal environments.

Adaptation, Physiological↗

PubMed1989

Rosacea: disturbed defense against brain overheating.

Tympanic (Tty), esophageal (Tes), forehead, and hand skin temperatures, as well as the forehead evaporation rate were recorded in six men (four suffering from rosacea and two healthy controls) before, during, and after 1 h of warm bath (38 degrees-39 degrees C). During the last 30 min of the bath, the subject's face was vigorously fanned (14 m/s). Blood flow was explored with ultrasonic Doppler in the emissary veins of the cranium during normothermia before entering the bath, and during hyperthermia just after leaving it. Under normothermic conditions, Tty was higher than Tes in all subjects. In three patients, no blood flow could be detected in the ophthalmic emissary veins whereas in the fourth patient as well as in both control subjects, blood flowed from the intracranium to the face. During hyperthermia, face fanning decreased Tty by 0.25 degrees +/- 0.05 degrees C (+/- SEM) below Tes in the control subjects whereas in all patients Tty remained warmer than Tes by 0.1 degrees C. Doppler recordings showed a rapid inward blood flow from the skin to the brain in the controls during hyperthermia. In patients, however, there was no change from normothermia in the blood flow patterns of vena angularis oculi. Their forehead temperature was permanently higher than in control subjects. Venous blood flow from the skin to the brain appears to be suppressed in rosacea, thus inhibiting selective brain cooling in hyperthermic conditions. The importance of this mechanism in the pathogenesis of rosacea and its significance as a means of investigation are discussed.

Adult↗

PubMed1988

Precedence of head homoeothermia over trunk homoeothermia in dehydrated men.

Three male humans were subjected repeatedly to 20 min exercise on a bicycle ergometer: twice when hydrated normally and twice when dehydrated. Tympanic (Tty) and oesophageal (Tes) temperatures were recorded and sweat rates on forehead and back were measured. Dehydration did not change the forehead sweat rate, but on the back it reduced significantly, resulting in an increase of Tes. However, Tty was decreased by dehydration. 20 min after the end of exercise subjects were allowed to drink water in order to trigger the potohidrotic response. A potohidrotic response was noted on the back of dehydrated subjects only. It is concluded that dehydration results in active inhibition of sweating on the body but not on the forehead, where evaporation is needed for selective cooling of the brain.

Body Temperature↗

PubMed1986

Effects of brain and trunk temperatures on exercise performance in goats.

In 40 experiments on seven goats head and trunk temperatures were altered independently of each other and the effects on exercise performance on a treadmill (speed: 3 km/h, slope: 16%-20%) were observed. Brain temperature between 38.5 degrees C and 42.0 degrees C and trunk temperature between 39 degrees C and 43.5 degrees C did not reduce exercise performance or running time. Blood lactate concentration increased with rising brain and trunk temperatures, but did not exceed 13.1 mmol/l-1. Blood pressure and heart rate did not show any dependence on brain or trunk temperatures. Brain temperature between 42.0 degrees C and 42.9 degrees C shortened running time in 3 out of 12 experiments and reduced performance during shortlasting upward deviations of temperature. This suggests that in this species, the thermal safety limit to exercise is very close to that range of temperature which is likely to induce heat stroke.

Animals↗

PubMed1986

Competition for cool nasal blood between trunk and brain in hyperthermic goats.

An influence of brain and trunk temperatures controlled independently of each other by means of artificial heat exchangers, on the intensity of natural selective brain cooling (SBC) was studied in 6 conscious goats. Intensity of SBC was markedly enhanced by increasing brain temperature. On the other hand, a rise of trunk temperature with the cerebral temperature clamped at 39 degrees C or 40 degrees C, reduced SBC intensity in spite of a simultaneous increase in the respiratory evaporative heat loss. When brain temperature was clamped at 41 degrees C, the magnitude of SBC was essentially independent of trunk temperature. These results suggest that during hyperthermia a competition exists between trunk and brain for cool nasal blood.

Animals↗

PubMed1985

Arylsulphatase A and acid phosphatase activities in plasma and leucocytes during LPS fever in the ox (Bos taurus).

Intravenous injection of E. coli LPS (0.5 micrograms/kg) produced the biphasic elevation of rectal temperature (TR) in conscious oxen. The fever was accompanied by a significant increase of the arylsulphatase A (AsA) activities in plasma and in mononuclear leucocytes. In polymorphonuclear cells a substantial decrease of the AsA activity after 1 hr fever was observed. After 3.5 hr of fever the polymorphonuclear activity of AsA restored to normal found before LPS administration. In contrast with AsA, the pyrogenic dose of LPS caused negligible changes of the acid phosphatase (AcP) activities in the sampled materials. Daily-repeated injections of pyrogen into the same oxen attenuated magnitudes of fever as well as AsA responses in plasma and granulocytes. Heat-induced hyperthermia provoked only minute changes of the AsA and AcP.

Acid Phosphatase↗

PubMed1980

Muscular work as thermal behavior in humans.

Human subjects were placed on a bicycle ergometer and left to pedal ad lib. for 43 min to warm themselves and thereby attain thermal comfort at an ambient temperature of 10 degrees C. Esophageal (Tes), tympanic (Tty), forehead, and hand skin temperatures were recorded. In addition, the work of pedaling was noted for each 2-min period. In some experiments sweating rate was also recorded. Two series of experiments were performed, the first with face fanning and the second with thermal insulation of the head. Face fanning resulted in decreased Tty, but in substantially increased Tes, which was 1.5 degrees C higher than Tty after an intense pedaling effort of 46-50 W. In experiments with head covering, a mild increase of both Tes and Tty was observed toward a position halfway between the extreme values obtained during face fanning. Simultaneously, pedaling intensity decreased to 16.7 W and the rate of sweating increased. In general, pedaling work was inversely proportional to intracranial temperature (Tty) and independent of trunk temperature (Tes). Therefore, motivation for muscular activity in humans exposed to cold appears to be goverened chiefly by the brain temperature.

Adolescent↗

PubMed1979

Natural selective cooling of the human brain: evidence of its occurrence and magnitude.

1. The technique of perceptual rating of thermal stimuli was used, in eight human subjects immersed in warm water, in order to appreciate whether they were hypo-, normo- or hyperthermic. Oesophageal, tympanic and forehead skin temperatures were recorded, as also was the temperature of the skin above the angularis oculi vein. Once the subjects gave clearly hyperthermic ratings, one arm was exposed to a 6 m/s wind. After 5--10 min the arm was re-immersed and the face was fanned. 2. Fanning of the arm resulted in lowering of body core temperature. However ratings of thermal stimuli remained hyperthermic. 3. Face fanning decreased forehead skin, angularis oculi vein and tympanic temperatures. Hyperthermic ratings were replaced by normothermic ratings, although oesophageal temperature continued to rise. 4. The upper limit of oesophageal temperature for normothermic ratings was 37.o6 +/- 0.09 degrees C during the control period without fanning. This temperature rose to 37.91 +/- 0.09 degrees C during facial ventilation. 5. These results suggest a selective cerebral cooling due to venous blood returning from facial skin via the ophthalmic vein to the cavernous sinus, where a cooling of arterial blood ascending to the brain can take place.

Body Temperature Regulation↗

PubMed1979

Open loop increase in trunk temperature produced by face cooling in working humans.

1. Five human subjects pedalled on a bicyle ergometer for at least two 74 min periods at 10 degrees C ambient temperature. During the first period the subjects cycled for 42 min with face fanning, followed by 32 min with the head thermally insulated. In the second period, this procedure was reversed. Oesophageal (tes), tympanic (Tty), forehead and hand skin temperatures were recorded. In addition, heart rate (H.R.) was counted throughout the experiments, and the technique of perceptual rating of cool and warm stimuli was used in order to appreciate whether the subjects were hypo-, normo-, or hyperthermic. 2. Face fanning resulted in decreased Tty, decreased H.R., mild skin vasoconstriction but increased Tes. 3. Head covering resulted in increased Tty and H.R., while Tes decreased slightly, due to peripheral vasodilatation. 4. When their faces were being fanned so that Tty was low and Tes was high, the subjects gave slightly hypothermic ratings. Ratings were clearly hyperthermic when their heads were covered and Tty was high and Tes was low. 5. The close correlation between vasomotor response and H.R. on the one hand and Tty on the other confirms that this variable is a better approximation of regulated core temperature than Tes. 6. Increase in Tes during face fanning and decrease in Tes during face insulation is new evidence for the possibility of the human brian being cooled during exercise by cool blood returning from the face. 7. We suggest that this selective brain cooling determines the apparent upper resetting of core temperature during exercise while brain temperature remains precisely regulated and constant.

Body Temperature Regulation↗

PubMed1979

Bradycardia during face cooling in man may be produced by selective brain cooling.

In human subjects, bradycardia was produced by immersing the subjects' faces in water at 15 degrees C when they were hyperthermic. When they were hypothermic, the same face cooling produced tachycardia. It is suggested that the difference in cardiac response originates in selective brain cooling during hyperthermia, by venous return from the face to the brain, via ophthalmic veins.

Adult↗

PubMed1978

[Reversal of human ophthalmic vein blood flow : selective cooling of the brain].

Direction of blood flow in angularis oculi veins was recorded in humans. In mild hypothermia, blood flow was weak and directed from brain to face. In hyperthermia, however, blood flowed rapidly in the opposite direction, angularis oculi vein collecting cool facial blood and supplying cavernous sinus. Therefore selective cooling of human brain is possible.

Adult↗

PubMed1976

Significance of cranial circulation for the brain homeothermia in rabbits. I. The brain-arterial blood temperature gradient.

The hypothalamic-arterial blood temperature gradient (THpr-TAC difference) was studied on 10 freely moving rabbits at ambient temperatures between 0 and 42 degrees Celsius. In cold environment, below 10 degrees Celsius the THpt-TAC gradient varied considerably, but some distinct correlations were found between vasomotor responses of the nasal mucosa and fluctuations of brain temperature, as well as between vasomotor responses of the ear pinnas and changes of the arterial blood temperature. Vasodilatation of the nasal mucosa or the ear pinna caused respectively a drop in brain temperature or in arterial blood temperature. Opposite changes were induced by vasoconstriction in those areas. Variations in THpt-TAC gradient resulted from oppositely directed vasomotor responses in the nasal mucosa and in the ear pinnas. At high ambient temperatures above 35 degrees Celsius thermal panting was accompanied by selective brain cooling with respect to the arterial blood. Blocking the heat loss from the nasal mucosa caused an increase of the THpt-TAC difference, and under these conditions brain temperature was determined solely by arterial blood temperature. The assumed mechanism of the selective brain cooling in rabbits is the exchange of heat through the neurocranial bottom, between the ventral brain and the spacious splanchnocranial venous lakes supplied with blood from the nasal mucosa.

Animals↗