B.C.G. in malignant melanoma.
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Biomedical subjects
Publications and source records attributed to M A Baker.
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1. Thermocouples were chronically implanted in various intracranial and extracranial structures in adult cats. Temperature of arterial blood on the proximal and distal sides of the carotid rete was determined by measuring temperature in the aortic arch and at the anterior cerebral arteries. Temperatures of brain stem regions supplied by the carotid rete and by the vertebral-basilar system were determined by measuring temperature in the anterior hypothalamus and the caudal medulla. Nasal mucosal temperature was measured with a thermocouple implanted in the nasal cavity.2. In a cool environment (25 degrees C), the temperature of anterior cerebral arterial blood was lower than aortic arterial temperature. Anterior cerebral temperature showed shifts which were not present in central (aortic) arterial blood and which were clearly associated with changes in heat loss from the nasal mucosa and with the behaviour of the animal. When the cats were relaxed or in e.e.g. slow-wave sleep, the nasal mucosal temperature was high and the temperature at the anterior cerebral arteries was as much as 0.30 degrees C less than aortic temperature. During behavioural arousal and paradoxical sleep, the nasal mucosal temperature fell and the anterior cerebral arterial temperature rose toward central arterial temperature. Shifts in hypothalamic temperature followed the changes in anterior cerebral arterial temperature. Medullary temperature was higher than aortic temperature and showed shifts which suggested that blood from the rostral circle of Willis mixed with vertebral blood in the basilar artery.3. When the ambient temperature was raised to 40-45 degrees C the cooling of cerebral arterial blood and brain increased as the rate of thermal panting increased. Respiratory rate increased tenfold and aortic temperature rose by 2.0-2.5 degrees C. Anterior cerebral arterial temperature fell below aortic temperature by as much as 1 degrees C, hypothalamic temperature dropping in parallel with cerebral arterial temperature. Medullary temperature cooled below aortic temperature during heat exposure, but the temperature drop in the medulla was not as high as in the rostral brain stem.4. Blowing air into the nasal cavity of anaesthetized cats produced a large, rapid temperature drop at the anterior cerebral arteries and in the hypothalamus, with little effect on central arterial temperature. The same experiments in a dead animal cooled the brain after a longer period of time, suggesting that an active process is involved in the brain cooling observed in living animals.5. It is concluded that the cooling of the rostral cerebral arterial blood and brain which occurs in cats in a cool environment and is accelerated during thermal panting, is a result of countercurrent heat exchange between arterial blood in the carotid rete and venous blood draining the evaporative surfaces of the upper respiratory passages. Such direct brain cooling during thermal panting has now been demonstrated in the cat, the sheep and the gazelle, and probably explains the high heat tolerance of the carnivores and hoofed mammals in which a rete is present.
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1. Adult cats were prepared for chronic micro-electrode recording in the nucleus ventralis posterolateralis (VPL) of the ventrobasal complex (VB) of the thalamus. Spontaneous and evoked activity of single neurones was recorded extracellularly while the animal stood in a hammock. The behavioural state of the animal and the electroencephalogram (e.e.g.) were observed and recorded.2. Three hundred and twenty-five single neurones sensitive to movement of hairs, depression of skin or movement of claws were isolated and studied. Peripheral receptive fields were on the contralateral surface of the body. They remained constant in size and location over long periods of time and despite changes in the behavioural state of the animal. Most of the receptive fields covered a cutaneous area at least as large as an entire paw and many covered an entire limb and extended on to the trunk. These fields are larger than those described by other investigators using natural stimulation in anaesthetized or paralysed animals.3. Moving hairs or touching skin in the peripheral receptive field elicited a burst of spikes at frequencies between 100 and 150/sec. Repeated stimulation did not result in obvious alteration or habituation of the response. There was no apparent change in responsiveness of neurones to peripheral stimulation when the animal was asleep.4. Except for claw-sensitive units, all neurones were active in the absence of intentional stimulation of the receptive field. When the animals were awake, VPL neurones fired more regularly than during sleeping. In slow sleep, with e.e.g. slow waves and spindles, firing patterns were characterized by the presence of more high-frequency bursts of spikes and more long interspike intervals than in waking. Claw-sensitive units, silent during waking, fired in bursts during sleep. When small doses of barbiturate were injected intravenously while recording the activity of neurones, the firing pattern changed to one in which all of the activity occurred in the form of high-frequency bursts. Interburst intervals were variable.5. The level of spontaneous activity in VB in conscious cats is greater than in sensory and sensorimotor cortex to which it projects. The pronounced effect of behavioural state on spontaneous activity of these neurones suggests that the background activity in somatosensory systems may play some role in the processing of afferent input.
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1. In chronically-prepared sheep, intracranial temperatures were measured in the cavernous sinus among the vessels of the carotid rete and at the circle of Willis extravascularly, and in the preoptic area and in other brain stem regions. Extracranial temperatures were measured intravascularly in the carotid or internal maxillary arteries and on the nasal mucosa and the skin of the ear.2. At 20 degrees C ambient temperature, shifts in temperature of the hypothalamus and of other brain sites paralleled temperature shifts in the cerebral arterial blood which was cooler than central arterial blood. During periods of arousal and of paradoxical sleep, vasoconstriction of the nasal mucosa and the ear skin occurred and temperatures at the cerebral arteries and in the brain rose without a comparable rise in central arterial blood temperature.3. Anaesthetic doses of barbiturate abolished the temperature oscillations in the cerebral arterial blood and the brain. When air was blown rapidly over the nasal mucosa in anaesthetized animals, temperatures dropped precipitously in the cavernous sinus, at the cerebral arteries, and in the brain, while central arterial temperature fell only slightly. Injections of latex into the facial venous system demonstrated a venous pathway from the nasal mucosa to the cavernous sinus.4. When sheep were exposed to 45-50 degrees C ambient temperature, respiratory rate increased 5-10 times and the temperature gradient between central and cerebral arterial blood widened.5. It is concluded that venous blood returning from the nasal mucosa and the skin of the head to the cavernous sinus cools the central arterial blood in the carotid rete. This is an important factor in the maintenance of hypothalamic temperature in the wool-covered, long-nosed, panting sheep and undoubtedly affects hypothalamic thermoreceptors and temperature regulation in artiodactyls.
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The rise in brain temperature in the rabbit during paradoxical sleep originates in a temperature rise of the cerebral arterial blood. Heat loss from the ear is a major factor in the regulation of arterial blood temperature in the rabbit, and the primary thermal event in paradoxical sleep is a vasoconstriction of the skin of the ear which results in a rise in arterial blood and brain temperatures. These thermal correlates of paradoxical sleep are not present in a cold environment when the ear skin is already maximally vasoconstricted. The persistence of peripheral vasoconstriction during paradoxical sleep in a hot environment suggests a disturbance in autonomic thermoregulatory control.