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Biomedical subjects

K G Foster

Publications and source records attributed to K G Foster.

At least 19 recordsLinked to original sources

Sweat responses in the aged.

The sweating responses to thermal stimulation and to the intradermal injection of acetyl choline or methacholine were measured in 28 men and 18 women aged 70 and over and were compared with the responses in young control subjects of both sexes. There was found to be a marked reduction in the sweating activity of the majority of aged men in comparison with the younger age groups and the body temperature threshold for the onset of sweating was increased. The reduced response and elevated threshold were even more pronounced in aged females. There is considerable variability in response in different subjects and at different bodily sites. Impairment of thermoregulatory function due to diminished or absent sweating is thought to be one of the factors responsible for increased mortality in the elderly population during heat-waves.

Acetylcholine↗

Factors affecting the quantitative response of human eccrine sweat glands to intradermal injections of acetylcholine and methacholine.

1. Using a ventilated capsule in conjunction with an infra-red water vapour analyser, and an indwelling intradermal needle, quantitative studies were made relating the magnitude of the sweat responses to the doses of acetylcholine or methacholine.2. Acetylcholine dose-response curves were constructed, and from these curves the threshold dose was defined. The threshold was similar in all subjects (10(-3) +/- S.E. 10(-4) mug/0.1 ml.).3. Factors affecting the acetylcholine dose-response curves were studied. Optimum conditions for stimulation in all subjects occurred using a capsule of 0.63 cm diameter, injection volume of 0.1 ml. and a solution temperature of 37 degrees C. When the skin temperature was 36 degrees C the maximal acetylcholine response was then the same as the maximal thermal response.4. No change in the acetylcholine dose-response curves occurred with repeated determinations at the same site on the same occasion.5. The dose-response relationship for methacholine was similar to that for acetylcholine. The methacholine response was, however, more prolonged and so the volumes secreted were greater.

Acetylcholine↗

Effects of cholinergic and adrenergic blocking agents on the activity of the eccrine sweat glands.

1. The effects of blocking agents on the responsiveness of the cast' pad and human forearm sweat glands have been studied.2. Of the anti-adrenergic substances examined (dibenamine, phenoxybenzamine, bretylium, guanethidine and phentolamine) only high doses of guanethidine and phentolamine produced any consistent and significant measure of blockade, and small doses of atropine were as effective as these large doses of guanethidine or phentolamine.3. It is concluded from the blockade of chemical stimulation as well as transmission by these substances that (1) there are only cholinergic fibres innervating eccrine sweat glands, and (2) any inhibitory action by anti-adrenergic substances is due to interaction with cholinergic receptors in the glands.

Animals↗

The response of the sweat glands of the newborn baby to thermal stimuli and to intradermal acetylcholine.

1. Measurements of evaporative sweat loss were made on fifty-six premature and full-term babies 1-67 days after birth with an infra-red analyser and a ventilated capsule placed on the thigh. Measurements were also made of total evaporative water loss while in a closed metabolic chamber and of the regional distribution of sweating with starch-iodine paper.2. No sweating to thermal stimuli could be detected in infants of less than 210 days post-conceptual age, even when rectal temperature rose as high as 37.8 degrees C. In older infants sweat was detected first on the forehead and temple, later on the chest, and usually by 240-260 days post-conceptual age on the legs (term approximately 268 days). Generalized sweating on the limbs appeared at an earlier post-conceptual age in the more prematurely born infants.3. The response of sweat glands on the thigh to an intradermal injection of 2 mug acetylcholine (ACh) was tested. No sweat response was detected in infants under 225 days post-conceptual age, while all infants born within 2 weeks of term responded. The response was often augmented after 2-5 tests at 5-10 min intervals; all the eight infants born within 2 weeks of term who were examined twice in the first 2 weeks of life showed a greater response on the second occasion.4. An average of 414 active sweat glands/cm(2) were detected on the thigh in eight babies 7-10 days old born within 2 weeks of term. This was 6(1/2) times the number found in adults. The mean peak sweat rate to chemical stimulation was however only 2.4 nl./gland.min, which was 3 times lower than the maximum rate recorded in adults.5. In five infants with congenital defects of the brain and complete absence of temperature control there was no sweat response to thermal or direct chemical stimulation of the glands.6. Functional maturation appears to depend on intact central innervation and is marginally hastened by post-natal factors. Immaturity of the sweat glands can account for the lack of any response to thermal stimuli in premature babies, but not for the modest thermal response obtained in babies at term.

Acetylcholine↗

Response of the cat's pad eccrine sweat glands to intravascular injections of catecholamines.

1. Using a sensitive method for detecting and monitoring sweat secretion, a study has been made of the effects of adrenaline and noradrenaline on the cat's pad sweat gland activity in the anaesthetized cat.2. Intravenous or intra-arterial injections of adrenaline or noradrenaline only very occasionally caused these glands to secrete.3. The predominant effect of these drugs on glands which are already secreting in response to plantar nerve stimulation is inhibitory.4. The catecholamine inhibition could be reduced or blocked by phentolamine, but not by propranolol, dibenamine or phenoxybenzamine.5. It is concluded that these glands can be directly activated by intravascular injections of adrenaline or noradrenaline, but that the inhibitory effect of concomitant vasoconstriction usually prevents a response being detected at the skin surface.

Animals↗