Biomedical subjects
Publications and source records attributed to J S Tindal.
A stereotaxic atlas has been prepared for the medulla oblongata of the adult goat's brain using the technique described previously (Tindal et al. 1968). The atlas consists of transverse stereotaxic planes passing caudally at 1 mm intervals from posterior 10 mm (P10) at the level of the junction between brainstem and cerebellum to posterior 20 mm (P20) at the level of the obex.
Transection of the ventral central grey and surrounding midbrain tegmentum in anaesthetized lactating rabbits caused repeated milk ejections which, on comparison with the effects of i.v. infusions of synthetic oxytocin, synthetic arginine-vasopressin or a mixture of the two, were attributed to continuous release of 1.25-2.5 mu. oxytocin/min, although it is not known whether lesser amounts of vasopressin might also have been released. It is suggested that the ascending midbrain reticular formation, which is known to project rostrally through this region, controls the central inhibition of oxytocin release via the previously described septo-hippocampo-subicular route to the hypothalamus.
Six rumen-fistulated, overnight-fasted, female British Saanen goats were used. In preliminary experiments on two of the goats, evidence was obtained that inflation of a balloon with water in the cranial sac of the rumen was accompanied by inhibition of GH release. In a definitive series of experiments on the other four goats (one goat on 1 day = one experiment), a total of 96 experiments were carried out, 48 of which were balloon inflations with 2.5 litres water at 37 degrees C in the cranial sac of the rumen for 40 min and 48 were control experiments on alternate days. It was found that the mean plasma GH concentration of the samples taken at the end of the 40-min inflation period was significantly (P less than 0.05) lower than the mean value of the samples taken at the start of inflation. Mean control values at the start and finish of inflation were not significantly different. There were no significant differences between mean plasma insulin concentrations at the start and finish of inflation in experimental and control groups. It is concluded that distension of the cranial rumen in the goat is a signal which can inhibit the release of GH.
Recording electrodes were implanted in contact with the dura mater overlying the parietal cortex of six female goats, four of which were lactating. After recovery from surgery and complete familiarization with the housing conditions, the personnel and the recording technique, each goat was observed continuously for 24 h with simultaneous recording of the cortical electroencephalogram (EEG). Remote blood sampling was carried out every 30 min without disturbing the animal. Apart from the release of growth hormone (GH) associated with morning milking in two of the goats, there was no consistent relationship between the apparently spontaneous, episodic release of GH and behvaiour, stages of sleep, cortical EEG, air temperature, time of day or night, obvious environmental stimuli which arose from the normal husbandry routine, or the levels of porlactin, insulin, glucose or free fatty acids in the blood. There was also no relationship between the release of prolactin and the stages of sleep.
Circulating prolactin levels were measured by radioimmunoassay after electrical stimulation of discrete sites in the forebrain of 420 lactating rats. The animals were prepared under initial anaesthesia, were decorticated except for frontal cortex and their brain stems were transected at the mid-collicular level.
When the afferent pathway of the milk-ejection reflex, which we had previously reported, was surgically severed bilaterally in the mid-brain of the lactating rabbit, the reflex release of oxytocin in response to suckling was blocked for up to 11 days; unilateral severance did not block the reflex. The position and discrete nature of the pathway were also further substained by electrical stimulation experiments in acute studies in the anaesthetized rabbit. Some animals, however, did not release oxytocin in response to stimulation of the pathway. Furthermore, whereas stimulation of this reflex pathway in the guinea-pig brain at intervals of a few minutes evokes release of oxytocin after each stimulation, in the present study the release of oxytocin in the rabbit in response to repeated electrical stimulation was either progressively attenuated or did not occur at all after the initial release. There appears, therefore, to be a powerful overriding central inhibitory mechanism in the rabbit which can prevent release of oxytocin, even when the appropriate stimulus for release is applied.
The daily milk yields and the yields of fat, lactose and protein in milk were studied in New Zealand White rabbits in which the pituitary stalk and its portal vessels had been interrupted by a radiofrequency lesion placed during the second or third weeks of lactation. In comparison with yields from control rabbits i.e. animals in which the lesion did not completely interrupt the stalk, the yields of milk anf of milk constituents were depressed after interruption of the stalk on day 11 or day 15 of lactation. When the lesion was placed on day 19 of lactation the molk yield was depressed whether or not the stalk was completely disrupted; the decline in yield exaggerated the normal decline of yield that occurs at this stage of lactation. After interruption of the pituitary stalk changes in milk composition were associated with changes in milk production, not evidence being obtained to support anearlier suggestion that section of the pituitary stalk in the rabbit alters the milk compostion whilst leaving milk output unaffected.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.