» Articles » PMID: 950597

Excitation of Phasically Firing Hypothalamic Supraoptic Neurones by Carotid Occlusion in Rats

Overview
Journal J Physiol
Specialty Physiology
Date 1976 May 1
PMID 950597
Citations 24
Authors
Affiliations
Soon will be listed here.
Abstract

1. The activity of supraoptic neurones has been recorded extracellularly during bilateral occlusion of the common carotid arteries in anaesthetized rats. 2. Experiments in lactating rats showed that occlusion liberated sufficient amounts of neurohypophysial hormones to cause a rise in intramammary pressure 15-25 s after the onset of occlusion. 3. Ninety-one percent of the phasic neurones (defined as those showing bursts of activity alternating with periods of silence) were activated by carotid occlusion less than 10 s after the onset of occlusion. Most randomly firing neurones were inhibited or were unaffected. 4. The activation of phasic neurones is unlikely to be just a nonspecific effect, because in the same animals, phasic neurones were excited whilst random neurones were not. 5. Moreover, in phasic neurones, statistical analysis shows (a) that the intervals during which an occlusion was performed were significantly shorter than the intervals between spontaneously occurring bursts, and (b) that this activation was followed by a period of reduced firing probability. 6. The results are discussed with reference to the correlation of supraoptic neuronal activity with hormone release. The possibility is considered of relating the tendency of some supraoptic neurones to fire in bursts with the secretion of vasopressin.

Citing Articles

Fifty Years of Advances in Neuroendocrinology.

Russell J Brain Neurosci Adv. 2020; 2:2398212818812014.

PMID: 32166160 PMC: 7058251. DOI: 10.1177/2398212818812014.


Electrophysiological properties of identified oxytocin and vasopressin neurones.

Armstrong W, Foehring R, Kirchner M, Sladek C J Neuroendocrinol. 2018; 31(3):e12666.

PMID: 30521104 PMC: 7251933. DOI: 10.1111/jne.12666.


Performance, properties and plasticity of identified oxytocin and vasopressin neurones in vitro.

Armstrong W, Wang L, Li C, Teruyama R J Neuroendocrinol. 2010; 22(5):330-42.

PMID: 20210845 PMC: 2910405. DOI: 10.1111/j.1365-2826.2010.01989.x.


Water deprivation in lactating rats: changes in nucleolar dry mass of paraventricular and supraoptic neurones.

Russell J Cell Tissue Res. 1980; 212(2):315-31.

PMID: 7428034 DOI: 10.1007/BF00233964.


Electrophysiological studies of paraventricular and supraoptic neurones recorded in vitro from slices of rat hypothalamus.

HALLER E, Wakerley J J Physiol. 1980; 302:347-62.

PMID: 7411456 PMC: 1282852. DOI: 10.1113/jphysiol.1980.sp013247.


References
1.
Share L, LEVY M . Cardiovascular receptors and blood titer of antidiuretic hormone. Am J Physiol. 1962; 203:425-8. DOI: 10.1152/ajplegacy.1962.203.3.425. View

2.
Dreifuss J, Kelly J . The activity of identified supraoptic neurones and their response to acetylcholine applied by iontophoresis. J Physiol. 1972; 220(1):105-18. PMC: 1331692. DOI: 10.1113/jphysiol.1972.sp009697. View

3.
Dreifuss J, Kelly J . Recurrent inhibition of antidromically identified rat supraoptic neurones. J Physiol. 1972; 220(1):87-103. PMC: 1331691. DOI: 10.1113/jphysiol.1972.sp009696. View

4.
HAYWARD J, Jennings D . Activity of magnocellular neuroendocrine cells in the hypothalamus of unanaesthetized monkeys. I. Functional cell types and their anatomical distribution in the supraoptic nucleus and the internuclear zone. J Physiol. 1973; 232(3):515-43. PMC: 1350507. DOI: 10.1113/jphysiol.1973.sp010284. View

5.
Dyball R . Oxytocin and ADH secretion in relation to electrical activity in antidromically identified supraoptic and paraventricular units. J Physiol. 1971; 214(2):245-56. PMC: 1331834. DOI: 10.1113/jphysiol.1971.sp009430. View