Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2004-4-5
pubmed:abstractText
Hypothalamic oxytocin neurones have dual physiological functions with associated characteristic activity patterns: a homeostatic osmoregulatory role involving continuous low frequency firing at a relatively constant rate, and roles associated with reproduction involving periodic, brief, synchronised, high frequency bursts of spikes. Apparently the same neurones maintain both roles during reproduction, when both activity patterns occur simultaneously, although sometimes factors linked to the homeostatic response predominate and prevent bursting. With the object of understanding how oxytocin neuronal networks manage both roles during lactation, we analysed basal activity between bursts in simultaneously recorded neurones to reveal potentially adaptive changes in network behaviour. Negative autocorrelation on a time scale of 0.5-2 s occurs in basal activity between bursts but also in non-bursting oxytocin neurones, and can therefore be associated with the system's homeostatic role. Although the system responds to the pups suckling by the induction of bursting, there are also increasing fluctuations in firing that are positively correlated in some simultaneously recorded neurones during basal activity between bursts. A few seconds before bursts, cross-correlation strengthens, irregularity of firing increases, and serial correlation (autocorrelation) weakens, all substantially. After pharmacological treatments known to facilitate bursting, cross-correlation and irregularity of firing increase and autocorrelation weakens, and the reverse occurs in conditions that delay bursting (hyperosmotic stress and pharmacological interventions). Our analyses suggest heterogeneity in the population of oxytocin neurones during lactation; the range including 'leader neurones' that readily display co-ordinated fluctuations in firing in response to suckling and escape from negative autocorrelation just before bursts, and 'follower neurones' that fire at a relatively constant rate in no apparent relationship to others, except when recruited late to bursting, probably in response to massive stimulation from already bursting neurones. The steep increases in correlation a few seconds before bursts reflect an accelerating process of recruitment of follower neurones to co-ordinated fluctuations, leading to the phase transition that constitutes the critical stage of burst generation.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0306-4522
pubmed:author
pubmed:issnType
Print
pubmed:volume
125
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
391-410
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:15062982-Acetylcholine, pubmed-meshheading:15062982-Action Potentials, pubmed-meshheading:15062982-Animals, pubmed-meshheading:15062982-Animals, Suckling, pubmed-meshheading:15062982-Cholecystokinin, pubmed-meshheading:15062982-Drug Administration Routes, pubmed-meshheading:15062982-Electrophysiology, pubmed-meshheading:15062982-Mathematics, pubmed-meshheading:15062982-Neurons, pubmed-meshheading:15062982-Nonlinear Dynamics, pubmed-meshheading:15062982-Oxytocin, pubmed-meshheading:15062982-Paraventricular Hypothalamic Nucleus, pubmed-meshheading:15062982-Rats, pubmed-meshheading:15062982-Rats, Wistar, pubmed-meshheading:15062982-Sodium, pubmed-meshheading:15062982-Statistics as Topic, pubmed-meshheading:15062982-Supraoptic Nucleus, pubmed-meshheading:15062982-Time Factors
pubmed:year
2004
pubmed:articleTitle
Oxytocin neurones are recruited into co-ordinated fluctuations of firing before bursting in the rat.
pubmed:affiliation
Laboratory Biologie des Neurones Endocrines, CNRS UMR 5101, CCIPE, 141, rue de la Cardonille, 34094 Montpellier Cedex 05, France. fmoos@ccipe.cnrs.fr
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't