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Autor(en) / Beteiligte
Titel
Noradrenergic inputs to the paraventricular hypothalamus contribute to HPA axis and central Fos activation in rats after acute systemic endotoxin exposure
Ist Teil von
  • Neuroscience, 2008-08, Vol.156 (4), p.1093-1102
Erscheinungsjahr
2008
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • Noradrenergic (NA) neurons within the nucleus of the solitary tract (NST) and caudal ventrolateral medulla (VLM) innervate the hypothalamic paraventricular nucleus (PVN) to initiate and modulate HPA axis responses to interoceptive stress. Systemic endotoxin (i.e., bacterial lipopolysaccharide, LPS) activates NA neurons within the NST and VLM that project to the PVN and other brain regions that receive interoceptive signals. The present study examined whether NA neurons with axonal inputs to the PVN are necessary for LPS to activate Fos expression within the PVN and other interoceptive-related brain regions, and to increase plasma corticosterone. Male Sprague-Dawley rats received bilateral stereotaxic microinjections of DSAP (saporin toxin conjugated to an antibody against dopamine-β-hydroxylase, DbH) into the PVN to destroy NA inputs. Control rats were microinjected with vehicle into the PVN or received no PVN injections. Two weeks later, DSAP and control rats were injected i.p. with LPS (200 µg/kg BW) or saline vehicle, and perfused with fixative 2.5–3 hrs later. Brain tissue sections were processed to reveal nuclear Fos protein and cytoplasmic DbH immunolabeling. DSAP lesions depleted NA terminals in the PVN and bed nucleus of the stria terminalis, reduced the number of NA cell bodies in the NST and VLM, attenuated PVN Fos activation after LPS, and attenuated LPS-induced increases in plasma corticosterone. These findings support the view that NA projections from hindbrain to hypothalamus are necessary for a full HPA axis response to systemic immune challenge.
Sprache
Englisch
Identifikatoren
ISSN: 0306-4522
DOI: 10.1016/j.neuroscience.2008.08.011
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2614295
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