Literature DB >> 8910738

Descending projections of the posterior nucleus of the hypothalamus: Phaseolus vulgaris leucoagglutinin analysis in the rat.

R P Vertes1, A M Crane.   

Abstract

No previous report in any species has systematically examined the descending projections of the posterior nucleus of the hypothalamus (PH). The present report describes the descending projections of the PH in the rat by using the anterograde anatomical tracer, Phaseolus vulgaris leucoagglutinin. PH fibers mainly descend to the brainstem through two routes: dorsally, within the central tegmental tract, and ventromedially, within the mammillo-tegmental tract and its caudal extension, ventral reticulo-tegmental tracts. PH fibers were found to distribute densely to several nuclei of the brainstem. They are (from rostral to caudal) 1) lateral/ ventrolateral regions of the diencephalo-mesopontine periaqueductal gray (PAG); 2) the peripeduncular nucleus; 3) discrete nuclei of pontomesencephalic central gray (dorsal raphe nucleus, laterodorsal tegmental nucleus, and Barrington's nucleus); 4) the longitudinal extent of the central core of the mesencephalic through meduallary reticular formation (RF); 5) the ventromedial medulla (nucleus gigantocellularis pars alpha, nucleus raphe magnus, and nucleus raphe pallidus); 6) the ventrolateral medulla (nucleus reticularis parvocellularis and the rostral ventrolateral medullary region); and 7) the inferior olivary nucleus. PH fibers originating from the caudal PH distribute much more heavily than those from the rostral PH to the lower brainstem. The PH has been linked to the control of several important functions, including respiration, cardiovascular activity, locomotion, antinociception, and arousal/wakefulness. It is likely that descending PH projections, particularly those to the PAG, the pontomesencephalic RF, Barrington's nucleus, and parts of the ventromedial and ventrolateral medulla, serve a role in a PH modulation of complex behaviors involving integration of respiratory, visceromotor, and somatomotor activity.

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Year:  1996        PMID: 8910738     DOI: 10.1002/(SICI)1096-9861(19961028)374:4<607::AID-CNE9>3.0.CO;2-5

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  18 in total

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Authors:  Hong-Wei Dong; Larry W Swanson
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3.  Effects of electrical stimulation of the posterior part of the hypothalamus on the spike activity of neurons in the oral nucleus of the pons.

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Journal:  Neurosci Behav Physiol       Date:  2005-10

4.  Serotonergic raphe magnus cell discharge reflects ongoing autonomic and respiratory activities.

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Review 5.  Distinct patterns of neuronal inputs and outputs of the juxtaparaventricular and suprafornical regions of the lateral hypothalamic area in the male rat.

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6.  Mapping cerebral blood flow changes during auditory-cued conditioned fear in the nontethered, nonrestrained rat.

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7.  Electrically induced static exercise elicits a pressor response in the decerebrate rat.

Authors:  S A Smith; J H Mitchell; M G Garry
Journal:  J Physiol       Date:  2001-12-15       Impact factor: 5.182

8.  Ingestion analgesia occurs when a bad taste turns good.

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Journal:  Behav Neurosci       Date:  2011-09-19       Impact factor: 1.912

Review 9.  Brain reward circuitry beyond the mesolimbic dopamine system: a neurobiological theory.

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Journal:  Neurosci Biobehav Rev       Date:  2010-02-10       Impact factor: 8.989

10.  The posterior hypothalamus exerts opposing effects on nociception via the A7 catecholamine cell group in rats.

Authors:  Y Jeong; J R Moes; M Wagner; J E Holden
Journal:  Neuroscience       Date:  2012-10-02       Impact factor: 3.590

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