Literature DB >> 6619341

Organization of the projections of a circumventricular organ: the area postrema in the rat.

D van der Kooy, L Y Koda.   

Abstract

The projections of the rat area postrema were analysed using anterograde and retrograde axonal transport techniques. Discrete injections of wheat germ agglutinin conjugated to horseradish peroxidase (WGA-HRP) into the area postrema produced anterograde labeling in specific medullary and pontine nuclei. In the medulla, anterograde labeling was present in the internal solitary zone and dorsal division of the medial solitary nucleus, both of which also contained a small number of retrogradely labeled perikarya. Prominent projections to the dorsal motor nucleus of the vagus were seen only if the WGA-HRP injections in the area postrema invaded dorsal solitary nuclei. In the pons, anterograde labeling was present in the parabrachial nuclei, the dorsolateral tegmental nucleus, and the pericentral division of the dorsal tegmental nucleus. By far the major pontine projection was to the dorsolateral region of the middle one-third of the rostrocaudal extent of the parabrachial nuclei. Retrograde fluorescent tracing studies indicated that most area postrema neurons take part in this parabrachial projection. The area postrema projection to the parabrachial nuclei was bilaterally distributed, whereas that from the dorsal solitary nuclei was primarily ipsilateral. The external solitary zone, immediately subadjacent to the area postrema, neither received area postrema projections nor participated in the projections to the parabrachial nuclei. Fluorescent retrograde double labeling studies confirmed the bilateral nature of the area postrema projection to the parabrachial nuclei. In addition, because no doubly labeled neurons were observed it appears that individual area postrema neurons project to either side but not both sides of the dorsal pons. Thus, numerous neuronal pathways exist for the transfer of blood-borne information (that cannot cross the blood-brain barrier) from the area postrema to other brain regions.

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Mesh:

Year:  1983        PMID: 6619341     DOI: 10.1002/cne.902190307

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


  31 in total

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Authors:  G Schulteis; J L Martinez
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2.  GABA-mediated inhibition of medullary vasomotor neurones by area postrema stimulation in rats.

Authors:  M K Sun; K M Spyer
Journal:  J Physiol       Date:  1991-05       Impact factor: 5.182

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4.  Glucagon-like peptide-1-responsive catecholamine neurons in the area postrema link peripheral glucagon-like peptide-1 with central autonomic control sites.

Authors:  Hiroshi Yamamoto; Toshiro Kishi; Charlotte E Lee; Brian J Choi; Hui Fang; Anthony N Hollenberg; Daniel J Drucker; Joel K Elmquist
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Review 5.  Comparative aspects of the area postrema: fine-structural considerations help to determine its function.

Authors:  R A Leslie
Journal:  Cell Mol Neurobiol       Date:  1986-06       Impact factor: 5.046

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Authors:  C M Kotz; M K Grace; J Briggs; A S Levine; C J Billington
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8.  Peripheral interleukin-1β inhibits arcuate kiss1 cells and LH pulses in female mice.

Authors:  Katherine N Makowski; Michael J Kreisman; Richard B McCosh; Ali A Raad; Kellie M Breen
Journal:  J Endocrinol       Date:  2020-08       Impact factor: 4.286

9.  Excitatory effect of ATP on rat area postrema neurons.

Authors:  Masaru Sorimachia; Minoru Wakamoria; Norio Akaikeb
Journal:  Purinergic Signal       Date:  2006-05-30       Impact factor: 3.765

10.  Taste responses in the nucleus tractus solitarius of sodium-deprived rats.

Authors:  K M Jacobs; G P Mark; T R Scott
Journal:  J Physiol       Date:  1988-12       Impact factor: 5.182

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