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  • Horseradish peroxidase  (2)
  • Medial preoptic area  (2)
  • 1
    ISSN: 1432-1106
    Keywords: Central noradrenergic innervation ; Rat spinal cord ; Horseradish peroxidase ; Monoamine oxidase staining
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The origin of the spinal cord noradrenaline (NA) has been investigated by means of the horseradish peroxidase (HRP) method, combined with monoamine oxidase staining (Glenner) to identify the NA neurons. Following the injection of HRP to the various levels of rat spinal cord, cervical to sacral cord, A1–3, 5–7 NA neuron groups were labeled with HRP. They showed almost the same distribution pattern regardless of difference in the injected segment. Labeled NA neurons in A6 were concentrated in the ventral division of the locus coeruleus, which continued to the labeled NA neurons in the subcoeruleus area. The HRP positive neurons in the pons outnumbered those of the medulla oblongata. As the NA neurons described above were considered to be the source of NA in the forebrain, such as the hypothalamus and preoptic area, the possibility that the same NA neurons might innervate both the forebrain and spinal cord has been presented.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1106
    Keywords: Afferent connection ; Lower brain stem ; Hypothalamus ; Horseradish peroxidase ; Histofluorescence
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Attempts were made to determine the afferent projections to the anterior hypothalamus including the preoptic area from the lower brain stem by means of the horseradish peroxidase method combined with monoamine oxidase staining to identify noradrenaline (NA) neurons. In addition to this technique, a histofluorescence analysis was performed. NA fibers in the medial part of the anterior hypothalamus were mainly supplied by A1 and A2 NA neuron groups, while the lateral part and periventricular zone received NA terminals from both pontine and medulla oblongata NA neuron groups. Furthermore, the present study indicated that there were direct projections to the anterior hypothalamus from non-noradrenergic neurons in the lower brain stem: nuclei raphe dorsalis, centralis superior, cells in the mesencephalic and pontine central gray matter, nuclei parabrachialis lateralis and medialis, cells around fasciculus longitudinalis medialis.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1106
    Keywords: Enkephalin ; Projection ; Medial preoptic area ; Arcuate nucleus ; Immunocytochemistry ; Double-staining method
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We studied the distribution of fibers with leucine-enkephalin — like immunoreactivity (L-ENKI) in the medial preoptic area (MPO) of the rat, and the origins of such fibers, using indirect immunofluorescence and a combination of a retrograde tracer with immunocytochemistry that we have developed. These fibers were very dense throughout the rostro-caudal part of the MPO. The distribution was uneven with the highest density in the lateral part. Destruction of the arcuate nucleus, which contains a group of L-ENKI neurons, resulted in the marked reduction of these fibers in the ipsilateral MPO, suggesting that most of these fibers originate in this nucleus. This was also suggested by the fact that injection of biotin-wheat germ agglutinin into the MPO labelled many neurons in the arcuate nucleus ipsilaterally. Simultaneous staining with antiserum showed that some of these neurons are L-ENKI.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-1106
    Keywords: Tuberomammillary nucleus ; Histaminergic system ; E groups ; Efferent projection ; Medial preoptic area ; Inferior colliculus ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The efferent projections of the five histaminergic neuronal subgroups in the tuberomammillary nucleus to the medial preoptic area (MPO) and inferior colliculus (IC) were examined by immunocytochemistry with antihistidine decarboxylase (HDC) antibodies combined with retrograde axonal tracing with Fast Blue (FB). The term “E groups” were used for the histaminergic neuronal subgroups. About 10% of the HDC-immunoreactive (HDCI) neurons were retrogradely labeled after FB injection into the MPO. The labeled neurons were not concentrated in any particular area, but were diffusely distributed bilaterally in all the subgroups. About two-thirds of the labeled neurons were observed on the side ipsilateral to the injection site and one-third on the contralateral side. The percentages of labeled neurons (double-labeled neurons/HDCI neurons) in the five subgroups were not significantly different with each other. The percentages in group E1 and E2 were particularly close, while that in group E4 resembled that in group E5. About 4% of the HDCI neurons were retrogradely labeled after the dye injections into the IC, and about half of the labeled neurons were detected on the ipsilateral side. The percentage of the double-labeled neurons in the five groups were not significantly different. Furthermore, those in E1 and E2, and in E4 and E5 were almost identical, respectively, to the situation following injection of FB into the MPO. These results indicate that each subgroup of histaminergic neurons in the tuberomammillary nucleus has similar efferent projections to the MPO and IC.
    Type of Medium: Electronic Resource
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