Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Anatomy and embryology 174 (1986), S. 123-144 
    ISSN: 1432-0568
    Keywords: Spinal cord ; Visceral afferents ; Somatic afferents ; Splanchnic nerve ; Dorsal column nuclei ; Sympathetic neurons ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The central projections of primary afferent fibers of the greater splanchnic nerve of the rat were investigated using the transganglionic horseradish peroxidase transport technique. In addition, the corresponding spinal ganglion cells and the preganglionic sympathetic neurons were demonstrated. For comparing visceral and somatic afferents, intercostal nerve afferents were labelled by the same technique. Splanchnic afferent dorsal root ganglion cells were found at segments T3 to T13 ipsilaterally, with the greatest density at T8 to T12. Labelled cells represented about 10%–15% of all neurons in the ganglia at maximal projection levels. They were randomly distributed within individual ganglia. The great majority were medium to small sized and round to slightly oval in shape. In the spinal cord, labelled visceral afferent axons were found maximally at T8 to T11, but could be detected in decreasing density up to T1 and down to L1. They were distributed over Lissauer's tract and the dorsal funiculus to a medial and lateral collateral pathway (MCP and LCP, respectively). The MCP, somewhat more prominent than the LCP, was destined primarily to clustered presumptive terminal fields in medial lamina I and outermost lamina IIa. Only a few axons continued further to laminae V and X. Splanchnic afferent axons, most likely derived from the MCP, formed a longitudinal bundle ventral to the central canal. The LCP consisted of more or less well-defined axon bundles emanating from the lateral Lissauer's tract and curving round the lateral edge of the dorsal horn and through the dorsolateral funiculus. Presumptive terminal sites of LCP axons are the lateral laminae I and IIa, the nucleus of the dorsolateral funiculus and the dorsal part of lamina V. A few LCP axons were seen in the vicinity of lateral dendrites of preganglionic sympathetic axons. Visceroafferent terminals were absent from laminae IIb–IV and VII. The possible consequences of the MCP/LCP duality for the central connections of splanchnic afferents are discussed. Some splanchnic afferents ascended to the gracile and cuneate nuclei, and rarely to the spinal trigeminal nucleus. These results fit into the general concept of visceroafferent terminal organization that has emerged during the last few years. Differences to other reports in the detailed arrangement of fibers and terminals are discussed. Somatoafferent cell bodies represented the vast majority of neurons in the respective spinal ganglia. Cell sizes encompassed the whole range from very small to very large without a clear predominance of one particular size class. Cell shapes of somatic neurons were more variable than those of visceral afferent neurons. Somatic afferent fibers and presumptive terminals in the spinal cord are distributed ipsilaterally to dorsal horn laminae I–V, most heavily II–IV, to the nucleus dorsalis Clarke, to the ventral horn, and also sparsely to the dorsal horn contralaterally. Labelled preganglionic sympathetic neurons were found in segments T3–T13. The vast majority was located in the intermediolateral nucleus. Fewer neurons occurred in the intercalated nucleus, and occasionally a neuron was labelled in the dorsal grey commissure.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Anatomy and embryology 170 (1984), S. 63-70 
    ISSN: 1432-0568
    Keywords: Esophagus ; Stomach ; Nucleus ambiguus ; Dorsal motor nucleus of the Vagus ; Nucleus solitarius
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The technique of retrograde labeling of nerve cells with HRP and nuclear yellow as well as transganglionic anterograde HRP-tracing of sensory projections into the CNS were used to establish the motor and sensory innervation pattern of two parts of the rat esophagus: the cervical and the abdominal segment. For comparison, also the innervation of the anterior wall of the stomach was studied. Application of HRP to the cervical part of the esophagus resulted in bilateral labeling of neurons in the nucleus ambiguns exclusively, while application of the tracer to the abdominal part was followed by labeling of cells in both the nucleus ambiguus and the dorsal motor nucleus of the vagus. Application of tracer to the wall of the stomach caused labeling of cells in the dorsal motor nucleus of the vagus exclusively. Labeling appeared always bilaterally. In all experiments there was a profuse labeling of primary afferent neurons with cell bodies in both nodose ganglia and endings in certain subnuclei of the solitary nucleus. Endings related to the cervical esophagus projected into the ventral subnuclei, projections from the abdominal esophagus were located in the ventral and medial subnuclei, those from the stomach in the medial subnucleus solely. The area postrema and the commissural nucleus received afferents from both organs, the esophagus and the stomach. Double labeling experiments with HRP and nuclear yellow provided no signs of overlap of sensory innervation areas of the sites investigated in this study. Within the wall of the esophagus no labeled intramural cells nor nerve fibers were found in sections beyond the injection sites.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...