Abstract
The distributions of brainstem cells of origin of the cervical vagus nerve, its cervical and thoracic branches, and of neurons projecting to the cricothyroid muscle and the stomach wall were identified and compared following injections of horseradish peroxidase (HRP) in 18 Rhesus monkeys. Physiologically and/or anatomically identified cardiopulmonary nerves were injected with 3-20 μl of HRP to identify the locations of vagal preganglionic cardioinhibitory neurons in 10 of these monkeys. After injections into cardiopulmonary nerves, retrogradely labelled cells were concentrated ipsilaterally in the most lateral parts of the dorsal motor nucleus of the vagus nerve (DMV) and in the ventrolateral nucleus ambiguus (NA). Fewer labelled neurons were identified close to or in the principal (dorsal) division of the NA and in the intermediate zone between the DMV and NA. The results indicate that monkey cardiopulmonary nerves have multiple origins; their somata are located primarily in the ventrolateral NA and to a lesser extent in the lateral DMV. In monkeys, there is a stronger representation in the lateral DMV than in cat, dog and pig. The viscerotopic organization of the cells of origin of primate vagal nerves is similar to that in other species. The cells of origin of vagal projections to the superior laryngeal nerve and cricothyroid muscle were located in the NA rostrally to those of the inferior laryngeal nerve. Injections into the superior laryngeal nerve also resulted in significant labelling in the DMV and intermediate zone (IZ). The cells of origin of projections to the anterior stomach wall were restricted to the DMV with a bilateral distribution of labelled cells, concentrated medially in the nucleus.
Original language | English |
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Pages (from-to) | 21-32 |
Number of pages | 12 |
Journal | Journal of the Autonomic Nervous System |
Volume | 68 |
Issue number | 1-2 |
DOIs | |
Publication status | Published - Jan 19 1998 |
Bibliographical note
Funding Information:Supported by MRC of Canada and the Nova Scotia Heart and Stroke Foundation. We thank D. Grantham, H.Y. Leung, S. MacDonald, K. McCleave, F. Sasinek for technical assistance and Dr. H.H. Ellenberger for reading the manuscript. B. Armstrong-Zwicker, L. Boylan and D. Carter helped prepare the manuscript.
ASJC Scopus Subject Areas
- General Neuroscience
- Physiology
- Clinical Neurology