Serotoninergic terminals: Ultrastructure and synaptic interaction with catecholamine‐containing neurons in the medial nuclei of the solitary tracts
- 9 May 1984
- journal article
- research article
- Published by Wiley in Journal of Comparative Neurology
- Vol. 225 (2) , 291-301
- https://doi.org/10.1002/cne.902250212
Abstract
The ultrastructural morphology of serotoninergic terminals and their synaptic relation with catecholaminergic neurons were examined in the medial nuclei of the solitary tracts (m‐NTS) using combined autoradiographic and immunocytochemical methods. Adult rats were pretreated with a monoamine oxidase inhibitor and subjected to a 2‐hour intraventricular infusion of 50 nM tritiated 5‐hydroxytryptamine (3H‐5HT). At the termination of the infusion, the brains were fixed by aortic arch perfusion with a mixture of 4% paraformaldehyde and 0.5% glutaraldehyde. Coronal Vibratome sections through the NTS and more rostral raphe nuclei were immunocytochemically labeled with specific antiserum to serotonin or tyrosine hydroxylase and then processed for autoradiography. By light microscopy, concentrations of reduced silver grains indicating uptake of 3H‐5HT usually paralleled the localization of peroxidase immunoreactivity for serotonin in neuronal perikarya of the rostral raphe nuclei and in varicosities in the brainstem. The 3H‐5HT‐containing varicosities were found throughout the medial and commissural portions of the NTS, where they were frequently associated with processes showing immunoreactivity for the catecholamine‐synthesizing enzyme tyrosine hydroxylase. Ultrastructural examination of the m‐NTS revealed that the silver grains for 3H‐5HT were accumulated over axon terminals. The 5HT‐labeled terminals contained a heterogeneous population of vesicles and formed both symmetric and asymmetric synapses with dendrites. The recipient dendrites were either unlabeled or showed immunoreactivity for tyrosine hydroxylase. These findings support a direct serotoninergic modulation of catecholaminergic neurons within the rat m‐NTS.Keywords
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