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Innervation of the Large Arteries and Heart of the Toad (Bufo Marinus) by Adrenergic and Peptide-containing Neurons

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Journal Cell Tissue Res
Date 1986 Jan 1
PMID 2417719
Citations 26
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Abstract

The innervation of the major arteries and heart of the toad (Bufo marinus) was examined by use of glyoxylic acid-induced catecholamine fluorescence and peptide immunohistochemistry. All arteries possessed a moderate to dense plexus of adrenergic axons, which also showed neuropeptide Y-like immunoreactivity (NPY-LI). Some adrenergic axons in the intracardiac vagal trunks showed NPY-LI, but the varicose adrenergic axons innervating the cardiac muscle of the atria and ventricle, and the coronary blood vessels did not display NPY-LI. About half of the nerve cell bodies in the anterior sympathetic chain ganglia with dopamine-beta-hydroxylase-LI (DBH-LI) also contained NPY-LI. The nerve cell bodies with DBH-LI alone were generally larger (median diameter 30 micron) than those with both DBH-LI and NPY-LI (median diameter 20 micron). Some cell bodies showing DBH-LI alone were surrounded by boutons with NPY-LI but not DBH-LI. Axons that displayed simultaneously both substance P-LI (SP-LI) and calcitonin gene-related peptide-LI (CGRP-LI) also formed a plexus around all arteries studied, being particularly dense around the mesenteric and pulmonary arteries. These axons are most likely sensory since SP-LI was reduced by capsaicin treatment, and nerve cell bodies with both SP-LI and CGRP-LI were found in dorsal root ganglia and the vagal ganglion. A dense plexus of axons showing somatostatin-LI was located around the pulmonary artery and its main intrapulmonary branches. A few nerves with vasoactive intestinal polypeptide-LI were found around the dorsal aorta and pulmonary artery. No perivascular nerves with enkephalin-LI were observed. Reversed-phase, high-pressure liquid chromatography of acid extracts of the large arteries showed that the major peaks of NPY-LI and SP-LI co-eluted with porcine NPY (1-36) and synthetic SP (1-11), respectively. Thus, the location and structure of these peptides in perivascular nerves has been highly conserved during vertebrate evolution.

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References
1.
Lundberg J, Terenius L, Hokfelt T, Martling C, Tatemoto K, Mutt V . Neuropeptide Y (NPY)-like immunoreactivity in peripheral noradrenergic neurons and effects of NPY on sympathetic function. Acta Physiol Scand. 1982; 116(4):477-80. DOI: 10.1111/j.1748-1716.1982.tb07171.x. View

2.
Jan Y, Bowers C, Branton D, Evans L, Jan L . Peptides in neuronal function: studies using frog autonomic ganglia. Cold Spring Harb Symp Quant Biol. 1983; 48 Pt 1:363-74. DOI: 10.1101/sqb.1983.048.01.040. View

3.
Wilson S, Klein R, Chang K, Gasparis M, Viveros O, Yang W . Are opioid peptides co-transmitters in noradrenergic vesicles of sympathetic nerves?. Nature. 1980; 288(5792):707-9. DOI: 10.1038/288707a0. View

4.
Morris J, Gibbins I, Clevers J . Resistance of adrenergic neurotransmission in the toad heart to adrenoceptor blockade. Naunyn Schmiedebergs Arch Pharmacol. 1981; 317(4):331-8. DOI: 10.1007/BF00501315. View

5.
Harmar A, Keen P . Chemical characterization of substance P-like immunoreactivity in primary afferent neurones. Brain Res. 1981; 220(1):203-7. DOI: 10.1016/0006-8993(81)90227-4. View