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Ultrastructure of substance P‐immunoreactive terminals and their relation to vascular smooth muscle cells of rat small mesenteric arteries
Author(s) -
Luff Susan E.,
Young Simone B.,
McLachlan Elspeth M.
Publication year - 2000
Publication title -
journal of comparative neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.855
H-Index - 209
eISSN - 1096-9861
pISSN - 0021-9967
DOI - 10.1002/(sici)1096-9861(20000117)416:3<277::aid-cne1>3.0.co;2-1
Subject(s) - adventitia , substance p , biology , axon , synaptic vesicle , calcitonin gene related peptide , anatomy , vascular smooth muscle , neuropeptide , ultrastructure , plexus , free nerve ending , mesenteric arteries , vesicle , artery , medicine , endocrinology , smooth muscle , receptor , membrane , biochemistry
Mesenteric arteries of the rat are surrounded by a plexus of primary afferent nerve terminals which contain both substance P (SP) and calcitonin gene‐related peptide (CGRP). The ultrastructural arrangement of the innervation was studied in second‐order branches of the rat mesenteric artery using immunohistochemical labelling with antibodies against SP. The structure and distribution of SP‐immunoreactive (SP+) and SP‐negative (SP−, i.e., virtually all noradrenergic) axons and their terminals within the adventitia of the artery have been determined. Sixteen percent of axons and 22% of varicosities in the perivascular plexus were SP+. Most of the SP+ varicosities lay between 0.4 and 2 μm from the smooth muscle cells, whereas most SP− varicosities lay much closer to the vessel (i.e., <1 μm). SP+ varicosities typically contained the same number and size of small synaptic vesicles and mitochondria as SP− varicosities, but there were more large dense‐cored vesicles in the SP+ varicosities. Unlike SP− varicosities, the peptidergic varicosities did not show clustering of synaptic vesicles toward one part of the axon membrane, and none of them formed junctions with the smooth muscle cells. Close relationships between SP+ and SP− varicosities lacked any detectable structural specialization. The arrangement of SP+ (primary afferent) terminals and their association with vascular smooth muscle cells indicates that peptide released from afferent terminals must diffuse further than noradrenaline from sympathetic terminals to reach the vascular smooth muscle. J. Comp. Neurol. 416:277–290, 2000. © 2000 Wiley‐Liss, Inc.