Literature DB >> 27209472

Pathological effects of chronic myocardial infarction on peripheral neurons mediating cardiac neurotransmission.

Keijiro Nakamura1, Olujimi A Ajijola2, Eric Aliotta1, J Andrew Armour1, Jeffrey L Ardell1, Kalyanam Shivkumar1.   

Abstract

OBJECTIVE: To determine whether chronic myocardial infarction (MI) induces structural and neurochemical changes in neurons within afferent and efferent ganglia mediating cardiac neurotransmission.
METHODS: Neuronal somata in i) right atrial (RAGP) and ii) ventral interventricular ganglionated plexi (VIVGP), iii) stellate ganglia (SG) and iv) T1-2 dorsal root ganglia (DRG) bilaterally derived from normal (n=8) vs. chronic MI (n=8) porcine subjects were studied. We examined whether the morphology and neuronal nitric oxide synthase (nNOS) expression in soma of RAGP, VIVGP, DRG and SG neurons were altered as a consequence of chronic MI. In DRG, we also examined immunoreactivity of calcitonin gene related peptide (CGRP), a marker of afferent neurons. Chronic MI increased neuronal size and nNOS immunoreactivity in VIVGP (but not RAGP), as well as in the SG bilaterally. Across these ganglia, the increase in neuronal size was more pronounced in nNOS immunoreactive neurons. In the DRG, chronic MI also caused neuronal enlargement, and increased CGRP immunoreactivity. Further, DRG neurons expressing both nNOS and CGRP were increased in MI animals compared to controls, and represented a shift from double negative neurons.
CONCLUSIONS: Chronic MI impacts diverse elements within the peripheral cardiac neuraxis. That chronic MI imposes such widespread, diverse remodeling of the peripheral cardiac neuraxis must be taken into consideration when contemplating neuronal regulation of the ischemic heart.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Autonomic nervous system; CGRP; Chronic myocardial infarction; Dorsal root ganglia; Intrinsic cardiac nervous system; Stellate ganglion; nNOS

Mesh:

Substances:

Year:  2016        PMID: 27209472      PMCID: PMC4903881          DOI: 10.1016/j.autneu.2016.05.001

Source DB:  PubMed          Journal:  Auton Neurosci        ISSN: 1566-0702            Impact factor:   3.145


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