Literature DB >> 20674686

Neuropeptide coding of sympathetic preganglionic neurons; focus on adrenally projecting populations.

N N Kumar1, K Allen, L Parker, H Damanhuri, A K Goodchild.   

Abstract

Chemical coding of sympathetic preganglionic neurons (SPN) suggests that the chemical content of subpopulations of SPN can define their function. Since neuropeptides, once synthesized are transported to the axon terminal, most demonstrated chemical coding has been identified using immunoreactive terminals at the target organ. Here, we use a different approach to identify and quantify the subpopulations of SPN that contain the mRNA for pituitary adenylate cyclase activating polypeptide (PACAP) or enkephalin. Using double-labeled immunohistochemistry combined with in situ hybridization (ISH) we firstly identified the distribution of these mRNAs in the spinal cord and determined quantitatively, in Sprague-Dawley rats, that many SPN at the T4-T10 spinal level contain preproPACAP (PPP+, 80 ± 3%, n=3), whereas a very small percentage contain preproenkephalin (PPE+, 4 ± 2%, n=4). A similar neurochemical distribution was found at C8-T3 spinal level. These data suggest that PACAP potentially regulates a large number of functions dictated by SPN whereas enkephalins are involved in few functions. We extended the study to explore those SPN that control adrenal chromaffin cells. We found 97 ± 5% of adrenally projecting SPN (AP-SPN) to be PPP+ (n=4) with only 47 ± 3% that were PPE+ (n=5). These data indicate that adrenally projecting PACAPergic SPN regulate both adrenal adrenaline (Ad) and noradrenaline (NAd) release whereas the enkephalinergic SPN subpopulation must control a (sub) population of chromaffin cells - most likely those that release Ad. The sensory innervation of the adrenal gland was also determined. Of the few adrenally projecting dorsal root ganglia (AP-DRG) observed, 74 ± 12% were PPP+ (n=3), whereas 1 ± 1% were PPE+ (n=3). Therefore, if sensory neurons release peptides to the adrenal medulla, PACAP is most likely involved. Together, these data provide a neurochemical basis for differential control of sympathetic outflow particularly that to the adrenal medulla.
Copyright © 2010 IBRO. Published by Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20674686     DOI: 10.1016/j.neuroscience.2010.07.047

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  4 in total

1.  Activation of PAC(1) and VPAC receptor subtypes elicits differential physiological responses from sympathetic preganglionic neurons in the anaesthetized rat.

Authors:  Melissa A Inglott; Ethan A Lerner; Paul M Pilowsky; Melissa M J Farnham
Journal:  Br J Pharmacol       Date:  2012-11       Impact factor: 8.739

Review 2.  PACAP is implicated in the stress axes.

Authors:  Hitoshi Hashimoto; Norihito Shintani; Mamoru Tanida; Atsuko Hayata; Ryota Hashimoto; Akemichi Baba
Journal:  Curr Pharm Des       Date:  2011       Impact factor: 3.116

Review 3.  Neural pathways that control the glucose counterregulatory response.

Authors:  Anthony J M Verberne; Azadeh Sabetghadam; Willian S Korim
Journal:  Front Neurosci       Date:  2014-02-26       Impact factor: 4.677

4.  Somatostatin 2 Receptors in the Spinal Cord Tonically Restrain Thermogenic, Cardiac and Other Sympathetic Outflows.

Authors:  Belinda R Bowman; Phillip Bokiniec; Simon McMullan; Ann K Goodchild; Peter G R Burke
Journal:  Front Neurosci       Date:  2019-02-20       Impact factor: 4.677

  4 in total

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