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The Journal of comparative neurology2010; 518(19); 4046-4066; doi: 10.1002/cne.22443

Sympathetic innervation of the ileocecal junction in horses.

Abstract: The distribution and chemical phenotypes of sympathetic and dorsal root ganglion (DRG) neurons innervating the equine ileocecal junction (ICJ) were studied by combining retrograde tracing and immunohistochemistry. Immunoreactivity (IR) for tyrosine hydroxylase (TH), dopamine beta-hydroxylase (DBH), neuronal nitric oxide synthase (nNOS), calcitonin gene-related peptide (CGRP), substance P (SP), and neuropeptide Y (NPY) was investigated. Sympathetic neurons projecting to the ICJ were distributed within the celiac (CG), cranial mesenteric (CranMG), and caudal mesenteric (CaudMG) ganglia, as well as in the last ganglia of the thoracic sympathetic chain and in the splanchnic ganglia. In the CG and CranMG 91 +/- 8% and 93 +/- 12% of the neurons innervating the ICJ expressed TH- and DBH-IR, respectively. In the CaudMG 90 +/- 15% and 94 +/- 5% of ICJ innervating neurons were TH- and DBH-IR, respectively. Sympathetic (TH-IR) fibers innervated the myenteric and submucosal ganglia, ileal blood vessels, and the muscle layers. They were more concentrated at the ICJ level and were also seen encircling myenteric plexus (MP) and submucosal plexus (SMP) descending neurons that were retrogradely labeled from the ICJ. Among the few retrogradely labeled DRG neurons, nNOS-, CGRP-, and SP-IR nerve cells were observed. Dense networks of CGRP-, nNOS-, and SP-IR varicosities were seen around retrogradely labeled prevertebral ganglia neurons. The CGRP-IR fibers are probably the endings of neurons projecting from the intestine to the prevertebral ganglia. These findings indicate that this crucial region of the intestinal tract is strongly influenced by the sympathetic system and that sensory information of visceral origin influences the sympathetic control of the ICJ.
Publication Date: 2010-08-26 PubMed ID: 20737599DOI: 10.1002/cne.22443Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research article delves into the details of how the nervous system, specifically the sympathetic system, influences the ileocecal junction (ICJ) in horses. The paper explores the distribution and different types of neurons associated with this region, along with how their presence impacts its function.

Research Methodology

  • The researchers used retrograde tracing and immunohistochemistry to study the distribution and chemical phenotypes of the sympathetic and dorsal root ganglion (DRG) neurons in the equine ileocecal junction.
  • Retrograde tracing is a method used in neuroscience to trace the path of nerve cells and neurons back to their sources. Immunohistochemistry involves the process of selectively identifying proteins in cells of a tissue section by exploiting the principle of antibodies binding specifically to antigens in biological tissues.
  • The researchers also investigated the immunoreactivity for tyrosine hydroxylase (TH), dopamine beta-hydroxylase (DBH), neuronal nitric oxide synthase (nNOS), calcitonin gene-related peptide (CGRP), substance P (SP), and neuropeptide Y (NPY). These are all specific markers for neural activity or neuronal cells.

Key Findings

  • The researchers found that sympathetic neurons projecting to the ICJ were located in the celiac, cranial mesenteric, and caudal mesenteric ganglia, as well as in the last ganglia of the thoracic sympathetic chain and in the splanchnic ganglia.
  • They discovered that most of the neurons in these regions expressed Tyrosine hydroxylase (TH) and Dopamine beta-hydroxylase (DBH) immunoreactivity, suggesting the presence of sympathetic activity.
  • The study also found that sympathetic fibers innervated the myenteric and submucosal ganglia, ileal blood vessels, and the muscle layers, indicating a strong influence of the sympathetic nervous system in these regions.
  • These fibers were noted to be more concentrated at the ICJ level and were seen to circle myenteric plexus and submucosal plexus neurons labeled from the ICJ.
  • There were also some retrogradely labeled DRG neurons that displayed nNOS-, CGRP-, and SP-immunoreactivity. In other words, these neurons showed activity markers associated with nitric oxide, calcitonin gene-related peptide, and substance P respectively.
  • Dense networks of neurons with the stated reactive proteins were found around labeled neurons in the prevertebral ganglia.

Conclusion and Implications

  • The findings of the study confirm that the ileocecal junction in horses is heavily influenced by the sympathetic system.
  • Additionally, the sensory information of visceral origin appears to affect the sympathetic control of the ICJ. This suggests a link between sensory conditions in the gut and sympathetic nervous control, an insight that could be crucial for understanding gastrointestinal diseases and conditions in horses.

Cite This Article

APA
Russo D, Bombardi C, Grandis A, Furness JB, Spadari A, Bernardini C, Chiocchetti R. (2010). Sympathetic innervation of the ileocecal junction in horses. J Comp Neurol, 518(19), 4046-4066. https://doi.org/10.1002/cne.22443

Publication

ISSN: 1096-9861
NlmUniqueID: 0406041
Country: United States
Language: English
Volume: 518
Issue: 19
Pages: 4046-4066

Researcher Affiliations

Russo, D
  • Department of Veterinary Morphophysiology and Animal Productions (UNI EN ISO 9001:2008), University of Bologna, 40064 Ozzano Emilia, Bologna, Italy.
Bombardi, C
    Grandis, A
      Furness, J B
        Spadari, A
          Bernardini, C
            Chiocchetti, R

              MeSH Terms

              • Animals
              • Calcitonin Gene-Related Peptide / metabolism
              • Cecum / innervation
              • Dopamine beta-Hydroxylase / metabolism
              • Female
              • Fluorescent Dyes / metabolism
              • Ganglia, Spinal / cytology
              • Horses / anatomy & histology
              • Ileum / innervation
              • Immunohistochemistry
              • Male
              • Nerve Fibers / metabolism
              • Nerve Fibers / ultrastructure
              • Neural Pathways / anatomy & histology
              • Neural Pathways / metabolism
              • Neurons / cytology
              • Neurons / metabolism
              • Neuropeptide Y / metabolism
              • Nitric Oxide Synthase Type I / metabolism
              • Spinal Cord / cytology
              • Spinal Cord / metabolism
              • Substance P / metabolism
              • Sympathetic Nervous System / anatomy & histology
              • Sympathetic Nervous System / physiology
              • Tyrosine 3-Monooxygenase / metabolism

              Citations

              This article has been cited 7 times.
              1. Diana A, Freccero F, Giancola F, Linta N, Pietra M, Luca V, Salamanca G, Cipone M, Chiocchetti R. Ex vivo ultrasonographic and histological morphometry of small intestinal wall layers in horses.. Vet Radiol Ultrasound 2022 May;63(3):353-363.
                doi: 10.1111/vru.13059pubmed: 35171532google scholar: lookup
              2. Chakrabarti S, Ai M, Henson FMD, Smith ESJ. Peripheral mechanisms of arthritic pain: A proposal to leverage large animals for in vitro studies.. Neurobiol Pain 2020 Aug-Dec;8:100051.
                doi: 10.1016/j.ynpai.2020.100051pubmed: 32817908google scholar: lookup
              3. de Brito MC, Chopard RP, Cury DP, Watanabe IS, Mendes CE, Castelucci P. Effects of aging on the architecture of the ileocecal junction in rats.. World J Gastrointest Pharmacol Ther 2016 Aug 6;7(3):416-27.
                doi: 10.4292/wjgpt.v7.i3.416pubmed: 27602243google scholar: lookup
              4. Byun H, Kwon S, Ahn HJ, Liu H, Forrest D, Demb JB, Kim IJ. Molecular features distinguish ten neuronal types in the mouse superficial superior colliculus.. J Comp Neurol 2016 Aug 1;524(11):2300-21.
                doi: 10.1002/cne.23952pubmed: 26713509google scholar: lookup
              5. Chiocchetti R, Giancola F, Mazzoni M, Sorteni C, Romagnoli N, Pietra M. Excitatory and inhibitory enteric innervation of horse lower esophageal sphincter.. Histochem Cell Biol 2015 Jun;143(6):625-35.
                doi: 10.1007/s00418-014-1306-ypubmed: 25578519google scholar: lookup
              6. Ragionieri L, Botti M, Gazza F, Sorteni C, Chiocchetti R, Clavenzani P, Minelli LB, Panu R. Localization of peripheral autonomic neurons innervating the boar urinary bladder trigone and neurochemical features of the sympathetic component.. Eur J Histochem 2013 May 6;57(2):e16.
                doi: 10.4081/ejh.2013.e16pubmed: 23807295google scholar: lookup
              7. Bruinstroop E, Cano G, Vanderhorst VG, Cavalcante JC, Wirth J, Sena-Esteves M, Saper CB. Spinal projections of the A5, A6 (locus coeruleus), and A7 noradrenergic cell groups in rats.. J Comp Neurol 2012 Jun 15;520(9):1985-2001.
                doi: 10.1002/cne.23024pubmed: 22173709google scholar: lookup