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Structural, neuronal, and functional adaptive changes in atrophic rat ileum
  1. K M Ekelund,
  2. E Ekblad
  1. Department of Physiology and Neuroscience, Section of Neuroendocrine Cell Biology, University of Lund, Lund University Hospital, E-blocket vån 5, S-221 85 Lund, Sweden
  1. Dr Ekblad

Abstract

BACKGROUND Inactivity of the gut leads to atrophic changes of which little is known.

AIMS To investigate structural, neuronal, and functional changes occurring in bypassed rat ileum.

METHODS Morphometry was used to characterise the atrophic changes. The numbers of enteric neurones, their expression of neurotransmitters, and the presence of interstitial cells of Cajal were studied using immunocytochemistry and in situ hybridisation. Motor activity was studied in vitro.

RESULTS Adaptive changes in bypassed ileum include atrophy and remodelling of the gut wall. The total numbers of submucous and myenteric neurones per unit length increased one and four weeks after bypass but were identical to sham operated intestine 10 weeks after bypass. Neurones expressing vasoactive intestinal peptide, neuropeptide Y, or pituitary adenylate cyclase activating peptide decreased gradually in number in bypassed ileum. Nitric oxide synthase expressing neurones were increased, particularly in the myenteric ganglia. No change in the frequency and distribution of interstitial cells of Cajal was noted. The contractile response elicited by electrical stimulation of sham operated ileum consisted of a fast cholinergic twitch followed by a slower non-adrenergic, non-cholinergic contraction. In the bypassed ileum an identical biphasic contraction was elicited; however, the entire response was non-adrenergic, non-cholinergic. The relaxatory response to electrical stimulation in sham operated ileum was nitric oxide mediated; after bypass it was non-nitrergic.

CONCLUSIONS Notable atrophic changes were seen in the rat ileum after bypass. The enteric nervous system reacted with neuronal cell death and plasticity in terms of release and expression of neurotransmitters.

  • neuronal plasticity
  • enteric nerves
  • interstitial cells of Cajal
  • atrophy
  • neuropeptides
  • nitric oxide
  • Abbreviations used in this paper

    ATP
    adenosine triphosphate
    CGRP
    calcitonin gene related peptide
    EFS
    electric field stimulation
    ENS
    enteric nervous system
    EtBr
    ethidium bromide
    GRP
    gastrin releasing peptide
    ICC
    interstitial cells of Cajal
    l-NAME
    l-N-nitro-arginine methyl ester
    NADPH
    nicotinamide adenine dinucleotide phosphate
    NANC
    non-adrenergic, non-cholinergic
    nNOS
    neuronal nitric oxide synthase
    NO
    nitric oxide
    NPY
    neuropeptide Y
    PACAP
    pituitary adenylate cyclase activating peptide
    SP
    substance P
    TTX
    tetrodotoxin
    VIP
    vasoactive intestinal peptide
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  • Abbreviations used in this paper

    ATP
    adenosine triphosphate
    CGRP
    calcitonin gene related peptide
    EFS
    electric field stimulation
    ENS
    enteric nervous system
    EtBr
    ethidium bromide
    GRP
    gastrin releasing peptide
    ICC
    interstitial cells of Cajal
    l-NAME
    l-N-nitro-arginine methyl ester
    NADPH
    nicotinamide adenine dinucleotide phosphate
    NANC
    non-adrenergic, non-cholinergic
    nNOS
    neuronal nitric oxide synthase
    NO
    nitric oxide
    NPY
    neuropeptide Y
    PACAP
    pituitary adenylate cyclase activating peptide
    SP
    substance P
    TTX
    tetrodotoxin
    VIP
    vasoactive intestinal peptide
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