Effect of age on the enteric nervous system of the human colon

The effect of age on the anatomy and function of the human colon is incompletely understood. The prevalence of disorders in adults such as constipation increase with age but it is unclear if this is due to confounding factors or age‐related structural defects. The aim of this study was to determine...

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Veröffentlicht in:Neurogastroenterology and motility 2009-07, Vol.21 (7), p.746-e46
Hauptverfasser: Bernard, C. E., Gibbons, S. J., Gomez‐pinilla, P. J., Lurken, M. S., Schmalz, P. F., Roeder, J. L., Linden, D., Cima, R. R., Dozois, E. J., Larson, D. W., Camilleri, M., Zinsmeister, A. R., Pozo, M. J., Hicks, G. A., Farrugia, G.
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container_end_page e46
container_issue 7
container_start_page 746
container_title Neurogastroenterology and motility
container_volume 21
creator Bernard, C. E.
Gibbons, S. J.
Gomez‐pinilla, P. J.
Lurken, M. S.
Schmalz, P. F.
Roeder, J. L.
Linden, D.
Cima, R. R.
Dozois, E. J.
Larson, D. W.
Camilleri, M.
Zinsmeister, A. R.
Pozo, M. J.
Hicks, G. A.
Farrugia, G.
description The effect of age on the anatomy and function of the human colon is incompletely understood. The prevalence of disorders in adults such as constipation increase with age but it is unclear if this is due to confounding factors or age‐related structural defects. The aim of this study was to determine number and subtypes of enteric neurons and neuronal volumes in the human colon of different ages. Normal colon (descending and sigmoid) from 16 patients (nine male) was studied; ages 33–99. Antibodies to HuC/D, choline acetyltransferase (ChAT), neuronal nitric oxide synthase (nNOS), and protein gene product 9.5 were used. Effect of age was determined by testing for linear trends using regression analysis. In the myenteric plexus, number of Hu‐positive neurons declined with age (slope = −1.3 neurons/mm/10 years, P = 0.03). The number of ChAT‐positive neurons also declined with age (slope = −1.1 neurons/mm/10 years of age, P = 0.02). The number of nNOS‐positive neurons did not decline with age. As a result, the ratio of nNOS to Hu increased (slope = 0.03 per 10 years of age, P = 0.01). In the submucosal plexus, the number of neurons did not decline with age (slope = −0.3 neurons/mm/10 years, P = 0.09). Volume of nerve fibres in the circular muscle and volume of neuronal structures in the myenteric plexus did not change with age. In conclusion, the number of neurons in the human colon declines with age with sparing of nNOS‐positive neurons. This change was not accompanied by changes in total volume of neuronal structures suggesting compensatory changes in the remaining neurons.
doi_str_mv 10.1111/j.1365-2982.2008.01245.x
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E. ; Gibbons, S. J. ; Gomez‐pinilla, P. J. ; Lurken, M. S. ; Schmalz, P. F. ; Roeder, J. L. ; Linden, D. ; Cima, R. R. ; Dozois, E. J. ; Larson, D. W. ; Camilleri, M. ; Zinsmeister, A. R. ; Pozo, M. J. ; Hicks, G. A. ; Farrugia, G.</creator><creatorcontrib>Bernard, C. E. ; Gibbons, S. J. ; Gomez‐pinilla, P. J. ; Lurken, M. S. ; Schmalz, P. F. ; Roeder, J. L. ; Linden, D. ; Cima, R. R. ; Dozois, E. J. ; Larson, D. W. ; Camilleri, M. ; Zinsmeister, A. R. ; Pozo, M. J. ; Hicks, G. A. ; Farrugia, G.</creatorcontrib><description>The effect of age on the anatomy and function of the human colon is incompletely understood. The prevalence of disorders in adults such as constipation increase with age but it is unclear if this is due to confounding factors or age‐related structural defects. The aim of this study was to determine number and subtypes of enteric neurons and neuronal volumes in the human colon of different ages. Normal colon (descending and sigmoid) from 16 patients (nine male) was studied; ages 33–99. Antibodies to HuC/D, choline acetyltransferase (ChAT), neuronal nitric oxide synthase (nNOS), and protein gene product 9.5 were used. Effect of age was determined by testing for linear trends using regression analysis. In the myenteric plexus, number of Hu‐positive neurons declined with age (slope = −1.3 neurons/mm/10 years, P = 0.03). The number of ChAT‐positive neurons also declined with age (slope = −1.1 neurons/mm/10 years of age, P = 0.02). The number of nNOS‐positive neurons did not decline with age. As a result, the ratio of nNOS to Hu increased (slope = 0.03 per 10 years of age, P = 0.01). In the submucosal plexus, the number of neurons did not decline with age (slope = −0.3 neurons/mm/10 years, P = 0.09). Volume of nerve fibres in the circular muscle and volume of neuronal structures in the myenteric plexus did not change with age. In conclusion, the number of neurons in the human colon declines with age with sparing of nNOS‐positive neurons. 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E.</creatorcontrib><creatorcontrib>Gibbons, S. J.</creatorcontrib><creatorcontrib>Gomez‐pinilla, P. J.</creatorcontrib><creatorcontrib>Lurken, M. S.</creatorcontrib><creatorcontrib>Schmalz, P. F.</creatorcontrib><creatorcontrib>Roeder, J. L.</creatorcontrib><creatorcontrib>Linden, D.</creatorcontrib><creatorcontrib>Cima, R. R.</creatorcontrib><creatorcontrib>Dozois, E. J.</creatorcontrib><creatorcontrib>Larson, D. W.</creatorcontrib><creatorcontrib>Camilleri, M.</creatorcontrib><creatorcontrib>Zinsmeister, A. R.</creatorcontrib><creatorcontrib>Pozo, M. J.</creatorcontrib><creatorcontrib>Hicks, G. A.</creatorcontrib><creatorcontrib>Farrugia, G.</creatorcontrib><title>Effect of age on the enteric nervous system of the human colon</title><title>Neurogastroenterology and motility</title><addtitle>Neurogastroenterol Motil</addtitle><description>The effect of age on the anatomy and function of the human colon is incompletely understood. The prevalence of disorders in adults such as constipation increase with age but it is unclear if this is due to confounding factors or age‐related structural defects. The aim of this study was to determine number and subtypes of enteric neurons and neuronal volumes in the human colon of different ages. Normal colon (descending and sigmoid) from 16 patients (nine male) was studied; ages 33–99. Antibodies to HuC/D, choline acetyltransferase (ChAT), neuronal nitric oxide synthase (nNOS), and protein gene product 9.5 were used. Effect of age was determined by testing for linear trends using regression analysis. In the myenteric plexus, number of Hu‐positive neurons declined with age (slope = −1.3 neurons/mm/10 years, P = 0.03). The number of ChAT‐positive neurons also declined with age (slope = −1.1 neurons/mm/10 years of age, P = 0.02). The number of nNOS‐positive neurons did not decline with age. 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This change was not accompanied by changes in total volume of neuronal structures suggesting compensatory changes in the remaining neurons.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Aging - metabolism</subject><subject>Aging - pathology</subject><subject>Cell Count</subject><subject>Choline O-Acetyltransferase - metabolism</subject><subject>Colon - cytology</subject><subject>Colon - innervation</subject><subject>Colon - metabolism</subject><subject>colonic transit</subject><subject>ELAV Proteins</subject><subject>Enteric Nervous System - cytology</subject><subject>Enteric Nervous System - metabolism</subject><subject>enteric neurons</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>myenteric plexus</subject><subject>Neurons - cytology</subject><subject>Neurons - metabolism</subject><subject>protein gene product 9.5</subject><issn>1350-1925</issn><issn>1365-2982</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1P3DAQhi1EBRT4C5VPvSX1R-yJD0VCiI9KtHuBs-U4EzarJKZxFth_j9NdbdtT64tHft95NeOHEMpZztP5ssq51CoTphS5YKzMGReFyt8OyMleOJxrxTJuhDomH2NcMca0KPQROU5vgoFSJ-TiumnQTzQ01D0hDQOdlkhxmHBsPR1wfAnrSOMmTtjPplldrns3UB-6MJyRD43rIp7v7lPyeHP9cHWX3S9uv11d3mdeaaMyowtW1lKjKwVUlahBSmFkBcDBVFCUdWUcQq2wAm2grLg0XgrJDfqCNVKekott7vO66rH2acDRdfZ5bHs3bmxwrf1bGdqlfQovVgBoYCIFfN4FjOHnGuNk-zZ67Do3YNrQaiikBFD_NAqWPq8oIBnLrdGPIcYRm_00nNmZkl3ZGYadYdiZkv1Fyb6l1k9_bvO7cYclGb5uDa9th5v_DrY_vi_mSr4D_CGf8g</recordid><startdate>200907</startdate><enddate>200907</enddate><creator>Bernard, C. 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A.</au><au>Farrugia, G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of age on the enteric nervous system of the human colon</atitle><jtitle>Neurogastroenterology and motility</jtitle><addtitle>Neurogastroenterol Motil</addtitle><date>2009-07</date><risdate>2009</risdate><volume>21</volume><issue>7</issue><spage>746</spage><epage>e46</epage><pages>746-e46</pages><issn>1350-1925</issn><eissn>1365-2982</eissn><abstract>The effect of age on the anatomy and function of the human colon is incompletely understood. The prevalence of disorders in adults such as constipation increase with age but it is unclear if this is due to confounding factors or age‐related structural defects. The aim of this study was to determine number and subtypes of enteric neurons and neuronal volumes in the human colon of different ages. Normal colon (descending and sigmoid) from 16 patients (nine male) was studied; ages 33–99. Antibodies to HuC/D, choline acetyltransferase (ChAT), neuronal nitric oxide synthase (nNOS), and protein gene product 9.5 were used. Effect of age was determined by testing for linear trends using regression analysis. In the myenteric plexus, number of Hu‐positive neurons declined with age (slope = −1.3 neurons/mm/10 years, P = 0.03). The number of ChAT‐positive neurons also declined with age (slope = −1.1 neurons/mm/10 years of age, P = 0.02). The number of nNOS‐positive neurons did not decline with age. As a result, the ratio of nNOS to Hu increased (slope = 0.03 per 10 years of age, P = 0.01). In the submucosal plexus, the number of neurons did not decline with age (slope = −0.3 neurons/mm/10 years, P = 0.09). Volume of nerve fibres in the circular muscle and volume of neuronal structures in the myenteric plexus did not change with age. In conclusion, the number of neurons in the human colon declines with age with sparing of nNOS‐positive neurons. This change was not accompanied by changes in total volume of neuronal structures suggesting compensatory changes in the remaining neurons.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>19220755</pmid><doi>10.1111/j.1365-2982.2008.01245.x</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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ispartof Neurogastroenterology and motility, 2009-07, Vol.21 (7), p.746-e46
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subjects Adult
Aged
Aged, 80 and over
Aging - metabolism
Aging - pathology
Cell Count
Choline O-Acetyltransferase - metabolism
Colon - cytology
Colon - innervation
Colon - metabolism
colonic transit
ELAV Proteins
Enteric Nervous System - cytology
Enteric Nervous System - metabolism
enteric neurons
Female
Humans
Male
Middle Aged
myenteric plexus
Neurons - cytology
Neurons - metabolism
protein gene product 9.5
title Effect of age on the enteric nervous system of the human colon
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