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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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. This change was not accompanied by changes in total volume of neuronal structures suggesting compensatory changes in the remaining neurons.</description><identifier>ISSN: 1350-1925</identifier><identifier>EISSN: 1365-2982</identifier><identifier>DOI: 10.1111/j.1365-2982.2008.01245.x</identifier><identifier>PMID: 19220755</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>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</subject><ispartof>Neurogastroenterology and motility, 2009-07, Vol.21 (7), p.746-e46</ispartof><rights>2009 The Mayo Foundation. Journal compilation © 2009 Blackwell Publishing Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5695-96408d36ea827bb2d733293b77179b748db9ae7d5eb76978b139c32319ec40f33</citedby><cites>FETCH-LOGICAL-c5695-96408d36ea827bb2d733293b77179b748db9ae7d5eb76978b139c32319ec40f33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2982.2008.01245.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2982.2008.01245.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,315,782,786,887,1419,1435,27931,27932,45581,45582,46416,46840</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19220755$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bernard, C. 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. 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.</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. E.</creator><creator>Gibbons, S. J.</creator><creator>Gomez‐pinilla, P. J.</creator><creator>Lurken, M. S.</creator><creator>Schmalz, P. F.</creator><creator>Roeder, J. L.</creator><creator>Linden, D.</creator><creator>Cima, R. R.</creator><creator>Dozois, E. J.</creator><creator>Larson, D. W.</creator><creator>Camilleri, M.</creator><creator>Zinsmeister, A. R.</creator><creator>Pozo, M. J.</creator><creator>Hicks, G. A.</creator><creator>Farrugia, G.</creator><general>Blackwell Publishing Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>200907</creationdate><title>Effect of age on the enteric nervous system of the human colon</title><author>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. 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A.</creatorcontrib><creatorcontrib>Farrugia, G.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Neurogastroenterology and motility</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bernard, C. E.</au><au>Gibbons, S. J.</au><au>Gomez‐pinilla, P. J.</au><au>Lurken, M. S.</au><au>Schmalz, P. F.</au><au>Roeder, J. L.</au><au>Linden, D.</au><au>Cima, R. R.</au><au>Dozois, E. J.</au><au>Larson, D. W.</au><au>Camilleri, M.</au><au>Zinsmeister, A. R.</au><au>Pozo, M. J.</au><au>Hicks, G. 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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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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