Convergent cholinergic activities in aging and Alzheimer's disease
Choline acetyltransferase (ChAT) and acetylcholinesterase (AChE) activities have been examined postmortem in a series of 66 individuals with no evidence of CNS disease, ranging in age from 24 gestational weeks to 95 years and in 33 cases of Alzheimer's disease (AD) aged 57–89 years. In the norm...
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Veröffentlicht in: | Neurobiology of aging 1992-05, Vol.13 (3), p.393-400 |
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creator | Perry, E.K. Johnson, M. Kerwin, J.M. Piggott, M.A. Court, J.A. Shaw, P.J. Ince, P.G. Brown, A. Perry, R.H. |
description | Choline acetyltransferase (ChAT) and acetylcholinesterase (AChE) activities have been examined postmortem in a series of 66 individuals with no evidence of CNS disease, ranging in age from 24 gestational weeks to 95 years and in 33 cases of Alzheimer's disease (AD) aged 57–89 years. In the normal human hippocampus a striking and highly significant age-related decline in ChAT occurred from middle to old age (between 40 and 100 years); a trend apparent at a later stage and to a lesser extent in the hippocampal gyrus. In both areas enzyme activity in AD was inversely related to age at death; reductions compared with the normal were on average 70–80% in the 60–70 year old groups compared with 30–40% in the 80–90 year old group. A similar trend was apparent with respect to acetylcholinesterase (AchE) histochemical activity associated with fibers and terminals (predominantly cholinergic and concentrated in CA3 and 4 of the hippocampus) but not with reactive perikarya (considered to be noncholinergic) present in both hippocampus and cortex. These data indicate that the normal aging human hippocampus may constitute a useful model for investigating the dysfunction or degeneration of basal forebrain cholinergic neurons in AD. |
doi_str_mv | 10.1016/0197-4580(92)90113-C |
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In the normal human hippocampus a striking and highly significant age-related decline in ChAT occurred from middle to old age (between 40 and 100 years); a trend apparent at a later stage and to a lesser extent in the hippocampal gyrus. In both areas enzyme activity in AD was inversely related to age at death; reductions compared with the normal were on average 70–80% in the 60–70 year old groups compared with 30–40% in the 80–90 year old group. A similar trend was apparent with respect to acetylcholinesterase (AchE) histochemical activity associated with fibers and terminals (predominantly cholinergic and concentrated in CA3 and 4 of the hippocampus) but not with reactive perikarya (considered to be noncholinergic) present in both hippocampus and cortex. These data indicate that the normal aging human hippocampus may constitute a useful model for investigating the dysfunction or degeneration of basal forebrain cholinergic neurons in AD.</description><identifier>ISSN: 0197-4580</identifier><identifier>EISSN: 1558-1497</identifier><identifier>DOI: 10.1016/0197-4580(92)90113-C</identifier><identifier>PMID: 1625768</identifier><identifier>CODEN: NEAGDO</identifier><language>eng</language><publisher>London: Elsevier Inc</publisher><subject>Acetylcholinesterase - analysis ; Acetylcholinesterase histochemistry ; Adolescent ; Adult ; Aged ; Aged, 80 and over ; Aging ; Aging - metabolism ; Alzheimer Disease - metabolism ; Alzheimer's disease ; Biological and medical sciences ; Child ; Child, Preschool ; Choline acetyltransferase ; Choline O-Acetyltransferase - analysis ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Entorhinal cortex ; Hippocampus ; Hippocampus - chemistry ; Humans ; Infant ; Infant, Newborn ; Medical sciences ; Middle Aged ; Neurology ; Senile plaques ; Silver Staining</subject><ispartof>Neurobiology of aging, 1992-05, Vol.13 (3), p.393-400</ispartof><rights>1992</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c468t-cc91ee204ec67044a5f8a8a6045e6016288dec8387cef180816ced5e7701277e3</citedby><cites>FETCH-LOGICAL-c468t-cc91ee204ec67044a5f8a8a6045e6016288dec8387cef180816ced5e7701277e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/019745809290113C$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5339870$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1625768$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Perry, E.K.</creatorcontrib><creatorcontrib>Johnson, M.</creatorcontrib><creatorcontrib>Kerwin, J.M.</creatorcontrib><creatorcontrib>Piggott, M.A.</creatorcontrib><creatorcontrib>Court, J.A.</creatorcontrib><creatorcontrib>Shaw, P.J.</creatorcontrib><creatorcontrib>Ince, P.G.</creatorcontrib><creatorcontrib>Brown, A.</creatorcontrib><creatorcontrib>Perry, R.H.</creatorcontrib><title>Convergent cholinergic activities in aging and Alzheimer's disease</title><title>Neurobiology of aging</title><addtitle>Neurobiol Aging</addtitle><description>Choline acetyltransferase (ChAT) and acetylcholinesterase (AChE) activities have been examined postmortem in a series of 66 individuals with no evidence of CNS disease, ranging in age from 24 gestational weeks to 95 years and in 33 cases of Alzheimer's disease (AD) aged 57–89 years. In the normal human hippocampus a striking and highly significant age-related decline in ChAT occurred from middle to old age (between 40 and 100 years); a trend apparent at a later stage and to a lesser extent in the hippocampal gyrus. In both areas enzyme activity in AD was inversely related to age at death; reductions compared with the normal were on average 70–80% in the 60–70 year old groups compared with 30–40% in the 80–90 year old group. A similar trend was apparent with respect to acetylcholinesterase (AchE) histochemical activity associated with fibers and terminals (predominantly cholinergic and concentrated in CA3 and 4 of the hippocampus) but not with reactive perikarya (considered to be noncholinergic) present in both hippocampus and cortex. These data indicate that the normal aging human hippocampus may constitute a useful model for investigating the dysfunction or degeneration of basal forebrain cholinergic neurons in AD.</description><subject>Acetylcholinesterase - analysis</subject><subject>Acetylcholinesterase histochemistry</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Aging</subject><subject>Aging - metabolism</subject><subject>Alzheimer Disease - metabolism</subject><subject>Alzheimer's disease</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Choline acetyltransferase</subject><subject>Choline O-Acetyltransferase - analysis</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Entorhinal cortex</subject><subject>Hippocampus</subject><subject>Hippocampus - chemistry</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Senile plaques</subject><subject>Silver Staining</subject><issn>0197-4580</issn><issn>1558-1497</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1LxDAQhoMouq7-A4UexI9DddLmqxdhLX6B4EXPIabTNdJN16S7oL_erl30pqdhmGeGeR9CDiicU6DiAmghU8YVnBbZWQGU5mm5QUaUc5VSVshNMvpBdshujG8AIJkU22SbioxLoUbkqmz9EsMUfZfY17Zxvm-cTYzt3NJ1DmPifGKmzk8T46tk0ny-opthOIlJ5SKaiHtkqzZNxP11HZPnm-un8i59eLy9LycPqWVCdam1BUXMgKEVEhgzvFZGGQGMo-jzZEpVaFWupMWaKlBUWKw4Sgk0kxLzMTke7s5D-77A2OmZixabxnhsF1HLHJgExf8FqRDACyF7kA2gDW2MAWs9D25mwoemoFeO9UqgXgnURaa_HeuyXztc31-8zLD6XRqk9vOj9dxEa5o6GG9d_MF4nhdKQo9dDhj20pYOg47Woe9Du4C201Xr_v7jC-Uclr0</recordid><startdate>19920501</startdate><enddate>19920501</enddate><creator>Perry, E.K.</creator><creator>Johnson, M.</creator><creator>Kerwin, J.M.</creator><creator>Piggott, M.A.</creator><creator>Court, J.A.</creator><creator>Shaw, P.J.</creator><creator>Ince, P.G.</creator><creator>Brown, A.</creator><creator>Perry, R.H.</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><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></search><sort><creationdate>19920501</creationdate><title>Convergent cholinergic activities in aging and Alzheimer's disease</title><author>Perry, E.K. ; Johnson, M. ; Kerwin, J.M. ; Piggott, M.A. ; Court, J.A. ; Shaw, P.J. ; Ince, P.G. ; Brown, A. ; Perry, R.H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c468t-cc91ee204ec67044a5f8a8a6045e6016288dec8387cef180816ced5e7701277e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Acetylcholinesterase - analysis</topic><topic>Acetylcholinesterase histochemistry</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Aging</topic><topic>Aging - metabolism</topic><topic>Alzheimer Disease - metabolism</topic><topic>Alzheimer's disease</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Choline acetyltransferase</topic><topic>Choline O-Acetyltransferase - analysis</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Entorhinal cortex</topic><topic>Hippocampus</topic><topic>Hippocampus - chemistry</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neurology</topic><topic>Senile plaques</topic><topic>Silver Staining</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Perry, E.K.</creatorcontrib><creatorcontrib>Johnson, M.</creatorcontrib><creatorcontrib>Kerwin, J.M.</creatorcontrib><creatorcontrib>Piggott, M.A.</creatorcontrib><creatorcontrib>Court, J.A.</creatorcontrib><creatorcontrib>Shaw, P.J.</creatorcontrib><creatorcontrib>Ince, P.G.</creatorcontrib><creatorcontrib>Brown, A.</creatorcontrib><creatorcontrib>Perry, R.H.</creatorcontrib><collection>Pascal-Francis</collection><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><jtitle>Neurobiology of aging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Perry, E.K.</au><au>Johnson, M.</au><au>Kerwin, J.M.</au><au>Piggott, M.A.</au><au>Court, J.A.</au><au>Shaw, P.J.</au><au>Ince, P.G.</au><au>Brown, A.</au><au>Perry, R.H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Convergent cholinergic activities in aging and Alzheimer's disease</atitle><jtitle>Neurobiology of aging</jtitle><addtitle>Neurobiol Aging</addtitle><date>1992-05-01</date><risdate>1992</risdate><volume>13</volume><issue>3</issue><spage>393</spage><epage>400</epage><pages>393-400</pages><issn>0197-4580</issn><eissn>1558-1497</eissn><coden>NEAGDO</coden><abstract>Choline acetyltransferase (ChAT) and acetylcholinesterase (AChE) activities have been examined postmortem in a series of 66 individuals with no evidence of CNS disease, ranging in age from 24 gestational weeks to 95 years and in 33 cases of Alzheimer's disease (AD) aged 57–89 years. In the normal human hippocampus a striking and highly significant age-related decline in ChAT occurred from middle to old age (between 40 and 100 years); a trend apparent at a later stage and to a lesser extent in the hippocampal gyrus. In both areas enzyme activity in AD was inversely related to age at death; reductions compared with the normal were on average 70–80% in the 60–70 year old groups compared with 30–40% in the 80–90 year old group. A similar trend was apparent with respect to acetylcholinesterase (AchE) histochemical activity associated with fibers and terminals (predominantly cholinergic and concentrated in CA3 and 4 of the hippocampus) but not with reactive perikarya (considered to be noncholinergic) present in both hippocampus and cortex. These data indicate that the normal aging human hippocampus may constitute a useful model for investigating the dysfunction or degeneration of basal forebrain cholinergic neurons in AD.</abstract><cop>London</cop><pub>Elsevier Inc</pub><pmid>1625768</pmid><doi>10.1016/0197-4580(92)90113-C</doi><tpages>8</tpages></addata></record> |
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subjects | Acetylcholinesterase - analysis Acetylcholinesterase histochemistry Adolescent Adult Aged Aged, 80 and over Aging Aging - metabolism Alzheimer Disease - metabolism Alzheimer's disease Biological and medical sciences Child Child, Preschool Choline acetyltransferase Choline O-Acetyltransferase - analysis Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Entorhinal cortex Hippocampus Hippocampus - chemistry Humans Infant Infant, Newborn Medical sciences Middle Aged Neurology Senile plaques Silver Staining |
title | Convergent cholinergic activities in aging and Alzheimer's disease |
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