Loading…

The cholinergic hypothesis of Alzheimer’s disease: a review of progress

Alzheimer’s disease is one of the most common causes of mental deterioration in elderly people, accounting for around 50%-60% of the overall cases of dementia among persons over 65 years of age. The past two decades have witnessed a considerable research effort directed towards discovering the cause...

Full description

Saved in:
Bibliographic Details
Published in:Journal of neurology, neurosurgery and psychiatry neurosurgery and psychiatry, 1999-02, Vol.66 (2), p.137-147
Main Authors: Francis, Paul T, Palmer, Alan M, Snape, Michael, Wilcock, Gordon K
Format: Article
Language:English
Subjects:
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-b621t-f8071d92d5d7e3f67290cf7c874f113c30b87dc46b468f90671a019bbf092b983
cites
container_end_page 147
container_issue 2
container_start_page 137
container_title Journal of neurology, neurosurgery and psychiatry
container_volume 66
creator Francis, Paul T
Palmer, Alan M
Snape, Michael
Wilcock, Gordon K
description Alzheimer’s disease is one of the most common causes of mental deterioration in elderly people, accounting for around 50%-60% of the overall cases of dementia among persons over 65 years of age. The past two decades have witnessed a considerable research effort directed towards discovering the cause of Alzheimer’s disease with the ultimate hope of developing safe and effective pharmacological treatments. This article examines the existing scientific applicability of the original cholinergic hypothesis of Alzheimer’s disease by describing the biochemical and histopathological changes of neurotransmitter markers that occur in the brains of patients with Alzheimer’s disease both at postmortem and neurosurgical cerebral biopsy and the behavioural consequences of cholinomimetic drugs and cholinergic lesions. Such studies have resulted in the discovery of an association between a decline in learning and memory, and a deficit in excitatory amino acid (EAA) neurotransmission, together with important roles for the cholinergic system in attentional processing and as a modulator of EAA neurotransmission. Accordingly, although there is presently no “cure” for Alzheimer’s disease, a large number of potential therapeutic interventions have emerged that are designed to correct loss of presynaptic cholinergic function. A few of these compounds have confirmed efficacy in delaying the deterioration of symptoms of Alzheimer’s disease, a valuable treatment target considering the progressive nature of the disease. Indeed, three compounds have received European approval for the treatment of the cognitive symptoms of Alzheimer’s disease, first tacrine and more recently, donepezil and rivastigmine, all of which are cholinesterase inhibitors.
doi_str_mv 10.1136/jnnp.66.2.137
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1736202</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>4025624521</sourcerecordid><originalsourceid>FETCH-LOGICAL-b621t-f8071d92d5d7e3f67290cf7c874f113c30b87dc46b468f90671a019bbf092b983</originalsourceid><addsrcrecordid>eNqFkc1u1DAUhS0EokPpkm0VCYTYZPDPxI5ZIJUBSqsKumgrdpbjXE88JHGwM4Wy4jV4PZ6kHs2oP2y4m7u4n849RwehZwRPCWH89bLvhynnUzolTDxAEzLjZc4Y_voQTTCmNGe4wDvoSYxLvJ5SPkY7BGNBsCQTdHTWQGYa37oewsKZrLka_NhAdDHzNjtofzXgOgh_f_-JWe0i6AhvMp0FuHTwY40MwS8CxPgUPbK6jbC33bvo_OOHs_mn_OTL4dH84CSvOCVjbsv0upa0LmoBzHJBJTZWmFLMbApkGK5KUZsZr1IQKzEXRGMiq8piSStZsl30dqM7rKoOagP9GHSrhuA6Ha6U107dv_SuUQt_qYhgnGKaBF5uBYL_voI4qs5FA22re_CrqLjkyWLBE_j8H3DpV6FP4ZJWSYqCUEkSlW8oE3yMAeyNFYLVuiK1rkhxrqhKFSV-_67_O_SmkwS82AI6Gt3aoHvj4i3Hi5JSdvvXxRF-3px1-Ka4YKJQny_m6vj96Rwfv-NKJv7Vhq-65X8sXgN3lbad</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1781551291</pqid></control><display><type>article</type><title>The cholinergic hypothesis of Alzheimer’s disease: a review of progress</title><source>PubMed Central</source><creator>Francis, Paul T ; Palmer, Alan M ; Snape, Michael ; Wilcock, Gordon K</creator><creatorcontrib>Francis, Paul T ; Palmer, Alan M ; Snape, Michael ; Wilcock, Gordon K</creatorcontrib><description>Alzheimer’s disease is one of the most common causes of mental deterioration in elderly people, accounting for around 50%-60% of the overall cases of dementia among persons over 65 years of age. The past two decades have witnessed a considerable research effort directed towards discovering the cause of Alzheimer’s disease with the ultimate hope of developing safe and effective pharmacological treatments. This article examines the existing scientific applicability of the original cholinergic hypothesis of Alzheimer’s disease by describing the biochemical and histopathological changes of neurotransmitter markers that occur in the brains of patients with Alzheimer’s disease both at postmortem and neurosurgical cerebral biopsy and the behavioural consequences of cholinomimetic drugs and cholinergic lesions. Such studies have resulted in the discovery of an association between a decline in learning and memory, and a deficit in excitatory amino acid (EAA) neurotransmission, together with important roles for the cholinergic system in attentional processing and as a modulator of EAA neurotransmission. Accordingly, although there is presently no “cure” for Alzheimer’s disease, a large number of potential therapeutic interventions have emerged that are designed to correct loss of presynaptic cholinergic function. A few of these compounds have confirmed efficacy in delaying the deterioration of symptoms of Alzheimer’s disease, a valuable treatment target considering the progressive nature of the disease. Indeed, three compounds have received European approval for the treatment of the cognitive symptoms of Alzheimer’s disease, first tacrine and more recently, donepezil and rivastigmine, all of which are cholinesterase inhibitors.</description><identifier>ISSN: 0022-3050</identifier><identifier>EISSN: 1468-330X</identifier><identifier>DOI: 10.1136/jnnp.66.2.137</identifier><identifier>PMID: 10071091</identifier><identifier>CODEN: JNNPAU</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd</publisher><subject>Alzheimer Disease ; Alzheimer's disease ; Biological and medical sciences ; Cholinergic Fibers ; Cholinergic system ; Cholinesterase Inhibitors - therapeutic use ; Cognitive ability ; Dementia ; Humans ; Hypotheses ; Medical sciences ; Neuropharmacology ; Neurotransmitters. Neurotransmission. Receptors ; Older people ; Pathology ; Patients ; Pharmacology. Drug treatments ; Quality of life ; Review</subject><ispartof>Journal of neurology, neurosurgery and psychiatry, 1999-02, Vol.66 (2), p.137-147</ispartof><rights>Journal of Neurology, Neurosurgery, and Psychiatry</rights><rights>1999 INIST-CNRS</rights><rights>Copyright: 1999 Journal of Neurology, Neurosurgery, and Psychiatry</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b621t-f8071d92d5d7e3f67290cf7c874f113c30b87dc46b468f90671a019bbf092b983</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1736202/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1736202/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,313,314,727,780,784,792,885,27920,27922,27923,53789,53791</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1658223$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10071091$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Francis, Paul T</creatorcontrib><creatorcontrib>Palmer, Alan M</creatorcontrib><creatorcontrib>Snape, Michael</creatorcontrib><creatorcontrib>Wilcock, Gordon K</creatorcontrib><title>The cholinergic hypothesis of Alzheimer’s disease: a review of progress</title><title>Journal of neurology, neurosurgery and psychiatry</title><addtitle>J Neurol Neurosurg Psychiatry</addtitle><description>Alzheimer’s disease is one of the most common causes of mental deterioration in elderly people, accounting for around 50%-60% of the overall cases of dementia among persons over 65 years of age. The past two decades have witnessed a considerable research effort directed towards discovering the cause of Alzheimer’s disease with the ultimate hope of developing safe and effective pharmacological treatments. This article examines the existing scientific applicability of the original cholinergic hypothesis of Alzheimer’s disease by describing the biochemical and histopathological changes of neurotransmitter markers that occur in the brains of patients with Alzheimer’s disease both at postmortem and neurosurgical cerebral biopsy and the behavioural consequences of cholinomimetic drugs and cholinergic lesions. Such studies have resulted in the discovery of an association between a decline in learning and memory, and a deficit in excitatory amino acid (EAA) neurotransmission, together with important roles for the cholinergic system in attentional processing and as a modulator of EAA neurotransmission. Accordingly, although there is presently no “cure” for Alzheimer’s disease, a large number of potential therapeutic interventions have emerged that are designed to correct loss of presynaptic cholinergic function. A few of these compounds have confirmed efficacy in delaying the deterioration of symptoms of Alzheimer’s disease, a valuable treatment target considering the progressive nature of the disease. Indeed, three compounds have received European approval for the treatment of the cognitive symptoms of Alzheimer’s disease, first tacrine and more recently, donepezil and rivastigmine, all of which are cholinesterase inhibitors.</description><subject>Alzheimer Disease</subject><subject>Alzheimer's disease</subject><subject>Biological and medical sciences</subject><subject>Cholinergic Fibers</subject><subject>Cholinergic system</subject><subject>Cholinesterase Inhibitors - therapeutic use</subject><subject>Cognitive ability</subject><subject>Dementia</subject><subject>Humans</subject><subject>Hypotheses</subject><subject>Medical sciences</subject><subject>Neuropharmacology</subject><subject>Neurotransmitters. Neurotransmission. Receptors</subject><subject>Older people</subject><subject>Pathology</subject><subject>Patients</subject><subject>Pharmacology. Drug treatments</subject><subject>Quality of life</subject><subject>Review</subject><issn>0022-3050</issn><issn>1468-330X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqFkc1u1DAUhS0EokPpkm0VCYTYZPDPxI5ZIJUBSqsKumgrdpbjXE88JHGwM4Wy4jV4PZ6kHs2oP2y4m7u4n849RwehZwRPCWH89bLvhynnUzolTDxAEzLjZc4Y_voQTTCmNGe4wDvoSYxLvJ5SPkY7BGNBsCQTdHTWQGYa37oewsKZrLka_NhAdDHzNjtofzXgOgh_f_-JWe0i6AhvMp0FuHTwY40MwS8CxPgUPbK6jbC33bvo_OOHs_mn_OTL4dH84CSvOCVjbsv0upa0LmoBzHJBJTZWmFLMbApkGK5KUZsZr1IQKzEXRGMiq8piSStZsl30dqM7rKoOagP9GHSrhuA6Ha6U107dv_SuUQt_qYhgnGKaBF5uBYL_voI4qs5FA22re_CrqLjkyWLBE_j8H3DpV6FP4ZJWSYqCUEkSlW8oE3yMAeyNFYLVuiK1rkhxrqhKFSV-_67_O_SmkwS82AI6Gt3aoHvj4i3Hi5JSdvvXxRF-3px1-Ka4YKJQny_m6vj96Rwfv-NKJv7Vhq-65X8sXgN3lbad</recordid><startdate>19990201</startdate><enddate>19990201</enddate><creator>Francis, Paul T</creator><creator>Palmer, Alan M</creator><creator>Snape, Michael</creator><creator>Wilcock, Gordon K</creator><general>BMJ Publishing Group Ltd</general><general>BMJ</general><general>BMJ Publishing Group LTD</general><general>BMJ Group</general><scope>BSCLL</scope><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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19990201</creationdate><title>The cholinergic hypothesis of Alzheimer’s disease: a review of progress</title><author>Francis, Paul T ; Palmer, Alan M ; Snape, Michael ; Wilcock, Gordon K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b621t-f8071d92d5d7e3f67290cf7c874f113c30b87dc46b468f90671a019bbf092b983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Alzheimer Disease</topic><topic>Alzheimer's disease</topic><topic>Biological and medical sciences</topic><topic>Cholinergic Fibers</topic><topic>Cholinergic system</topic><topic>Cholinesterase Inhibitors - therapeutic use</topic><topic>Cognitive ability</topic><topic>Dementia</topic><topic>Humans</topic><topic>Hypotheses</topic><topic>Medical sciences</topic><topic>Neuropharmacology</topic><topic>Neurotransmitters. Neurotransmission. Receptors</topic><topic>Older people</topic><topic>Pathology</topic><topic>Patients</topic><topic>Pharmacology. Drug treatments</topic><topic>Quality of life</topic><topic>Review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Francis, Paul T</creatorcontrib><creatorcontrib>Palmer, Alan M</creatorcontrib><creatorcontrib>Snape, Michael</creatorcontrib><creatorcontrib>Wilcock, Gordon K</creatorcontrib><collection>Istex</collection><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>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing &amp; Allied Health Database</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Science Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of neurology, neurosurgery and psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Francis, Paul T</au><au>Palmer, Alan M</au><au>Snape, Michael</au><au>Wilcock, Gordon K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The cholinergic hypothesis of Alzheimer’s disease: a review of progress</atitle><jtitle>Journal of neurology, neurosurgery and psychiatry</jtitle><addtitle>J Neurol Neurosurg Psychiatry</addtitle><date>1999-02-01</date><risdate>1999</risdate><volume>66</volume><issue>2</issue><spage>137</spage><epage>147</epage><pages>137-147</pages><issn>0022-3050</issn><eissn>1468-330X</eissn><coden>JNNPAU</coden><abstract>Alzheimer’s disease is one of the most common causes of mental deterioration in elderly people, accounting for around 50%-60% of the overall cases of dementia among persons over 65 years of age. The past two decades have witnessed a considerable research effort directed towards discovering the cause of Alzheimer’s disease with the ultimate hope of developing safe and effective pharmacological treatments. This article examines the existing scientific applicability of the original cholinergic hypothesis of Alzheimer’s disease by describing the biochemical and histopathological changes of neurotransmitter markers that occur in the brains of patients with Alzheimer’s disease both at postmortem and neurosurgical cerebral biopsy and the behavioural consequences of cholinomimetic drugs and cholinergic lesions. Such studies have resulted in the discovery of an association between a decline in learning and memory, and a deficit in excitatory amino acid (EAA) neurotransmission, together with important roles for the cholinergic system in attentional processing and as a modulator of EAA neurotransmission. Accordingly, although there is presently no “cure” for Alzheimer’s disease, a large number of potential therapeutic interventions have emerged that are designed to correct loss of presynaptic cholinergic function. A few of these compounds have confirmed efficacy in delaying the deterioration of symptoms of Alzheimer’s disease, a valuable treatment target considering the progressive nature of the disease. Indeed, three compounds have received European approval for the treatment of the cognitive symptoms of Alzheimer’s disease, first tacrine and more recently, donepezil and rivastigmine, all of which are cholinesterase inhibitors.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd</pub><pmid>10071091</pmid><doi>10.1136/jnnp.66.2.137</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0022-3050
ispartof Journal of neurology, neurosurgery and psychiatry, 1999-02, Vol.66 (2), p.137-147
issn 0022-3050
1468-330X
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1736202
source PubMed Central
subjects Alzheimer Disease
Alzheimer's disease
Biological and medical sciences
Cholinergic Fibers
Cholinergic system
Cholinesterase Inhibitors - therapeutic use
Cognitive ability
Dementia
Humans
Hypotheses
Medical sciences
Neuropharmacology
Neurotransmitters. Neurotransmission. Receptors
Older people
Pathology
Patients
Pharmacology. Drug treatments
Quality of life
Review
title The cholinergic hypothesis of Alzheimer’s disease: a review of progress
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T17%3A46%3A10IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20cholinergic%20hypothesis%20of%20Alzheimer%E2%80%99s%20disease:%20a%20review%20of%20progress&rft.jtitle=Journal%20of%20neurology,%20neurosurgery%20and%20psychiatry&rft.au=Francis,%20Paul%20T&rft.date=1999-02-01&rft.volume=66&rft.issue=2&rft.spage=137&rft.epage=147&rft.pages=137-147&rft.issn=0022-3050&rft.eissn=1468-330X&rft.coden=JNNPAU&rft_id=info:doi/10.1136/jnnp.66.2.137&rft_dat=%3Cproquest_pubme%3E4025624521%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-b621t-f8071d92d5d7e3f67290cf7c874f113c30b87dc46b468f90671a019bbf092b983%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1781551291&rft_id=info:pmid/10071091&rfr_iscdi=true