New approaches and challenges to targeting the endocannabinoid system
Dysregulation of the endocannabinoid system has been implicated in numerous diseases, particularly pain, psychiatric and neurological disorders, but therapeutic intervention in this complex system has proved challenging. In this Perspective article, Di Marzo discusses the lessons learned from the de...
Gespeichert in:
Veröffentlicht in: | Nature reviews. Drug discovery 2018-09, Vol.17 (9), p.623-639 |
---|---|
1. Verfasser: | |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 639 |
---|---|
container_issue | 9 |
container_start_page | 623 |
container_title | Nature reviews. Drug discovery |
container_volume | 17 |
creator | Di Marzo, Vincenzo |
description | Dysregulation of the endocannabinoid system has been implicated in numerous diseases, particularly pain, psychiatric and neurological disorders, but therapeutic intervention in this complex system has proved challenging. In this Perspective article, Di Marzo discusses the lessons learned from the development of drugs that alter endocannabinoid signalling and highlights novel opportunities for pharmacologically manipulating the endocannabinoid system, such as the use of multi-target drugs.
The endocannabinoid signalling system was discovered because receptors in this system are the targets of compounds present in psychotropic preparations of
Cannabis sativa
. The search for new therapeutics that target endocannabinoid signalling is both challenging and potentially rewarding, as endocannabinoids are implicated in numerous physiological and pathological processes. Hundreds of mediators chemically related to the endocannabinoids, often with similar metabolic pathways but different targets, have complicated the development of inhibitors of endocannabinoid metabolic enzymes but have also stimulated the rational design of multi-target drugs. Meanwhile, drugs based on botanical cannabinoids have come to the clinical forefront, synthetic agonists designed to bind cannabinoid receptor 1 with very high affinity have become a societal threat and the gut microbiome has been found to signal in part through the endocannabinoid network. The current development of drugs that alter endocannabinoid signalling and how this complex system could be pharmacologically manipulated in the future are described in this Opinion article. |
doi_str_mv | 10.1038/nrd.2018.115 |
format | Article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_2089851583</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A572646245</galeid><sourcerecordid>A572646245</sourcerecordid><originalsourceid>FETCH-LOGICAL-c490t-a80495705204dab306d7fcf6cd33a74a85dd543b0bad68334a7ccd1abdc8af793</originalsourceid><addsrcrecordid>eNptkclLxDAYxYMoLqM3z1Lw4sGOSbP2KIMbiF70HL4m6UylTcakg_jfm2FcUCSHbL_38sJD6JjgKcFUXfhopxUmakoI30L7hElWEqnY9vdaij10kNILxkQQWe2iPYoJEZjV--jqwb0VsFzGAGbhUgHeFmYBfe_8PG_HUIwQ527s_LwYF65w3gYD3kPT-dDZIr2n0Q2HaKeFPrmjz3mCnq-vnma35f3jzd3s8r40rMZjCSq_ySXmFWYWGoqFla1phbGUgmSguLWc0QY3YIWilIE0xhJorFHQyppO0NnGN-d9Xbk06qFLxvU9eBdWSVdY1YoTnrUTdPoHfQmr6HM6XZFK1IxLwn6oOfROd74NYwSzNtWXXFaCiYrxTE3_ofKwbuhM8K7t8vkvwflGYGJIKbpWL2M3QHzXBOt1azq3ptet6dxaxk8-s66awdlv-KumDJQbIOWrXEz8-cy_hh-FTZ-T</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2126945714</pqid></control><display><type>article</type><title>New approaches and challenges to targeting the endocannabinoid system</title><source>Springer Nature - Complete Springer Journals</source><source>Nature</source><creator>Di Marzo, Vincenzo</creator><creatorcontrib>Di Marzo, Vincenzo</creatorcontrib><description>Dysregulation of the endocannabinoid system has been implicated in numerous diseases, particularly pain, psychiatric and neurological disorders, but therapeutic intervention in this complex system has proved challenging. In this Perspective article, Di Marzo discusses the lessons learned from the development of drugs that alter endocannabinoid signalling and highlights novel opportunities for pharmacologically manipulating the endocannabinoid system, such as the use of multi-target drugs.
The endocannabinoid signalling system was discovered because receptors in this system are the targets of compounds present in psychotropic preparations of
Cannabis sativa
. The search for new therapeutics that target endocannabinoid signalling is both challenging and potentially rewarding, as endocannabinoids are implicated in numerous physiological and pathological processes. Hundreds of mediators chemically related to the endocannabinoids, often with similar metabolic pathways but different targets, have complicated the development of inhibitors of endocannabinoid metabolic enzymes but have also stimulated the rational design of multi-target drugs. Meanwhile, drugs based on botanical cannabinoids have come to the clinical forefront, synthetic agonists designed to bind cannabinoid receptor 1 with very high affinity have become a societal threat and the gut microbiome has been found to signal in part through the endocannabinoid network. The current development of drugs that alter endocannabinoid signalling and how this complex system could be pharmacologically manipulated in the future are described in this Opinion article.</description><identifier>ISSN: 1474-1776</identifier><identifier>EISSN: 1474-1784</identifier><identifier>DOI: 10.1038/nrd.2018.115</identifier><identifier>PMID: 30116049</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/154 ; 631/154/436 ; 692/699/375 ; 692/699/476 ; Biomedicine ; Biotechnology ; Cancer Research ; Cannabinoids ; Cellular signal transduction ; Enzymes ; Hallucinogenic drugs ; Health aspects ; Innovations ; Marijuana ; Medicinal Chemistry ; Metabolism ; Molecular Medicine ; Molecular targeted therapy ; opinion-2 ; Pharmaceutical research ; Pharmacology/Toxicology ; Phenols (Class of compounds) ; Psychotropic drugs ; Therapeutics ; Type 2 diabetes</subject><ispartof>Nature reviews. Drug discovery, 2018-09, Vol.17 (9), p.623-639</ispartof><rights>Springer Nature Limited 2018</rights><rights>COPYRIGHT 2018 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Sep 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c490t-a80495705204dab306d7fcf6cd33a74a85dd543b0bad68334a7ccd1abdc8af793</citedby><cites>FETCH-LOGICAL-c490t-a80495705204dab306d7fcf6cd33a74a85dd543b0bad68334a7ccd1abdc8af793</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/nrd.2018.115$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/nrd.2018.115$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30116049$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Di Marzo, Vincenzo</creatorcontrib><title>New approaches and challenges to targeting the endocannabinoid system</title><title>Nature reviews. Drug discovery</title><addtitle>Nat Rev Drug Discov</addtitle><addtitle>Nat Rev Drug Discov</addtitle><description>Dysregulation of the endocannabinoid system has been implicated in numerous diseases, particularly pain, psychiatric and neurological disorders, but therapeutic intervention in this complex system has proved challenging. In this Perspective article, Di Marzo discusses the lessons learned from the development of drugs that alter endocannabinoid signalling and highlights novel opportunities for pharmacologically manipulating the endocannabinoid system, such as the use of multi-target drugs.
The endocannabinoid signalling system was discovered because receptors in this system are the targets of compounds present in psychotropic preparations of
Cannabis sativa
. The search for new therapeutics that target endocannabinoid signalling is both challenging and potentially rewarding, as endocannabinoids are implicated in numerous physiological and pathological processes. Hundreds of mediators chemically related to the endocannabinoids, often with similar metabolic pathways but different targets, have complicated the development of inhibitors of endocannabinoid metabolic enzymes but have also stimulated the rational design of multi-target drugs. Meanwhile, drugs based on botanical cannabinoids have come to the clinical forefront, synthetic agonists designed to bind cannabinoid receptor 1 with very high affinity have become a societal threat and the gut microbiome has been found to signal in part through the endocannabinoid network. The current development of drugs that alter endocannabinoid signalling and how this complex system could be pharmacologically manipulated in the future are described in this Opinion article.</description><subject>631/154</subject><subject>631/154/436</subject><subject>692/699/375</subject><subject>692/699/476</subject><subject>Biomedicine</subject><subject>Biotechnology</subject><subject>Cancer Research</subject><subject>Cannabinoids</subject><subject>Cellular signal transduction</subject><subject>Enzymes</subject><subject>Hallucinogenic drugs</subject><subject>Health aspects</subject><subject>Innovations</subject><subject>Marijuana</subject><subject>Medicinal Chemistry</subject><subject>Metabolism</subject><subject>Molecular Medicine</subject><subject>Molecular targeted therapy</subject><subject>opinion-2</subject><subject>Pharmaceutical research</subject><subject>Pharmacology/Toxicology</subject><subject>Phenols (Class of compounds)</subject><subject>Psychotropic drugs</subject><subject>Therapeutics</subject><subject>Type 2 diabetes</subject><issn>1474-1776</issn><issn>1474-1784</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNptkclLxDAYxYMoLqM3z1Lw4sGOSbP2KIMbiF70HL4m6UylTcakg_jfm2FcUCSHbL_38sJD6JjgKcFUXfhopxUmakoI30L7hElWEqnY9vdaij10kNILxkQQWe2iPYoJEZjV--jqwb0VsFzGAGbhUgHeFmYBfe_8PG_HUIwQ527s_LwYF65w3gYD3kPT-dDZIr2n0Q2HaKeFPrmjz3mCnq-vnma35f3jzd3s8r40rMZjCSq_ySXmFWYWGoqFla1phbGUgmSguLWc0QY3YIWilIE0xhJorFHQyppO0NnGN-d9Xbk06qFLxvU9eBdWSVdY1YoTnrUTdPoHfQmr6HM6XZFK1IxLwn6oOfROd74NYwSzNtWXXFaCiYrxTE3_ofKwbuhM8K7t8vkvwflGYGJIKbpWL2M3QHzXBOt1azq3ptet6dxaxk8-s66awdlv-KumDJQbIOWrXEz8-cy_hh-FTZ-T</recordid><startdate>20180901</startdate><enddate>20180901</enddate><creator>Di Marzo, Vincenzo</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><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>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20180901</creationdate><title>New approaches and challenges to targeting the endocannabinoid system</title><author>Di Marzo, Vincenzo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c490t-a80495705204dab306d7fcf6cd33a74a85dd543b0bad68334a7ccd1abdc8af793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>631/154</topic><topic>631/154/436</topic><topic>692/699/375</topic><topic>692/699/476</topic><topic>Biomedicine</topic><topic>Biotechnology</topic><topic>Cancer Research</topic><topic>Cannabinoids</topic><topic>Cellular signal transduction</topic><topic>Enzymes</topic><topic>Hallucinogenic drugs</topic><topic>Health aspects</topic><topic>Innovations</topic><topic>Marijuana</topic><topic>Medicinal Chemistry</topic><topic>Metabolism</topic><topic>Molecular Medicine</topic><topic>Molecular targeted therapy</topic><topic>opinion-2</topic><topic>Pharmaceutical research</topic><topic>Pharmacology/Toxicology</topic><topic>Phenols (Class of compounds)</topic><topic>Psychotropic drugs</topic><topic>Therapeutics</topic><topic>Type 2 diabetes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Di Marzo, Vincenzo</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</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</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & 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>MEDLINE - Academic</collection><jtitle>Nature reviews. Drug discovery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Di Marzo, Vincenzo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New approaches and challenges to targeting the endocannabinoid system</atitle><jtitle>Nature reviews. Drug discovery</jtitle><stitle>Nat Rev Drug Discov</stitle><addtitle>Nat Rev Drug Discov</addtitle><date>2018-09-01</date><risdate>2018</risdate><volume>17</volume><issue>9</issue><spage>623</spage><epage>639</epage><pages>623-639</pages><issn>1474-1776</issn><eissn>1474-1784</eissn><abstract>Dysregulation of the endocannabinoid system has been implicated in numerous diseases, particularly pain, psychiatric and neurological disorders, but therapeutic intervention in this complex system has proved challenging. In this Perspective article, Di Marzo discusses the lessons learned from the development of drugs that alter endocannabinoid signalling and highlights novel opportunities for pharmacologically manipulating the endocannabinoid system, such as the use of multi-target drugs.
The endocannabinoid signalling system was discovered because receptors in this system are the targets of compounds present in psychotropic preparations of
Cannabis sativa
. The search for new therapeutics that target endocannabinoid signalling is both challenging and potentially rewarding, as endocannabinoids are implicated in numerous physiological and pathological processes. Hundreds of mediators chemically related to the endocannabinoids, often with similar metabolic pathways but different targets, have complicated the development of inhibitors of endocannabinoid metabolic enzymes but have also stimulated the rational design of multi-target drugs. Meanwhile, drugs based on botanical cannabinoids have come to the clinical forefront, synthetic agonists designed to bind cannabinoid receptor 1 with very high affinity have become a societal threat and the gut microbiome has been found to signal in part through the endocannabinoid network. The current development of drugs that alter endocannabinoid signalling and how this complex system could be pharmacologically manipulated in the future are described in this Opinion article.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>30116049</pmid><doi>10.1038/nrd.2018.115</doi><tpages>17</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1474-1776 |
ispartof | Nature reviews. Drug discovery, 2018-09, Vol.17 (9), p.623-639 |
issn | 1474-1776 1474-1784 |
language | eng |
recordid | cdi_proquest_miscellaneous_2089851583 |
source | Springer Nature - Complete Springer Journals; Nature |
subjects | 631/154 631/154/436 692/699/375 692/699/476 Biomedicine Biotechnology Cancer Research Cannabinoids Cellular signal transduction Enzymes Hallucinogenic drugs Health aspects Innovations Marijuana Medicinal Chemistry Metabolism Molecular Medicine Molecular targeted therapy opinion-2 Pharmaceutical research Pharmacology/Toxicology Phenols (Class of compounds) Psychotropic drugs Therapeutics Type 2 diabetes |
title | New approaches and challenges to targeting the endocannabinoid system |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T22%3A25%3A36IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=New%20approaches%20and%20challenges%20to%20targeting%20the%20endocannabinoid%20system&rft.jtitle=Nature%20reviews.%20Drug%20discovery&rft.au=Di%20Marzo,%20Vincenzo&rft.date=2018-09-01&rft.volume=17&rft.issue=9&rft.spage=623&rft.epage=639&rft.pages=623-639&rft.issn=1474-1776&rft.eissn=1474-1784&rft_id=info:doi/10.1038/nrd.2018.115&rft_dat=%3Cgale_proqu%3EA572646245%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2126945714&rft_id=info:pmid/30116049&rft_galeid=A572646245&rfr_iscdi=true |