Will peripherally restricted kappa-opioid receptor agonists (pKORAs) relieve pain with less opioid adverse effects and abuse potential?
Summary What is known and objective Optimal utilization of opioid analgesics is significantly limited by the central nervous system adverse effects and misuse/abuse potential of currently available drugs. It has been postulated that opioid‐associated adverse effects and abuse potential would be grea...
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Veröffentlicht in: | Journal of clinical pharmacy and therapeutics 2016-08, Vol.41 (4), p.371-382 |
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container_title | Journal of clinical pharmacy and therapeutics |
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creator | Albert-Vartanian, A. Boyd, M. R. Hall, A. L. Morgado, S. J. Nguyen, E. Nguyen, V. P. H. Patel, S. P. Russo, L. J. Shao, A. J. Raffa, R. B. |
description | Summary
What is known and objective
Optimal utilization of opioid analgesics is significantly limited by the central nervous system adverse effects and misuse/abuse potential of currently available drugs. It has been postulated that opioid‐associated adverse effects and abuse potential would be greatly reduced if opioids could be excluded from reaching the brain. We review the basic science and clinical evidence of one such approach – peripherally restricted kappa‐opioid receptor (KOR) agonists (pKORAs).
Methods
Published and unpublished literature, websites and other sources were searched for basic science and clinical information related to the potential benefits and development of peripherally restricted kappa‐opioid receptor agonists. Each source was summarized, reviewed and assessed.
Results
The historical development of pKORAs can be traced from the design of increasingly KOR‐selective agonists, elucidation of the pharmacologic attributes of such compounds and strategies to restrict passage across the blood–brain barrier. Novel compounds are under development and have progressed to clinical trials.
What is new and conclusions
The results from recent clinical trials suggest that peripherally restricted opioids can be successfully designed and that they can retain analgesic efficacy with a more favourable adverse effect profile.
It has been postulated that opioid‐associated adverse effects and abuse potential would be greatly reduced if opioids could be excluded from reaching the brain. We review the basic science and clinical evidence of one such approach – peripherally restricted kappa‐opioid receptor (KOR) agonists (pKORAs). |
doi_str_mv | 10.1111/jcpt.12404 |
format | Article |
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What is known and objective
Optimal utilization of opioid analgesics is significantly limited by the central nervous system adverse effects and misuse/abuse potential of currently available drugs. It has been postulated that opioid‐associated adverse effects and abuse potential would be greatly reduced if opioids could be excluded from reaching the brain. We review the basic science and clinical evidence of one such approach – peripherally restricted kappa‐opioid receptor (KOR) agonists (pKORAs).
Methods
Published and unpublished literature, websites and other sources were searched for basic science and clinical information related to the potential benefits and development of peripherally restricted kappa‐opioid receptor agonists. Each source was summarized, reviewed and assessed.
Results
The historical development of pKORAs can be traced from the design of increasingly KOR‐selective agonists, elucidation of the pharmacologic attributes of such compounds and strategies to restrict passage across the blood–brain barrier. Novel compounds are under development and have progressed to clinical trials.
What is new and conclusions
The results from recent clinical trials suggest that peripherally restricted opioids can be successfully designed and that they can retain analgesic efficacy with a more favourable adverse effect profile.
It has been postulated that opioid‐associated adverse effects and abuse potential would be greatly reduced if opioids could be excluded from reaching the brain. We review the basic science and clinical evidence of one such approach – peripherally restricted kappa‐opioid receptor (KOR) agonists (pKORAs).</description><identifier>ISSN: 0269-4727</identifier><identifier>EISSN: 1365-2710</identifier><identifier>DOI: 10.1111/jcpt.12404</identifier><identifier>PMID: 27245498</identifier><identifier>CODEN: JCPTED</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>analgesic ; Analgesics, Opioid - adverse effects ; Analgesics, Opioid - pharmacology ; Analgesics, Opioid - therapeutic use ; Animals ; Blood-Brain Barrier - metabolism ; Drug Design ; efficacy ; Humans ; kappa-opioid ; Opioid-Related Disorders - epidemiology ; Opioid-Related Disorders - prevention & control ; Pain - drug therapy ; peripheral ; Receptors, Opioid, kappa - agonists ; safety ; Tissue Distribution</subject><ispartof>Journal of clinical pharmacy and therapeutics, 2016-08, Vol.41 (4), p.371-382</ispartof><rights>2016 John Wiley & Sons Ltd</rights><rights>2016 John Wiley & Sons Ltd.</rights><rights>Copyright © 2016 John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5344-320fb2703e51c16cd92304d8b299843ebece5ef49abf231eb056d9d044f4b3683</citedby><cites>FETCH-LOGICAL-c5344-320fb2703e51c16cd92304d8b299843ebece5ef49abf231eb056d9d044f4b3683</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%2Fjcpt.12404$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjcpt.12404$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27245498$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Albert-Vartanian, A.</creatorcontrib><creatorcontrib>Boyd, M. R.</creatorcontrib><creatorcontrib>Hall, A. L.</creatorcontrib><creatorcontrib>Morgado, S. J.</creatorcontrib><creatorcontrib>Nguyen, E.</creatorcontrib><creatorcontrib>Nguyen, V. P. H.</creatorcontrib><creatorcontrib>Patel, S. P.</creatorcontrib><creatorcontrib>Russo, L. J.</creatorcontrib><creatorcontrib>Shao, A. J.</creatorcontrib><creatorcontrib>Raffa, R. B.</creatorcontrib><title>Will peripherally restricted kappa-opioid receptor agonists (pKORAs) relieve pain with less opioid adverse effects and abuse potential?</title><title>Journal of clinical pharmacy and therapeutics</title><addtitle>J Clin Pharm Ther</addtitle><description>Summary
What is known and objective
Optimal utilization of opioid analgesics is significantly limited by the central nervous system adverse effects and misuse/abuse potential of currently available drugs. It has been postulated that opioid‐associated adverse effects and abuse potential would be greatly reduced if opioids could be excluded from reaching the brain. We review the basic science and clinical evidence of one such approach – peripherally restricted kappa‐opioid receptor (KOR) agonists (pKORAs).
Methods
Published and unpublished literature, websites and other sources were searched for basic science and clinical information related to the potential benefits and development of peripherally restricted kappa‐opioid receptor agonists. Each source was summarized, reviewed and assessed.
Results
The historical development of pKORAs can be traced from the design of increasingly KOR‐selective agonists, elucidation of the pharmacologic attributes of such compounds and strategies to restrict passage across the blood–brain barrier. Novel compounds are under development and have progressed to clinical trials.
What is new and conclusions
The results from recent clinical trials suggest that peripherally restricted opioids can be successfully designed and that they can retain analgesic efficacy with a more favourable adverse effect profile.
It has been postulated that opioid‐associated adverse effects and abuse potential would be greatly reduced if opioids could be excluded from reaching the brain. We review the basic science and clinical evidence of one such approach – peripherally restricted kappa‐opioid receptor (KOR) agonists (pKORAs).</description><subject>analgesic</subject><subject>Analgesics, Opioid - adverse effects</subject><subject>Analgesics, Opioid - pharmacology</subject><subject>Analgesics, Opioid - therapeutic use</subject><subject>Animals</subject><subject>Blood-Brain Barrier - metabolism</subject><subject>Drug Design</subject><subject>efficacy</subject><subject>Humans</subject><subject>kappa-opioid</subject><subject>Opioid-Related Disorders - epidemiology</subject><subject>Opioid-Related Disorders - prevention & control</subject><subject>Pain - drug therapy</subject><subject>peripheral</subject><subject>Receptors, Opioid, kappa - agonists</subject><subject>safety</subject><subject>Tissue Distribution</subject><issn>0269-4727</issn><issn>1365-2710</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkV9PFDEUxRujkQV98QOYJr6AyWD_TTt9ImSjKBARXOWx6czckS7dmdrOgvsJ_NoWduHBB70vNzn9nZPeHIReUbJP87ybN2Hcp0wQ8QRNKJdlwRQlT9GEMKkLoZjaQtspzQkhUjH-HG0xxUQpdDVBvy-d9zhAdOEKovV-hSOkMbpmhBZf2xBsMQQ3uDbrDYRxiNj-GHqXxoR3w8nZxWHay0_ewQ3gYF2Pb914hT2khDdG295ATICh66DJNttnrV5mJQwj9KOz_uAFetZZn-DlZu-gbx_ez6Yfi9Ozo0_Tw9OiKbkQBWekq5kiHEraUNm0mnEi2qpmWleCQ53_WEIntK07xinUpJStbokQnai5rPgO2l3nhjj8XOZLzcKlBry3PQzLZGhFKkWorvT_UaV1KRmVIqNv_kLnwzL2-ZB7igpOJM_U2zXVxCGlCJ0J0S1sXBlKzF2T5q5Jc99khl9vIpf1AtpH9KG6DNA1cOs8rP4RZY6nX2YPocXak-uDX48eG6-NVFyV5vLzkfl6oWcn38-PzTn_AyGDuQM</recordid><startdate>201608</startdate><enddate>201608</enddate><creator>Albert-Vartanian, A.</creator><creator>Boyd, M. R.</creator><creator>Hall, A. L.</creator><creator>Morgado, S. J.</creator><creator>Nguyen, E.</creator><creator>Nguyen, V. P. H.</creator><creator>Patel, S. P.</creator><creator>Russo, L. J.</creator><creator>Shao, A. J.</creator><creator>Raffa, R. B.</creator><general>Blackwell Publishing Ltd</general><general>Hindawi Limited</general><scope>BSCLL</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>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>7X8</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>201608</creationdate><title>Will peripherally restricted kappa-opioid receptor agonists (pKORAs) relieve pain with less opioid adverse effects and abuse potential?</title><author>Albert-Vartanian, A. ; Boyd, M. R. ; Hall, A. L. ; Morgado, S. J. ; Nguyen, E. ; Nguyen, V. P. H. ; Patel, S. P. ; Russo, L. J. ; Shao, A. J. ; Raffa, R. B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5344-320fb2703e51c16cd92304d8b299843ebece5ef49abf231eb056d9d044f4b3683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>analgesic</topic><topic>Analgesics, Opioid - adverse effects</topic><topic>Analgesics, Opioid - pharmacology</topic><topic>Analgesics, Opioid - therapeutic use</topic><topic>Animals</topic><topic>Blood-Brain Barrier - metabolism</topic><topic>Drug Design</topic><topic>efficacy</topic><topic>Humans</topic><topic>kappa-opioid</topic><topic>Opioid-Related Disorders - epidemiology</topic><topic>Opioid-Related Disorders - prevention & control</topic><topic>Pain - drug therapy</topic><topic>peripheral</topic><topic>Receptors, Opioid, kappa - agonists</topic><topic>safety</topic><topic>Tissue Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Albert-Vartanian, A.</creatorcontrib><creatorcontrib>Boyd, M. R.</creatorcontrib><creatorcontrib>Hall, A. L.</creatorcontrib><creatorcontrib>Morgado, S. J.</creatorcontrib><creatorcontrib>Nguyen, E.</creatorcontrib><creatorcontrib>Nguyen, V. P. H.</creatorcontrib><creatorcontrib>Patel, S. P.</creatorcontrib><creatorcontrib>Russo, L. J.</creatorcontrib><creatorcontrib>Shao, A. J.</creatorcontrib><creatorcontrib>Raffa, R. B.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Journal of clinical pharmacy and therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Albert-Vartanian, A.</au><au>Boyd, M. R.</au><au>Hall, A. L.</au><au>Morgado, S. J.</au><au>Nguyen, E.</au><au>Nguyen, V. P. H.</au><au>Patel, S. P.</au><au>Russo, L. J.</au><au>Shao, A. J.</au><au>Raffa, R. B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Will peripherally restricted kappa-opioid receptor agonists (pKORAs) relieve pain with less opioid adverse effects and abuse potential?</atitle><jtitle>Journal of clinical pharmacy and therapeutics</jtitle><addtitle>J Clin Pharm Ther</addtitle><date>2016-08</date><risdate>2016</risdate><volume>41</volume><issue>4</issue><spage>371</spage><epage>382</epage><pages>371-382</pages><issn>0269-4727</issn><eissn>1365-2710</eissn><coden>JCPTED</coden><abstract>Summary
What is known and objective
Optimal utilization of opioid analgesics is significantly limited by the central nervous system adverse effects and misuse/abuse potential of currently available drugs. It has been postulated that opioid‐associated adverse effects and abuse potential would be greatly reduced if opioids could be excluded from reaching the brain. We review the basic science and clinical evidence of one such approach – peripherally restricted kappa‐opioid receptor (KOR) agonists (pKORAs).
Methods
Published and unpublished literature, websites and other sources were searched for basic science and clinical information related to the potential benefits and development of peripherally restricted kappa‐opioid receptor agonists. Each source was summarized, reviewed and assessed.
Results
The historical development of pKORAs can be traced from the design of increasingly KOR‐selective agonists, elucidation of the pharmacologic attributes of such compounds and strategies to restrict passage across the blood–brain barrier. Novel compounds are under development and have progressed to clinical trials.
What is new and conclusions
The results from recent clinical trials suggest that peripherally restricted opioids can be successfully designed and that they can retain analgesic efficacy with a more favourable adverse effect profile.
It has been postulated that opioid‐associated adverse effects and abuse potential would be greatly reduced if opioids could be excluded from reaching the brain. We review the basic science and clinical evidence of one such approach – peripherally restricted kappa‐opioid receptor (KOR) agonists (pKORAs).</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>27245498</pmid><doi>10.1111/jcpt.12404</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | analgesic Analgesics, Opioid - adverse effects Analgesics, Opioid - pharmacology Analgesics, Opioid - therapeutic use Animals Blood-Brain Barrier - metabolism Drug Design efficacy Humans kappa-opioid Opioid-Related Disorders - epidemiology Opioid-Related Disorders - prevention & control Pain - drug therapy peripheral Receptors, Opioid, kappa - agonists safety Tissue Distribution |
title | Will peripherally restricted kappa-opioid receptor agonists (pKORAs) relieve pain with less opioid adverse effects and abuse potential? |
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