Possible role of proenkephalin in psoriasis
Summary Background Psoriasis is a common chronic skin disease that can also affect the mucous membranes and joints. It is multifactorial in origin, occurring in genetically predisposed individuals, and triggered by various endogenous and exogenous factors. Proenkephalin (PENK) is an endogenous opioi...
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Veröffentlicht in: | Clinical and experimental dermatology 2016-03, Vol.41 (2), p.124-128 |
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creator | Nagui, N. A. Ezzat, M. A. Abdel Raheem, H. M. Rashed, L. A. Abozaid, N. A. |
description | Summary
Background
Psoriasis is a common chronic skin disease that can also affect the mucous membranes and joints. It is multifactorial in origin, occurring in genetically predisposed individuals, and triggered by various endogenous and exogenous factors. Proenkephalin (PENK) is an endogenous opioid polypeptide hormone that acts on specific opiate receptors found on nerve and mucosal cells, and on various cells in the immune system. PENK receptors are expressed on skin cells, and their activation can regulate keratinocyte and melanocyte activities. PENK expression has been found to be increased in keratinocytes in psoriatic skin, and together with its inflammatory basis, this suggests that PENK may be regulated by inflammatory stimuli.
Aim
To assess the possible role of PENK in the pathogenesis of psoriasis and to assess if it is related to the severity of psoriatic lesions.
Methods
Serum and tissue PENK levels were estimated in 20 patients with psoriasis vulgaris, and compared with those of 20 healthy controls (HCs).
Results
PENK levels were found to be significantly increased both in serum and in psoriatic lesions in patients compared with HCs. No significant correlation was found between PENK levels and patient age, disease duration or disease severity (Psoriasis Area and Severity Index).
Conclusion
Our results support the role of PENK in the aetiopathogenesis of psoriasis, and indicate that giving anti‐PENK drugs in addition to current antipsoriatic therapies might be of value in treating this common chronic skin disease. |
doi_str_mv | 10.1111/ced.12679 |
format | Article |
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Background
Psoriasis is a common chronic skin disease that can also affect the mucous membranes and joints. It is multifactorial in origin, occurring in genetically predisposed individuals, and triggered by various endogenous and exogenous factors. Proenkephalin (PENK) is an endogenous opioid polypeptide hormone that acts on specific opiate receptors found on nerve and mucosal cells, and on various cells in the immune system. PENK receptors are expressed on skin cells, and their activation can regulate keratinocyte and melanocyte activities. PENK expression has been found to be increased in keratinocytes in psoriatic skin, and together with its inflammatory basis, this suggests that PENK may be regulated by inflammatory stimuli.
Aim
To assess the possible role of PENK in the pathogenesis of psoriasis and to assess if it is related to the severity of psoriatic lesions.
Methods
Serum and tissue PENK levels were estimated in 20 patients with psoriasis vulgaris, and compared with those of 20 healthy controls (HCs).
Results
PENK levels were found to be significantly increased both in serum and in psoriatic lesions in patients compared with HCs. No significant correlation was found between PENK levels and patient age, disease duration or disease severity (Psoriasis Area and Severity Index).
Conclusion
Our results support the role of PENK in the aetiopathogenesis of psoriasis, and indicate that giving anti‐PENK drugs in addition to current antipsoriatic therapies might be of value in treating this common chronic skin disease.</description><identifier>ISSN: 0307-6938</identifier><identifier>EISSN: 1365-2230</identifier><identifier>DOI: 10.1111/ced.12679</identifier><identifier>PMID: 26011402</identifier><identifier>CODEN: CEDEDE</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Adolescent ; Adult ; Aged ; Case-Control Studies ; Enkephalins - blood ; Enkephalins - physiology ; Female ; Humans ; Male ; Middle Aged ; Protein Precursors - blood ; Protein Precursors - physiology ; Psoriasis ; Psoriasis - metabolism ; Risk Factors ; Severity of Illness Index ; Skin - metabolism ; Skin diseases ; Young Adult</subject><ispartof>Clinical and experimental dermatology, 2016-03, Vol.41 (2), p.124-128</ispartof><rights>2015 British Association of Dermatologists</rights><rights>2015 British Association of Dermatologists.</rights><rights>Copyright © 2016 British Association of Dermatologists</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4249-b11f74cea18069ac8f39c3cae764c95ab5cba445c20bda7aea65025b09f8031f3</citedby><cites>FETCH-LOGICAL-c4249-b11f74cea18069ac8f39c3cae764c95ab5cba445c20bda7aea65025b09f8031f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27907,27908</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26011402$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nagui, N. A.</creatorcontrib><creatorcontrib>Ezzat, M. A.</creatorcontrib><creatorcontrib>Abdel Raheem, H. M.</creatorcontrib><creatorcontrib>Rashed, L. A.</creatorcontrib><creatorcontrib>Abozaid, N. A.</creatorcontrib><title>Possible role of proenkephalin in psoriasis</title><title>Clinical and experimental dermatology</title><addtitle>Clin Exp Dermatol</addtitle><description>Summary
Background
Psoriasis is a common chronic skin disease that can also affect the mucous membranes and joints. It is multifactorial in origin, occurring in genetically predisposed individuals, and triggered by various endogenous and exogenous factors. Proenkephalin (PENK) is an endogenous opioid polypeptide hormone that acts on specific opiate receptors found on nerve and mucosal cells, and on various cells in the immune system. PENK receptors are expressed on skin cells, and their activation can regulate keratinocyte and melanocyte activities. PENK expression has been found to be increased in keratinocytes in psoriatic skin, and together with its inflammatory basis, this suggests that PENK may be regulated by inflammatory stimuli.
Aim
To assess the possible role of PENK in the pathogenesis of psoriasis and to assess if it is related to the severity of psoriatic lesions.
Methods
Serum and tissue PENK levels were estimated in 20 patients with psoriasis vulgaris, and compared with those of 20 healthy controls (HCs).
Results
PENK levels were found to be significantly increased both in serum and in psoriatic lesions in patients compared with HCs. No significant correlation was found between PENK levels and patient age, disease duration or disease severity (Psoriasis Area and Severity Index).
Conclusion
Our results support the role of PENK in the aetiopathogenesis of psoriasis, and indicate that giving anti‐PENK drugs in addition to current antipsoriatic therapies might be of value in treating this common chronic skin disease.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Case-Control Studies</subject><subject>Enkephalins - blood</subject><subject>Enkephalins - physiology</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Protein Precursors - blood</subject><subject>Protein Precursors - physiology</subject><subject>Psoriasis</subject><subject>Psoriasis - metabolism</subject><subject>Risk Factors</subject><subject>Severity of Illness Index</subject><subject>Skin - metabolism</subject><subject>Skin diseases</subject><subject>Young Adult</subject><issn>0307-6938</issn><issn>1365-2230</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE1Lw0AQhhdRbK0e_ANS8KJI2tnv5Ki1tqL4AUrBy7LZbjBtmsTdFu2_d2tbD4LDMAPDMy8zL0LHGDo4RNfYcQcTIZMd1MRU8IgQCruoCRRkJBIaN9CB9xMATLHk-6hBBGDMgDTRxVPlfZ4Wtu2qUKqsXbvKllNbv-siL9sha1-5XPvcH6K9TBfeHm16C73e9F96w-j-cXDbu7yPDCMsiVKMM8mM1TgGkWgTZzQx1GgrBTMJ1yk3qWaMGwLpWEttteBAeApJFgPFGW2hs7VuOOVjYf1czXJvbFHo0lYLr7AUHEPMKAT09A86qRauDNetKCZIzIEG6nxNGRe-dTZTtctn2i0VBrVyUAUH1Y-DgT3ZKC7SWZhuya1lAeiugc-8sMv_lVSvf72VjNYbuZ_br98N7aZKSCq5Gj0M1NudHA05flZX9BspMIda</recordid><startdate>201603</startdate><enddate>201603</enddate><creator>Nagui, N. A.</creator><creator>Ezzat, M. A.</creator><creator>Abdel Raheem, H. M.</creator><creator>Rashed, L. A.</creator><creator>Abozaid, N. A.</creator><general>Blackwell Publishing Ltd</general><general>Oxford University Press</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>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201603</creationdate><title>Possible role of proenkephalin in psoriasis</title><author>Nagui, N. A. ; Ezzat, M. A. ; Abdel Raheem, H. M. ; Rashed, L. A. ; Abozaid, N. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4249-b11f74cea18069ac8f39c3cae764c95ab5cba445c20bda7aea65025b09f8031f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Case-Control Studies</topic><topic>Enkephalins - blood</topic><topic>Enkephalins - physiology</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Protein Precursors - blood</topic><topic>Protein Precursors - physiology</topic><topic>Psoriasis</topic><topic>Psoriasis - metabolism</topic><topic>Risk Factors</topic><topic>Severity of Illness Index</topic><topic>Skin - metabolism</topic><topic>Skin diseases</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nagui, N. A.</creatorcontrib><creatorcontrib>Ezzat, M. A.</creatorcontrib><creatorcontrib>Abdel Raheem, H. M.</creatorcontrib><creatorcontrib>Rashed, L. A.</creatorcontrib><creatorcontrib>Abozaid, N. A.</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>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical and experimental dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nagui, N. A.</au><au>Ezzat, M. A.</au><au>Abdel Raheem, H. M.</au><au>Rashed, L. A.</au><au>Abozaid, N. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Possible role of proenkephalin in psoriasis</atitle><jtitle>Clinical and experimental dermatology</jtitle><addtitle>Clin Exp Dermatol</addtitle><date>2016-03</date><risdate>2016</risdate><volume>41</volume><issue>2</issue><spage>124</spage><epage>128</epage><pages>124-128</pages><issn>0307-6938</issn><eissn>1365-2230</eissn><coden>CEDEDE</coden><abstract>Summary
Background
Psoriasis is a common chronic skin disease that can also affect the mucous membranes and joints. It is multifactorial in origin, occurring in genetically predisposed individuals, and triggered by various endogenous and exogenous factors. Proenkephalin (PENK) is an endogenous opioid polypeptide hormone that acts on specific opiate receptors found on nerve and mucosal cells, and on various cells in the immune system. PENK receptors are expressed on skin cells, and their activation can regulate keratinocyte and melanocyte activities. PENK expression has been found to be increased in keratinocytes in psoriatic skin, and together with its inflammatory basis, this suggests that PENK may be regulated by inflammatory stimuli.
Aim
To assess the possible role of PENK in the pathogenesis of psoriasis and to assess if it is related to the severity of psoriatic lesions.
Methods
Serum and tissue PENK levels were estimated in 20 patients with psoriasis vulgaris, and compared with those of 20 healthy controls (HCs).
Results
PENK levels were found to be significantly increased both in serum and in psoriatic lesions in patients compared with HCs. No significant correlation was found between PENK levels and patient age, disease duration or disease severity (Psoriasis Area and Severity Index).
Conclusion
Our results support the role of PENK in the aetiopathogenesis of psoriasis, and indicate that giving anti‐PENK drugs in addition to current antipsoriatic therapies might be of value in treating this common chronic skin disease.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>26011402</pmid><doi>10.1111/ced.12679</doi><tpages>5</tpages></addata></record> |
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source | MEDLINE; Oxford University Press Journals All Titles (1996-Current); Alma/SFX Local Collection |
subjects | Adolescent Adult Aged Case-Control Studies Enkephalins - blood Enkephalins - physiology Female Humans Male Middle Aged Protein Precursors - blood Protein Precursors - physiology Psoriasis Psoriasis - metabolism Risk Factors Severity of Illness Index Skin - metabolism Skin diseases Young Adult |
title | Possible role of proenkephalin in psoriasis |
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