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
Hauptverfasser: Nagui, N. A., Ezzat, M. A., Abdel Raheem, H. M., Rashed, L. A., Abozaid, N. A.
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container_end_page 128
container_issue 2
container_start_page 124
container_title Clinical and experimental dermatology
container_volume 41
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
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A. ; Ezzat, M. A. ; Abdel Raheem, H. M. ; Rashed, L. A. ; Abozaid, N. A.</creator><creatorcontrib>Nagui, N. A. ; Ezzat, M. A. ; Abdel Raheem, H. M. ; Rashed, L. A. ; Abozaid, N. A.</creatorcontrib><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><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. 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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). 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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 &amp; 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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