Pathology of Nerve Terminal Degeneration in the Skin
To characterize the pathology of epidermal nerve degeneration and regeneration, we investigated temporal and spatial changes in skin innervation of the mouse footpad. Within 24 hours after sciatic nerve axotomy, terminals of epidermal nerves appeared swollen and there was a mild reduction in epiderm...
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Veröffentlicht in: | Journal of neuropathology and experimental neurology 2000-04, Vol.59 (4), p.297-307 |
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description | To characterize the pathology of epidermal nerve degeneration and regeneration, we investigated temporal and spatial changes in skin innervation of the mouse footpad. Within 24 hours after sciatic nerve axotomy, terminals of epidermal nerves appeared swollen and there was a mild reduction in epidermal nerve density (5.7 ± 2.8 vs 12.7 ± 2.2 fibers/mm, p < 0.04). Epidermal nerves completely disappeared by 48 hours (0.2 ± 0.2 vs 14.2 ± 0.9 fibers/mm, p < 0.001). Concomitant with the disappearance of epidermal nerves, the immunocytochemical pattern of the subepidermal nerve plexus became fragmented. At the electron microscopic level, the axoplasm of degenerating dermal nerves was distended with organelles and later became amorphous. Beginning from day 28 after axotomy, collateral sprouts from the adjacent saphenous nerve territory extended into the denervated area with a beaded appearance. They never penetrated the epidermal-dermal junction to innervate the epidermis. In contrast, 3 months after nerve crushing, the epidermis on the surgery side resumed a normal innervation pattern as the epidermis on the control side (10.3 ± 3.9 vs 10.6 ± 1.5 fibers/mm, p = 0.1). This study demonstrates the characteristics of degenerating and regenerating nerves, and suggests that successful reinnervation mainly originates from regenerating nerves of the original nerve trunks. All these findings provide qualitative and quantitative information for interpreting the pathology of cutaneous nerves. |
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Within 24 hours after sciatic nerve axotomy, terminals of epidermal nerves appeared swollen and there was a mild reduction in epidermal nerve density (5.7 ± 2.8 vs 12.7 ± 2.2 fibers/mm, p < 0.04). Epidermal nerves completely disappeared by 48 hours (0.2 ± 0.2 vs 14.2 ± 0.9 fibers/mm, p < 0.001). Concomitant with the disappearance of epidermal nerves, the immunocytochemical pattern of the subepidermal nerve plexus became fragmented. At the electron microscopic level, the axoplasm of degenerating dermal nerves was distended with organelles and later became amorphous. Beginning from day 28 after axotomy, collateral sprouts from the adjacent saphenous nerve territory extended into the denervated area with a beaded appearance. They never penetrated the epidermal-dermal junction to innervate the epidermis. In contrast, 3 months after nerve crushing, the epidermis on the surgery side resumed a normal innervation pattern as the epidermis on the control side (10.3 ± 3.9 vs 10.6 ± 1.5 fibers/mm, p = 0.1). This study demonstrates the characteristics of degenerating and regenerating nerves, and suggests that successful reinnervation mainly originates from regenerating nerves of the original nerve trunks. All these findings provide qualitative and quantitative information for interpreting the pathology of cutaneous nerves.</description><identifier>ISSN: 0022-3069</identifier><identifier>EISSN: 1554-6578</identifier><identifier>DOI: 10.1093/jnen/59.4.297</identifier><identifier>PMID: 10759185</identifier><identifier>CODEN: JNENAD</identifier><language>eng</language><publisher>Hagerstown, MD: American Association of Neuropathologists, Inc</publisher><subject>Animals ; Axons - ultrastructure ; Axotomy ; Biological and medical sciences ; Cytochemistry ; Denervation ; Hindlimb - innervation ; Immunohistochemistry ; Injuries of the nervous system and the skull. Diseases due to physical agents ; Male ; Medical sciences ; Mice ; Mice, Inbred ICR ; Nerve Crush ; Nerve Endings - metabolism ; Nerve Endings - pathology ; Nerve Endings - ultrastructure ; Nerve Regeneration - physiology ; Physiological aspects ; Sciatic Nerve - metabolism ; Sciatic Nerve - physiology ; Sciatic Nerve - surgery ; Sciatic Nerve - ultrastructure ; Skin ; Skin - innervation ; Skin - pathology ; Skin - ultrastructure ; Thiolester Hydrolases - metabolism ; Traumas. Diseases due to physical agents ; Tropical medicine ; Ubiquitin Thiolesterase ; Wallerian Degeneration - pathology</subject><ispartof>Journal of neuropathology and experimental neurology, 2000-04, Vol.59 (4), p.297-307</ispartof><rights>2000 American Association of Neuropathologists, Inc</rights><rights>2000 INIST-CNRS</rights><rights>COPYRIGHT 2000 Oxford University Press</rights><rights>Copyright American Association of Neuropathologists, Inc. Apr 2000</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5655-72833f0b9e44fc611ef33b3a1938e23935b359be7d1e15b3b48e1b47e03801833</citedby><cites>FETCH-LOGICAL-c5655-72833f0b9e44fc611ef33b3a1938e23935b359be7d1e15b3b48e1b47e03801833</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1332080$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10759185$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>HSIEH, SUNG-TSANG</creatorcontrib><creatorcontrib>CHIANG, HOU-YU</creatorcontrib><creatorcontrib>LIN, WHEI-MIN</creatorcontrib><title>Pathology of Nerve Terminal Degeneration in the Skin</title><title>Journal of neuropathology and experimental neurology</title><addtitle>J Neuropathol Exp Neurol</addtitle><description>To characterize the pathology of epidermal nerve degeneration and regeneration, we investigated temporal and spatial changes in skin innervation of the mouse footpad. Within 24 hours after sciatic nerve axotomy, terminals of epidermal nerves appeared swollen and there was a mild reduction in epidermal nerve density (5.7 ± 2.8 vs 12.7 ± 2.2 fibers/mm, p < 0.04). Epidermal nerves completely disappeared by 48 hours (0.2 ± 0.2 vs 14.2 ± 0.9 fibers/mm, p < 0.001). Concomitant with the disappearance of epidermal nerves, the immunocytochemical pattern of the subepidermal nerve plexus became fragmented. At the electron microscopic level, the axoplasm of degenerating dermal nerves was distended with organelles and later became amorphous. Beginning from day 28 after axotomy, collateral sprouts from the adjacent saphenous nerve territory extended into the denervated area with a beaded appearance. They never penetrated the epidermal-dermal junction to innervate the epidermis. In contrast, 3 months after nerve crushing, the epidermis on the surgery side resumed a normal innervation pattern as the epidermis on the control side (10.3 ± 3.9 vs 10.6 ± 1.5 fibers/mm, p = 0.1). This study demonstrates the characteristics of degenerating and regenerating nerves, and suggests that successful reinnervation mainly originates from regenerating nerves of the original nerve trunks. All these findings provide qualitative and quantitative information for interpreting the pathology of cutaneous nerves.</description><subject>Animals</subject><subject>Axons - ultrastructure</subject><subject>Axotomy</subject><subject>Biological and medical sciences</subject><subject>Cytochemistry</subject><subject>Denervation</subject><subject>Hindlimb - innervation</subject><subject>Immunohistochemistry</subject><subject>Injuries of the nervous system and the skull. Diseases due to physical agents</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred ICR</subject><subject>Nerve Crush</subject><subject>Nerve Endings - metabolism</subject><subject>Nerve Endings - pathology</subject><subject>Nerve Endings - ultrastructure</subject><subject>Nerve Regeneration - physiology</subject><subject>Physiological aspects</subject><subject>Sciatic Nerve - metabolism</subject><subject>Sciatic Nerve - physiology</subject><subject>Sciatic Nerve - surgery</subject><subject>Sciatic Nerve - ultrastructure</subject><subject>Skin</subject><subject>Skin - innervation</subject><subject>Skin - pathology</subject><subject>Skin - ultrastructure</subject><subject>Thiolester Hydrolases - metabolism</subject><subject>Traumas. Diseases due to physical agents</subject><subject>Tropical medicine</subject><subject>Ubiquitin Thiolesterase</subject><subject>Wallerian Degeneration - pathology</subject><issn>0022-3069</issn><issn>1554-6578</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkU1v1DAQhi0EotvCkSuKEOot2_FXHB-rli-pAiTK2XKyk11vvXaxE6r-exyyEogLskYejZ557ZmXkFcU1hQ0v9gHDBdSr8WaafWErKiUom6kap-SFQBjNYdGn5DTnPcAoEGL5-SEgpKatnJFxFc77qKP28cqDtVnTD-xusV0cMH66hq3GDDZ0cVQuVCNO6y-3bnwgjwbrM_48nifke_v391efaxvvnz4dHV5U_eykbJWrOV8gE6jEEPfUIoD5x23VPMWGddcdlzqDtWGIi15J1qknVAIvAVaes_I-aJ7n-KPCfNoDi736L0NGKdsFAUhWwr_BakWRU-0BXzzD7iPUyqzZsPK_ihXlBVovUBb69G4MMQx2b6cDR5cHwMOrtQvJW-oUpzPqvXS0KeYc8LB3Cd3sOnRUDCzS2Z2yUhthCmvFP718RdTd8DNX_RiSwHeHgGbe-uHZEPv8h-OcwbtPLZYsIfoR0z5zk8PmMwOrR93ptgNEhSr2ZyJEvXvEv8FhommNA</recordid><startdate>200004</startdate><enddate>200004</enddate><creator>HSIEH, SUNG-TSANG</creator><creator>CHIANG, HOU-YU</creator><creator>LIN, WHEI-MIN</creator><general>American Association of Neuropathologists, Inc</general><general>Lippincott Williams & Wilkins</general><general>Oxford University Press</general><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>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>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>S0X</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>200004</creationdate><title>Pathology of Nerve Terminal Degeneration in the Skin</title><author>HSIEH, SUNG-TSANG ; CHIANG, HOU-YU ; LIN, WHEI-MIN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5655-72833f0b9e44fc611ef33b3a1938e23935b359be7d1e15b3b48e1b47e03801833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Animals</topic><topic>Axons - ultrastructure</topic><topic>Axotomy</topic><topic>Biological and medical sciences</topic><topic>Cytochemistry</topic><topic>Denervation</topic><topic>Hindlimb - innervation</topic><topic>Immunohistochemistry</topic><topic>Injuries of the nervous system and the skull. Diseases due to physical agents</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred ICR</topic><topic>Nerve Crush</topic><topic>Nerve Endings - metabolism</topic><topic>Nerve Endings - pathology</topic><topic>Nerve Endings - ultrastructure</topic><topic>Nerve Regeneration - physiology</topic><topic>Physiological aspects</topic><topic>Sciatic Nerve - metabolism</topic><topic>Sciatic Nerve - physiology</topic><topic>Sciatic Nerve - surgery</topic><topic>Sciatic Nerve - ultrastructure</topic><topic>Skin</topic><topic>Skin - innervation</topic><topic>Skin - pathology</topic><topic>Skin - ultrastructure</topic><topic>Thiolester Hydrolases - metabolism</topic><topic>Traumas. Diseases due to physical agents</topic><topic>Tropical medicine</topic><topic>Ubiquitin Thiolesterase</topic><topic>Wallerian Degeneration - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>HSIEH, SUNG-TSANG</creatorcontrib><creatorcontrib>CHIANG, HOU-YU</creatorcontrib><creatorcontrib>LIN, WHEI-MIN</creatorcontrib><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>Health & 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>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 & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</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 Basic</collection><collection>SIRS Editorial</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neuropathology and experimental neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>HSIEH, SUNG-TSANG</au><au>CHIANG, HOU-YU</au><au>LIN, WHEI-MIN</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pathology of Nerve Terminal Degeneration in the Skin</atitle><jtitle>Journal of neuropathology and experimental neurology</jtitle><addtitle>J Neuropathol Exp Neurol</addtitle><date>2000-04</date><risdate>2000</risdate><volume>59</volume><issue>4</issue><spage>297</spage><epage>307</epage><pages>297-307</pages><issn>0022-3069</issn><eissn>1554-6578</eissn><coden>JNENAD</coden><abstract>To characterize the pathology of epidermal nerve degeneration and regeneration, we investigated temporal and spatial changes in skin innervation of the mouse footpad. Within 24 hours after sciatic nerve axotomy, terminals of epidermal nerves appeared swollen and there was a mild reduction in epidermal nerve density (5.7 ± 2.8 vs 12.7 ± 2.2 fibers/mm, p < 0.04). Epidermal nerves completely disappeared by 48 hours (0.2 ± 0.2 vs 14.2 ± 0.9 fibers/mm, p < 0.001). Concomitant with the disappearance of epidermal nerves, the immunocytochemical pattern of the subepidermal nerve plexus became fragmented. At the electron microscopic level, the axoplasm of degenerating dermal nerves was distended with organelles and later became amorphous. Beginning from day 28 after axotomy, collateral sprouts from the adjacent saphenous nerve territory extended into the denervated area with a beaded appearance. They never penetrated the epidermal-dermal junction to innervate the epidermis. In contrast, 3 months after nerve crushing, the epidermis on the surgery side resumed a normal innervation pattern as the epidermis on the control side (10.3 ± 3.9 vs 10.6 ± 1.5 fibers/mm, p = 0.1). This study demonstrates the characteristics of degenerating and regenerating nerves, and suggests that successful reinnervation mainly originates from regenerating nerves of the original nerve trunks. All these findings provide qualitative and quantitative information for interpreting the pathology of cutaneous nerves.</abstract><cop>Hagerstown, MD</cop><pub>American Association of Neuropathologists, Inc</pub><pmid>10759185</pmid><doi>10.1093/jnen/59.4.297</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Journals@Ovid Complete |
subjects | Animals Axons - ultrastructure Axotomy Biological and medical sciences Cytochemistry Denervation Hindlimb - innervation Immunohistochemistry Injuries of the nervous system and the skull. Diseases due to physical agents Male Medical sciences Mice Mice, Inbred ICR Nerve Crush Nerve Endings - metabolism Nerve Endings - pathology Nerve Endings - ultrastructure Nerve Regeneration - physiology Physiological aspects Sciatic Nerve - metabolism Sciatic Nerve - physiology Sciatic Nerve - surgery Sciatic Nerve - ultrastructure Skin Skin - innervation Skin - pathology Skin - ultrastructure Thiolester Hydrolases - metabolism Traumas. Diseases due to physical agents Tropical medicine Ubiquitin Thiolesterase Wallerian Degeneration - pathology |
title | Pathology of Nerve Terminal Degeneration in the Skin |
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