Simvastatin in an experimental spinal cord injury model: a histopathological and biochemical evidence based study
In this study we tried to determine the possible neuroprotective effects of simvastatin in a rat model of Spinal Cord Injury (SCI) with the help of biochemical and histopathological tests. Rats were divided into 5 groups:1) SCI control, 2) Sham operated, 3) SCI with 10 mg/kg intraperitoneal simvasta...
Gespeichert in:
Veröffentlicht in: | Bratislava Medical Journal 2020, Vol.121 (10), p.722-726 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 726 |
---|---|
container_issue | 10 |
container_start_page | 722 |
container_title | Bratislava Medical Journal |
container_volume | 121 |
creator | Tascioglu, T Karatay, M Erdem, Y Tekiner, A Celik, H Sahin, O Sertbas, I Bayar, M A |
description | In this study we tried to determine the possible neuroprotective effects of simvastatin in a rat model of Spinal Cord Injury (SCI) with the help of biochemical and histopathological tests.
Rats were divided into 5 groups:1) SCI control, 2) Sham operated, 3) SCI with 10 mg/kg intraperitoneal simvastatin, 4) SCI with 10 mg/kg oral simvastatin, 5) SCI with 10 mg/kg subcutaneous simvastatin. After the treatment period, all rats were sacrificed; their blood and spinal cord samples were taken for biochemical and histopathological assessment.
When the groups were compared in terms of oedema and inflammation status, the scores of groups receiving simvastatin were better than the control and sham groups (p = 0.001 and p = 0.038 respectively). When the 3 treatment groups (oral, intraperitoneal and subcutaneous simvastatin groups) were compared with each other in terms of inflammation, haemorrhage and oedema, there were no significant differences between groups (p = 0.112, p = 0.797 and p = 0.188, respectively). NSE and S100B levels were significantly lower in the treatment groups compared to the sham group (p = 0.039 and p = 0.004 respectively).
According to our biochemical and histopathological findings, simvastatin 10 mg/kg has a positive impact in the spinal cord injury model in rats, regardless of route of application (Tab. 1, Fig. 5, Ref. 26). |
doi_str_mv | 10.4149/BLL_2020_118 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2444882814</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2444882814</sourcerecordid><originalsourceid>FETCH-LOGICAL-c286t-239d9c035ca2604b91a32f88ed28a736d94e879ed0ab1fac946baa0421048e3d3</originalsourceid><addsrcrecordid>eNpNkEtLw0AUhQdRbH3sXMssXRidV9IZd1p8QcGFug43M7d2SpJJM0mx_95oqwgXDpfzcRYfIWecXSmuzPXdbJYLJljOud4jYy5lljCp0n0yZoxliRFKj8hRjEvGlEx5dkhGUpg0NUyNyerVV2uIHXS-psNBTfGzwdZXWHdQ0tj4eggbWjfUy77d0Co4LG8o0IWPXWigW4QyfHg7YFA7WvhgF1j9_Lj2DmuLtICIjsaud5sTcjCHMuLpLo_J-8P92_Qpmb08Pk9vZ4kVOusSIY0zlsnUgsiYKgwHKeZaoxMaJjJzRqGeGHQMCj4Ha1RWADAlOFMapZPH5GK727Rh1WPs8spHi2UJNYY-5kIppbXQXA3o5Ra1bYixxXneDAKg3eSc5d-S8_-SB_x8t9wXFbo_-Neq_AIRjHlI</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2444882814</pqid></control><display><type>article</type><title>Simvastatin in an experimental spinal cord injury model: a histopathological and biochemical evidence based study</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Tascioglu, T ; Karatay, M ; Erdem, Y ; Tekiner, A ; Celik, H ; Sahin, O ; Sertbas, I ; Bayar, M A</creator><creatorcontrib>Tascioglu, T ; Karatay, M ; Erdem, Y ; Tekiner, A ; Celik, H ; Sahin, O ; Sertbas, I ; Bayar, M A</creatorcontrib><description>In this study we tried to determine the possible neuroprotective effects of simvastatin in a rat model of Spinal Cord Injury (SCI) with the help of biochemical and histopathological tests.
Rats were divided into 5 groups:1) SCI control, 2) Sham operated, 3) SCI with 10 mg/kg intraperitoneal simvastatin, 4) SCI with 10 mg/kg oral simvastatin, 5) SCI with 10 mg/kg subcutaneous simvastatin. After the treatment period, all rats were sacrificed; their blood and spinal cord samples were taken for biochemical and histopathological assessment.
When the groups were compared in terms of oedema and inflammation status, the scores of groups receiving simvastatin were better than the control and sham groups (p = 0.001 and p = 0.038 respectively). When the 3 treatment groups (oral, intraperitoneal and subcutaneous simvastatin groups) were compared with each other in terms of inflammation, haemorrhage and oedema, there were no significant differences between groups (p = 0.112, p = 0.797 and p = 0.188, respectively). NSE and S100B levels were significantly lower in the treatment groups compared to the sham group (p = 0.039 and p = 0.004 respectively).
According to our biochemical and histopathological findings, simvastatin 10 mg/kg has a positive impact in the spinal cord injury model in rats, regardless of route of application (Tab. 1, Fig. 5, Ref. 26).</description><identifier>ISSN: 0006-9248</identifier><identifier>ISSN: 1336-0345</identifier><identifier>EISSN: 1336-0345</identifier><identifier>DOI: 10.4149/BLL_2020_118</identifier><identifier>PMID: 32955904</identifier><language>eng</language><publisher>Slovakia</publisher><subject>Animals ; Disease Models, Animal ; Neuroprotective Agents - pharmacology ; Rats ; Rats, Sprague-Dawley ; Simvastatin - pharmacology ; Spinal Cord ; Spinal Cord Injuries - drug therapy</subject><ispartof>Bratislava Medical Journal, 2020, Vol.121 (10), p.722-726</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32955904$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tascioglu, T</creatorcontrib><creatorcontrib>Karatay, M</creatorcontrib><creatorcontrib>Erdem, Y</creatorcontrib><creatorcontrib>Tekiner, A</creatorcontrib><creatorcontrib>Celik, H</creatorcontrib><creatorcontrib>Sahin, O</creatorcontrib><creatorcontrib>Sertbas, I</creatorcontrib><creatorcontrib>Bayar, M A</creatorcontrib><title>Simvastatin in an experimental spinal cord injury model: a histopathological and biochemical evidence based study</title><title>Bratislava Medical Journal</title><addtitle>Bratisl Lek Listy</addtitle><description>In this study we tried to determine the possible neuroprotective effects of simvastatin in a rat model of Spinal Cord Injury (SCI) with the help of biochemical and histopathological tests.
Rats were divided into 5 groups:1) SCI control, 2) Sham operated, 3) SCI with 10 mg/kg intraperitoneal simvastatin, 4) SCI with 10 mg/kg oral simvastatin, 5) SCI with 10 mg/kg subcutaneous simvastatin. After the treatment period, all rats were sacrificed; their blood and spinal cord samples were taken for biochemical and histopathological assessment.
When the groups were compared in terms of oedema and inflammation status, the scores of groups receiving simvastatin were better than the control and sham groups (p = 0.001 and p = 0.038 respectively). When the 3 treatment groups (oral, intraperitoneal and subcutaneous simvastatin groups) were compared with each other in terms of inflammation, haemorrhage and oedema, there were no significant differences between groups (p = 0.112, p = 0.797 and p = 0.188, respectively). NSE and S100B levels were significantly lower in the treatment groups compared to the sham group (p = 0.039 and p = 0.004 respectively).
According to our biochemical and histopathological findings, simvastatin 10 mg/kg has a positive impact in the spinal cord injury model in rats, regardless of route of application (Tab. 1, Fig. 5, Ref. 26).</description><subject>Animals</subject><subject>Disease Models, Animal</subject><subject>Neuroprotective Agents - pharmacology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Simvastatin - pharmacology</subject><subject>Spinal Cord</subject><subject>Spinal Cord Injuries - drug therapy</subject><issn>0006-9248</issn><issn>1336-0345</issn><issn>1336-0345</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkEtLw0AUhQdRbH3sXMssXRidV9IZd1p8QcGFug43M7d2SpJJM0mx_95oqwgXDpfzcRYfIWecXSmuzPXdbJYLJljOud4jYy5lljCp0n0yZoxliRFKj8hRjEvGlEx5dkhGUpg0NUyNyerVV2uIHXS-psNBTfGzwdZXWHdQ0tj4eggbWjfUy77d0Co4LG8o0IWPXWigW4QyfHg7YFA7WvhgF1j9_Lj2DmuLtICIjsaud5sTcjCHMuLpLo_J-8P92_Qpmb08Pk9vZ4kVOusSIY0zlsnUgsiYKgwHKeZaoxMaJjJzRqGeGHQMCj4Ha1RWADAlOFMapZPH5GK727Rh1WPs8spHi2UJNYY-5kIppbXQXA3o5Ra1bYixxXneDAKg3eSc5d-S8_-SB_x8t9wXFbo_-Neq_AIRjHlI</recordid><startdate>2020</startdate><enddate>2020</enddate><creator>Tascioglu, T</creator><creator>Karatay, M</creator><creator>Erdem, Y</creator><creator>Tekiner, A</creator><creator>Celik, H</creator><creator>Sahin, O</creator><creator>Sertbas, I</creator><creator>Bayar, M A</creator><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>7X8</scope></search><sort><creationdate>2020</creationdate><title>Simvastatin in an experimental spinal cord injury model: a histopathological and biochemical evidence based study</title><author>Tascioglu, T ; Karatay, M ; Erdem, Y ; Tekiner, A ; Celik, H ; Sahin, O ; Sertbas, I ; Bayar, M A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c286t-239d9c035ca2604b91a32f88ed28a736d94e879ed0ab1fac946baa0421048e3d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Disease Models, Animal</topic><topic>Neuroprotective Agents - pharmacology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Simvastatin - pharmacology</topic><topic>Spinal Cord</topic><topic>Spinal Cord Injuries - drug therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tascioglu, T</creatorcontrib><creatorcontrib>Karatay, M</creatorcontrib><creatorcontrib>Erdem, Y</creatorcontrib><creatorcontrib>Tekiner, A</creatorcontrib><creatorcontrib>Celik, H</creatorcontrib><creatorcontrib>Sahin, O</creatorcontrib><creatorcontrib>Sertbas, I</creatorcontrib><creatorcontrib>Bayar, M A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Bratislava Medical Journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tascioglu, T</au><au>Karatay, M</au><au>Erdem, Y</au><au>Tekiner, A</au><au>Celik, H</au><au>Sahin, O</au><au>Sertbas, I</au><au>Bayar, M A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Simvastatin in an experimental spinal cord injury model: a histopathological and biochemical evidence based study</atitle><jtitle>Bratislava Medical Journal</jtitle><addtitle>Bratisl Lek Listy</addtitle><date>2020</date><risdate>2020</risdate><volume>121</volume><issue>10</issue><spage>722</spage><epage>726</epage><pages>722-726</pages><issn>0006-9248</issn><issn>1336-0345</issn><eissn>1336-0345</eissn><abstract>In this study we tried to determine the possible neuroprotective effects of simvastatin in a rat model of Spinal Cord Injury (SCI) with the help of biochemical and histopathological tests.
Rats were divided into 5 groups:1) SCI control, 2) Sham operated, 3) SCI with 10 mg/kg intraperitoneal simvastatin, 4) SCI with 10 mg/kg oral simvastatin, 5) SCI with 10 mg/kg subcutaneous simvastatin. After the treatment period, all rats were sacrificed; their blood and spinal cord samples were taken for biochemical and histopathological assessment.
When the groups were compared in terms of oedema and inflammation status, the scores of groups receiving simvastatin were better than the control and sham groups (p = 0.001 and p = 0.038 respectively). When the 3 treatment groups (oral, intraperitoneal and subcutaneous simvastatin groups) were compared with each other in terms of inflammation, haemorrhage and oedema, there were no significant differences between groups (p = 0.112, p = 0.797 and p = 0.188, respectively). NSE and S100B levels were significantly lower in the treatment groups compared to the sham group (p = 0.039 and p = 0.004 respectively).
According to our biochemical and histopathological findings, simvastatin 10 mg/kg has a positive impact in the spinal cord injury model in rats, regardless of route of application (Tab. 1, Fig. 5, Ref. 26).</abstract><cop>Slovakia</cop><pmid>32955904</pmid><doi>10.4149/BLL_2020_118</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0006-9248 |
ispartof | Bratislava Medical Journal, 2020, Vol.121 (10), p.722-726 |
issn | 0006-9248 1336-0345 1336-0345 |
language | eng |
recordid | cdi_proquest_miscellaneous_2444882814 |
source | MEDLINE; EZB-FREE-00999 freely available EZB journals |
subjects | Animals Disease Models, Animal Neuroprotective Agents - pharmacology Rats Rats, Sprague-Dawley Simvastatin - pharmacology Spinal Cord Spinal Cord Injuries - drug therapy |
title | Simvastatin in an experimental spinal cord injury model: a histopathological and biochemical evidence based study |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-03T13%3A09%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Simvastatin%20in%20an%20experimental%20spinal%20cord%20injury%20model:%20a%20histopathological%20and%20biochemical%20evidence%20based%20study&rft.jtitle=Bratislava%20Medical%20Journal&rft.au=Tascioglu,%20T&rft.date=2020&rft.volume=121&rft.issue=10&rft.spage=722&rft.epage=726&rft.pages=722-726&rft.issn=0006-9248&rft.eissn=1336-0345&rft_id=info:doi/10.4149/BLL_2020_118&rft_dat=%3Cproquest_cross%3E2444882814%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2444882814&rft_id=info:pmid/32955904&rfr_iscdi=true |