Effects of an anticoagulant and a lipid-lowering agent on the prevention of steroid-induced osteonecrosis in rabbits

Summary This study was designed to evaluate the effects of the combined treatment with an anti‐coagulant (enoxaparin) agent and a lipid‐lowering agent (lovastatin) on prevention or decrease in the occurrence of steroid‐induced osteonecrosis in rabbits. A total of 112 rabbits, which were injected int...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:International journal of experimental pathology 2010-06, Vol.91 (3), p.235-243
Hauptverfasser: Kang, Pengde, Gao, Hong, Pei, Fuxing, Shen, Bin, Yang, Jing, Zhou, Zongke
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 243
container_issue 3
container_start_page 235
container_title International journal of experimental pathology
container_volume 91
creator Kang, Pengde
Gao, Hong
Pei, Fuxing
Shen, Bin
Yang, Jing
Zhou, Zongke
description Summary This study was designed to evaluate the effects of the combined treatment with an anti‐coagulant (enoxaparin) agent and a lipid‐lowering agent (lovastatin) on prevention or decrease in the occurrence of steroid‐induced osteonecrosis in rabbits. A total of 112 rabbits, which were injected intramuscularly with 20 mg/kg of methylprednisolone acetate were divided into four groups and treated as follows: one group received enoxaparin combined with lovastatin (EL; n = 30), another received enoxaparin alone (EA; n = 28), another received lovastatin alone (LA; n = 28) and the last received no treatment (non‐prophylactic; NP, n = 26). Haematological examination for serum lipid levels and prothrombin time was carried out and both femora and humeri were examined histopathologically for the presence of osteonecrosis (ON) before injection and at 2, 4, 8 and 12 weeks after the injection. The incidence of ON in the EL group (15%) was significantly lower than that observed in the NP group (68%). The incidence in the EA and LA groups was also significantly lower than that in the NP group (31%, 35%vs. 68%). The fat cell sizes of the bone marrow in both EL (46.49 ± 1.27 μm) and LA (50.8 ± 2.31 μm) groups were lower than in the NP group (59.89 ± 6.33 μm). The prothrombin time was prolonged and plasma lipid levels were reduced in the EL group during the study. Combination treatment with an anti‐coagulant agent and a lipid‐lowering agent can reduce the incidence of steroid‐induced ON in rabbits. Future evaluation in clinical practice is necessary.
doi_str_mv 10.1111/j.1365-2613.2010.00705.x
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2884091</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>745938408</sourcerecordid><originalsourceid>FETCH-LOGICAL-c6085-5fd4ed069510aaccfccb1db471c248a3bc64049e0652feebd0bfc31a559ff4e73</originalsourceid><addsrcrecordid>eNqNUk1vEzEQtRCIhsJfQL5x2mCv1_shISRaQimKgAMfEpeR1ztOHTbr1N5t03_PhJQIbliWPON573nsZ8a4FHNJ4-V6LlWps7yUap4L2hWiEnq-e8Bmx8JDNhONbrKmrNQJe5LSWgipclk9Zie5UFoVuZ6xceEc2jHx4LgZaI7eBrOaeooo67jhvd_6LuvDLUY_rLhZIZXCwMcr5NuIN5R6SkkgjRgDYf3QTRY7HmgjDGhjSD5xP_Bo2taP6Sl75Eyf8Nn9esq-vlt8OX-fLT9dXJ6_WWa2FLXOtOsK7ETZaCmMsdZZ28quLSpp86I2qrVlIYoGRalzh9h2onVWSaN141yBlTplrw-626ndYGep02h62Ea_MfEOgvHwb2XwV7AKN5DXdSEaSQIv7gViuJ4wjbDxyWJPr4NhSlAVulEErQlZH5D7y6aI7niKFLD3DNawtwb21sDeM_jtGeyI-vzvLo_EPyYR4NUBcOt7vPtvYbhcfKaA6NmB7smO3ZFu4k-gr1Fp-P7xAqoP386aH8u3cKZ-ARj6uGc</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>745938408</pqid></control><display><type>article</type><title>Effects of an anticoagulant and a lipid-lowering agent on the prevention of steroid-induced osteonecrosis in rabbits</title><source>Wiley-Blackwell Journals</source><source>PubMed Central (Open Access)</source><source>MEDLINE</source><creator>Kang, Pengde ; Gao, Hong ; Pei, Fuxing ; Shen, Bin ; Yang, Jing ; Zhou, Zongke</creator><creatorcontrib>Kang, Pengde ; Gao, Hong ; Pei, Fuxing ; Shen, Bin ; Yang, Jing ; Zhou, Zongke</creatorcontrib><description>Summary This study was designed to evaluate the effects of the combined treatment with an anti‐coagulant (enoxaparin) agent and a lipid‐lowering agent (lovastatin) on prevention or decrease in the occurrence of steroid‐induced osteonecrosis in rabbits. A total of 112 rabbits, which were injected intramuscularly with 20 mg/kg of methylprednisolone acetate were divided into four groups and treated as follows: one group received enoxaparin combined with lovastatin (EL; n = 30), another received enoxaparin alone (EA; n = 28), another received lovastatin alone (LA; n = 28) and the last received no treatment (non‐prophylactic; NP, n = 26). Haematological examination for serum lipid levels and prothrombin time was carried out and both femora and humeri were examined histopathologically for the presence of osteonecrosis (ON) before injection and at 2, 4, 8 and 12 weeks after the injection. The incidence of ON in the EL group (15%) was significantly lower than that observed in the NP group (68%). The incidence in the EA and LA groups was also significantly lower than that in the NP group (31%, 35%vs. 68%). The fat cell sizes of the bone marrow in both EL (46.49 ± 1.27 μm) and LA (50.8 ± 2.31 μm) groups were lower than in the NP group (59.89 ± 6.33 μm). The prothrombin time was prolonged and plasma lipid levels were reduced in the EL group during the study. Combination treatment with an anti‐coagulant agent and a lipid‐lowering agent can reduce the incidence of steroid‐induced ON in rabbits. Future evaluation in clinical practice is necessary.</description><identifier>ISSN: 0959-9673</identifier><identifier>EISSN: 1365-2613</identifier><identifier>DOI: 10.1111/j.1365-2613.2010.00705.x</identifier><identifier>PMID: 20353425</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Animals ; Anticholesteremic Agents - therapeutic use ; Anticoagulants - therapeutic use ; Bone Marrow Cells - pathology ; Cholesterol - blood ; corticosteroid ; enoxaparin ; Enoxaparin - therapeutic use ; Fatty Acids, Nonesterified - blood ; Glucocorticoids - adverse effects ; lovastatin ; Lovastatin - therapeutic use ; Male ; Methylprednisolone - adverse effects ; Original ; osteonecrosis ; Osteonecrosis - chemically induced ; Osteonecrosis - pathology ; Osteonecrosis - prevention &amp; control ; Rabbits ; Triglycerides - blood</subject><ispartof>International journal of experimental pathology, 2010-06, Vol.91 (3), p.235-243</ispartof><rights>2010 The Authors. Journal compilation © 2010 Blackwell Publishing Ltd</rights><rights>Journal compilation © 2010 Blackwell Publishing Ltd 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6085-5fd4ed069510aaccfccb1db471c248a3bc64049e0652feebd0bfc31a559ff4e73</citedby><cites>FETCH-LOGICAL-c6085-5fd4ed069510aaccfccb1db471c248a3bc64049e0652feebd0bfc31a559ff4e73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2884091/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2884091/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,1417,27924,27925,45574,45575,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20353425$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kang, Pengde</creatorcontrib><creatorcontrib>Gao, Hong</creatorcontrib><creatorcontrib>Pei, Fuxing</creatorcontrib><creatorcontrib>Shen, Bin</creatorcontrib><creatorcontrib>Yang, Jing</creatorcontrib><creatorcontrib>Zhou, Zongke</creatorcontrib><title>Effects of an anticoagulant and a lipid-lowering agent on the prevention of steroid-induced osteonecrosis in rabbits</title><title>International journal of experimental pathology</title><addtitle>Int J Exp Pathol</addtitle><description>Summary This study was designed to evaluate the effects of the combined treatment with an anti‐coagulant (enoxaparin) agent and a lipid‐lowering agent (lovastatin) on prevention or decrease in the occurrence of steroid‐induced osteonecrosis in rabbits. A total of 112 rabbits, which were injected intramuscularly with 20 mg/kg of methylprednisolone acetate were divided into four groups and treated as follows: one group received enoxaparin combined with lovastatin (EL; n = 30), another received enoxaparin alone (EA; n = 28), another received lovastatin alone (LA; n = 28) and the last received no treatment (non‐prophylactic; NP, n = 26). Haematological examination for serum lipid levels and prothrombin time was carried out and both femora and humeri were examined histopathologically for the presence of osteonecrosis (ON) before injection and at 2, 4, 8 and 12 weeks after the injection. The incidence of ON in the EL group (15%) was significantly lower than that observed in the NP group (68%). The incidence in the EA and LA groups was also significantly lower than that in the NP group (31%, 35%vs. 68%). The fat cell sizes of the bone marrow in both EL (46.49 ± 1.27 μm) and LA (50.8 ± 2.31 μm) groups were lower than in the NP group (59.89 ± 6.33 μm). The prothrombin time was prolonged and plasma lipid levels were reduced in the EL group during the study. Combination treatment with an anti‐coagulant agent and a lipid‐lowering agent can reduce the incidence of steroid‐induced ON in rabbits. Future evaluation in clinical practice is necessary.</description><subject>Animals</subject><subject>Anticholesteremic Agents - therapeutic use</subject><subject>Anticoagulants - therapeutic use</subject><subject>Bone Marrow Cells - pathology</subject><subject>Cholesterol - blood</subject><subject>corticosteroid</subject><subject>enoxaparin</subject><subject>Enoxaparin - therapeutic use</subject><subject>Fatty Acids, Nonesterified - blood</subject><subject>Glucocorticoids - adverse effects</subject><subject>lovastatin</subject><subject>Lovastatin - therapeutic use</subject><subject>Male</subject><subject>Methylprednisolone - adverse effects</subject><subject>Original</subject><subject>osteonecrosis</subject><subject>Osteonecrosis - chemically induced</subject><subject>Osteonecrosis - pathology</subject><subject>Osteonecrosis - prevention &amp; control</subject><subject>Rabbits</subject><subject>Triglycerides - blood</subject><issn>0959-9673</issn><issn>1365-2613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNUk1vEzEQtRCIhsJfQL5x2mCv1_shISRaQimKgAMfEpeR1ztOHTbr1N5t03_PhJQIbliWPON573nsZ8a4FHNJ4-V6LlWps7yUap4L2hWiEnq-e8Bmx8JDNhONbrKmrNQJe5LSWgipclk9Zie5UFoVuZ6xceEc2jHx4LgZaI7eBrOaeooo67jhvd_6LuvDLUY_rLhZIZXCwMcr5NuIN5R6SkkgjRgDYf3QTRY7HmgjDGhjSD5xP_Bo2taP6Sl75Eyf8Nn9esq-vlt8OX-fLT9dXJ6_WWa2FLXOtOsK7ETZaCmMsdZZ28quLSpp86I2qrVlIYoGRalzh9h2onVWSaN141yBlTplrw-626ndYGep02h62Ea_MfEOgvHwb2XwV7AKN5DXdSEaSQIv7gViuJ4wjbDxyWJPr4NhSlAVulEErQlZH5D7y6aI7niKFLD3DNawtwb21sDeM_jtGeyI-vzvLo_EPyYR4NUBcOt7vPtvYbhcfKaA6NmB7smO3ZFu4k-gr1Fp-P7xAqoP386aH8u3cKZ-ARj6uGc</recordid><startdate>201006</startdate><enddate>201006</enddate><creator>Kang, Pengde</creator><creator>Gao, Hong</creator><creator>Pei, Fuxing</creator><creator>Shen, Bin</creator><creator>Yang, Jing</creator><creator>Zhou, Zongke</creator><general>Blackwell Publishing Ltd</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>7QP</scope><scope>5PM</scope></search><sort><creationdate>201006</creationdate><title>Effects of an anticoagulant and a lipid-lowering agent on the prevention of steroid-induced osteonecrosis in rabbits</title><author>Kang, Pengde ; Gao, Hong ; Pei, Fuxing ; Shen, Bin ; Yang, Jing ; Zhou, Zongke</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6085-5fd4ed069510aaccfccb1db471c248a3bc64049e0652feebd0bfc31a559ff4e73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Anticholesteremic Agents - therapeutic use</topic><topic>Anticoagulants - therapeutic use</topic><topic>Bone Marrow Cells - pathology</topic><topic>Cholesterol - blood</topic><topic>corticosteroid</topic><topic>enoxaparin</topic><topic>Enoxaparin - therapeutic use</topic><topic>Fatty Acids, Nonesterified - blood</topic><topic>Glucocorticoids - adverse effects</topic><topic>lovastatin</topic><topic>Lovastatin - therapeutic use</topic><topic>Male</topic><topic>Methylprednisolone - adverse effects</topic><topic>Original</topic><topic>osteonecrosis</topic><topic>Osteonecrosis - chemically induced</topic><topic>Osteonecrosis - pathology</topic><topic>Osteonecrosis - prevention &amp; control</topic><topic>Rabbits</topic><topic>Triglycerides - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kang, Pengde</creatorcontrib><creatorcontrib>Gao, Hong</creatorcontrib><creatorcontrib>Pei, Fuxing</creatorcontrib><creatorcontrib>Shen, Bin</creatorcontrib><creatorcontrib>Yang, Jing</creatorcontrib><creatorcontrib>Zhou, Zongke</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>Calcium &amp; Calcified Tissue Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of experimental pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kang, Pengde</au><au>Gao, Hong</au><au>Pei, Fuxing</au><au>Shen, Bin</au><au>Yang, Jing</au><au>Zhou, Zongke</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of an anticoagulant and a lipid-lowering agent on the prevention of steroid-induced osteonecrosis in rabbits</atitle><jtitle>International journal of experimental pathology</jtitle><addtitle>Int J Exp Pathol</addtitle><date>2010-06</date><risdate>2010</risdate><volume>91</volume><issue>3</issue><spage>235</spage><epage>243</epage><pages>235-243</pages><issn>0959-9673</issn><eissn>1365-2613</eissn><abstract>Summary This study was designed to evaluate the effects of the combined treatment with an anti‐coagulant (enoxaparin) agent and a lipid‐lowering agent (lovastatin) on prevention or decrease in the occurrence of steroid‐induced osteonecrosis in rabbits. A total of 112 rabbits, which were injected intramuscularly with 20 mg/kg of methylprednisolone acetate were divided into four groups and treated as follows: one group received enoxaparin combined with lovastatin (EL; n = 30), another received enoxaparin alone (EA; n = 28), another received lovastatin alone (LA; n = 28) and the last received no treatment (non‐prophylactic; NP, n = 26). Haematological examination for serum lipid levels and prothrombin time was carried out and both femora and humeri were examined histopathologically for the presence of osteonecrosis (ON) before injection and at 2, 4, 8 and 12 weeks after the injection. The incidence of ON in the EL group (15%) was significantly lower than that observed in the NP group (68%). The incidence in the EA and LA groups was also significantly lower than that in the NP group (31%, 35%vs. 68%). The fat cell sizes of the bone marrow in both EL (46.49 ± 1.27 μm) and LA (50.8 ± 2.31 μm) groups were lower than in the NP group (59.89 ± 6.33 μm). The prothrombin time was prolonged and plasma lipid levels were reduced in the EL group during the study. Combination treatment with an anti‐coagulant agent and a lipid‐lowering agent can reduce the incidence of steroid‐induced ON in rabbits. Future evaluation in clinical practice is necessary.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>20353425</pmid><doi>10.1111/j.1365-2613.2010.00705.x</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0959-9673
ispartof International journal of experimental pathology, 2010-06, Vol.91 (3), p.235-243
issn 0959-9673
1365-2613
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2884091
source Wiley-Blackwell Journals; PubMed Central (Open Access); MEDLINE
subjects Animals
Anticholesteremic Agents - therapeutic use
Anticoagulants - therapeutic use
Bone Marrow Cells - pathology
Cholesterol - blood
corticosteroid
enoxaparin
Enoxaparin - therapeutic use
Fatty Acids, Nonesterified - blood
Glucocorticoids - adverse effects
lovastatin
Lovastatin - therapeutic use
Male
Methylprednisolone - adverse effects
Original
osteonecrosis
Osteonecrosis - chemically induced
Osteonecrosis - pathology
Osteonecrosis - prevention & control
Rabbits
Triglycerides - blood
title Effects of an anticoagulant and a lipid-lowering agent on the prevention of steroid-induced osteonecrosis in rabbits
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T08%3A38%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Effects%20of%20an%20anticoagulant%20and%20a%20lipid-lowering%20agent%20on%20the%20prevention%20of%20steroid-induced%20osteonecrosis%20in%20rabbits&rft.jtitle=International%20journal%20of%20experimental%20pathology&rft.au=Kang,%20Pengde&rft.date=2010-06&rft.volume=91&rft.issue=3&rft.spage=235&rft.epage=243&rft.pages=235-243&rft.issn=0959-9673&rft.eissn=1365-2613&rft_id=info:doi/10.1111/j.1365-2613.2010.00705.x&rft_dat=%3Cproquest_pubme%3E745938408%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=745938408&rft_id=info:pmid/20353425&rfr_iscdi=true