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Dose-response Effects of Bleomycin on Inflammation and Pulmonary Fibrosis in Mice
Many studies have reported that bleomycin, anti-cancer drug, induces pulmonary fibrosis as a side effect. However, few investigations have focused on the dose-response effects of bleomycin on pulmonary fibrosis. Therefore, in the present study, we investigated the effects of different doses of bleom...
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Published in: | Toxicological research (Seoul) 2010, 26(3), , pp.217-222 |
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creator | Kim, S.N., KIT Jeongeup Campus, Jeongeup, Republic of Korea Lee, J.S., KIT Jeongeup Campus, Jeongeup, Republic of Korea Yang, H.S., KIT Jeongeup Campus, Jeongeup, Republic of Korea Cho, J.W., Korea Institute of Toxicology, Daejeon, Republic of Korea Kwon, S.J., KIT Jeongeup Campus, Jeongeup, Republic of Korea Kim, Y.B., Korea Institute of Toxicology, Daejeon, Republic of Korea Her, J.D., KIT Jeongeup Campus, Jeongeup, Republic of Korea Cho, K.H., KIT Jeongeup Campus, Jeongeup, Republic of Korea Song, C.W., KIT Jeongeup Campus, Jeongeup, Republic of Korea Lee, K.H., KIT Jeongeup Campus, Jeongeup, Republic of Korea |
description | Many studies have reported that bleomycin, anti-cancer drug, induces pulmonary fibrosis as a side effect. However, few investigations have focused on the dose-response effects of bleomycin on pulmonary fibrosis. Therefore, in the present study, we investigated the effects of different doses of bleomycin in male mice. ICR mice were given 3 consecutive doses of bleomycin: 1, 2, or 4 mg/kg in bleomycin-treated (BT) groups and saline only in vehicle control (VC) groups. The animals were sacrificed at 7 and 24 days postinstillation. The severity of pulmonary fibrosis was evaluated according to inflammatory cell count and lactate dehydrogenase (LDH) activity in the broncho alveolar lavage fluid (BALF), and lung tissues were histologically evaluated after hematoxylin and eosin (HnE), and Masson's trichrome staining. BT groups exhibited changed cellular profiles in BAL fluid compared to the VC group, which had an increased number of total cells, neutrophils, and lymphocytes and a modest increase in the number of macrophages at 7 days post-bleomycin instillation. Moreover, BT groups showed a dose-dependent increase in LDH levels and inflammatory cell counts. However, at 24 days after treatment, collagen deposition, interstitial thickening, and granulomatous lesions were observed in the alveolar spaces in addition to a decrease in inflammatory cells. These results indicate that pulmonary fibrosis induced by 4 mg/kg bleomycin was more severe than that induced by 1 or 2 mg/kg. These data will be utilized in experimental animal models and as basic data to evaluate therapeutic candidates through non-invasive monitoring using the pulmonary fibrosis mouse model established in this study. |
doi_str_mv | 10.5487/tr.2010.26.3.217 |
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However, few investigations have focused on the dose-response effects of bleomycin on pulmonary fibrosis. Therefore, in the present study, we investigated the effects of different doses of bleomycin in male mice. ICR mice were given 3 consecutive doses of bleomycin: 1, 2, or 4 mg/kg in bleomycin-treated (BT) groups and saline only in vehicle control (VC) groups. The animals were sacrificed at 7 and 24 days postinstillation. The severity of pulmonary fibrosis was evaluated according to inflammatory cell count and lactate dehydrogenase (LDH) activity in the broncho alveolar lavage fluid (BALF), and lung tissues were histologically evaluated after hematoxylin and eosin (HnE), and Masson's trichrome staining. BT groups exhibited changed cellular profiles in BAL fluid compared to the VC group, which had an increased number of total cells, neutrophils, and lymphocytes and a modest increase in the number of macrophages at 7 days post-bleomycin instillation. Moreover, BT groups showed a dose-dependent increase in LDH levels and inflammatory cell counts. However, at 24 days after treatment, collagen deposition, interstitial thickening, and granulomatous lesions were observed in the alveolar spaces in addition to a decrease in inflammatory cells. These results indicate that pulmonary fibrosis induced by 4 mg/kg bleomycin was more severe than that induced by 1 or 2 mg/kg. These data will be utilized in experimental animal models and as basic data to evaluate therapeutic candidates through non-invasive monitoring using the pulmonary fibrosis mouse model established in this study.</description><identifier>ISSN: 1976-8257</identifier><identifier>EISSN: 2234-2753</identifier><identifier>DOI: 10.5487/tr.2010.26.3.217</identifier><identifier>PMID: 24278527</identifier><language>eng</language><publisher>Singapore: 한국독성학회</publisher><subject>Biomedicine ; Bleomycin ; INFLAMACION ; INFLAMMATION ; Mouse model ; Pharmacology/Toxicology ; Pulmonary fibrosis ; 예방의학</subject><ispartof>한국독성학회지, 2010, 26(3), , pp.217-222</ispartof><rights>Korean Society of Toxicology 2010</rights><rights>Copyright ©2010, The Korean Society of Toxicology 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c589t-9604af97444b8ff5d1819f19a6dc8c518fe5b495b02e7dfcbf753a2b885428c3</citedby><cites>FETCH-LOGICAL-c589t-9604af97444b8ff5d1819f19a6dc8c518fe5b495b02e7dfcbf753a2b885428c3</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/PMC3834487/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834487/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24278527$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART001473954$$DAccess content in National Research Foundation of Korea (NRF)$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, S.N., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creatorcontrib><creatorcontrib>Lee, J.S., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creatorcontrib><creatorcontrib>Yang, H.S., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creatorcontrib><creatorcontrib>Cho, J.W., Korea Institute of Toxicology, Daejeon, Republic of Korea</creatorcontrib><creatorcontrib>Kwon, S.J., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creatorcontrib><creatorcontrib>Kim, Y.B., Korea Institute of Toxicology, Daejeon, Republic of Korea</creatorcontrib><creatorcontrib>Her, J.D., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creatorcontrib><creatorcontrib>Cho, K.H., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creatorcontrib><creatorcontrib>Song, C.W., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creatorcontrib><creatorcontrib>Lee, K.H., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creatorcontrib><title>Dose-response Effects of Bleomycin on Inflammation and Pulmonary Fibrosis in Mice</title><title>Toxicological research (Seoul)</title><addtitle>Toxicol Res</addtitle><addtitle>Toxicol Res</addtitle><description>Many studies have reported that bleomycin, anti-cancer drug, induces pulmonary fibrosis as a side effect. However, few investigations have focused on the dose-response effects of bleomycin on pulmonary fibrosis. Therefore, in the present study, we investigated the effects of different doses of bleomycin in male mice. ICR mice were given 3 consecutive doses of bleomycin: 1, 2, or 4 mg/kg in bleomycin-treated (BT) groups and saline only in vehicle control (VC) groups. The animals were sacrificed at 7 and 24 days postinstillation. The severity of pulmonary fibrosis was evaluated according to inflammatory cell count and lactate dehydrogenase (LDH) activity in the broncho alveolar lavage fluid (BALF), and lung tissues were histologically evaluated after hematoxylin and eosin (HnE), and Masson's trichrome staining. BT groups exhibited changed cellular profiles in BAL fluid compared to the VC group, which had an increased number of total cells, neutrophils, and lymphocytes and a modest increase in the number of macrophages at 7 days post-bleomycin instillation. Moreover, BT groups showed a dose-dependent increase in LDH levels and inflammatory cell counts. However, at 24 days after treatment, collagen deposition, interstitial thickening, and granulomatous lesions were observed in the alveolar spaces in addition to a decrease in inflammatory cells. These results indicate that pulmonary fibrosis induced by 4 mg/kg bleomycin was more severe than that induced by 1 or 2 mg/kg. These data will be utilized in experimental animal models and as basic data to evaluate therapeutic candidates through non-invasive monitoring using the pulmonary fibrosis mouse model established in this study.</description><subject>Biomedicine</subject><subject>Bleomycin</subject><subject>INFLAMACION</subject><subject>INFLAMMATION</subject><subject>Mouse model</subject><subject>Pharmacology/Toxicology</subject><subject>Pulmonary fibrosis</subject><subject>예방의학</subject><issn>1976-8257</issn><issn>2234-2753</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNp9kk1vEzEQhi0EolHonQtoL0hcNthee-29IPUjpRGFQpS75fXawe2uHdkbpP57Jt02gguWpdFo3nmsd8YIvSV4wZkUn8a0oBgSWi-qBSXiBZpRWrGSCl69RDPSiLqUlIsTdJrzHYbDmahx8xqdUEaF5FTM0M_LmG2ZbN7FkG2xdM6aMRfRFee9jcOD8aGIoVgF1-th0KOHRIeu-LHvhxh0eiiufJti9rkA5Tdv7Bv0yuk-29OnOEebq-Xm4rq8uf2yuji7KQ2XzVg2NWbaNYIx1krneEckaRxpdN0ZaTiRzvKWNbzF1IrOmdaBLU1bKTmj0lRz9HHChuTUvfEqav8Yt1HdJ3W23qwUwaSCO0efJ-lu3w62MzaMSfdql_wABh4b_60E_wswv1UlKwaTBgCeAAac5mTdsZdgddiF2qzVYReK1qpSsAtoef_3m8eG58mDgEyCDKWwtUndxX0KMLH_QT88ed4DznZeH7nfby-XmHBCiDgYfjfpnI5Kb5PP6usaUAT-QCVp9QcIUqpi</recordid><startdate>20100901</startdate><enddate>20100901</enddate><creator>Kim, S.N., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creator><creator>Lee, J.S., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creator><creator>Yang, H.S., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creator><creator>Cho, J.W., Korea Institute of Toxicology, Daejeon, Republic of Korea</creator><creator>Kwon, S.J., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creator><creator>Kim, Y.B., Korea Institute of Toxicology, Daejeon, Republic of Korea</creator><creator>Her, J.D., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creator><creator>Cho, K.H., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creator><creator>Song, C.W., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creator><creator>Lee, K.H., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creator><general>한국독성학회</general><general>Springer Singapore</general><general>The Korean Society of Toxicology</general><scope>FBQ</scope><scope>DBRKI</scope><scope>TDB</scope><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><scope>ACYCR</scope></search><sort><creationdate>20100901</creationdate><title>Dose-response Effects of Bleomycin on Inflammation and Pulmonary Fibrosis in Mice</title><author>Kim, S.N., KIT Jeongeup Campus, Jeongeup, Republic of Korea ; Lee, J.S., KIT Jeongeup Campus, Jeongeup, Republic of Korea ; Yang, H.S., KIT Jeongeup Campus, Jeongeup, Republic of Korea ; Cho, J.W., Korea Institute of Toxicology, Daejeon, Republic of Korea ; Kwon, S.J., KIT Jeongeup Campus, Jeongeup, Republic of Korea ; Kim, Y.B., Korea Institute of Toxicology, Daejeon, Republic of Korea ; Her, J.D., KIT Jeongeup Campus, Jeongeup, Republic of Korea ; Cho, K.H., KIT Jeongeup Campus, Jeongeup, Republic of Korea ; Song, C.W., KIT Jeongeup Campus, Jeongeup, Republic of Korea ; Lee, K.H., KIT Jeongeup Campus, Jeongeup, Republic of Korea</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c589t-9604af97444b8ff5d1819f19a6dc8c518fe5b495b02e7dfcbf753a2b885428c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Biomedicine</topic><topic>Bleomycin</topic><topic>INFLAMACION</topic><topic>INFLAMMATION</topic><topic>Mouse model</topic><topic>Pharmacology/Toxicology</topic><topic>Pulmonary fibrosis</topic><topic>예방의학</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, S.N., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creatorcontrib><creatorcontrib>Lee, J.S., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creatorcontrib><creatorcontrib>Yang, H.S., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creatorcontrib><creatorcontrib>Cho, J.W., Korea Institute of Toxicology, Daejeon, Republic of Korea</creatorcontrib><creatorcontrib>Kwon, S.J., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creatorcontrib><creatorcontrib>Kim, Y.B., Korea Institute of Toxicology, Daejeon, Republic of Korea</creatorcontrib><creatorcontrib>Her, J.D., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creatorcontrib><creatorcontrib>Cho, K.H., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creatorcontrib><creatorcontrib>Song, C.W., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creatorcontrib><creatorcontrib>Lee, K.H., KIT Jeongeup Campus, Jeongeup, Republic of Korea</creatorcontrib><collection>AGRIS</collection><collection>DBPIA - 디비피아</collection><collection>Korean Database (DBpia)</collection><collection>SpringerOpen</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Korean Citation Index</collection><jtitle>Toxicological research (Seoul)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, S.N., KIT Jeongeup Campus, Jeongeup, Republic of Korea</au><au>Lee, J.S., KIT Jeongeup Campus, Jeongeup, Republic of Korea</au><au>Yang, H.S., KIT Jeongeup Campus, Jeongeup, Republic of Korea</au><au>Cho, J.W., Korea Institute of Toxicology, Daejeon, Republic of Korea</au><au>Kwon, S.J., KIT Jeongeup Campus, Jeongeup, Republic of Korea</au><au>Kim, Y.B., Korea Institute of Toxicology, Daejeon, Republic of Korea</au><au>Her, J.D., KIT Jeongeup Campus, Jeongeup, Republic of Korea</au><au>Cho, K.H., KIT Jeongeup Campus, Jeongeup, Republic of Korea</au><au>Song, C.W., KIT Jeongeup Campus, Jeongeup, Republic of Korea</au><au>Lee, K.H., KIT Jeongeup Campus, Jeongeup, Republic of Korea</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dose-response Effects of Bleomycin on Inflammation and Pulmonary Fibrosis in Mice</atitle><jtitle>Toxicological research (Seoul)</jtitle><stitle>Toxicol Res</stitle><addtitle>Toxicol Res</addtitle><date>2010-09-01</date><risdate>2010</risdate><volume>26</volume><issue>3</issue><spage>217</spage><epage>222</epage><pages>217-222</pages><issn>1976-8257</issn><eissn>2234-2753</eissn><abstract>Many studies have reported that bleomycin, anti-cancer drug, induces pulmonary fibrosis as a side effect. However, few investigations have focused on the dose-response effects of bleomycin on pulmonary fibrosis. Therefore, in the present study, we investigated the effects of different doses of bleomycin in male mice. ICR mice were given 3 consecutive doses of bleomycin: 1, 2, or 4 mg/kg in bleomycin-treated (BT) groups and saline only in vehicle control (VC) groups. The animals were sacrificed at 7 and 24 days postinstillation. The severity of pulmonary fibrosis was evaluated according to inflammatory cell count and lactate dehydrogenase (LDH) activity in the broncho alveolar lavage fluid (BALF), and lung tissues were histologically evaluated after hematoxylin and eosin (HnE), and Masson's trichrome staining. BT groups exhibited changed cellular profiles in BAL fluid compared to the VC group, which had an increased number of total cells, neutrophils, and lymphocytes and a modest increase in the number of macrophages at 7 days post-bleomycin instillation. Moreover, BT groups showed a dose-dependent increase in LDH levels and inflammatory cell counts. However, at 24 days after treatment, collagen deposition, interstitial thickening, and granulomatous lesions were observed in the alveolar spaces in addition to a decrease in inflammatory cells. These results indicate that pulmonary fibrosis induced by 4 mg/kg bleomycin was more severe than that induced by 1 or 2 mg/kg. These data will be utilized in experimental animal models and as basic data to evaluate therapeutic candidates through non-invasive monitoring using the pulmonary fibrosis mouse model established in this study.</abstract><cop>Singapore</cop><pub>한국독성학회</pub><pmid>24278527</pmid><doi>10.5487/tr.2010.26.3.217</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biomedicine Bleomycin INFLAMACION INFLAMMATION Mouse model Pharmacology/Toxicology Pulmonary fibrosis 예방의학 |
title | Dose-response Effects of Bleomycin on Inflammation and Pulmonary Fibrosis in Mice |
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