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Effects of polymyxin B on clinical signs, serum TNF-α, haptoglobin and plasma lactate concentrations in experimental endotoxaemia in sheep
The experiment evaluated the effects of intravenous administration of polymyxin B on experimental endotoxaemia in sheep.Material and Methods Twenty clinically healthy fat-tailed sheep were randomly divided into: a group treated with 6,000 U/kg of polymyxin B, a group at 12,000 U/kg, and positive and...
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Published in: | Journal of veterinary research 2018-03, Vol.62 (1), p.79-85 |
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description | The experiment evaluated the effects of intravenous administration of polymyxin B on experimental endotoxaemia in sheep.Material and Methods Twenty clinically healthy fat-tailed sheep were randomly divided into: a group treated with 6,000 U/kg of polymyxin B, a group at 12,000 U/kg, and positive and negative controls. Endotoxaemia was induced by intravenous administration of lipopolysaccharide (LPS) from E. coli serotype O55:B5 at 0.5 μg/kg. polymyxin was infused intravenously along with 2.5 L of isotonic intravenous fluids at 20 mL/kg/h. The positive control group received LPS and 2.5 L of isotonic fluids, the negatives receiving just 2.5 L of isotonic fluids. Clinical signs were evaluated before and at 1.5, 3, 4.5, 6, 24, and 48 h after LPS administration. Blood was also sampled at the denoted hours and serum haptoglobin, tumour necrosis factor-α (TNF-α), and plasma lactate concentrations were assayed.Results The serum concentration of TNF-α in the positive control group increased significantly up to 48 h after LPS administration. The concentration of TNF-α was significantly different from those of the polymyxin B and positive control groups from 3 to 48 h; also, the concentrations of haptoglobin at different times in the polymyxin groups were lower than those of the positive control group and were significant at hours 3 to 48 (P < 0.05). Following the LPS administration, haptoglobin and TNF-α concentrations changed without significant difference between the two polymyxin B groups.Conclusion Polymyxin B (6,000 U/kg) restrained blood lactate concentrations. Furthermore, it significantly improved the clinical signs in endotoxaemic animals, including rectal temperature and heart and respiratory rates. Polymyxin B may be an antiendotoxic in fat-tailed sheep. |
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Endotoxaemia was induced by intravenous administration of lipopolysaccharide (LPS) from E. coli serotype O55:B5 at 0.5 μg/kg. polymyxin was infused intravenously along with 2.5 L of isotonic intravenous fluids at 20 mL/kg/h. The positive control group received LPS and 2.5 L of isotonic fluids, the negatives receiving just 2.5 L of isotonic fluids. Clinical signs were evaluated before and at 1.5, 3, 4.5, 6, 24, and 48 h after LPS administration. Blood was also sampled at the denoted hours and serum haptoglobin, tumour necrosis factor-α (TNF-α), and plasma lactate concentrations were assayed.Results The serum concentration of TNF-α in the positive control group increased significantly up to 48 h after LPS administration. The concentration of TNF-α was significantly different from those of the polymyxin B and positive control groups from 3 to 48 h; also, the concentrations of haptoglobin at different times in the polymyxin groups were lower than those of the positive control group and were significant at hours 3 to 48 (P < 0.05). Following the LPS administration, haptoglobin and TNF-α concentrations changed without significant difference between the two polymyxin B groups.Conclusion Polymyxin B (6,000 U/kg) restrained blood lactate concentrations. Furthermore, it significantly improved the clinical signs in endotoxaemic animals, including rectal temperature and heart and respiratory rates. Polymyxin B may be an antiendotoxic in fat-tailed sheep.</description><identifier>ISSN: 2450-8608</identifier><identifier>ISSN: 2450-7393</identifier><identifier>EISSN: 2450-8608</identifier><identifier>DOI: 10.2478/jvetres-2018-0011</identifier><language>eng</language><publisher>Pulawy: Sciendo</publisher><subject>clinical signs ; Haptoglobin ; inflammatory biomarkers ; Intravenous administration ; Lactic acid ; lipopolysaccharide ; Lipopolysaccharides ; Polymyxin B ; Sheep ; Tumor necrosis factor-TNF ; Tumor necrosis factor-α ; Tumors</subject><ispartof>Journal of veterinary research, 2018-03, Vol.62 (1), p.79-85</ispartof><rights>2018. This work is published under http://creativecommons.org/licenses/by-nc-nd/3.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c367t-5adb7e600564a32706727619693c7b04d6f574cfce9ee3f99411370403d89dba3</citedby><cites>FETCH-LOGICAL-c367t-5adb7e600564a32706727619693c7b04d6f574cfce9ee3f99411370403d89dba3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2544556278?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,777,781,25734,27905,27906,36993,44571</link.rule.ids></links><search><creatorcontrib>Hajimohammadi, Ali</creatorcontrib><creatorcontrib>Badiei, Khalil</creatorcontrib><creatorcontrib>Kheibari, Parviz</creatorcontrib><creatorcontrib>Pourjafar, Meherdad</creatorcontrib><creatorcontrib>Chalmeh, Aliasghar</creatorcontrib><title>Effects of polymyxin B on clinical signs, serum TNF-α, haptoglobin and plasma lactate concentrations in experimental endotoxaemia in sheep</title><title>Journal of veterinary research</title><description>The experiment evaluated the effects of intravenous administration of polymyxin B on experimental endotoxaemia in sheep.Material and Methods Twenty clinically healthy fat-tailed sheep were randomly divided into: a group treated with 6,000 U/kg of polymyxin B, a group at 12,000 U/kg, and positive and negative controls. Endotoxaemia was induced by intravenous administration of lipopolysaccharide (LPS) from E. coli serotype O55:B5 at 0.5 μg/kg. polymyxin was infused intravenously along with 2.5 L of isotonic intravenous fluids at 20 mL/kg/h. The positive control group received LPS and 2.5 L of isotonic fluids, the negatives receiving just 2.5 L of isotonic fluids. Clinical signs were evaluated before and at 1.5, 3, 4.5, 6, 24, and 48 h after LPS administration. Blood was also sampled at the denoted hours and serum haptoglobin, tumour necrosis factor-α (TNF-α), and plasma lactate concentrations were assayed.Results The serum concentration of TNF-α in the positive control group increased significantly up to 48 h after LPS administration. The concentration of TNF-α was significantly different from those of the polymyxin B and positive control groups from 3 to 48 h; also, the concentrations of haptoglobin at different times in the polymyxin groups were lower than those of the positive control group and were significant at hours 3 to 48 (P < 0.05). Following the LPS administration, haptoglobin and TNF-α concentrations changed without significant difference between the two polymyxin B groups.Conclusion Polymyxin B (6,000 U/kg) restrained blood lactate concentrations. Furthermore, it significantly improved the clinical signs in endotoxaemic animals, including rectal temperature and heart and respiratory rates. Polymyxin B may be an antiendotoxic in fat-tailed sheep.</description><subject>clinical signs</subject><subject>Haptoglobin</subject><subject>inflammatory biomarkers</subject><subject>Intravenous administration</subject><subject>Lactic acid</subject><subject>lipopolysaccharide</subject><subject>Lipopolysaccharides</subject><subject>Polymyxin B</subject><subject>Sheep</subject><subject>Tumor necrosis factor-TNF</subject><subject>Tumor necrosis factor-α</subject><subject>Tumors</subject><issn>2450-8608</issn><issn>2450-7393</issn><issn>2450-8608</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1kU1uFDEQhVsIJKIkB2BniW0a7LbbPxskiBKIFMEmrK1qu3rSox67sT0wc4achotwJjyZCNiwqlLV916V9JrmFaNvOqH02_V3LAlz21GmW0oZe9acdKKnrZZUP_-nf9mc57ymFVFcGcZPmoercURXMokjWeK83-x3UyAfSAzEzVOYHMwkT6uQL0jGtN2Qu8_X7a-fF-QelhJXcxwqDsGTZYa8ATKDK1CQuBgchpKgTDFkUiHcLZimTR1WSww-lrgD3ExwWOZ7xOWseTHCnPH8qZ42X6-v7i4_tbdfPt5cvr9tHZeqtD34QaGktJcCeKeoVJ2SzEjDnRqo8HLslXCjQ4PIR2MEY1xRQbnXxg_AT5ubo6-PsLZLfQrS3kaY7OMgppWFVCY3ozXokAsjtJBMcBy0RqW1RxCDNzD21ev10WtJ8dsWc7HruE2hvm-7Xoi-l53SlWJHyqWYc8Lxz1VG7SFC-xShPURoDxFWzbuj5gfMBZPHVdrua_P3wH-1smPK8N_ZOKe2</recordid><startdate>20180330</startdate><enddate>20180330</enddate><creator>Hajimohammadi, Ali</creator><creator>Badiei, Khalil</creator><creator>Kheibari, Parviz</creator><creator>Pourjafar, Meherdad</creator><creator>Chalmeh, Aliasghar</creator><general>Sciendo</general><general>De Gruyter Poland</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>DOA</scope></search><sort><creationdate>20180330</creationdate><title>Effects of polymyxin B on clinical signs, serum TNF-α, haptoglobin and plasma lactate concentrations in experimental endotoxaemia in sheep</title><author>Hajimohammadi, Ali ; Badiei, Khalil ; Kheibari, Parviz ; Pourjafar, Meherdad ; Chalmeh, Aliasghar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c367t-5adb7e600564a32706727619693c7b04d6f574cfce9ee3f99411370403d89dba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>clinical signs</topic><topic>Haptoglobin</topic><topic>inflammatory biomarkers</topic><topic>Intravenous administration</topic><topic>Lactic acid</topic><topic>lipopolysaccharide</topic><topic>Lipopolysaccharides</topic><topic>Polymyxin B</topic><topic>Sheep</topic><topic>Tumor necrosis factor-TNF</topic><topic>Tumor necrosis factor-α</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hajimohammadi, Ali</creatorcontrib><creatorcontrib>Badiei, Khalil</creatorcontrib><creatorcontrib>Kheibari, Parviz</creatorcontrib><creatorcontrib>Pourjafar, Meherdad</creatorcontrib><creatorcontrib>Chalmeh, Aliasghar</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</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>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content (ProQuest)</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 China</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of veterinary research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hajimohammadi, Ali</au><au>Badiei, Khalil</au><au>Kheibari, Parviz</au><au>Pourjafar, Meherdad</au><au>Chalmeh, Aliasghar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of polymyxin B on clinical signs, serum TNF-α, haptoglobin and plasma lactate concentrations in experimental endotoxaemia in sheep</atitle><jtitle>Journal of veterinary research</jtitle><date>2018-03-30</date><risdate>2018</risdate><volume>62</volume><issue>1</issue><spage>79</spage><epage>85</epage><pages>79-85</pages><issn>2450-8608</issn><issn>2450-7393</issn><eissn>2450-8608</eissn><abstract>The experiment evaluated the effects of intravenous administration of polymyxin B on experimental endotoxaemia in sheep.Material and Methods Twenty clinically healthy fat-tailed sheep were randomly divided into: a group treated with 6,000 U/kg of polymyxin B, a group at 12,000 U/kg, and positive and negative controls. Endotoxaemia was induced by intravenous administration of lipopolysaccharide (LPS) from E. coli serotype O55:B5 at 0.5 μg/kg. polymyxin was infused intravenously along with 2.5 L of isotonic intravenous fluids at 20 mL/kg/h. The positive control group received LPS and 2.5 L of isotonic fluids, the negatives receiving just 2.5 L of isotonic fluids. Clinical signs were evaluated before and at 1.5, 3, 4.5, 6, 24, and 48 h after LPS administration. Blood was also sampled at the denoted hours and serum haptoglobin, tumour necrosis factor-α (TNF-α), and plasma lactate concentrations were assayed.Results The serum concentration of TNF-α in the positive control group increased significantly up to 48 h after LPS administration. The concentration of TNF-α was significantly different from those of the polymyxin B and positive control groups from 3 to 48 h; also, the concentrations of haptoglobin at different times in the polymyxin groups were lower than those of the positive control group and were significant at hours 3 to 48 (P < 0.05). Following the LPS administration, haptoglobin and TNF-α concentrations changed without significant difference between the two polymyxin B groups.Conclusion Polymyxin B (6,000 U/kg) restrained blood lactate concentrations. Furthermore, it significantly improved the clinical signs in endotoxaemic animals, including rectal temperature and heart and respiratory rates. Polymyxin B may be an antiendotoxic in fat-tailed sheep.</abstract><cop>Pulawy</cop><pub>Sciendo</pub><doi>10.2478/jvetres-2018-0011</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | clinical signs Haptoglobin inflammatory biomarkers Intravenous administration Lactic acid lipopolysaccharide Lipopolysaccharides Polymyxin B Sheep Tumor necrosis factor-TNF Tumor necrosis factor-α Tumors |
title | Effects of polymyxin B on clinical signs, serum TNF-α, haptoglobin and plasma lactate concentrations in experimental endotoxaemia in sheep |
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