Long-term flaxseed oil supplementation diet protects BALB/c mice against Streptococcus pneumoniae infection
Intense host immune response to infection contributes significantly to the pathology of pneumococcal pneumonia. Therefore, the regulation of host immune response is critical for the successful outcome of pneumonia in such patients. The aim of the present study was to investigate the effect of n-3 PU...
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description | Intense host immune response to infection contributes significantly to the pathology of pneumococcal pneumonia. Therefore, the regulation of host immune response is critical for the successful outcome of pneumonia in such patients. The aim of the present study was to investigate the effect of n-3 PUFA, i.e. flaxseed oil supplementation for short (4 weeks) as well as long (9 weeks) term, on the course of
S. pneumoniae
D39 serotype 2 infection in mice. The efficacy of flaxseed oil supplementation was investigated in terms of survival of animals and production of various inflammatory molecules (malondialdehyde, myeloperoxidase, nitric oxide) in the lung homogenate of animals. This was correlated with bacteriological and histopathological parameters. The immunomodulation was studied in terms of cytokines in the lungs following infection with
Streptococcus pneumoniae
. Results suggest that long-term flaxseed supplementation protected the mice against bacterial colonization of lungs with
Streptococcus pneumoniae
with reduced histopathological involvement of lung tissue. Moderate pneumonia was observed in supplemented, infected mice compared to severe pneumonia seen in control mice. This was accompanied by decreased inflammatory markers (malondialdehyde, myeloperoxidase, nitric oxide) as the disease progressed. In addition, difference in the levels of pro-inflammatory (TNF-α and IL-1β) and anti-inflammatory (IL-10) cytokines was observed in the flaxseed fed animals. On the contrary, short-term supplementation did not show such an effect on lung colonization. |
doi_str_mv | 10.1007/s00430-009-0132-7 |
format | Article |
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S. pneumoniae
D39 serotype 2 infection in mice. The efficacy of flaxseed oil supplementation was investigated in terms of survival of animals and production of various inflammatory molecules (malondialdehyde, myeloperoxidase, nitric oxide) in the lung homogenate of animals. This was correlated with bacteriological and histopathological parameters. The immunomodulation was studied in terms of cytokines in the lungs following infection with
Streptococcus pneumoniae
. Results suggest that long-term flaxseed supplementation protected the mice against bacterial colonization of lungs with
Streptococcus pneumoniae
with reduced histopathological involvement of lung tissue. Moderate pneumonia was observed in supplemented, infected mice compared to severe pneumonia seen in control mice. This was accompanied by decreased inflammatory markers (malondialdehyde, myeloperoxidase, nitric oxide) as the disease progressed. In addition, difference in the levels of pro-inflammatory (TNF-α and IL-1β) and anti-inflammatory (IL-10) cytokines was observed in the flaxseed fed animals. On the contrary, short-term supplementation did not show such an effect on lung colonization.</description><identifier>ISSN: 0300-8584</identifier><identifier>EISSN: 1432-1831</identifier><identifier>DOI: 10.1007/s00430-009-0132-7</identifier><identifier>PMID: 19921254</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Animals ; Biomedical and Life Sciences ; Biomedicine ; Colonization ; Cytokines ; Cytokines - analysis ; Diet - methods ; Dietary supplements ; Diets ; Flax ; Immune response ; Immunologic Factors - administration & dosage ; Immunology ; Immunomodulation ; Infection ; Inflammation ; Inflammation Mediators - analysis ; Interleukin 1 ; Interleukin 10 ; Linseed Oil - administration & dosage ; Lung ; Lung - chemistry ; Lung - immunology ; Lung - microbiology ; Lung - pathology ; Malondialdehyde ; Medical Microbiology ; Mice ; Mice, Inbred BALB C ; Nitric oxide ; Oil ; Original Investigation ; Peroxidase ; Pneumococcal Infections - drug therapy ; Pneumococcal Infections - pathology ; Pneumonia ; Rodents ; Seeds ; Serotypes ; Streptococcus infections ; Streptococcus pneumoniae ; Streptococcus pneumoniae - drug effects ; Streptococcus pneumoniae - immunology ; Survival ; Survival Analysis ; Tumor necrosis factor-a ; Virology</subject><ispartof>Medical microbiology and immunology, 2010-02, Vol.199 (1), p.27-34</ispartof><rights>Springer-Verlag 2009</rights><rights>Springer-Verlag 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-p210t-312330e19d23092690811d2a9998f752ca3d0e507ff15e88b2c1142db23449c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00430-009-0132-7$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00430-009-0132-7$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,778,782,27911,27912,41475,42544,51306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19921254$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Saini, Archana</creatorcontrib><creatorcontrib>Harjai, Kusum</creatorcontrib><creatorcontrib>Mohan, Harsh</creatorcontrib><creatorcontrib>Punia, Raj Pal Singh</creatorcontrib><creatorcontrib>Chhibber, Sanjay</creatorcontrib><title>Long-term flaxseed oil supplementation diet protects BALB/c mice against Streptococcus pneumoniae infection</title><title>Medical microbiology and immunology</title><addtitle>Med Microbiol Immunol</addtitle><addtitle>Med Microbiol Immunol</addtitle><description>Intense host immune response to infection contributes significantly to the pathology of pneumococcal pneumonia. Therefore, the regulation of host immune response is critical for the successful outcome of pneumonia in such patients. The aim of the present study was to investigate the effect of n-3 PUFA, i.e. flaxseed oil supplementation for short (4 weeks) as well as long (9 weeks) term, on the course of
S. pneumoniae
D39 serotype 2 infection in mice. The efficacy of flaxseed oil supplementation was investigated in terms of survival of animals and production of various inflammatory molecules (malondialdehyde, myeloperoxidase, nitric oxide) in the lung homogenate of animals. This was correlated with bacteriological and histopathological parameters. The immunomodulation was studied in terms of cytokines in the lungs following infection with
Streptococcus pneumoniae
. Results suggest that long-term flaxseed supplementation protected the mice against bacterial colonization of lungs with
Streptococcus pneumoniae
with reduced histopathological involvement of lung tissue. Moderate pneumonia was observed in supplemented, infected mice compared to severe pneumonia seen in control mice. This was accompanied by decreased inflammatory markers (malondialdehyde, myeloperoxidase, nitric oxide) as the disease progressed. In addition, difference in the levels of pro-inflammatory (TNF-α and IL-1β) and anti-inflammatory (IL-10) cytokines was observed in the flaxseed fed animals. On the contrary, short-term supplementation did not show such an effect on lung colonization.</description><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Colonization</subject><subject>Cytokines</subject><subject>Cytokines - analysis</subject><subject>Diet - methods</subject><subject>Dietary supplements</subject><subject>Diets</subject><subject>Flax</subject><subject>Immune response</subject><subject>Immunologic Factors - administration & dosage</subject><subject>Immunology</subject><subject>Immunomodulation</subject><subject>Infection</subject><subject>Inflammation</subject><subject>Inflammation Mediators - analysis</subject><subject>Interleukin 1</subject><subject>Interleukin 10</subject><subject>Linseed Oil - administration & dosage</subject><subject>Lung</subject><subject>Lung - chemistry</subject><subject>Lung - immunology</subject><subject>Lung - microbiology</subject><subject>Lung - pathology</subject><subject>Malondialdehyde</subject><subject>Medical Microbiology</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Nitric oxide</subject><subject>Oil</subject><subject>Original Investigation</subject><subject>Peroxidase</subject><subject>Pneumococcal Infections - drug therapy</subject><subject>Pneumococcal Infections - pathology</subject><subject>Pneumonia</subject><subject>Rodents</subject><subject>Seeds</subject><subject>Serotypes</subject><subject>Streptococcus infections</subject><subject>Streptococcus pneumoniae</subject><subject>Streptococcus pneumoniae - drug effects</subject><subject>Streptococcus pneumoniae - immunology</subject><subject>Survival</subject><subject>Survival Analysis</subject><subject>Tumor necrosis factor-a</subject><subject>Virology</subject><issn>0300-8584</issn><issn>1432-1831</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkUFr3DAQhUVpaTZpf0AvQfTSk5MZSV5Lx2Rp08JCD81daOXxosSWXEuG5t9HYVMKPc3AfPPmMY-xTwhXCNBdZwAloQEwDaAUTfeGbVDVBrXEt2wDEqDRrVZn7DznBwDstgLeszM0RqBo1YY97lM8NoWWiQ-j-5OJep7CyPM6zyNNFIsrIUXeByp8XlIhXzK_vdnfXns-BU_cHV2IufBfZaG5JJ-8XzOfI61TisERD3GoS1XkA3s3uDHTx9d6we6_fb3ffW_2P-9-7G72zSwQSiNRSAmEphcSjNga0Ii9cMYYPXSt8E72QC10w4AtaX0QHlGJ_iCkUsbLC_blJFvt_l4pFzuF7GkcXaS0Ztupbb1j2m0lP_9HPqR1idWbFQJ0a7TqKnT5Cq2HiXo7L2Fyy5P9-8MKiBOQ6ygeafmngmBfgrKnoGwNyr4EZTv5DNiygsc</recordid><startdate>20100201</startdate><enddate>20100201</enddate><creator>Saini, Archana</creator><creator>Harjai, Kusum</creator><creator>Mohan, Harsh</creator><creator>Punia, Raj Pal Singh</creator><creator>Chhibber, Sanjay</creator><general>Springer-Verlag</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7T5</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</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>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7QL</scope><scope>C1K</scope></search><sort><creationdate>20100201</creationdate><title>Long-term flaxseed oil supplementation diet protects BALB/c mice against Streptococcus pneumoniae infection</title><author>Saini, Archana ; Harjai, Kusum ; Mohan, Harsh ; Punia, Raj Pal Singh ; Chhibber, Sanjay</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p210t-312330e19d23092690811d2a9998f752ca3d0e507ff15e88b2c1142db23449c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Colonization</topic><topic>Cytokines</topic><topic>Cytokines - 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Therefore, the regulation of host immune response is critical for the successful outcome of pneumonia in such patients. The aim of the present study was to investigate the effect of n-3 PUFA, i.e. flaxseed oil supplementation for short (4 weeks) as well as long (9 weeks) term, on the course of
S. pneumoniae
D39 serotype 2 infection in mice. The efficacy of flaxseed oil supplementation was investigated in terms of survival of animals and production of various inflammatory molecules (malondialdehyde, myeloperoxidase, nitric oxide) in the lung homogenate of animals. This was correlated with bacteriological and histopathological parameters. The immunomodulation was studied in terms of cytokines in the lungs following infection with
Streptococcus pneumoniae
. Results suggest that long-term flaxseed supplementation protected the mice against bacterial colonization of lungs with
Streptococcus pneumoniae
with reduced histopathological involvement of lung tissue. Moderate pneumonia was observed in supplemented, infected mice compared to severe pneumonia seen in control mice. This was accompanied by decreased inflammatory markers (malondialdehyde, myeloperoxidase, nitric oxide) as the disease progressed. In addition, difference in the levels of pro-inflammatory (TNF-α and IL-1β) and anti-inflammatory (IL-10) cytokines was observed in the flaxseed fed animals. On the contrary, short-term supplementation did not show such an effect on lung colonization.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>19921254</pmid><doi>10.1007/s00430-009-0132-7</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Biomedical and Life Sciences Biomedicine Colonization Cytokines Cytokines - analysis Diet - methods Dietary supplements Diets Flax Immune response Immunologic Factors - administration & dosage Immunology Immunomodulation Infection Inflammation Inflammation Mediators - analysis Interleukin 1 Interleukin 10 Linseed Oil - administration & dosage Lung Lung - chemistry Lung - immunology Lung - microbiology Lung - pathology Malondialdehyde Medical Microbiology Mice Mice, Inbred BALB C Nitric oxide Oil Original Investigation Peroxidase Pneumococcal Infections - drug therapy Pneumococcal Infections - pathology Pneumonia Rodents Seeds Serotypes Streptococcus infections Streptococcus pneumoniae Streptococcus pneumoniae - drug effects Streptococcus pneumoniae - immunology Survival Survival Analysis Tumor necrosis factor-a Virology |
title | Long-term flaxseed oil supplementation diet protects BALB/c mice against Streptococcus pneumoniae infection |
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