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Antagonistic Effects Of Baicalin On Mycoplasma gallisepticum -Induced Inflammation And Apoptosis By Restoring Energy Metabolism In The Chicken Lungs
Baicalin possesses potential anti-inflammatory, anti-tumor and anti-oxidant activities. In the present study, we attempted to investigate the preventive effects of baicalin against (MG)-induced inflammation, apoptosis and energy metabolism dysfunction in chicken lungs. Experimental chickens were ran...
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Published in: | Infection and drug resistance 2019-01, Vol.12, p.3075-3089 |
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description | Baicalin possesses potential anti-inflammatory, anti-tumor and anti-oxidant activities. In the present study, we attempted to investigate the preventive effects of baicalin against
(MG)-induced inflammation, apoptosis and energy metabolism dysfunction in chicken lungs.
Experimental chickens were randomly divided into 1) control group, 2) MG infection group, 3) MG-infected group treated with baicalin at a dose of 450 mg/kg and 4) baicalin alone treated group (450 mg/kg). After 7 days of post-treatment, serum and lung tissues were collected for different experimental analyses. The hallmarks of inflammation, apoptosis and energy metabolism dysfunction were detected by histological and ultrastructural examination, qRT-PCR, Western blotting and terminal deoxynucleotidyl transferase-mediated dUTP nick endlabeling (TUNEL) assay.
The level of serum inflammatory markers were increased with MG infection. Histological and ultrastructural analysis showed excessive inflammatory cells infiltrates, alveolar wall thickening, hemorrhages, mitochondrial and nuclear damage, including mitochondrial swelling and condensation of DNA in the lungs of chickens infected with MG. TUNEL assay positive-stained nuclei were significantly increased in MG infection group. In addition, the mRNA and protein expression level of energy metabolism-related genes and ATPase activities were significantly reduced. Meanwhile, MG-induced morphological and ultrastructural changes were partially disappeared with baicalin-treatment, and the level of serum inflammatory markers were significantly reduced. It has been noted that baicalin significantly attenuated MG-induced inflammation and apoptosis in the chicken lungs through the suppression of nuclear factor-kappa B and reduced extensive positive-stained apoptotic nuclei. More importantly, ATPase activities and mRNA and protein expression level of energy metabolism-related genes were significantly improved with baicalin-treatment in the lungs of chickens infected with MG.
Conclusively, it has been suggested from these results that baicalin-treatment efficiently prevented MG-induced inflammation, apoptosis and energy metabolism dysfunction in the chicken lungs and provide basis for new therapeutic targets to control MG infection. |
doi_str_mv | 10.2147/IDR.S223085 |
format | article |
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(MG)-induced inflammation, apoptosis and energy metabolism dysfunction in chicken lungs.
Experimental chickens were randomly divided into 1) control group, 2) MG infection group, 3) MG-infected group treated with baicalin at a dose of 450 mg/kg and 4) baicalin alone treated group (450 mg/kg). After 7 days of post-treatment, serum and lung tissues were collected for different experimental analyses. The hallmarks of inflammation, apoptosis and energy metabolism dysfunction were detected by histological and ultrastructural examination, qRT-PCR, Western blotting and terminal deoxynucleotidyl transferase-mediated dUTP nick endlabeling (TUNEL) assay.
The level of serum inflammatory markers were increased with MG infection. Histological and ultrastructural analysis showed excessive inflammatory cells infiltrates, alveolar wall thickening, hemorrhages, mitochondrial and nuclear damage, including mitochondrial swelling and condensation of DNA in the lungs of chickens infected with MG. TUNEL assay positive-stained nuclei were significantly increased in MG infection group. In addition, the mRNA and protein expression level of energy metabolism-related genes and ATPase activities were significantly reduced. Meanwhile, MG-induced morphological and ultrastructural changes were partially disappeared with baicalin-treatment, and the level of serum inflammatory markers were significantly reduced. It has been noted that baicalin significantly attenuated MG-induced inflammation and apoptosis in the chicken lungs through the suppression of nuclear factor-kappa B and reduced extensive positive-stained apoptotic nuclei. More importantly, ATPase activities and mRNA and protein expression level of energy metabolism-related genes were significantly improved with baicalin-treatment in the lungs of chickens infected with MG.
Conclusively, it has been suggested from these results that baicalin-treatment efficiently prevented MG-induced inflammation, apoptosis and energy metabolism dysfunction in the chicken lungs and provide basis for new therapeutic targets to control MG infection.</description><identifier>ISSN: 1178-6973</identifier><identifier>EISSN: 1178-6973</identifier><identifier>DOI: 10.2147/IDR.S223085</identifier><identifier>PMID: 31632098</identifier><language>eng</language><publisher>New Zealand: Dove Medical Press Limited</publisher><subject>Adenosine triphosphatase ; Alveoli ; Analysis ; Anti-inflammatory agents ; Apoptosis ; ATPases ; Bacterial infections ; Baicalin ; Cancer ; Chemokines ; Cytokines ; Dehydrogenases ; DNA ; DNA nucleotidylexotransferase ; Energy ; Energy metabolism ; Enzymes ; Gene expression ; Genes ; Genetic research ; Health aspects ; Infection ; Infections ; Inflammation ; Kinases ; Laboratory animals ; Lungs ; Messenger RNA ; Metabolism ; Mitochondria ; mRNA ; Mycoplasma gallisepticum ; NF-κB protein ; Nuclei ; Original Research ; Physiological aspects ; Poultry ; Protein turnover ; Researchers ; RNA ; Studies ; Therapeutic applications ; Tumor necrosis factor-TNF ; Tumors ; Veterinary medicine ; Western blotting</subject><ispartof>Infection and drug resistance, 2019-01, Vol.12, p.3075-3089</ispartof><rights>2019 Ishfaq et al.</rights><rights>COPYRIGHT 2019 Dove Medical Press Limited</rights><rights>2019. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2019 Ishfaq et al. 2019 Ishfaq et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c573t-f646160b26a653c883f26a4f65377deecd68e0b39e866c894dd37dba89cb67173</citedby><orcidid>0000-0002-1779-1190</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2299560391/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2299560391?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25751,27922,27923,37010,37011,44588,53789,53791,74896</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31632098$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ishfaq, Muhammad</creatorcontrib><creatorcontrib>Zhang, Wei</creatorcontrib><creatorcontrib>Hu, Wanying</creatorcontrib><creatorcontrib>Waqas Ali Shah, Syed</creatorcontrib><creatorcontrib>Liu, Yuhao</creatorcontrib><creatorcontrib>Wang, Jian</creatorcontrib><creatorcontrib>Wu, Zhiyong</creatorcontrib><creatorcontrib>Ahmad, Ijaz</creatorcontrib><creatorcontrib>Li, Jichang</creatorcontrib><title>Antagonistic Effects Of Baicalin On Mycoplasma gallisepticum -Induced Inflammation And Apoptosis By Restoring Energy Metabolism In The Chicken Lungs</title><title>Infection and drug resistance</title><addtitle>Infect Drug Resist</addtitle><description>Baicalin possesses potential anti-inflammatory, anti-tumor and anti-oxidant activities. In the present study, we attempted to investigate the preventive effects of baicalin against
(MG)-induced inflammation, apoptosis and energy metabolism dysfunction in chicken lungs.
Experimental chickens were randomly divided into 1) control group, 2) MG infection group, 3) MG-infected group treated with baicalin at a dose of 450 mg/kg and 4) baicalin alone treated group (450 mg/kg). After 7 days of post-treatment, serum and lung tissues were collected for different experimental analyses. The hallmarks of inflammation, apoptosis and energy metabolism dysfunction were detected by histological and ultrastructural examination, qRT-PCR, Western blotting and terminal deoxynucleotidyl transferase-mediated dUTP nick endlabeling (TUNEL) assay.
The level of serum inflammatory markers were increased with MG infection. Histological and ultrastructural analysis showed excessive inflammatory cells infiltrates, alveolar wall thickening, hemorrhages, mitochondrial and nuclear damage, including mitochondrial swelling and condensation of DNA in the lungs of chickens infected with MG. TUNEL assay positive-stained nuclei were significantly increased in MG infection group. In addition, the mRNA and protein expression level of energy metabolism-related genes and ATPase activities were significantly reduced. Meanwhile, MG-induced morphological and ultrastructural changes were partially disappeared with baicalin-treatment, and the level of serum inflammatory markers were significantly reduced. It has been noted that baicalin significantly attenuated MG-induced inflammation and apoptosis in the chicken lungs through the suppression of nuclear factor-kappa B and reduced extensive positive-stained apoptotic nuclei. More importantly, ATPase activities and mRNA and protein expression level of energy metabolism-related genes were significantly improved with baicalin-treatment in the lungs of chickens infected with MG.
Conclusively, it has been suggested from these results that baicalin-treatment efficiently prevented MG-induced inflammation, apoptosis and energy metabolism dysfunction in the chicken lungs and provide basis for new therapeutic targets to control MG infection.</description><subject>Adenosine triphosphatase</subject><subject>Alveoli</subject><subject>Analysis</subject><subject>Anti-inflammatory agents</subject><subject>Apoptosis</subject><subject>ATPases</subject><subject>Bacterial infections</subject><subject>Baicalin</subject><subject>Cancer</subject><subject>Chemokines</subject><subject>Cytokines</subject><subject>Dehydrogenases</subject><subject>DNA</subject><subject>DNA nucleotidylexotransferase</subject><subject>Energy</subject><subject>Energy metabolism</subject><subject>Enzymes</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Genetic research</subject><subject>Health aspects</subject><subject>Infection</subject><subject>Infections</subject><subject>Inflammation</subject><subject>Kinases</subject><subject>Laboratory animals</subject><subject>Lungs</subject><subject>Messenger RNA</subject><subject>Metabolism</subject><subject>Mitochondria</subject><subject>mRNA</subject><subject>Mycoplasma gallisepticum</subject><subject>NF-κB protein</subject><subject>Nuclei</subject><subject>Original Research</subject><subject>Physiological aspects</subject><subject>Poultry</subject><subject>Protein turnover</subject><subject>Researchers</subject><subject>RNA</subject><subject>Studies</subject><subject>Therapeutic applications</subject><subject>Tumor necrosis factor-TNF</subject><subject>Tumors</subject><subject>Veterinary medicine</subject><subject>Western blotting</subject><issn>1178-6973</issn><issn>1178-6973</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptUl2LEzEUHURxl3WffJeAIIK0zkym-XgRurVqoUthXZ9DJrmZpmaSOpkR-j_8wabburZi8pCb5Nxzk3NPlr0s8nFZVPT94uPd-GtZ4pxNnmSXRUHZiHCKn57EF9l1jJs8DcxJRcvn2QUuCC5zzi6zX1PfyyZ4G3ur0NwYUH1EK4NupFXSWY9WHt3uVNg6GVuJGumcjbBN6KFFo4XXgwKNFt442bayt8Gjqddoug3bPkQb0c0O3UHsQ2d9g-YeumaHbqGXdUhEbcpE92tAs7VV38Gj5eCb-CJ7ZqSLcH1cr7Jvn-b3sy-j5erzYjZdjtSE4n5kSEUKktclkWSCFWPYpLAyaUOpBlCaMMhrzIERohivtMZU15JxVRNaUHyVLQ68OsiN2Ha2ld1OBGnFw0HoGiG79FMHAoysGdSKs1JXFSGcGE6SoAVnuOSMJ64PB67tULegFfi-k-6M9PzG27Vowk9BKEutKhLB2yNBF34MSTHR2qjAOekhDFGkHlPMeZ7va73-B7oJQ-eTVKIsOZ88POwvKvUMhPUmpLpqTyqmJK9wMSnJXoPxf1BpamitCh6MTednCW9OEtYgXb-OwQ371sdz4LsDUHUhxg7MoxhFLvbmFcm84mjehH51qt8j9o9V8W8ywugq</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Ishfaq, Muhammad</creator><creator>Zhang, Wei</creator><creator>Hu, Wanying</creator><creator>Waqas Ali Shah, Syed</creator><creator>Liu, Yuhao</creator><creator>Wang, Jian</creator><creator>Wu, Zhiyong</creator><creator>Ahmad, Ijaz</creator><creator>Li, Jichang</creator><general>Dove Medical Press Limited</general><general>Taylor & Francis Ltd</general><general>Dove</general><general>Dove Medical Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</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>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-1779-1190</orcidid></search><sort><creationdate>20190101</creationdate><title>Antagonistic Effects Of Baicalin On Mycoplasma gallisepticum -Induced Inflammation And Apoptosis By Restoring Energy Metabolism In The Chicken Lungs</title><author>Ishfaq, Muhammad ; Zhang, Wei ; Hu, Wanying ; Waqas Ali Shah, Syed ; Liu, Yuhao ; Wang, Jian ; Wu, Zhiyong ; Ahmad, Ijaz ; Li, Jichang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c573t-f646160b26a653c883f26a4f65377deecd68e0b39e866c894dd37dba89cb67173</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adenosine triphosphatase</topic><topic>Alveoli</topic><topic>Analysis</topic><topic>Anti-inflammatory agents</topic><topic>Apoptosis</topic><topic>ATPases</topic><topic>Bacterial infections</topic><topic>Baicalin</topic><topic>Cancer</topic><topic>Chemokines</topic><topic>Cytokines</topic><topic>Dehydrogenases</topic><topic>DNA</topic><topic>DNA nucleotidylexotransferase</topic><topic>Energy</topic><topic>Energy metabolism</topic><topic>Enzymes</topic><topic>Gene expression</topic><topic>Genes</topic><topic>Genetic research</topic><topic>Health aspects</topic><topic>Infection</topic><topic>Infections</topic><topic>Inflammation</topic><topic>Kinases</topic><topic>Laboratory animals</topic><topic>Lungs</topic><topic>Messenger RNA</topic><topic>Metabolism</topic><topic>Mitochondria</topic><topic>mRNA</topic><topic>Mycoplasma gallisepticum</topic><topic>NF-κB protein</topic><topic>Nuclei</topic><topic>Original Research</topic><topic>Physiological aspects</topic><topic>Poultry</topic><topic>Protein turnover</topic><topic>Researchers</topic><topic>RNA</topic><topic>Studies</topic><topic>Therapeutic applications</topic><topic>Tumor necrosis factor-TNF</topic><topic>Tumors</topic><topic>Veterinary medicine</topic><topic>Western blotting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ishfaq, Muhammad</creatorcontrib><creatorcontrib>Zhang, Wei</creatorcontrib><creatorcontrib>Hu, Wanying</creatorcontrib><creatorcontrib>Waqas Ali Shah, Syed</creatorcontrib><creatorcontrib>Liu, Yuhao</creatorcontrib><creatorcontrib>Wang, Jian</creatorcontrib><creatorcontrib>Wu, Zhiyong</creatorcontrib><creatorcontrib>Ahmad, Ijaz</creatorcontrib><creatorcontrib>Li, Jichang</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>ProQuest Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Infection and drug resistance</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ishfaq, Muhammad</au><au>Zhang, Wei</au><au>Hu, Wanying</au><au>Waqas Ali Shah, Syed</au><au>Liu, Yuhao</au><au>Wang, Jian</au><au>Wu, Zhiyong</au><au>Ahmad, Ijaz</au><au>Li, Jichang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antagonistic Effects Of Baicalin On Mycoplasma gallisepticum -Induced Inflammation And Apoptosis By Restoring Energy Metabolism In The Chicken Lungs</atitle><jtitle>Infection and drug resistance</jtitle><addtitle>Infect Drug Resist</addtitle><date>2019-01-01</date><risdate>2019</risdate><volume>12</volume><spage>3075</spage><epage>3089</epage><pages>3075-3089</pages><issn>1178-6973</issn><eissn>1178-6973</eissn><abstract>Baicalin possesses potential anti-inflammatory, anti-tumor and anti-oxidant activities. In the present study, we attempted to investigate the preventive effects of baicalin against
(MG)-induced inflammation, apoptosis and energy metabolism dysfunction in chicken lungs.
Experimental chickens were randomly divided into 1) control group, 2) MG infection group, 3) MG-infected group treated with baicalin at a dose of 450 mg/kg and 4) baicalin alone treated group (450 mg/kg). After 7 days of post-treatment, serum and lung tissues were collected for different experimental analyses. The hallmarks of inflammation, apoptosis and energy metabolism dysfunction were detected by histological and ultrastructural examination, qRT-PCR, Western blotting and terminal deoxynucleotidyl transferase-mediated dUTP nick endlabeling (TUNEL) assay.
The level of serum inflammatory markers were increased with MG infection. Histological and ultrastructural analysis showed excessive inflammatory cells infiltrates, alveolar wall thickening, hemorrhages, mitochondrial and nuclear damage, including mitochondrial swelling and condensation of DNA in the lungs of chickens infected with MG. TUNEL assay positive-stained nuclei were significantly increased in MG infection group. In addition, the mRNA and protein expression level of energy metabolism-related genes and ATPase activities were significantly reduced. Meanwhile, MG-induced morphological and ultrastructural changes were partially disappeared with baicalin-treatment, and the level of serum inflammatory markers were significantly reduced. It has been noted that baicalin significantly attenuated MG-induced inflammation and apoptosis in the chicken lungs through the suppression of nuclear factor-kappa B and reduced extensive positive-stained apoptotic nuclei. More importantly, ATPase activities and mRNA and protein expression level of energy metabolism-related genes were significantly improved with baicalin-treatment in the lungs of chickens infected with MG.
Conclusively, it has been suggested from these results that baicalin-treatment efficiently prevented MG-induced inflammation, apoptosis and energy metabolism dysfunction in the chicken lungs and provide basis for new therapeutic targets to control MG infection.</abstract><cop>New Zealand</cop><pub>Dove Medical Press Limited</pub><pmid>31632098</pmid><doi>10.2147/IDR.S223085</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-1779-1190</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adenosine triphosphatase Alveoli Analysis Anti-inflammatory agents Apoptosis ATPases Bacterial infections Baicalin Cancer Chemokines Cytokines Dehydrogenases DNA DNA nucleotidylexotransferase Energy Energy metabolism Enzymes Gene expression Genes Genetic research Health aspects Infection Infections Inflammation Kinases Laboratory animals Lungs Messenger RNA Metabolism Mitochondria mRNA Mycoplasma gallisepticum NF-κB protein Nuclei Original Research Physiological aspects Poultry Protein turnover Researchers RNA Studies Therapeutic applications Tumor necrosis factor-TNF Tumors Veterinary medicine Western blotting |
title | Antagonistic Effects Of Baicalin On Mycoplasma gallisepticum -Induced Inflammation And Apoptosis By Restoring Energy Metabolism In The Chicken Lungs |
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