Loading…
Low Glucose plus β-Hydroxybutyrate Induces an Enhanced Inflammatory Response in Yak Alveolar Macrophages via Activating the GPR109A/NF-κB Signaling Pathway
Yaks are often subject to long-term starvation and a high prevalence of respiratory diseases and mortality in the withered season, yet the mechanisms that cause this remain unclear. Research has demonstrated that β-hydroxybutyrate (BHB) plays a significant role in regulating the immune system. Hence...
Saved in:
Published in: | International journal of molecular sciences 2023-07, Vol.24 (14), p.11331 |
---|---|
Main Authors: | , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c505t-dc801fffe7ff72608ad68f462eb7382c1ab8cec6d0875dcd1bd436115f86d0253 |
container_end_page | |
container_issue | 14 |
container_start_page | 11331 |
container_title | International journal of molecular sciences |
container_volume | 24 |
creator | Qi, Jiancheng Yang, Qiyuan Xia, Qing Huang, Fangyuan Guo, Hongrui Cui, Hengmin Xie, Yue Ren, Zhihua Gou, Liping Cai, Dongjie Kumbhar, Maqsood Ahmed Fang, Jing Zuo, Zhicai |
description | Yaks are often subject to long-term starvation and a high prevalence of respiratory diseases and mortality in the withered season, yet the mechanisms that cause this remain unclear. Research has demonstrated that β-hydroxybutyrate (BHB) plays a significant role in regulating the immune system. Hence, we hypothesize that the low glucose and high BHB condition induced by severe starvation might have an effect on the pro-inflammatory response of the alveolar macrophages (AMs) in yaks. To validate our hypothesis, we isolated and identified primary AMs from freshly slaughtered yaks and cultured them in a medium with 5.5 mM of glucose or 2.8 mM of glucose plus 1-4 mM of BHB. Utilizing a real-time quantitative polymerase chain reaction (RT-qPCR), immunoblot assay, and enzyme-linked immunosorbent assay (ELISA), we evaluated the gene and protein expression levels of GPR109A (G-protein-coupled receptor 109A), NF-κB p65, p38, and PPARγ and the concentrations of pro-inflammatory cytokines interleukin (IL)-1β and IL-6 and tumor necrosis factor (TNF)-α in the supernatant. The results demonstrated that AMs exposed to low glucose plus BHB had significantly higher levels of IL-1β, IL-6, and TNF-α (
< 0.05) and higher activity of the GPR109A/NF-κB signaling pathway. A pretreatment of either pertussis toxin (PTX, inhibitor of GPR109A) or pyrrolidinedithiocarbamic (PDTC, inhibitor of NF-κB p65) was effective in preventing the elevated secretion of pro-inflammatory cytokines induced by low glucose plus BHB (
< 0.05). These results indicated that the low glucose plus BHB condition would induce an enhanced pro-inflammatory response through the activation of the GPR109A/NF-κB signaling pathway in primary yak AMs, which is probably the reason why yaks experience a higher rate of respiratory diseases and mortality. This study will offer new insight into the prevention and treatment of bovine respiratory diseases. |
doi_str_mv | 10.3390/ijms241411331 |
format | article |
fullrecord | <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_a62c0c0758504656877e8c5ef5ce57ff</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A759152814</galeid><doaj_id>oai_doaj_org_article_a62c0c0758504656877e8c5ef5ce57ff</doaj_id><sourcerecordid>A759152814</sourcerecordid><originalsourceid>FETCH-LOGICAL-c505t-dc801fffe7ff72608ad68f462eb7382c1ab8cec6d0875dcd1bd436115f86d0253</originalsourceid><addsrcrecordid>eNptks9uEzEQxlcIREvhyBVZ4sJlW_9Zr50TSqs2rRSgKnDgtJp47cRh1w72bso-DC_BkYfoM-E0pTQI-WDrm29-47Eny14SfMjYCB_ZZRtpQQpCGCOPsn1SUJpjXIrHD8572bMYlxhTRvnoabbHBCcEj8h-9mPqr9Gk6ZWPGq2aPqKbn_n5UAf_fZj13RCg0-jC1b3SEYFDp24BTuk6aaaBtoXOhwFd6bjyLhGsQ1_gKxo3a-0bCOgdqOBXC5in7LUFNFadXUNn3Rx1C40ml1fpGuOj92f5za9j9NHOHTSb4CV0i2sYnmdPDDRRv7jbD7LPZ6efTs7z6YfJxcl4miuOeZfXSmJijNHCGEFLLKEupSlKqmeCSaoIzKTSqqyxFLxWNZnVBSsJ4UYmjXJ2kF1subWHZbUKtoUwVB5sdSv4MK8gdFY1uoKSKqyw4JLjouSlFEJLxbXhSvNUP7HeblmrftbqWmnXBWh2oLsRZxfV3K8rgpkYMSES4c0dIfhvvY5d1dqodNOA076PFZVFgeWowCRZX_9jXfo-pEe8dTEsGKbir2sOqQPrjE-F1QZajQUfEU4lKZLr8D-utGrdWuWdNjbpOwn5NiH9cYxBm_smCa42w1ntDGfyv3r4MvfuP9PIfgMZe-Fx</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2843073027</pqid></control><display><type>article</type><title>Low Glucose plus β-Hydroxybutyrate Induces an Enhanced Inflammatory Response in Yak Alveolar Macrophages via Activating the GPR109A/NF-κB Signaling Pathway</title><source>Publicly Available Content Database</source><source>PubMed Central</source><source>Coronavirus Research Database</source><creator>Qi, Jiancheng ; Yang, Qiyuan ; Xia, Qing ; Huang, Fangyuan ; Guo, Hongrui ; Cui, Hengmin ; Xie, Yue ; Ren, Zhihua ; Gou, Liping ; Cai, Dongjie ; Kumbhar, Maqsood Ahmed ; Fang, Jing ; Zuo, Zhicai</creator><creatorcontrib>Qi, Jiancheng ; Yang, Qiyuan ; Xia, Qing ; Huang, Fangyuan ; Guo, Hongrui ; Cui, Hengmin ; Xie, Yue ; Ren, Zhihua ; Gou, Liping ; Cai, Dongjie ; Kumbhar, Maqsood Ahmed ; Fang, Jing ; Zuo, Zhicai</creatorcontrib><description>Yaks are often subject to long-term starvation and a high prevalence of respiratory diseases and mortality in the withered season, yet the mechanisms that cause this remain unclear. Research has demonstrated that β-hydroxybutyrate (BHB) plays a significant role in regulating the immune system. Hence, we hypothesize that the low glucose and high BHB condition induced by severe starvation might have an effect on the pro-inflammatory response of the alveolar macrophages (AMs) in yaks. To validate our hypothesis, we isolated and identified primary AMs from freshly slaughtered yaks and cultured them in a medium with 5.5 mM of glucose or 2.8 mM of glucose plus 1-4 mM of BHB. Utilizing a real-time quantitative polymerase chain reaction (RT-qPCR), immunoblot assay, and enzyme-linked immunosorbent assay (ELISA), we evaluated the gene and protein expression levels of GPR109A (G-protein-coupled receptor 109A), NF-κB p65, p38, and PPARγ and the concentrations of pro-inflammatory cytokines interleukin (IL)-1β and IL-6 and tumor necrosis factor (TNF)-α in the supernatant. The results demonstrated that AMs exposed to low glucose plus BHB had significantly higher levels of IL-1β, IL-6, and TNF-α (
< 0.05) and higher activity of the GPR109A/NF-κB signaling pathway. A pretreatment of either pertussis toxin (PTX, inhibitor of GPR109A) or pyrrolidinedithiocarbamic (PDTC, inhibitor of NF-κB p65) was effective in preventing the elevated secretion of pro-inflammatory cytokines induced by low glucose plus BHB (
< 0.05). These results indicated that the low glucose plus BHB condition would induce an enhanced pro-inflammatory response through the activation of the GPR109A/NF-κB signaling pathway in primary yak AMs, which is probably the reason why yaks experience a higher rate of respiratory diseases and mortality. This study will offer new insight into the prevention and treatment of bovine respiratory diseases.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms241411331</identifier><identifier>PMID: 37511091</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>China ; Cultural heritage ; Cytokines ; Dextrose ; Genetic research ; Glucose ; Health aspects ; Interleukins ; low glucose ; Macrophages ; Mortality ; Pathogens ; primary alveolar macrophages (AMs) ; pro-inflammatory response ; Protein expression ; Proteins ; Respiratory diseases ; Tumor necrosis factor-TNF ; yak ; β-hydroxybutyrate (BHB)</subject><ispartof>International journal of molecular sciences, 2023-07, Vol.24 (14), p.11331</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c505t-dc801fffe7ff72608ad68f462eb7382c1ab8cec6d0875dcd1bd436115f86d0253</cites><orcidid>0000-0003-1674-8497 ; 0000-0002-3992-3529 ; 0000-0003-2249-6484</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2843073027/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2843073027?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,38516,43895,44590,53791,53793,74412,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37511091$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Qi, Jiancheng</creatorcontrib><creatorcontrib>Yang, Qiyuan</creatorcontrib><creatorcontrib>Xia, Qing</creatorcontrib><creatorcontrib>Huang, Fangyuan</creatorcontrib><creatorcontrib>Guo, Hongrui</creatorcontrib><creatorcontrib>Cui, Hengmin</creatorcontrib><creatorcontrib>Xie, Yue</creatorcontrib><creatorcontrib>Ren, Zhihua</creatorcontrib><creatorcontrib>Gou, Liping</creatorcontrib><creatorcontrib>Cai, Dongjie</creatorcontrib><creatorcontrib>Kumbhar, Maqsood Ahmed</creatorcontrib><creatorcontrib>Fang, Jing</creatorcontrib><creatorcontrib>Zuo, Zhicai</creatorcontrib><title>Low Glucose plus β-Hydroxybutyrate Induces an Enhanced Inflammatory Response in Yak Alveolar Macrophages via Activating the GPR109A/NF-κB Signaling Pathway</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Yaks are often subject to long-term starvation and a high prevalence of respiratory diseases and mortality in the withered season, yet the mechanisms that cause this remain unclear. Research has demonstrated that β-hydroxybutyrate (BHB) plays a significant role in regulating the immune system. Hence, we hypothesize that the low glucose and high BHB condition induced by severe starvation might have an effect on the pro-inflammatory response of the alveolar macrophages (AMs) in yaks. To validate our hypothesis, we isolated and identified primary AMs from freshly slaughtered yaks and cultured them in a medium with 5.5 mM of glucose or 2.8 mM of glucose plus 1-4 mM of BHB. Utilizing a real-time quantitative polymerase chain reaction (RT-qPCR), immunoblot assay, and enzyme-linked immunosorbent assay (ELISA), we evaluated the gene and protein expression levels of GPR109A (G-protein-coupled receptor 109A), NF-κB p65, p38, and PPARγ and the concentrations of pro-inflammatory cytokines interleukin (IL)-1β and IL-6 and tumor necrosis factor (TNF)-α in the supernatant. The results demonstrated that AMs exposed to low glucose plus BHB had significantly higher levels of IL-1β, IL-6, and TNF-α (
< 0.05) and higher activity of the GPR109A/NF-κB signaling pathway. A pretreatment of either pertussis toxin (PTX, inhibitor of GPR109A) or pyrrolidinedithiocarbamic (PDTC, inhibitor of NF-κB p65) was effective in preventing the elevated secretion of pro-inflammatory cytokines induced by low glucose plus BHB (
< 0.05). These results indicated that the low glucose plus BHB condition would induce an enhanced pro-inflammatory response through the activation of the GPR109A/NF-κB signaling pathway in primary yak AMs, which is probably the reason why yaks experience a higher rate of respiratory diseases and mortality. This study will offer new insight into the prevention and treatment of bovine respiratory diseases.</description><subject>China</subject><subject>Cultural heritage</subject><subject>Cytokines</subject><subject>Dextrose</subject><subject>Genetic research</subject><subject>Glucose</subject><subject>Health aspects</subject><subject>Interleukins</subject><subject>low glucose</subject><subject>Macrophages</subject><subject>Mortality</subject><subject>Pathogens</subject><subject>primary alveolar macrophages (AMs)</subject><subject>pro-inflammatory response</subject><subject>Protein expression</subject><subject>Proteins</subject><subject>Respiratory diseases</subject><subject>Tumor necrosis factor-TNF</subject><subject>yak</subject><subject>β-hydroxybutyrate (BHB)</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>COVID</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptks9uEzEQxlcIREvhyBVZ4sJlW_9Zr50TSqs2rRSgKnDgtJp47cRh1w72bso-DC_BkYfoM-E0pTQI-WDrm29-47Eny14SfMjYCB_ZZRtpQQpCGCOPsn1SUJpjXIrHD8572bMYlxhTRvnoabbHBCcEj8h-9mPqr9Gk6ZWPGq2aPqKbn_n5UAf_fZj13RCg0-jC1b3SEYFDp24BTuk6aaaBtoXOhwFd6bjyLhGsQ1_gKxo3a-0bCOgdqOBXC5in7LUFNFadXUNn3Rx1C40ml1fpGuOj92f5za9j9NHOHTSb4CV0i2sYnmdPDDRRv7jbD7LPZ6efTs7z6YfJxcl4miuOeZfXSmJijNHCGEFLLKEupSlKqmeCSaoIzKTSqqyxFLxWNZnVBSsJ4UYmjXJ2kF1subWHZbUKtoUwVB5sdSv4MK8gdFY1uoKSKqyw4JLjouSlFEJLxbXhSvNUP7HeblmrftbqWmnXBWh2oLsRZxfV3K8rgpkYMSES4c0dIfhvvY5d1dqodNOA076PFZVFgeWowCRZX_9jXfo-pEe8dTEsGKbir2sOqQPrjE-F1QZajQUfEU4lKZLr8D-utGrdWuWdNjbpOwn5NiH9cYxBm_smCa42w1ntDGfyv3r4MvfuP9PIfgMZe-Fx</recordid><startdate>20230701</startdate><enddate>20230701</enddate><creator>Qi, Jiancheng</creator><creator>Yang, Qiyuan</creator><creator>Xia, Qing</creator><creator>Huang, Fangyuan</creator><creator>Guo, Hongrui</creator><creator>Cui, Hengmin</creator><creator>Xie, Yue</creator><creator>Ren, Zhihua</creator><creator>Gou, Liping</creator><creator>Cai, Dongjie</creator><creator>Kumbhar, Maqsood Ahmed</creator><creator>Fang, Jing</creator><creator>Zuo, Zhicai</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>COVID</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</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/0000-0003-1674-8497</orcidid><orcidid>https://orcid.org/0000-0002-3992-3529</orcidid><orcidid>https://orcid.org/0000-0003-2249-6484</orcidid></search><sort><creationdate>20230701</creationdate><title>Low Glucose plus β-Hydroxybutyrate Induces an Enhanced Inflammatory Response in Yak Alveolar Macrophages via Activating the GPR109A/NF-κB Signaling Pathway</title><author>Qi, Jiancheng ; Yang, Qiyuan ; Xia, Qing ; Huang, Fangyuan ; Guo, Hongrui ; Cui, Hengmin ; Xie, Yue ; Ren, Zhihua ; Gou, Liping ; Cai, Dongjie ; Kumbhar, Maqsood Ahmed ; Fang, Jing ; Zuo, Zhicai</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c505t-dc801fffe7ff72608ad68f462eb7382c1ab8cec6d0875dcd1bd436115f86d0253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>China</topic><topic>Cultural heritage</topic><topic>Cytokines</topic><topic>Dextrose</topic><topic>Genetic research</topic><topic>Glucose</topic><topic>Health aspects</topic><topic>Interleukins</topic><topic>low glucose</topic><topic>Macrophages</topic><topic>Mortality</topic><topic>Pathogens</topic><topic>primary alveolar macrophages (AMs)</topic><topic>pro-inflammatory response</topic><topic>Protein expression</topic><topic>Proteins</topic><topic>Respiratory diseases</topic><topic>Tumor necrosis factor-TNF</topic><topic>yak</topic><topic>β-hydroxybutyrate (BHB)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Qi, Jiancheng</creatorcontrib><creatorcontrib>Yang, Qiyuan</creatorcontrib><creatorcontrib>Xia, Qing</creatorcontrib><creatorcontrib>Huang, Fangyuan</creatorcontrib><creatorcontrib>Guo, Hongrui</creatorcontrib><creatorcontrib>Cui, Hengmin</creatorcontrib><creatorcontrib>Xie, Yue</creatorcontrib><creatorcontrib>Ren, Zhihua</creatorcontrib><creatorcontrib>Gou, Liping</creatorcontrib><creatorcontrib>Cai, Dongjie</creatorcontrib><creatorcontrib>Kumbhar, Maqsood Ahmed</creatorcontrib><creatorcontrib>Fang, Jing</creatorcontrib><creatorcontrib>Zuo, Zhicai</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</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>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Coronavirus Research Database</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>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</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>Directory of Open Access Journals (DOAJ)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Qi, Jiancheng</au><au>Yang, Qiyuan</au><au>Xia, Qing</au><au>Huang, Fangyuan</au><au>Guo, Hongrui</au><au>Cui, Hengmin</au><au>Xie, Yue</au><au>Ren, Zhihua</au><au>Gou, Liping</au><au>Cai, Dongjie</au><au>Kumbhar, Maqsood Ahmed</au><au>Fang, Jing</au><au>Zuo, Zhicai</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Low Glucose plus β-Hydroxybutyrate Induces an Enhanced Inflammatory Response in Yak Alveolar Macrophages via Activating the GPR109A/NF-κB Signaling Pathway</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2023-07-01</date><risdate>2023</risdate><volume>24</volume><issue>14</issue><spage>11331</spage><pages>11331-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Yaks are often subject to long-term starvation and a high prevalence of respiratory diseases and mortality in the withered season, yet the mechanisms that cause this remain unclear. Research has demonstrated that β-hydroxybutyrate (BHB) plays a significant role in regulating the immune system. Hence, we hypothesize that the low glucose and high BHB condition induced by severe starvation might have an effect on the pro-inflammatory response of the alveolar macrophages (AMs) in yaks. To validate our hypothesis, we isolated and identified primary AMs from freshly slaughtered yaks and cultured them in a medium with 5.5 mM of glucose or 2.8 mM of glucose plus 1-4 mM of BHB. Utilizing a real-time quantitative polymerase chain reaction (RT-qPCR), immunoblot assay, and enzyme-linked immunosorbent assay (ELISA), we evaluated the gene and protein expression levels of GPR109A (G-protein-coupled receptor 109A), NF-κB p65, p38, and PPARγ and the concentrations of pro-inflammatory cytokines interleukin (IL)-1β and IL-6 and tumor necrosis factor (TNF)-α in the supernatant. The results demonstrated that AMs exposed to low glucose plus BHB had significantly higher levels of IL-1β, IL-6, and TNF-α (
< 0.05) and higher activity of the GPR109A/NF-κB signaling pathway. A pretreatment of either pertussis toxin (PTX, inhibitor of GPR109A) or pyrrolidinedithiocarbamic (PDTC, inhibitor of NF-κB p65) was effective in preventing the elevated secretion of pro-inflammatory cytokines induced by low glucose plus BHB (
< 0.05). These results indicated that the low glucose plus BHB condition would induce an enhanced pro-inflammatory response through the activation of the GPR109A/NF-κB signaling pathway in primary yak AMs, which is probably the reason why yaks experience a higher rate of respiratory diseases and mortality. This study will offer new insight into the prevention and treatment of bovine respiratory diseases.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>37511091</pmid><doi>10.3390/ijms241411331</doi><orcidid>https://orcid.org/0000-0003-1674-8497</orcidid><orcidid>https://orcid.org/0000-0002-3992-3529</orcidid><orcidid>https://orcid.org/0000-0003-2249-6484</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1422-0067 |
ispartof | International journal of molecular sciences, 2023-07, Vol.24 (14), p.11331 |
issn | 1422-0067 1661-6596 1422-0067 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_a62c0c0758504656877e8c5ef5ce57ff |
source | Publicly Available Content Database; PubMed Central; Coronavirus Research Database |
subjects | China Cultural heritage Cytokines Dextrose Genetic research Glucose Health aspects Interleukins low glucose Macrophages Mortality Pathogens primary alveolar macrophages (AMs) pro-inflammatory response Protein expression Proteins Respiratory diseases Tumor necrosis factor-TNF yak β-hydroxybutyrate (BHB) |
title | Low Glucose plus β-Hydroxybutyrate Induces an Enhanced Inflammatory Response in Yak Alveolar Macrophages via Activating the GPR109A/NF-κB Signaling Pathway |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T15%3A05%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Low%20Glucose%20plus%20%CE%B2-Hydroxybutyrate%20Induces%20an%20Enhanced%20Inflammatory%20Response%20in%20Yak%20Alveolar%20Macrophages%20via%20Activating%20the%20GPR109A/NF-%CE%BAB%20Signaling%20Pathway&rft.jtitle=International%20journal%20of%20molecular%20sciences&rft.au=Qi,%20Jiancheng&rft.date=2023-07-01&rft.volume=24&rft.issue=14&rft.spage=11331&rft.pages=11331-&rft.issn=1422-0067&rft.eissn=1422-0067&rft_id=info:doi/10.3390/ijms241411331&rft_dat=%3Cgale_doaj_%3EA759152814%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c505t-dc801fffe7ff72608ad68f462eb7382c1ab8cec6d0875dcd1bd436115f86d0253%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2843073027&rft_id=info:pmid/37511091&rft_galeid=A759152814&rfr_iscdi=true |