An Animal Model of Aspiration and Aspiration Pneumonia using LacZ Gene Expression in Lungs by Adenoviral vectors
To examine the relationship between disturbed upper airway reflexes and aspiration pneumonia, we administered a total volume of 20μl of Ad-CMV-lacZ (Ad vector) or 20μl of phosphate buffer solution (PBS) intranasal to C57 black mice. In nostrils, the lacZ gene expression was investigated in each mous...
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Veröffentlicht in: | Nihon Rōnen Igakkai zasshi 1998/04/25, Vol.35(4), pp.303-306 |
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description | To examine the relationship between disturbed upper airway reflexes and aspiration pneumonia, we administered a total volume of 20μl of Ad-CMV-lacZ (Ad vector) or 20μl of phosphate buffer solution (PBS) intranasal to C57 black mice. In nostrils, the lacZ gene expression was investigated in each mouse with or without anesthesia. Under anesthesia, the lacZ gene expression was detected by Xgal staining in the lungs of every mouse given the Ad vector. However, no gene expression was measured in the lungs of those given the Ad vector without anesthesia. In mice treated with PBS, there was no lacZ gene expression in the nostrils, trachea, or lungs, irrespective of anesthesia. These results suggest that unconsciousness or disturbed upper airway reflexes caused by anesthesia caused aspiration, resulting in an intranasal bolus that can reached the lower airways, This process can be analyzed in mice tracted with adenovirus vectors carrying the E. coli LacZ gene. Mice given Ad-CMV-lacZ transnasally can be used to study aspiration pneumonia in relation to unconsciousness. |
doi_str_mv | 10.3143/geriatrics.35.303 |
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In nostrils, the lacZ gene expression was investigated in each mouse with or without anesthesia. Under anesthesia, the lacZ gene expression was detected by Xgal staining in the lungs of every mouse given the Ad vector. However, no gene expression was measured in the lungs of those given the Ad vector without anesthesia. In mice treated with PBS, there was no lacZ gene expression in the nostrils, trachea, or lungs, irrespective of anesthesia. These results suggest that unconsciousness or disturbed upper airway reflexes caused by anesthesia caused aspiration, resulting in an intranasal bolus that can reached the lower airways, This process can be analyzed in mice tracted with adenovirus vectors carrying the E. coli LacZ gene. Mice given Ad-CMV-lacZ transnasally can be used to study aspiration pneumonia in relation to unconsciousness.</description><identifier>ISSN: 0300-9173</identifier><identifier>DOI: 10.3143/geriatrics.35.303</identifier><identifier>PMID: 9643015</identifier><language>jpn</language><publisher>Japan: The Japan Geriatrics Society</publisher><subject>Adenoviridae ; adenovirus vector ; Administration, Intranasal ; anesthesia ; Animals ; aspiration ; aspiration pneumonia ; Disease Models, Animal ; Genetic Vectors ; intranasal administration ; Lac Operon - genetics ; LacZ gene ; Lung - metabolism ; Male ; Mice ; Mice, Inbred C57BL ; Pneumonia, Aspiration - genetics</subject><ispartof>Nippon Ronen Igakkai Zasshi. 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In nostrils, the lacZ gene expression was investigated in each mouse with or without anesthesia. Under anesthesia, the lacZ gene expression was detected by Xgal staining in the lungs of every mouse given the Ad vector. However, no gene expression was measured in the lungs of those given the Ad vector without anesthesia. In mice treated with PBS, there was no lacZ gene expression in the nostrils, trachea, or lungs, irrespective of anesthesia. These results suggest that unconsciousness or disturbed upper airway reflexes caused by anesthesia caused aspiration, resulting in an intranasal bolus that can reached the lower airways, This process can be analyzed in mice tracted with adenovirus vectors carrying the E. coli LacZ gene. Mice given Ad-CMV-lacZ transnasally can be used to study aspiration pneumonia in relation to unconsciousness.</description><subject>Adenoviridae</subject><subject>adenovirus vector</subject><subject>Administration, Intranasal</subject><subject>anesthesia</subject><subject>Animals</subject><subject>aspiration</subject><subject>aspiration pneumonia</subject><subject>Disease Models, Animal</subject><subject>Genetic Vectors</subject><subject>intranasal administration</subject><subject>Lac Operon - genetics</subject><subject>LacZ gene</subject><subject>Lung - metabolism</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Pneumonia, Aspiration - genetics</subject><issn>0300-9173</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkM9PwjAUx3vQIKJ_gAeTnryB7dqt7LgQRQ1GD3rx0pTuDUtGO9uNyH9vEUQur3n5_sjrB6ErSkaMcna7AG9U640OI5aOGGEnqE8YIcOcCnaGzkNYEpKmPEt6qJdnnBGa9lFTWFxYs1I1fnYl1NhVuAiN8ao1zmJly-P11UK3ctYo3AVjF3im9AeeggV89914CGFrMhbPOrsIeL7BRQnWrWO8xmvQrfPhAp1Wqg5wuX8H6P3-7m3yMJy9TB8nxWyoWbx9mIpEJ0nJs5wCTxORz3OV6XIsqooLPc_ij1XG9VhXldYJz4SgNBOKRCdLxglnA3Sz6228--ogtHJlgoa6VhZcF6TII4MxYdFId0btXQgeKtn4yMNvJCVyS1b-k5Uslew3c70v7-YrKA-JPdaoP-30ZWjVAg668q3RNRw10hjZtv4Nwg4m_am8BMt-AGxxk90</recordid><startdate>1998</startdate><enddate>1998</enddate><creator>Teramoto, Shinji</creator><creator>Ito, Hideki</creator><creator>Matsuse, Takeshi</creator><creator>Mastui, Hirotoshi</creator><creator>Ohga, Eijiro</creator><creator>Katayama, Hirofumi</creator><creator>Oka, Teruaki</creator><creator>Ouchi, Yasuyoshi</creator><general>The Japan Geriatrics Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>1998</creationdate><title>An Animal Model of Aspiration and Aspiration Pneumonia using LacZ Gene Expression in Lungs by Adenoviral vectors</title><author>Teramoto, Shinji ; Ito, Hideki ; Matsuse, Takeshi ; Mastui, Hirotoshi ; Ohga, Eijiro ; Katayama, Hirofumi ; Oka, Teruaki ; Ouchi, Yasuyoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3303-572c22d4691e45279b9a6cd87ff47cb6143a64c8cffcc246771167a0279328243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>jpn</language><creationdate>1998</creationdate><topic>Adenoviridae</topic><topic>adenovirus vector</topic><topic>Administration, Intranasal</topic><topic>anesthesia</topic><topic>Animals</topic><topic>aspiration</topic><topic>aspiration pneumonia</topic><topic>Disease Models, Animal</topic><topic>Genetic Vectors</topic><topic>intranasal administration</topic><topic>Lac Operon - genetics</topic><topic>LacZ gene</topic><topic>Lung - metabolism</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Pneumonia, Aspiration - genetics</topic><toplevel>online_resources</toplevel><creatorcontrib>Teramoto, Shinji</creatorcontrib><creatorcontrib>Ito, Hideki</creatorcontrib><creatorcontrib>Matsuse, Takeshi</creatorcontrib><creatorcontrib>Mastui, Hirotoshi</creatorcontrib><creatorcontrib>Ohga, Eijiro</creatorcontrib><creatorcontrib>Katayama, Hirofumi</creatorcontrib><creatorcontrib>Oka, Teruaki</creatorcontrib><creatorcontrib>Ouchi, Yasuyoshi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Nihon Rōnen Igakkai zasshi</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Teramoto, Shinji</au><au>Ito, Hideki</au><au>Matsuse, Takeshi</au><au>Mastui, Hirotoshi</au><au>Ohga, Eijiro</au><au>Katayama, Hirofumi</au><au>Oka, Teruaki</au><au>Ouchi, Yasuyoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An Animal Model of Aspiration and Aspiration Pneumonia using LacZ Gene Expression in Lungs by Adenoviral vectors</atitle><jtitle>Nihon Rōnen Igakkai zasshi</jtitle><addtitle>Nippon Ronen Igakkai Zasshi</addtitle><date>1998</date><risdate>1998</risdate><volume>35</volume><issue>4</issue><spage>303</spage><epage>306</epage><pages>303-306</pages><issn>0300-9173</issn><abstract>To examine the relationship between disturbed upper airway reflexes and aspiration pneumonia, we administered a total volume of 20μl of Ad-CMV-lacZ (Ad vector) or 20μl of phosphate buffer solution (PBS) intranasal to C57 black mice. In nostrils, the lacZ gene expression was investigated in each mouse with or without anesthesia. Under anesthesia, the lacZ gene expression was detected by Xgal staining in the lungs of every mouse given the Ad vector. However, no gene expression was measured in the lungs of those given the Ad vector without anesthesia. In mice treated with PBS, there was no lacZ gene expression in the nostrils, trachea, or lungs, irrespective of anesthesia. These results suggest that unconsciousness or disturbed upper airway reflexes caused by anesthesia caused aspiration, resulting in an intranasal bolus that can reached the lower airways, This process can be analyzed in mice tracted with adenovirus vectors carrying the E. coli LacZ gene. 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subjects | Adenoviridae adenovirus vector Administration, Intranasal anesthesia Animals aspiration aspiration pneumonia Disease Models, Animal Genetic Vectors intranasal administration Lac Operon - genetics LacZ gene Lung - metabolism Male Mice Mice, Inbred C57BL Pneumonia, Aspiration - genetics |
title | An Animal Model of Aspiration and Aspiration Pneumonia using LacZ Gene Expression in Lungs by Adenoviral vectors |
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