PTU-171 Oestrogen plays a critical role in murine epithelial healing in a buccal model of reflux injury
IntroductionSevere oesophagitis, oesophageal adenocarcinoma (OAC) are more common in men and post-menopausal women. Female sex hormones may protect pre-menopausal women from gastro-oesophageal reflux mediated mucosal damage, delaying the onset of BO and development of OAC in women. We have demonstra...
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Veröffentlicht in: | Gut 2012-07, Vol.61 (Suppl 2), p.A254-A255 |
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description | IntroductionSevere oesophagitis, oesophageal adenocarcinoma (OAC) are more common in men and post-menopausal women. Female sex hormones may protect pre-menopausal women from gastro-oesophageal reflux mediated mucosal damage, delaying the onset of BO and development of OAC in women. We have demonstrated more rapid mucosal healing and less inflammatory response in females in a murine buccal model of reflux injury. We have used a model comparing intact female mice with oestrogen deprived mice (by removal of their ovaries) to determine if this effect may be oestrogen driven.MethodsFemale mice (C57 strain) were divided into three groups of 5: ovariectomised (OVX), OVX with oestrogen replacement (OVX+E) (50 μg oestradiol per day dorsal implants) and intact females. 1.5 mm buccal ulcers were induced using a punch biopsy and treated with 1 M hydrochloric acid. Wounds were harvested at day 4. Wound planimetry and immunohistochemistry for macrophages and neutrophils were compared in a blinded fashion.ResultsResults: Re-epithelialisation was greatest in the intact group (mean 0.88 mm SEM ± 0.22) compared to the OVX (0.51 mm ± 0.13) or OVX+E (0.79 mm ± 0.12) groups. The difference between intact and OVX groups was statistically significant (p=0.04). Neutrophil wound infiltration (cells/wound area) was greater in the OVX group (1842±75) than the intact group (1279±169, p There was a greater number of macrophages in the OVX wounds (1556±128) than both OVX+E (984±95 (p=0.02) and the intact group (1026±91, p=0.01).ConclusionLack of systemic oestrogen delays mucosal healing in buccal wounds. This may explain gender differences in the oesophageal epithelial response to gastro-oesophageal reflux injury.Competing interestsNone declared. |
doi_str_mv | 10.1136/gutjnl-2012-302514c.171 |
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Female sex hormones may protect pre-menopausal women from gastro-oesophageal reflux mediated mucosal damage, delaying the onset of BO and development of OAC in women. We have demonstrated more rapid mucosal healing and less inflammatory response in females in a murine buccal model of reflux injury. We have used a model comparing intact female mice with oestrogen deprived mice (by removal of their ovaries) to determine if this effect may be oestrogen driven.MethodsFemale mice (C57 strain) were divided into three groups of 5: ovariectomised (OVX), OVX with oestrogen replacement (OVX+E) (50 μg oestradiol per day dorsal implants) and intact females. 1.5 mm buccal ulcers were induced using a punch biopsy and treated with 1 M hydrochloric acid. Wounds were harvested at day 4. Wound planimetry and immunohistochemistry for macrophages and neutrophils were compared in a blinded fashion.ResultsResults: Re-epithelialisation was greatest in the intact group (mean 0.88 mm SEM ± 0.22) compared to the OVX (0.51 mm ± 0.13) or OVX+E (0.79 mm ± 0.12) groups. The difference between intact and OVX groups was statistically significant (p=0.04). Neutrophil wound infiltration (cells/wound area) was greater in the OVX group (1842±75) than the intact group (1279±169, p There was a greater number of macrophages in the OVX wounds (1556±128) than both OVX+E (984±95 (p=0.02) and the intact group (1026±91, p=0.01).ConclusionLack of systemic oestrogen delays mucosal healing in buccal wounds. This may explain gender differences in the oesophageal epithelial response to gastro-oesophageal reflux injury.Competing interestsNone declared.</description><identifier>ISSN: 0017-5749</identifier><identifier>EISSN: 1468-3288</identifier><identifier>DOI: 10.1136/gutjnl-2012-302514c.171</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and British Society of Gastroenterology</publisher><subject>Adenocarcinoma ; Biopsy ; Esophageal cancer ; Esophagitis ; Esophagus ; Estrogens ; Females ; Gastroesophageal reflux ; Hydrochloric acid ; Immunohistochemistry ; Inflammation ; Leukocytes (neutrophilic) ; Macrophages ; Mucosa ; Ovariectomy ; Ovaries ; Rodents ; Sex differences ; Sex hormones ; Statistical analysis ; Ulcers ; Wound healing</subject><ispartof>Gut, 2012-07, Vol.61 (Suppl 2), p.A254-A255</ispartof><rights>2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.</rights><rights>Copyright: 2012 © 2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://gut.bmj.com/content/61/Suppl_2/A254.3.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://gut.bmj.com/content/61/Suppl_2/A254.3.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,780,784,3194,23570,27923,27924,77371,77402</link.rule.ids></links><search><creatorcontrib>Theron, B T</creatorcontrib><creatorcontrib>Trudgill, N</creatorcontrib><title>PTU-171 Oestrogen plays a critical role in murine epithelial healing in a buccal model of reflux injury</title><title>Gut</title><addtitle>Gut</addtitle><description>IntroductionSevere oesophagitis, oesophageal adenocarcinoma (OAC) are more common in men and post-menopausal women. Female sex hormones may protect pre-menopausal women from gastro-oesophageal reflux mediated mucosal damage, delaying the onset of BO and development of OAC in women. We have demonstrated more rapid mucosal healing and less inflammatory response in females in a murine buccal model of reflux injury. We have used a model comparing intact female mice with oestrogen deprived mice (by removal of their ovaries) to determine if this effect may be oestrogen driven.MethodsFemale mice (C57 strain) were divided into three groups of 5: ovariectomised (OVX), OVX with oestrogen replacement (OVX+E) (50 μg oestradiol per day dorsal implants) and intact females. 1.5 mm buccal ulcers were induced using a punch biopsy and treated with 1 M hydrochloric acid. Wounds were harvested at day 4. Wound planimetry and immunohistochemistry for macrophages and neutrophils were compared in a blinded fashion.ResultsResults: Re-epithelialisation was greatest in the intact group (mean 0.88 mm SEM ± 0.22) compared to the OVX (0.51 mm ± 0.13) or OVX+E (0.79 mm ± 0.12) groups. The difference between intact and OVX groups was statistically significant (p=0.04). Neutrophil wound infiltration (cells/wound area) was greater in the OVX group (1842±75) than the intact group (1279±169, p There was a greater number of macrophages in the OVX wounds (1556±128) than both OVX+E (984±95 (p=0.02) and the intact group (1026±91, p=0.01).ConclusionLack of systemic oestrogen delays mucosal healing in buccal wounds. This may explain gender differences in the oesophageal epithelial response to gastro-oesophageal reflux injury.Competing interestsNone declared.</description><subject>Adenocarcinoma</subject><subject>Biopsy</subject><subject>Esophageal cancer</subject><subject>Esophagitis</subject><subject>Esophagus</subject><subject>Estrogens</subject><subject>Females</subject><subject>Gastroesophageal reflux</subject><subject>Hydrochloric acid</subject><subject>Immunohistochemistry</subject><subject>Inflammation</subject><subject>Leukocytes (neutrophilic)</subject><subject>Macrophages</subject><subject>Mucosa</subject><subject>Ovariectomy</subject><subject>Ovaries</subject><subject>Rodents</subject><subject>Sex differences</subject><subject>Sex hormones</subject><subject>Statistical analysis</subject><subject>Ulcers</subject><subject>Wound healing</subject><issn>0017-5749</issn><issn>1468-3288</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkMtOxCAUhonRxPHyDJK4RjlACyzNxFviLXE07gjt0JHKtCNtE2fnxhf1SWRS49rVWfzfzzl8CB0BPQHg-eli6OsmEEaBEU5ZBqI8AQlbaAIiV4QzpbbRhFKQJJNC76K9rqsppUppmCD_MHsiCf_-_Lp3XR_bhWvwKth1hy0uo-99aQOObXDYN3g5RN847Fa-f3XBp-TV2eCbxSa0uBjKDb1s5y7gtsLRVWH4SFk9xPUB2qls6Nzh79xHs4vz2fSK3NxfXk_PbkjBaA6kAleBnHOQqmRQaK2rTFiuldCi4CVkFXea29LqnBUin4OaV5RZBYV0TAq-j47HZ1exfR_Sl0zdDrFJGw2jXMlcKJ4lSo5UGduuS3eaVfRLG9cGqNloNaNWs9FqfrWa5Ck1ydj0Xe8-_mo2vplccpmZu-epuX3JuLqjD-Yx8Wzki2X97yU_pWGMeQ</recordid><startdate>201207</startdate><enddate>201207</enddate><creator>Theron, B T</creator><creator>Trudgill, N</creator><general>BMJ Publishing Group Ltd and British Society of Gastroenterology</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</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>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope></search><sort><creationdate>201207</creationdate><title>PTU-171 Oestrogen plays a critical role in murine epithelial healing in a buccal model of reflux injury</title><author>Theron, B T ; Trudgill, N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b2061-f1ef17d3178c21b999f54a398494b3c15f3e93aca962b46d18df02a81b7e2743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adenocarcinoma</topic><topic>Biopsy</topic><topic>Esophageal cancer</topic><topic>Esophagitis</topic><topic>Esophagus</topic><topic>Estrogens</topic><topic>Females</topic><topic>Gastroesophageal reflux</topic><topic>Hydrochloric acid</topic><topic>Immunohistochemistry</topic><topic>Inflammation</topic><topic>Leukocytes (neutrophilic)</topic><topic>Macrophages</topic><topic>Mucosa</topic><topic>Ovariectomy</topic><topic>Ovaries</topic><topic>Rodents</topic><topic>Sex differences</topic><topic>Sex hormones</topic><topic>Statistical analysis</topic><topic>Ulcers</topic><topic>Wound healing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Theron, B T</creatorcontrib><creatorcontrib>Trudgill, N</creatorcontrib><collection>Istex</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>Science Database (Alumni Edition)</collection><collection>STEM Database</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 UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>BMJ Journals</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>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science 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><jtitle>Gut</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Theron, B T</au><au>Trudgill, N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PTU-171 Oestrogen plays a critical role in murine epithelial healing in a buccal model of reflux injury</atitle><jtitle>Gut</jtitle><addtitle>Gut</addtitle><date>2012-07</date><risdate>2012</risdate><volume>61</volume><issue>Suppl 2</issue><spage>A254</spage><epage>A255</epage><pages>A254-A255</pages><issn>0017-5749</issn><eissn>1468-3288</eissn><abstract>IntroductionSevere oesophagitis, oesophageal adenocarcinoma (OAC) are more common in men and post-menopausal women. Female sex hormones may protect pre-menopausal women from gastro-oesophageal reflux mediated mucosal damage, delaying the onset of BO and development of OAC in women. We have demonstrated more rapid mucosal healing and less inflammatory response in females in a murine buccal model of reflux injury. We have used a model comparing intact female mice with oestrogen deprived mice (by removal of their ovaries) to determine if this effect may be oestrogen driven.MethodsFemale mice (C57 strain) were divided into three groups of 5: ovariectomised (OVX), OVX with oestrogen replacement (OVX+E) (50 μg oestradiol per day dorsal implants) and intact females. 1.5 mm buccal ulcers were induced using a punch biopsy and treated with 1 M hydrochloric acid. Wounds were harvested at day 4. Wound planimetry and immunohistochemistry for macrophages and neutrophils were compared in a blinded fashion.ResultsResults: Re-epithelialisation was greatest in the intact group (mean 0.88 mm SEM ± 0.22) compared to the OVX (0.51 mm ± 0.13) or OVX+E (0.79 mm ± 0.12) groups. The difference between intact and OVX groups was statistically significant (p=0.04). Neutrophil wound infiltration (cells/wound area) was greater in the OVX group (1842±75) than the intact group (1279±169, p There was a greater number of macrophages in the OVX wounds (1556±128) than both OVX+E (984±95 (p=0.02) and the intact group (1026±91, p=0.01).ConclusionLack of systemic oestrogen delays mucosal healing in buccal wounds. This may explain gender differences in the oesophageal epithelial response to gastro-oesophageal reflux injury.Competing interestsNone declared.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and British Society of Gastroenterology</pub><doi>10.1136/gutjnl-2012-302514c.171</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma Biopsy Esophageal cancer Esophagitis Esophagus Estrogens Females Gastroesophageal reflux Hydrochloric acid Immunohistochemistry Inflammation Leukocytes (neutrophilic) Macrophages Mucosa Ovariectomy Ovaries Rodents Sex differences Sex hormones Statistical analysis Ulcers Wound healing |
title | PTU-171 Oestrogen plays a critical role in murine epithelial healing in a buccal model of reflux injury |
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