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Effect of growth hormone, hyperbaric oxygen and combined therapy on the gastric serosa
To investigate the role of growth hormone (GH), hyperbaric oxygen therapy (HBOT) and combined therapy on the intestinal neomucosa formation of the gastric serosa. Forty-eight male Wistar-albino rats, weighing 250-280 g, were used in this study. The rats were divided into four groups (n = 12): Group...
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Published in: | World journal of gastroenterology : WJG 2013-05, Vol.19 (19), p.2904-2912 |
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description | To investigate the role of growth hormone (GH), hyperbaric oxygen therapy (HBOT) and combined therapy on the intestinal neomucosa formation of the gastric serosa.
Forty-eight male Wistar-albino rats, weighing 250-280 g, were used in this study. The rats were divided into four groups (n = 12): Group 1, control, gastric serosal patch; Group 2, gastric serosal patch + GH; Group 3, gastric serosal patch + HBOT; and Group 4, gastric serosal patch + GH + HBOT. Abdominal access was achieved through a midline incision, and after the 1-cm-long defect was created in the jejunum, a 1 cm × 1 cm patch of the gastric corpus was anastomosed to the jejunal defect. Venous blood samples were taken to determine the insulin-like growth factor 1 (IGF-1) and insulin-like growth factor binding protein 3 (IGFBP-3) basal levels. HBOT was performed in Groups 3 and 4. In Groups 2 and 4, human GH was given subcutaneously at a dose of 2 mg per kg/d for 28 d, beginning on the operation day. All animals were sacrificed 60 d after surgery. The jejunal segment and the gastric anastomotic area were excised for histological examination. The inflammatory process, granulation, collagen deposition and fibroblast activity at the neomucosa formation were studied and scored. Additionally, the villus density, villus height, and crypt depth were counted and recorded. The measurements of villus height and crypt depth were calculated with an ocular micrometer. New vessel growth was determined by calculatingeach new vessel in a 1 mm(2) area.
In the histological comparison of groups, no significant differences were observed between the control group and Groups 2 and 3 with respect to epithelialization, granulation, fibroblastic activity and the inflammatory process, but significant differences were present between the control group and all others groups (Groups 2-4) with respect to angiogenesis (P < 0.01) and collagen deposition (P < 0.05, P < 0.01). Significant differences between the control group and Group 4 were also observed with respect to epithelialization and fibroblastic activity (P < 0.01 and P < 0.05, respectively). There were significant differences in villus density in all of groups compared with the control group (P < 0.05). Crypt depth was significantly greater in Group 4 than in the control group (P < 0.05), but no other groups had deeper crypts. However, villus height was significantly longer in Groups 2 and 4 than in the control group (P < 0.05). The comparison of groups revealed, sig |
doi_str_mv | 10.3748/wjg.v19.i19.2904 |
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Forty-eight male Wistar-albino rats, weighing 250-280 g, were used in this study. The rats were divided into four groups (n = 12): Group 1, control, gastric serosal patch; Group 2, gastric serosal patch + GH; Group 3, gastric serosal patch + HBOT; and Group 4, gastric serosal patch + GH + HBOT. Abdominal access was achieved through a midline incision, and after the 1-cm-long defect was created in the jejunum, a 1 cm × 1 cm patch of the gastric corpus was anastomosed to the jejunal defect. Venous blood samples were taken to determine the insulin-like growth factor 1 (IGF-1) and insulin-like growth factor binding protein 3 (IGFBP-3) basal levels. HBOT was performed in Groups 3 and 4. In Groups 2 and 4, human GH was given subcutaneously at a dose of 2 mg per kg/d for 28 d, beginning on the operation day. All animals were sacrificed 60 d after surgery. The jejunal segment and the gastric anastomotic area were excised for histological examination. The inflammatory process, granulation, collagen deposition and fibroblast activity at the neomucosa formation were studied and scored. Additionally, the villus density, villus height, and crypt depth were counted and recorded. The measurements of villus height and crypt depth were calculated with an ocular micrometer. New vessel growth was determined by calculatingeach new vessel in a 1 mm(2) area.
In the histological comparison of groups, no significant differences were observed between the control group and Groups 2 and 3 with respect to epithelialization, granulation, fibroblastic activity and the inflammatory process, but significant differences were present between the control group and all others groups (Groups 2-4) with respect to angiogenesis (P < 0.01) and collagen deposition (P < 0.05, P < 0.01). Significant differences between the control group and Group 4 were also observed with respect to epithelialization and fibroblastic activity (P < 0.01 and P < 0.05, respectively). There were significant differences in villus density in all of groups compared with the control group (P < 0.05). Crypt depth was significantly greater in Group 4 than in the control group (P < 0.05), but no other groups had deeper crypts. However, villus height was significantly longer in Groups 2 and 4 than in the control group (P < 0.05). The comparison of groups revealed, significant difference between control group and Groups 2 and 4) with respect to the levels of IGF-1 and IGFBP-3 (P < 0.01) 3 wk after the operation.
HBOT or GH and combined therapy augmented on neomucosal formation. The use of combined therapy produced a synergistic effect on the histological, morphological and functional parameters.]]></description><identifier>ISSN: 1007-9327</identifier><identifier>EISSN: 2219-2840</identifier><identifier>DOI: 10.3748/wjg.v19.i19.2904</identifier><identifier>PMID: 23704823</identifier><language>eng</language><publisher>United States: Baishideng Publishing Group Co., Limited</publisher><subject>Anastomosis, Surgical ; Animals ; Combined Modality Therapy ; Disease Models, Animal ; Human Growth Hormone - pharmacology ; Hyperbaric Oxygenation ; Insulin-Like Growth Factor Binding Protein 3 - blood ; Insulin-Like Growth Factor I - metabolism ; Intestinal Mucosa - drug effects ; Intestinal Mucosa - metabolism ; Intestinal Mucosa - pathology ; Intestinal Mucosa - surgery ; Jejunum - drug effects ; Jejunum - metabolism ; Jejunum - pathology ; Jejunum - surgery ; Male ; Original ; Rats ; Rats, Wistar ; Regeneration - drug effects ; Serous Membrane - drug effects ; Serous Membrane - metabolism ; Serous Membrane - pathology ; Serous Membrane - surgery ; Short Bowel Syndrome - etiology ; Short Bowel Syndrome - metabolism ; Short Bowel Syndrome - pathology ; Short Bowel Syndrome - therapy ; Stomach - drug effects ; Stomach - metabolism ; Stomach - pathology ; Stomach - surgery ; Time Factors</subject><ispartof>World journal of gastroenterology : WJG, 2013-05, Vol.19 (19), p.2904-2912</ispartof><rights>2013 Baishideng Publishing Group Co., Limited. All rights reserved. 2013</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-23afc81946fba249ef0210241e206025d47a6aaee13f48d37609fa392c34233f3</citedby><cites>FETCH-LOGICAL-c396t-23afc81946fba249ef0210241e206025d47a6aaee13f48d37609fa392c34233f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3660815/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3660815/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23704823$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Adas, Gokhan</creatorcontrib><creatorcontrib>Adas, Mine</creatorcontrib><creatorcontrib>Arikan, Soykan</creatorcontrib><creatorcontrib>Sarvan, Ahu Kemik</creatorcontrib><creatorcontrib>Toklu, Akin Savas</creatorcontrib><creatorcontrib>Mert, Selva</creatorcontrib><creatorcontrib>Barut, Gul</creatorcontrib><creatorcontrib>Kamali, Sedat</creatorcontrib><creatorcontrib>Koc, Bora</creatorcontrib><creatorcontrib>Tutal, Firat</creatorcontrib><title>Effect of growth hormone, hyperbaric oxygen and combined therapy on the gastric serosa</title><title>World journal of gastroenterology : WJG</title><addtitle>World J Gastroenterol</addtitle><description><![CDATA[To investigate the role of growth hormone (GH), hyperbaric oxygen therapy (HBOT) and combined therapy on the intestinal neomucosa formation of the gastric serosa.
Forty-eight male Wistar-albino rats, weighing 250-280 g, were used in this study. The rats were divided into four groups (n = 12): Group 1, control, gastric serosal patch; Group 2, gastric serosal patch + GH; Group 3, gastric serosal patch + HBOT; and Group 4, gastric serosal patch + GH + HBOT. Abdominal access was achieved through a midline incision, and after the 1-cm-long defect was created in the jejunum, a 1 cm × 1 cm patch of the gastric corpus was anastomosed to the jejunal defect. Venous blood samples were taken to determine the insulin-like growth factor 1 (IGF-1) and insulin-like growth factor binding protein 3 (IGFBP-3) basal levels. HBOT was performed in Groups 3 and 4. In Groups 2 and 4, human GH was given subcutaneously at a dose of 2 mg per kg/d for 28 d, beginning on the operation day. All animals were sacrificed 60 d after surgery. The jejunal segment and the gastric anastomotic area were excised for histological examination. The inflammatory process, granulation, collagen deposition and fibroblast activity at the neomucosa formation were studied and scored. Additionally, the villus density, villus height, and crypt depth were counted and recorded. The measurements of villus height and crypt depth were calculated with an ocular micrometer. New vessel growth was determined by calculatingeach new vessel in a 1 mm(2) area.
In the histological comparison of groups, no significant differences were observed between the control group and Groups 2 and 3 with respect to epithelialization, granulation, fibroblastic activity and the inflammatory process, but significant differences were present between the control group and all others groups (Groups 2-4) with respect to angiogenesis (P < 0.01) and collagen deposition (P < 0.05, P < 0.01). Significant differences between the control group and Group 4 were also observed with respect to epithelialization and fibroblastic activity (P < 0.01 and P < 0.05, respectively). There were significant differences in villus density in all of groups compared with the control group (P < 0.05). Crypt depth was significantly greater in Group 4 than in the control group (P < 0.05), but no other groups had deeper crypts. However, villus height was significantly longer in Groups 2 and 4 than in the control group (P < 0.05). The comparison of groups revealed, significant difference between control group and Groups 2 and 4) with respect to the levels of IGF-1 and IGFBP-3 (P < 0.01) 3 wk after the operation.
HBOT or GH and combined therapy augmented on neomucosal formation. The use of combined therapy produced a synergistic effect on the histological, morphological and functional parameters.]]></description><subject>Anastomosis, Surgical</subject><subject>Animals</subject><subject>Combined Modality Therapy</subject><subject>Disease Models, Animal</subject><subject>Human Growth Hormone - pharmacology</subject><subject>Hyperbaric Oxygenation</subject><subject>Insulin-Like Growth Factor Binding Protein 3 - blood</subject><subject>Insulin-Like Growth Factor I - metabolism</subject><subject>Intestinal Mucosa - drug effects</subject><subject>Intestinal Mucosa - metabolism</subject><subject>Intestinal Mucosa - pathology</subject><subject>Intestinal Mucosa - surgery</subject><subject>Jejunum - drug effects</subject><subject>Jejunum - metabolism</subject><subject>Jejunum - pathology</subject><subject>Jejunum - surgery</subject><subject>Male</subject><subject>Original</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Regeneration - drug effects</subject><subject>Serous Membrane - drug effects</subject><subject>Serous Membrane - metabolism</subject><subject>Serous Membrane - pathology</subject><subject>Serous Membrane - surgery</subject><subject>Short Bowel Syndrome - etiology</subject><subject>Short Bowel Syndrome - metabolism</subject><subject>Short Bowel Syndrome - pathology</subject><subject>Short Bowel Syndrome - therapy</subject><subject>Stomach - drug effects</subject><subject>Stomach - metabolism</subject><subject>Stomach - pathology</subject><subject>Stomach - surgery</subject><subject>Time Factors</subject><issn>1007-9327</issn><issn>2219-2840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNpVkUlPwzAQhS0EoqVw54R85ECKtyy-IKGKTULiAlwt1xknqZI42CnQf48rCoKDNZb85o3ffAidUjLnuSguP1bV_J3KeRMPk0TsoSljVCasEGQfTSkheSI5yyfoKIQVIYzzlB2iCeM5EQXjU_R6Yy2YETuLK-8-xhrXzneuhwtcbwbwS-0bg93npoIe677ExnXLpocSjzV4PWyw67dXXOkwbqUBvAv6GB1Y3QY42dUZerm9eV7cJ49Pdw-L68fEcJmNCePamoJKkdmlZkKCJYwSJigwkhGWliLXmdYAlFtRlDzPiLSaS2a4iFksn6Grb99hveygNNCPXrdq8E2n_UY53aj_L31Tq8q9K55lpKBpNDjfGXj3toYwqq4JBtpW9-DWQVGepqKgeSajlHxLTUwYPNjfMZSoLQ4VcaiIQ0Ucaosjtpz9_d5vw8_--Rf-Uoie</recordid><startdate>20130521</startdate><enddate>20130521</enddate><creator>Adas, Gokhan</creator><creator>Adas, Mine</creator><creator>Arikan, Soykan</creator><creator>Sarvan, Ahu Kemik</creator><creator>Toklu, Akin Savas</creator><creator>Mert, Selva</creator><creator>Barut, Gul</creator><creator>Kamali, Sedat</creator><creator>Koc, Bora</creator><creator>Tutal, Firat</creator><general>Baishideng Publishing Group Co., Limited</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><scope>5PM</scope></search><sort><creationdate>20130521</creationdate><title>Effect of growth hormone, hyperbaric oxygen and combined therapy on the gastric serosa</title><author>Adas, Gokhan ; Adas, Mine ; Arikan, Soykan ; Sarvan, Ahu Kemik ; Toklu, Akin Savas ; Mert, Selva ; Barut, Gul ; Kamali, Sedat ; Koc, Bora ; Tutal, Firat</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-23afc81946fba249ef0210241e206025d47a6aaee13f48d37609fa392c34233f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Anastomosis, Surgical</topic><topic>Animals</topic><topic>Combined Modality Therapy</topic><topic>Disease Models, Animal</topic><topic>Human Growth Hormone - pharmacology</topic><topic>Hyperbaric Oxygenation</topic><topic>Insulin-Like Growth Factor Binding Protein 3 - blood</topic><topic>Insulin-Like Growth Factor I - metabolism</topic><topic>Intestinal Mucosa - drug effects</topic><topic>Intestinal Mucosa - metabolism</topic><topic>Intestinal Mucosa - pathology</topic><topic>Intestinal Mucosa - surgery</topic><topic>Jejunum - drug effects</topic><topic>Jejunum - metabolism</topic><topic>Jejunum - pathology</topic><topic>Jejunum - surgery</topic><topic>Male</topic><topic>Original</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Regeneration - drug effects</topic><topic>Serous Membrane - drug effects</topic><topic>Serous Membrane - metabolism</topic><topic>Serous Membrane - pathology</topic><topic>Serous Membrane - surgery</topic><topic>Short Bowel Syndrome - etiology</topic><topic>Short Bowel Syndrome - metabolism</topic><topic>Short Bowel Syndrome - pathology</topic><topic>Short Bowel Syndrome - therapy</topic><topic>Stomach - drug effects</topic><topic>Stomach - metabolism</topic><topic>Stomach - pathology</topic><topic>Stomach - surgery</topic><topic>Time Factors</topic><toplevel>online_resources</toplevel><creatorcontrib>Adas, Gokhan</creatorcontrib><creatorcontrib>Adas, Mine</creatorcontrib><creatorcontrib>Arikan, Soykan</creatorcontrib><creatorcontrib>Sarvan, Ahu Kemik</creatorcontrib><creatorcontrib>Toklu, Akin Savas</creatorcontrib><creatorcontrib>Mert, Selva</creatorcontrib><creatorcontrib>Barut, Gul</creatorcontrib><creatorcontrib>Kamali, Sedat</creatorcontrib><creatorcontrib>Koc, Bora</creatorcontrib><creatorcontrib>Tutal, Firat</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>World journal of gastroenterology : WJG</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Adas, Gokhan</au><au>Adas, Mine</au><au>Arikan, Soykan</au><au>Sarvan, Ahu Kemik</au><au>Toklu, Akin Savas</au><au>Mert, Selva</au><au>Barut, Gul</au><au>Kamali, Sedat</au><au>Koc, Bora</au><au>Tutal, Firat</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of growth hormone, hyperbaric oxygen and combined therapy on the gastric serosa</atitle><jtitle>World journal of gastroenterology : WJG</jtitle><addtitle>World J Gastroenterol</addtitle><date>2013-05-21</date><risdate>2013</risdate><volume>19</volume><issue>19</issue><spage>2904</spage><epage>2912</epage><pages>2904-2912</pages><issn>1007-9327</issn><eissn>2219-2840</eissn><abstract><![CDATA[To investigate the role of growth hormone (GH), hyperbaric oxygen therapy (HBOT) and combined therapy on the intestinal neomucosa formation of the gastric serosa.
Forty-eight male Wistar-albino rats, weighing 250-280 g, were used in this study. The rats were divided into four groups (n = 12): Group 1, control, gastric serosal patch; Group 2, gastric serosal patch + GH; Group 3, gastric serosal patch + HBOT; and Group 4, gastric serosal patch + GH + HBOT. Abdominal access was achieved through a midline incision, and after the 1-cm-long defect was created in the jejunum, a 1 cm × 1 cm patch of the gastric corpus was anastomosed to the jejunal defect. Venous blood samples were taken to determine the insulin-like growth factor 1 (IGF-1) and insulin-like growth factor binding protein 3 (IGFBP-3) basal levels. HBOT was performed in Groups 3 and 4. In Groups 2 and 4, human GH was given subcutaneously at a dose of 2 mg per kg/d for 28 d, beginning on the operation day. All animals were sacrificed 60 d after surgery. The jejunal segment and the gastric anastomotic area were excised for histological examination. The inflammatory process, granulation, collagen deposition and fibroblast activity at the neomucosa formation were studied and scored. Additionally, the villus density, villus height, and crypt depth were counted and recorded. The measurements of villus height and crypt depth were calculated with an ocular micrometer. New vessel growth was determined by calculatingeach new vessel in a 1 mm(2) area.
In the histological comparison of groups, no significant differences were observed between the control group and Groups 2 and 3 with respect to epithelialization, granulation, fibroblastic activity and the inflammatory process, but significant differences were present between the control group and all others groups (Groups 2-4) with respect to angiogenesis (P < 0.01) and collagen deposition (P < 0.05, P < 0.01). Significant differences between the control group and Group 4 were also observed with respect to epithelialization and fibroblastic activity (P < 0.01 and P < 0.05, respectively). There were significant differences in villus density in all of groups compared with the control group (P < 0.05). Crypt depth was significantly greater in Group 4 than in the control group (P < 0.05), but no other groups had deeper crypts. However, villus height was significantly longer in Groups 2 and 4 than in the control group (P < 0.05). The comparison of groups revealed, significant difference between control group and Groups 2 and 4) with respect to the levels of IGF-1 and IGFBP-3 (P < 0.01) 3 wk after the operation.
HBOT or GH and combined therapy augmented on neomucosal formation. The use of combined therapy produced a synergistic effect on the histological, morphological and functional parameters.]]></abstract><cop>United States</cop><pub>Baishideng Publishing Group Co., Limited</pub><pmid>23704823</pmid><doi>10.3748/wjg.v19.i19.2904</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anastomosis, Surgical Animals Combined Modality Therapy Disease Models, Animal Human Growth Hormone - pharmacology Hyperbaric Oxygenation Insulin-Like Growth Factor Binding Protein 3 - blood Insulin-Like Growth Factor I - metabolism Intestinal Mucosa - drug effects Intestinal Mucosa - metabolism Intestinal Mucosa - pathology Intestinal Mucosa - surgery Jejunum - drug effects Jejunum - metabolism Jejunum - pathology Jejunum - surgery Male Original Rats Rats, Wistar Regeneration - drug effects Serous Membrane - drug effects Serous Membrane - metabolism Serous Membrane - pathology Serous Membrane - surgery Short Bowel Syndrome - etiology Short Bowel Syndrome - metabolism Short Bowel Syndrome - pathology Short Bowel Syndrome - therapy Stomach - drug effects Stomach - metabolism Stomach - pathology Stomach - surgery Time Factors |
title | Effect of growth hormone, hyperbaric oxygen and combined therapy on the gastric serosa |
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