Green tea polyphenols ameliorate pancreatic injury in cerulein-induced murine acute pancreatitis
Green tea polyphenols (GTPs) are naturally occurring antioxidants acting through pathways that include reactive oxygen species and nuclear factor kappa B (NF-kappaB). This study investigates the effect of GTPs in a cerulein-induced murine model of acute pancreatitis (AP). Male CD mice (median weight...
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Veröffentlicht in: | Pancreas 2009-11, Vol.38 (8), p.954-967 |
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creator | Babu, Benoy I Malleo, Giuseppe Genovese, Tiziana Mazzon, Emanuela Di Paola, Rosanna Crisafulli, Concetta Caminiti, Rocco Siriwardena, Ajith K Cuzzocrea, Salvatore |
description | Green tea polyphenols (GTPs) are naturally occurring antioxidants acting through pathways that include reactive oxygen species and nuclear factor kappa B (NF-kappaB). This study investigates the effect of GTPs in a cerulein-induced murine model of acute pancreatitis (AP).
Male CD mice (median weight, 37.7 g) were divided into 4 groups: mice administered with cerulein alone, cerulein and GTP, saline alone (sham), and GTP alone. Acute pancreatitis was induced by serial intraperitoneal administration of cerulein (50 microg/kg, x6). Green tea polyphenol was administered intraperitoneally at 25 mg/kg on the first, third, and sixth hours after pancreatitis induction.We analyzed histologic and biochemical features of AP, NF-kappaB pathway activity, leukocyte-mediated damage, cytokine levels, oxidative stress injury, lipid peroxidation, expression of poly-(adenosine diphosphate-ribose) synthetase, and presence of apoptosis.
Treatment with GTP reduced the histologic and biochemical features of AP. Western blot revealed significant NF-kappaB inactivation. Immunostaining for P selectin and intercellular adhesion molecule 1, tumor necrosis factor alpha, transforming growth factor beta, vascular endothelial growth factor, nitrotirosine, poly-(adenosine diphosphate ribose) synthetase, and malondialdheide levels were significantly reduced. There was a significant down-regulation of apoptotic markers.
Our results demonstrated that GTP significantly ameliorated the effects of cerulein-induced AP in mice. These effects of GTP are mediated by actions at the NF-kappaB/IkB (inhibitor kB) proteins and oxidative stress pathways. |
doi_str_mv | 10.1097/MPA.0b013e3181b28d11 |
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Male CD mice (median weight, 37.7 g) were divided into 4 groups: mice administered with cerulein alone, cerulein and GTP, saline alone (sham), and GTP alone. Acute pancreatitis was induced by serial intraperitoneal administration of cerulein (50 microg/kg, x6). Green tea polyphenol was administered intraperitoneally at 25 mg/kg on the first, third, and sixth hours after pancreatitis induction.We analyzed histologic and biochemical features of AP, NF-kappaB pathway activity, leukocyte-mediated damage, cytokine levels, oxidative stress injury, lipid peroxidation, expression of poly-(adenosine diphosphate-ribose) synthetase, and presence of apoptosis.
Treatment with GTP reduced the histologic and biochemical features of AP. Western blot revealed significant NF-kappaB inactivation. Immunostaining for P selectin and intercellular adhesion molecule 1, tumor necrosis factor alpha, transforming growth factor beta, vascular endothelial growth factor, nitrotirosine, poly-(adenosine diphosphate ribose) synthetase, and malondialdheide levels were significantly reduced. There was a significant down-regulation of apoptotic markers.
Our results demonstrated that GTP significantly ameliorated the effects of cerulein-induced AP in mice. These effects of GTP are mediated by actions at the NF-kappaB/IkB (inhibitor kB) proteins and oxidative stress pathways.</description><identifier>ISSN: 0885-3177</identifier><identifier>EISSN: 1536-4828</identifier><identifier>DOI: 10.1097/MPA.0b013e3181b28d11</identifier><identifier>PMID: 19672210</identifier><language>eng</language><publisher>United States</publisher><subject>Acute Disease ; Animals ; Apoptosis - drug effects ; Blotting, Western ; Ceruletide ; I-kappa B Proteins - metabolism ; Immunohistochemistry ; In Situ Nick-End Labeling ; Injections, Intraperitoneal ; Intercellular Adhesion Molecule-1 - metabolism ; Lipid Peroxidation - drug effects ; Male ; Mice ; Neutrophil Infiltration - drug effects ; NF-kappa B - metabolism ; P-Selectin - metabolism ; Pancreas - drug effects ; Pancreas - metabolism ; Pancreas - pathology ; Pancreatitis - chemically induced ; Pancreatitis - prevention & control ; Phenol - administration & dosage ; Phenol - pharmacology ; Poly(ADP-ribose) Polymerases - metabolism ; Tea - chemistry ; Time Factors ; Transforming Growth Factor beta - metabolism ; Tumor Necrosis Factor-alpha - metabolism ; Vascular Endothelial Growth Factor A - metabolism</subject><ispartof>Pancreas, 2009-11, Vol.38 (8), p.954-967</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-e58f7942d6be2ec734d14d377a75244929fe6ad47d8d67b0899fe7e46a6db08c3</citedby><cites>FETCH-LOGICAL-c372t-e58f7942d6be2ec734d14d377a75244929fe6ad47d8d67b0899fe7e46a6db08c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19672210$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Babu, Benoy I</creatorcontrib><creatorcontrib>Malleo, Giuseppe</creatorcontrib><creatorcontrib>Genovese, Tiziana</creatorcontrib><creatorcontrib>Mazzon, Emanuela</creatorcontrib><creatorcontrib>Di Paola, Rosanna</creatorcontrib><creatorcontrib>Crisafulli, Concetta</creatorcontrib><creatorcontrib>Caminiti, Rocco</creatorcontrib><creatorcontrib>Siriwardena, Ajith K</creatorcontrib><creatorcontrib>Cuzzocrea, Salvatore</creatorcontrib><title>Green tea polyphenols ameliorate pancreatic injury in cerulein-induced murine acute pancreatitis</title><title>Pancreas</title><addtitle>Pancreas</addtitle><description>Green tea polyphenols (GTPs) are naturally occurring antioxidants acting through pathways that include reactive oxygen species and nuclear factor kappa B (NF-kappaB). This study investigates the effect of GTPs in a cerulein-induced murine model of acute pancreatitis (AP).
Male CD mice (median weight, 37.7 g) were divided into 4 groups: mice administered with cerulein alone, cerulein and GTP, saline alone (sham), and GTP alone. Acute pancreatitis was induced by serial intraperitoneal administration of cerulein (50 microg/kg, x6). Green tea polyphenol was administered intraperitoneally at 25 mg/kg on the first, third, and sixth hours after pancreatitis induction.We analyzed histologic and biochemical features of AP, NF-kappaB pathway activity, leukocyte-mediated damage, cytokine levels, oxidative stress injury, lipid peroxidation, expression of poly-(adenosine diphosphate-ribose) synthetase, and presence of apoptosis.
Treatment with GTP reduced the histologic and biochemical features of AP. Western blot revealed significant NF-kappaB inactivation. Immunostaining for P selectin and intercellular adhesion molecule 1, tumor necrosis factor alpha, transforming growth factor beta, vascular endothelial growth factor, nitrotirosine, poly-(adenosine diphosphate ribose) synthetase, and malondialdheide levels were significantly reduced. There was a significant down-regulation of apoptotic markers.
Our results demonstrated that GTP significantly ameliorated the effects of cerulein-induced AP in mice. These effects of GTP are mediated by actions at the NF-kappaB/IkB (inhibitor kB) proteins and oxidative stress pathways.</description><subject>Acute Disease</subject><subject>Animals</subject><subject>Apoptosis - drug effects</subject><subject>Blotting, Western</subject><subject>Ceruletide</subject><subject>I-kappa B Proteins - metabolism</subject><subject>Immunohistochemistry</subject><subject>In Situ Nick-End Labeling</subject><subject>Injections, Intraperitoneal</subject><subject>Intercellular Adhesion Molecule-1 - metabolism</subject><subject>Lipid Peroxidation - drug effects</subject><subject>Male</subject><subject>Mice</subject><subject>Neutrophil Infiltration - drug effects</subject><subject>NF-kappa B - metabolism</subject><subject>P-Selectin - metabolism</subject><subject>Pancreas - drug effects</subject><subject>Pancreas - metabolism</subject><subject>Pancreas - pathology</subject><subject>Pancreatitis - chemically induced</subject><subject>Pancreatitis - prevention & control</subject><subject>Phenol - administration & dosage</subject><subject>Phenol - pharmacology</subject><subject>Poly(ADP-ribose) Polymerases - metabolism</subject><subject>Tea - chemistry</subject><subject>Time Factors</subject><subject>Transforming Growth Factor beta - metabolism</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><subject>Vascular Endothelial Growth Factor A - metabolism</subject><issn>0885-3177</issn><issn>1536-4828</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkEtLAzEUhYMotlb_gUh2rqbmNZNkWYpWoaILXY-Z5A6mzMtkZtF_b6QFxdXhXM45Fz6ErilZUqLl3fPrakkqQjlwqmjFlKP0BM1pzotMKKZO0ZwolWecSjlDFzHuCKGS5_oczaguJGOUzNHHJgB0eASDh77ZD5_Q9U3EpoXG98GMgAfT2QBm9Bb7bjeFfRJsIUwN-C7znZssONxOwXeAjZ3-VkYfL9FZbZoIV0ddoPeH-7f1Y7Z92TytV9vMcsnGDHJVSy2YKypgYCUXjgrHpTQyZ0JopmsojBPSKVfIiiidDhJEYQqXnOULdHvYHUL_NUEcy9ZHC01jOuinWKZFmmBxnZLikLShjzFAXQ7BtybsS0rKH7RlQlv-R5tqN8cHU9WC-y0dWfJv-I13mg</recordid><startdate>200911</startdate><enddate>200911</enddate><creator>Babu, Benoy I</creator><creator>Malleo, Giuseppe</creator><creator>Genovese, Tiziana</creator><creator>Mazzon, Emanuela</creator><creator>Di Paola, Rosanna</creator><creator>Crisafulli, Concetta</creator><creator>Caminiti, Rocco</creator><creator>Siriwardena, Ajith K</creator><creator>Cuzzocrea, Salvatore</creator><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>200911</creationdate><title>Green tea polyphenols ameliorate pancreatic injury in cerulein-induced murine acute pancreatitis</title><author>Babu, Benoy I ; Malleo, Giuseppe ; Genovese, Tiziana ; Mazzon, Emanuela ; Di Paola, Rosanna ; Crisafulli, Concetta ; Caminiti, Rocco ; Siriwardena, Ajith K ; Cuzzocrea, Salvatore</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c372t-e58f7942d6be2ec734d14d377a75244929fe6ad47d8d67b0899fe7e46a6db08c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Acute Disease</topic><topic>Animals</topic><topic>Apoptosis - drug effects</topic><topic>Blotting, Western</topic><topic>Ceruletide</topic><topic>I-kappa B Proteins - metabolism</topic><topic>Immunohistochemistry</topic><topic>In Situ Nick-End Labeling</topic><topic>Injections, Intraperitoneal</topic><topic>Intercellular Adhesion Molecule-1 - metabolism</topic><topic>Lipid Peroxidation - drug effects</topic><topic>Male</topic><topic>Mice</topic><topic>Neutrophil Infiltration - drug effects</topic><topic>NF-kappa B - metabolism</topic><topic>P-Selectin - metabolism</topic><topic>Pancreas - drug effects</topic><topic>Pancreas - metabolism</topic><topic>Pancreas - pathology</topic><topic>Pancreatitis - chemically induced</topic><topic>Pancreatitis - prevention & control</topic><topic>Phenol - administration & dosage</topic><topic>Phenol - pharmacology</topic><topic>Poly(ADP-ribose) Polymerases - metabolism</topic><topic>Tea - chemistry</topic><topic>Time Factors</topic><topic>Transforming Growth Factor beta - metabolism</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><topic>Vascular Endothelial Growth Factor A - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Babu, Benoy I</creatorcontrib><creatorcontrib>Malleo, Giuseppe</creatorcontrib><creatorcontrib>Genovese, Tiziana</creatorcontrib><creatorcontrib>Mazzon, Emanuela</creatorcontrib><creatorcontrib>Di Paola, Rosanna</creatorcontrib><creatorcontrib>Crisafulli, Concetta</creatorcontrib><creatorcontrib>Caminiti, Rocco</creatorcontrib><creatorcontrib>Siriwardena, Ajith K</creatorcontrib><creatorcontrib>Cuzzocrea, Salvatore</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>Pancreas</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Babu, Benoy I</au><au>Malleo, Giuseppe</au><au>Genovese, Tiziana</au><au>Mazzon, Emanuela</au><au>Di Paola, Rosanna</au><au>Crisafulli, Concetta</au><au>Caminiti, Rocco</au><au>Siriwardena, Ajith K</au><au>Cuzzocrea, Salvatore</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Green tea polyphenols ameliorate pancreatic injury in cerulein-induced murine acute pancreatitis</atitle><jtitle>Pancreas</jtitle><addtitle>Pancreas</addtitle><date>2009-11</date><risdate>2009</risdate><volume>38</volume><issue>8</issue><spage>954</spage><epage>967</epage><pages>954-967</pages><issn>0885-3177</issn><eissn>1536-4828</eissn><abstract>Green tea polyphenols (GTPs) are naturally occurring antioxidants acting through pathways that include reactive oxygen species and nuclear factor kappa B (NF-kappaB). This study investigates the effect of GTPs in a cerulein-induced murine model of acute pancreatitis (AP).
Male CD mice (median weight, 37.7 g) were divided into 4 groups: mice administered with cerulein alone, cerulein and GTP, saline alone (sham), and GTP alone. Acute pancreatitis was induced by serial intraperitoneal administration of cerulein (50 microg/kg, x6). Green tea polyphenol was administered intraperitoneally at 25 mg/kg on the first, third, and sixth hours after pancreatitis induction.We analyzed histologic and biochemical features of AP, NF-kappaB pathway activity, leukocyte-mediated damage, cytokine levels, oxidative stress injury, lipid peroxidation, expression of poly-(adenosine diphosphate-ribose) synthetase, and presence of apoptosis.
Treatment with GTP reduced the histologic and biochemical features of AP. Western blot revealed significant NF-kappaB inactivation. Immunostaining for P selectin and intercellular adhesion molecule 1, tumor necrosis factor alpha, transforming growth factor beta, vascular endothelial growth factor, nitrotirosine, poly-(adenosine diphosphate ribose) synthetase, and malondialdheide levels were significantly reduced. There was a significant down-regulation of apoptotic markers.
Our results demonstrated that GTP significantly ameliorated the effects of cerulein-induced AP in mice. These effects of GTP are mediated by actions at the NF-kappaB/IkB (inhibitor kB) proteins and oxidative stress pathways.</abstract><cop>United States</cop><pmid>19672210</pmid><doi>10.1097/MPA.0b013e3181b28d11</doi><tpages>14</tpages></addata></record> |
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subjects | Acute Disease Animals Apoptosis - drug effects Blotting, Western Ceruletide I-kappa B Proteins - metabolism Immunohistochemistry In Situ Nick-End Labeling Injections, Intraperitoneal Intercellular Adhesion Molecule-1 - metabolism Lipid Peroxidation - drug effects Male Mice Neutrophil Infiltration - drug effects NF-kappa B - metabolism P-Selectin - metabolism Pancreas - drug effects Pancreas - metabolism Pancreas - pathology Pancreatitis - chemically induced Pancreatitis - prevention & control Phenol - administration & dosage Phenol - pharmacology Poly(ADP-ribose) Polymerases - metabolism Tea - chemistry Time Factors Transforming Growth Factor beta - metabolism Tumor Necrosis Factor-alpha - metabolism Vascular Endothelial Growth Factor A - metabolism |
title | Green tea polyphenols ameliorate pancreatic injury in cerulein-induced murine acute pancreatitis |
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