The effect of antibiotic and probiotic combination therapy on secondary pancreatic infections and oxidative stress parameters in experimental acute necrotizing pancreatitis
Ciprofloxacin and meropenem have effects on intestinal bacteria that are responsible for pancreatic infection, and on the basis of recent data it has been argued that probiotics, especially those used in the food industry, could improve efforts to prevent and treat secondary pancreatic infections by...
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Veröffentlicht in: | Pancreas 2003-05, Vol.26 (4), p.363-367 |
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creator | AKYOL, Sedat MAS, M. Refik KOCAR, I. Hakki COMERT, Bilgin ATESKAN, Ümit YASAR, Mehmet AYDOGAN, Hakan DEVECI, Salih AKAY, Cemal MAS, Nuket YENER, Nuran |
description | Ciprofloxacin and meropenem have effects on intestinal bacteria that are responsible for pancreatic infection, and on the basis of recent data it has been argued that probiotics, especially those used in the food industry, could improve efforts to prevent and treat secondary pancreatic infections by inhibiting bacterial translocation.
To evaluate the effects of probiotic treatment alone or in combination with early administration of two different antibiotics on serum amylase, pancreatic histopathology, bacterial translocation, and oxidative markers.
Acute pancreatitis was induced in rats with 3% sodium taurocholate (1 mL/kg intraductally), except in group VI (sham group). After the stabilization period, the rats were divided into seven groups (n = 20) randomly. At hour 6 after injection, group I rats received probiotic Saccharomyces boulardii (25 mg/d orally q.d.), group II received meropenem (60 mg/kg intraperitoneally b.i.d.), group III received ciprofloxacin (40 mg/kg intraperitoneally b.i.d.), group IV received the same dose of probiotic plus meropenem, and group V received probiotic plus ciprofloxacin. Treatment was not given to group VI (sham group) and group VII (pancreatitis group). At hour 48 after induction, specimens were collected.
Although histopathologic scores in treatment groups were found to be lower than in group VII, the difference was statistically significant only in group V (p < 0.001). In evaluation of oxidative stress, we found that MDA levels decreased and SOD levels increased in treatment groups in comparison with levels in group VII. Probiotic treatment alone reduced bacterial translocation. Probiotic-antibiotic combination therapy was shown to improve histopathologic scores and oxidative parameters. |
doi_str_mv | 10.1097/00006676-200305000-00009 |
format | Article |
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To evaluate the effects of probiotic treatment alone or in combination with early administration of two different antibiotics on serum amylase, pancreatic histopathology, bacterial translocation, and oxidative markers.
Acute pancreatitis was induced in rats with 3% sodium taurocholate (1 mL/kg intraductally), except in group VI (sham group). After the stabilization period, the rats were divided into seven groups (n = 20) randomly. At hour 6 after injection, group I rats received probiotic Saccharomyces boulardii (25 mg/d orally q.d.), group II received meropenem (60 mg/kg intraperitoneally b.i.d.), group III received ciprofloxacin (40 mg/kg intraperitoneally b.i.d.), group IV received the same dose of probiotic plus meropenem, and group V received probiotic plus ciprofloxacin. Treatment was not given to group VI (sham group) and group VII (pancreatitis group). At hour 48 after induction, specimens were collected.
Although histopathologic scores in treatment groups were found to be lower than in group VII, the difference was statistically significant only in group V (p < 0.001). In evaluation of oxidative stress, we found that MDA levels decreased and SOD levels increased in treatment groups in comparison with levels in group VII. Probiotic treatment alone reduced bacterial translocation. Probiotic-antibiotic combination therapy was shown to improve histopathologic scores and oxidative parameters.</description><identifier>ISSN: 0885-3177</identifier><identifier>EISSN: 1536-4828</identifier><identifier>DOI: 10.1097/00006676-200305000-00009</identifier><identifier>PMID: 12717269</identifier><identifier>CODEN: PANCE4</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Analysis of Variance ; Animals ; Anti-Bacterial Agents - pharmacology ; Anti-Bacterial Agents - therapeutic use ; Bacterial Infections - microbiology ; Bacterial Infections - prevention & control ; Bacterial Translocation - drug effects ; Biological and medical sciences ; Ciprofloxacin - pharmacology ; Ciprofloxacin - therapeutic use ; Combined Modality Therapy ; Gastroenterology. Liver. Pancreas. Abdomen ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Male ; Malondialdehyde - metabolism ; Medical sciences ; Meropenem ; Other diseases. Semiology ; Oxidative Stress - drug effects ; Pancreatitis, Acute Necrotizing - drug therapy ; Pancreatitis, Acute Necrotizing - metabolism ; Pancreatitis, Acute Necrotizing - microbiology ; Probiotics - pharmacology ; Probiotics - therapeutic use ; Rats ; Rats, Sprague-Dawley ; Saccharomyces - physiology ; Superoxide Dismutase - metabolism ; Taurocholic Acid ; Thienamycins - pharmacology ; Thienamycins - therapeutic use</subject><ispartof>Pancreas, 2003-05, Vol.26 (4), p.363-367</ispartof><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-26842f0b1e7d588a3c2e05b69c004ef696be1735f9db78ed31df8e7ef47725a23</citedby><cites>FETCH-LOGICAL-c372t-26842f0b1e7d588a3c2e05b69c004ef696be1735f9db78ed31df8e7ef47725a23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14770948$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12717269$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>AKYOL, Sedat</creatorcontrib><creatorcontrib>MAS, M. Refik</creatorcontrib><creatorcontrib>KOCAR, I. Hakki</creatorcontrib><creatorcontrib>COMERT, Bilgin</creatorcontrib><creatorcontrib>ATESKAN, Ümit</creatorcontrib><creatorcontrib>YASAR, Mehmet</creatorcontrib><creatorcontrib>AYDOGAN, Hakan</creatorcontrib><creatorcontrib>DEVECI, Salih</creatorcontrib><creatorcontrib>AKAY, Cemal</creatorcontrib><creatorcontrib>MAS, Nuket</creatorcontrib><creatorcontrib>YENER, Nuran</creatorcontrib><title>The effect of antibiotic and probiotic combination therapy on secondary pancreatic infections and oxidative stress parameters in experimental acute necrotizing pancreatitis</title><title>Pancreas</title><addtitle>Pancreas</addtitle><description>Ciprofloxacin and meropenem have effects on intestinal bacteria that are responsible for pancreatic infection, and on the basis of recent data it has been argued that probiotics, especially those used in the food industry, could improve efforts to prevent and treat secondary pancreatic infections by inhibiting bacterial translocation.
To evaluate the effects of probiotic treatment alone or in combination with early administration of two different antibiotics on serum amylase, pancreatic histopathology, bacterial translocation, and oxidative markers.
Acute pancreatitis was induced in rats with 3% sodium taurocholate (1 mL/kg intraductally), except in group VI (sham group). After the stabilization period, the rats were divided into seven groups (n = 20) randomly. At hour 6 after injection, group I rats received probiotic Saccharomyces boulardii (25 mg/d orally q.d.), group II received meropenem (60 mg/kg intraperitoneally b.i.d.), group III received ciprofloxacin (40 mg/kg intraperitoneally b.i.d.), group IV received the same dose of probiotic plus meropenem, and group V received probiotic plus ciprofloxacin. Treatment was not given to group VI (sham group) and group VII (pancreatitis group). At hour 48 after induction, specimens were collected.
Although histopathologic scores in treatment groups were found to be lower than in group VII, the difference was statistically significant only in group V (p < 0.001). In evaluation of oxidative stress, we found that MDA levels decreased and SOD levels increased in treatment groups in comparison with levels in group VII. Probiotic treatment alone reduced bacterial translocation. Probiotic-antibiotic combination therapy was shown to improve histopathologic scores and oxidative parameters.</description><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>Bacterial Infections - microbiology</subject><subject>Bacterial Infections - prevention & control</subject><subject>Bacterial Translocation - drug effects</subject><subject>Biological and medical sciences</subject><subject>Ciprofloxacin - pharmacology</subject><subject>Ciprofloxacin - therapeutic use</subject><subject>Combined Modality Therapy</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Male</subject><subject>Malondialdehyde - metabolism</subject><subject>Medical sciences</subject><subject>Meropenem</subject><subject>Other diseases. Semiology</subject><subject>Oxidative Stress - drug effects</subject><subject>Pancreatitis, Acute Necrotizing - drug therapy</subject><subject>Pancreatitis, Acute Necrotizing - metabolism</subject><subject>Pancreatitis, Acute Necrotizing - microbiology</subject><subject>Probiotics - pharmacology</subject><subject>Probiotics - therapeutic use</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Saccharomyces - physiology</subject><subject>Superoxide Dismutase - metabolism</subject><subject>Taurocholic Acid</subject><subject>Thienamycins - pharmacology</subject><subject>Thienamycins - therapeutic use</subject><issn>0885-3177</issn><issn>1536-4828</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkctu1TAQhi0EoqeFV0DewC7Fl8SXJaooIFViU9aR44ypUeIE2we1PBMPyaQNHG88M_rmnxshlLNLzqx-z_AppVUjGJOsQ6_ZQvYZOfBOqqY1wjwnB2ZM10iu9Rk5L-UHY1zLzr4kZ1xoroWyB_Ln9g4ohAC-0iVQl2oc4lKjR3Oka152zy_zEJOrcUm03kF26wNFs4Bf0ujyA11d8hncxsa0ySFZHkWW-zhi_BfQUjOUgmh2M1TIBVEK9yvkOEOqbqLOHyvQBD5j1d8xfT_p1lhekRfBTQVe7_8F-Xb98fbqc3Pz9dOXqw83jZda1EYo04rABg567Ixx0gtg3aCsZ6yFoKwaYNtEsOOgDYySj8GAhtBqLTon5AV596SL8_88Qqn9HIuHaXIJlmPptRSiM1ohaJ5A7LeUDKFfcRRcR89Zv12q_3ep_v-lHkMWU9_sNY7DDOMpcT8NAm93wBXvppBxEbGcOGyW2dbIv_EYoTI</recordid><startdate>20030501</startdate><enddate>20030501</enddate><creator>AKYOL, Sedat</creator><creator>MAS, M. Refik</creator><creator>KOCAR, I. Hakki</creator><creator>COMERT, Bilgin</creator><creator>ATESKAN, Ümit</creator><creator>YASAR, Mehmet</creator><creator>AYDOGAN, Hakan</creator><creator>DEVECI, Salih</creator><creator>AKAY, Cemal</creator><creator>MAS, Nuket</creator><creator>YENER, Nuran</creator><general>Lippincott Williams & Wilkins</general><scope>IQODW</scope><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>20030501</creationdate><title>The effect of antibiotic and probiotic combination therapy on secondary pancreatic infections and oxidative stress parameters in experimental acute necrotizing pancreatitis</title><author>AKYOL, Sedat ; MAS, M. Refik ; KOCAR, I. Hakki ; COMERT, Bilgin ; ATESKAN, Ümit ; YASAR, Mehmet ; AYDOGAN, Hakan ; DEVECI, Salih ; AKAY, Cemal ; MAS, Nuket ; YENER, Nuran</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c372t-26842f0b1e7d588a3c2e05b69c004ef696be1735f9db78ed31df8e7ef47725a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>Bacterial Infections - microbiology</topic><topic>Bacterial Infections - prevention & control</topic><topic>Bacterial Translocation - drug effects</topic><topic>Biological and medical sciences</topic><topic>Ciprofloxacin - pharmacology</topic><topic>Ciprofloxacin - therapeutic use</topic><topic>Combined Modality Therapy</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Male</topic><topic>Malondialdehyde - metabolism</topic><topic>Medical sciences</topic><topic>Meropenem</topic><topic>Other diseases. Semiology</topic><topic>Oxidative Stress - drug effects</topic><topic>Pancreatitis, Acute Necrotizing - drug therapy</topic><topic>Pancreatitis, Acute Necrotizing - metabolism</topic><topic>Pancreatitis, Acute Necrotizing - microbiology</topic><topic>Probiotics - pharmacology</topic><topic>Probiotics - therapeutic use</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Saccharomyces - physiology</topic><topic>Superoxide Dismutase - metabolism</topic><topic>Taurocholic Acid</topic><topic>Thienamycins - pharmacology</topic><topic>Thienamycins - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>AKYOL, Sedat</creatorcontrib><creatorcontrib>MAS, M. Refik</creatorcontrib><creatorcontrib>KOCAR, I. Hakki</creatorcontrib><creatorcontrib>COMERT, Bilgin</creatorcontrib><creatorcontrib>ATESKAN, Ümit</creatorcontrib><creatorcontrib>YASAR, Mehmet</creatorcontrib><creatorcontrib>AYDOGAN, Hakan</creatorcontrib><creatorcontrib>DEVECI, Salih</creatorcontrib><creatorcontrib>AKAY, Cemal</creatorcontrib><creatorcontrib>MAS, Nuket</creatorcontrib><creatorcontrib>YENER, Nuran</creatorcontrib><collection>Pascal-Francis</collection><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>AKYOL, Sedat</au><au>MAS, M. Refik</au><au>KOCAR, I. Hakki</au><au>COMERT, Bilgin</au><au>ATESKAN, Ümit</au><au>YASAR, Mehmet</au><au>AYDOGAN, Hakan</au><au>DEVECI, Salih</au><au>AKAY, Cemal</au><au>MAS, Nuket</au><au>YENER, Nuran</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effect of antibiotic and probiotic combination therapy on secondary pancreatic infections and oxidative stress parameters in experimental acute necrotizing pancreatitis</atitle><jtitle>Pancreas</jtitle><addtitle>Pancreas</addtitle><date>2003-05-01</date><risdate>2003</risdate><volume>26</volume><issue>4</issue><spage>363</spage><epage>367</epage><pages>363-367</pages><issn>0885-3177</issn><eissn>1536-4828</eissn><coden>PANCE4</coden><abstract>Ciprofloxacin and meropenem have effects on intestinal bacteria that are responsible for pancreatic infection, and on the basis of recent data it has been argued that probiotics, especially those used in the food industry, could improve efforts to prevent and treat secondary pancreatic infections by inhibiting bacterial translocation.
To evaluate the effects of probiotic treatment alone or in combination with early administration of two different antibiotics on serum amylase, pancreatic histopathology, bacterial translocation, and oxidative markers.
Acute pancreatitis was induced in rats with 3% sodium taurocholate (1 mL/kg intraductally), except in group VI (sham group). After the stabilization period, the rats were divided into seven groups (n = 20) randomly. At hour 6 after injection, group I rats received probiotic Saccharomyces boulardii (25 mg/d orally q.d.), group II received meropenem (60 mg/kg intraperitoneally b.i.d.), group III received ciprofloxacin (40 mg/kg intraperitoneally b.i.d.), group IV received the same dose of probiotic plus meropenem, and group V received probiotic plus ciprofloxacin. Treatment was not given to group VI (sham group) and group VII (pancreatitis group). At hour 48 after induction, specimens were collected.
Although histopathologic scores in treatment groups were found to be lower than in group VII, the difference was statistically significant only in group V (p < 0.001). In evaluation of oxidative stress, we found that MDA levels decreased and SOD levels increased in treatment groups in comparison with levels in group VII. Probiotic treatment alone reduced bacterial translocation. Probiotic-antibiotic combination therapy was shown to improve histopathologic scores and oxidative parameters.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>12717269</pmid><doi>10.1097/00006676-200305000-00009</doi><tpages>5</tpages></addata></record> |
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subjects | Analysis of Variance Animals Anti-Bacterial Agents - pharmacology Anti-Bacterial Agents - therapeutic use Bacterial Infections - microbiology Bacterial Infections - prevention & control Bacterial Translocation - drug effects Biological and medical sciences Ciprofloxacin - pharmacology Ciprofloxacin - therapeutic use Combined Modality Therapy Gastroenterology. Liver. Pancreas. Abdomen Liver. Biliary tract. Portal circulation. Exocrine pancreas Male Malondialdehyde - metabolism Medical sciences Meropenem Other diseases. Semiology Oxidative Stress - drug effects Pancreatitis, Acute Necrotizing - drug therapy Pancreatitis, Acute Necrotizing - metabolism Pancreatitis, Acute Necrotizing - microbiology Probiotics - pharmacology Probiotics - therapeutic use Rats Rats, Sprague-Dawley Saccharomyces - physiology Superoxide Dismutase - metabolism Taurocholic Acid Thienamycins - pharmacology Thienamycins - therapeutic use |
title | The effect of antibiotic and probiotic combination therapy on secondary pancreatic infections and oxidative stress parameters in experimental acute necrotizing pancreatitis |
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