Therapeutic effects of Clostridium butyricum on experimental colitis induced by oxazolone in rats

AIM: To evaluate the therapeutic effects of a probiotic supplement (Clostridium butyricum, CGMCC0313 ) in a chemically-induced rat model of experimental colitis. METHODS: An experimental ulcerative colitis model was established by rectal injection of oxazolone into the colon of 40 Wistar rats random...

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Veröffentlicht in:World journal of gastroenterology : WJG 2009-04, Vol.15 (15), p.1821-1828
Hauptverfasser: Zhang, Hai-Qiang, Ding, Tomas T, Zhao, Jun-Sheng, Yang, Xin, Zhang, Hai-Xia, Zhang, Juan-Juan, Cui, Yun-Long
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container_issue 15
container_start_page 1821
container_title World journal of gastroenterology : WJG
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creator Zhang, Hai-Qiang
Ding, Tomas T
Zhao, Jun-Sheng
Yang, Xin
Zhang, Hai-Xia
Zhang, Juan-Juan
Cui, Yun-Long
description AIM: To evaluate the therapeutic effects of a probiotic supplement (Clostridium butyricum, CGMCC0313 ) in a chemically-induced rat model of experimental colitis. METHODS: An experimental ulcerative colitis model was established by rectal injection of oxazolone into the colon of 40 Wistar rats randomly divided into four groups. The positive control group was sacrificed 3 d after colitis onset. The remaining groups were fed daily with either 2 mL of C. butyricum (2.3 × 10^11 CFU/L), 2 mL of mesalamine (100 g/L), or 1 mL of sodium butyrate (50 mmol/L) for 21 d. The animals' body weight, behavior, and bowel movements were recorded weekly. After sacrifice, visual and microscopic observations of pathological changes of colon tissue were made, body weight and wet colon mass index were measured and recorded, and serum levels of interleukin-23 (IL-23) and TNF-α were measured using ELISA. Expression of calcitonin gene-related peptide in colon tissue was measured by RT-PCR. Finally, changes in rat intestinal microflora status were measured in all groups.lowered the serum levels of both IL-23 and tumor necrosis factor-α (TNF-α) with similar or even better efficiency than that of mesalamine or sodium butyrate. The rat intestinal flora appeared to recover more quickly in the group treated with C. butyricum than in the mesalamine and sodium butyrate groups. Finally, we found that the expression level of calcitonin gene related peptide was elevated in colon tissue in the sodium butyrate treated group but not in the C. butyricum or mesalamine treated groups, indicating a sensitization of colon following sodium butyrate treatment. CONCLUSION: In our experimental colitis model, treatment with C. butyricum CGMCC0313, a probiotic supplement, is at least as efficient as treatment with mesalamine.
doi_str_mv 10.3748/wjg.15.1821
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METHODS: An experimental ulcerative colitis model was established by rectal injection of oxazolone into the colon of 40 Wistar rats randomly divided into four groups. The positive control group was sacrificed 3 d after colitis onset. The remaining groups were fed daily with either 2 mL of C. butyricum (2.3 × 10^11 CFU/L), 2 mL of mesalamine (100 g/L), or 1 mL of sodium butyrate (50 mmol/L) for 21 d. The animals' body weight, behavior, and bowel movements were recorded weekly. After sacrifice, visual and microscopic observations of pathological changes of colon tissue were made, body weight and wet colon mass index were measured and recorded, and serum levels of interleukin-23 (IL-23) and TNF-α were measured using ELISA. Expression of calcitonin gene-related peptide in colon tissue was measured by RT-PCR. Finally, changes in rat intestinal microflora status were measured in all groups.lowered the serum levels of both IL-23 and tumor necrosis factor-α (TNF-α) with similar or even better efficiency than that of mesalamine or sodium butyrate. The rat intestinal flora appeared to recover more quickly in the group treated with C. butyricum than in the mesalamine and sodium butyrate groups. Finally, we found that the expression level of calcitonin gene related peptide was elevated in colon tissue in the sodium butyrate treated group but not in the C. butyricum or mesalamine treated groups, indicating a sensitization of colon following sodium butyrate treatment. CONCLUSION: In our experimental colitis model, treatment with C. butyricum CGMCC0313, a probiotic supplement, is at least as efficient as treatment with mesalamine.</description><identifier>ISSN: 1007-9327</identifier><identifier>EISSN: 2219-2840</identifier><identifier>DOI: 10.3748/wjg.15.1821</identifier><identifier>PMID: 19370778</identifier><language>eng</language><publisher>United States: Qingdao Research Center of Microecology-Engineering Technology, Jiaonan 266400, Shandong Province, China%BRITE/Department of Pharmaceutical Sciences, North Carolina Central University, Durham, NC 27707, United States%Pathology Department of Peoplej's Hospital, Jiaonan 266400, Shandong Province, China%Qingdao East Sea Pharmaceutical Co. Ltd, Jiaonan 266400, Shandong Province, China</publisher><subject>Animals ; Anti-Inflammatory Agents, Non-Steroidal - therapeutic use ; Butyrates - therapeutic use ; Calcitonin Gene-Related Peptide - metabolism ; Clostridium butyricum - metabolism ; Colitis - chemically induced ; Colitis - drug therapy ; Colitis - metabolism ; Colitis - pathology ; Colon - anatomy &amp; histology ; Colon - chemistry ; Colon - metabolism ; Disease Models, Animal ; Feces - microbiology ; Interleukin-23 - blood ; Mesalamine - therapeutic use ; Organ Size ; Original ; Oxazolone - adverse effects ; Random Allocation ; Rats ; Rats, Wistar ; Tumor Necrosis Factor-alpha - blood ; 大鼠模型 ; 实验性结肠炎 ; 恶唑酮 ; 治疗效果 ; 溃疡性结肠炎模型 ; 白细胞介素23 ; 酪酸梭菌 ; 降钙素基因相关肽</subject><ispartof>World journal of gastroenterology : WJG, 2009-04, Vol.15 (15), p.1821-1828</ispartof><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><rights>2009 The WJG Press and Baishideng. All rights reserved. 2009</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c501t-1c7d0b53ed430a5cd3c644a2b3e8a7e274c3f8456ecd3a17f5b3177e064997a03</citedby><cites>FETCH-LOGICAL-c501t-1c7d0b53ed430a5cd3c644a2b3e8a7e274c3f8456ecd3a17f5b3177e064997a03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/84123X/84123X.jpg</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2670408/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2670408/$$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/19370778$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Hai-Qiang</creatorcontrib><creatorcontrib>Ding, Tomas T</creatorcontrib><creatorcontrib>Zhao, Jun-Sheng</creatorcontrib><creatorcontrib>Yang, Xin</creatorcontrib><creatorcontrib>Zhang, Hai-Xia</creatorcontrib><creatorcontrib>Zhang, Juan-Juan</creatorcontrib><creatorcontrib>Cui, Yun-Long</creatorcontrib><title>Therapeutic effects of Clostridium butyricum on experimental colitis induced by oxazolone in rats</title><title>World journal of gastroenterology : WJG</title><addtitle>World Journal of Gastroenterology</addtitle><description>AIM: To evaluate the therapeutic effects of a probiotic supplement (Clostridium butyricum, CGMCC0313 ) in a chemically-induced rat model of experimental colitis. METHODS: An experimental ulcerative colitis model was established by rectal injection of oxazolone into the colon of 40 Wistar rats randomly divided into four groups. The positive control group was sacrificed 3 d after colitis onset. The remaining groups were fed daily with either 2 mL of C. butyricum (2.3 × 10^11 CFU/L), 2 mL of mesalamine (100 g/L), or 1 mL of sodium butyrate (50 mmol/L) for 21 d. The animals' body weight, behavior, and bowel movements were recorded weekly. After sacrifice, visual and microscopic observations of pathological changes of colon tissue were made, body weight and wet colon mass index were measured and recorded, and serum levels of interleukin-23 (IL-23) and TNF-α were measured using ELISA. Expression of calcitonin gene-related peptide in colon tissue was measured by RT-PCR. Finally, changes in rat intestinal microflora status were measured in all groups.lowered the serum levels of both IL-23 and tumor necrosis factor-α (TNF-α) with similar or even better efficiency than that of mesalamine or sodium butyrate. The rat intestinal flora appeared to recover more quickly in the group treated with C. butyricum than in the mesalamine and sodium butyrate groups. Finally, we found that the expression level of calcitonin gene related peptide was elevated in colon tissue in the sodium butyrate treated group but not in the C. butyricum or mesalamine treated groups, indicating a sensitization of colon following sodium butyrate treatment. CONCLUSION: In our experimental colitis model, treatment with C. butyricum CGMCC0313, a probiotic supplement, is at least as efficient as treatment with mesalamine.</description><subject>Animals</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</subject><subject>Butyrates - therapeutic use</subject><subject>Calcitonin Gene-Related Peptide - metabolism</subject><subject>Clostridium butyricum - metabolism</subject><subject>Colitis - chemically induced</subject><subject>Colitis - drug therapy</subject><subject>Colitis - metabolism</subject><subject>Colitis - pathology</subject><subject>Colon - anatomy &amp; histology</subject><subject>Colon - chemistry</subject><subject>Colon - metabolism</subject><subject>Disease Models, Animal</subject><subject>Feces - microbiology</subject><subject>Interleukin-23 - blood</subject><subject>Mesalamine - therapeutic use</subject><subject>Organ Size</subject><subject>Original</subject><subject>Oxazolone - adverse effects</subject><subject>Random Allocation</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Tumor Necrosis Factor-alpha - blood</subject><subject>大鼠模型</subject><subject>实验性结肠炎</subject><subject>恶唑酮</subject><subject>治疗效果</subject><subject>溃疡性结肠炎模型</subject><subject>白细胞介素23</subject><subject>酪酸梭菌</subject><subject>降钙素基因相关肽</subject><issn>1007-9327</issn><issn>2219-2840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkUtvEzEURi1ERUNhxR5ZiB2acP0az2yQUMRLqtRNWVsez3XiMBkHe6Zt-PV1lAjoypbv0XeP_BHyhsFSaNl8vN-ul0wtWcPZM7LgnLUVbyQ8JwsGoKtWcH1JXua8BeBCKP6CXLJWaNC6WRB7u8Fk9zhPwVH0Ht2UafR0NcQ8pdCHeUe7eTqk4MotjhQf9pjCDsfJDtTFIUwh0zD2s8OedgcaH-yfOMQRyyNNdsqvyIW3Q8bX5_OK_Pz65Xb1vbq--fZj9fm6cgrYVDGne-iUwF4KsMr1wtVSWt4JbKxGrqUTvpGqxjKyTHvVCaY1Qi3bVlsQV-TTKXc_dzvsXTFMdjD7ImvTwUQbzNPJGDZmHe8MrzVIaErA-1PAvR29HddmG-c0FmVTfpgDtEwB1AX7cMJcijkn9H9XMDDHQo64YcocCyn02_-t_rHnBgrw7hy3ieP6dyh7O-t--TCgEcB4y4vaI5rylK4</recordid><startdate>20090421</startdate><enddate>20090421</enddate><creator>Zhang, Hai-Qiang</creator><creator>Ding, Tomas T</creator><creator>Zhao, Jun-Sheng</creator><creator>Yang, Xin</creator><creator>Zhang, Hai-Xia</creator><creator>Zhang, Juan-Juan</creator><creator>Cui, Yun-Long</creator><general>Qingdao Research Center of Microecology-Engineering Technology, Jiaonan 266400, Shandong Province, China%BRITE/Department of Pharmaceutical Sciences, North Carolina Central University, Durham, NC 27707, United States%Pathology Department of Peoplej's Hospital, Jiaonan 266400, Shandong Province, China%Qingdao East Sea Pharmaceutical Co. 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METHODS: An experimental ulcerative colitis model was established by rectal injection of oxazolone into the colon of 40 Wistar rats randomly divided into four groups. The positive control group was sacrificed 3 d after colitis onset. The remaining groups were fed daily with either 2 mL of C. butyricum (2.3 × 10^11 CFU/L), 2 mL of mesalamine (100 g/L), or 1 mL of sodium butyrate (50 mmol/L) for 21 d. The animals' body weight, behavior, and bowel movements were recorded weekly. After sacrifice, visual and microscopic observations of pathological changes of colon tissue were made, body weight and wet colon mass index were measured and recorded, and serum levels of interleukin-23 (IL-23) and TNF-α were measured using ELISA. Expression of calcitonin gene-related peptide in colon tissue was measured by RT-PCR. Finally, changes in rat intestinal microflora status were measured in all groups.lowered the serum levels of both IL-23 and tumor necrosis factor-α (TNF-α) with similar or even better efficiency than that of mesalamine or sodium butyrate. The rat intestinal flora appeared to recover more quickly in the group treated with C. butyricum than in the mesalamine and sodium butyrate groups. Finally, we found that the expression level of calcitonin gene related peptide was elevated in colon tissue in the sodium butyrate treated group but not in the C. butyricum or mesalamine treated groups, indicating a sensitization of colon following sodium butyrate treatment. CONCLUSION: In our experimental colitis model, treatment with C. butyricum CGMCC0313, a probiotic supplement, is at least as efficient as treatment with mesalamine.</abstract><cop>United States</cop><pub>Qingdao Research Center of Microecology-Engineering Technology, Jiaonan 266400, Shandong Province, China%BRITE/Department of Pharmaceutical Sciences, North Carolina Central University, Durham, NC 27707, United States%Pathology Department of Peoplej's Hospital, Jiaonan 266400, Shandong Province, China%Qingdao East Sea Pharmaceutical Co. Ltd, Jiaonan 266400, Shandong Province, China</pub><pmid>19370778</pmid><doi>10.3748/wjg.15.1821</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Baishideng "World Journal of" online journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Alma/SFX Local Collection
subjects Animals
Anti-Inflammatory Agents, Non-Steroidal - therapeutic use
Butyrates - therapeutic use
Calcitonin Gene-Related Peptide - metabolism
Clostridium butyricum - metabolism
Colitis - chemically induced
Colitis - drug therapy
Colitis - metabolism
Colitis - pathology
Colon - anatomy & histology
Colon - chemistry
Colon - metabolism
Disease Models, Animal
Feces - microbiology
Interleukin-23 - blood
Mesalamine - therapeutic use
Organ Size
Original
Oxazolone - adverse effects
Random Allocation
Rats
Rats, Wistar
Tumor Necrosis Factor-alpha - blood
大鼠模型
实验性结肠炎
恶唑酮
治疗效果
溃疡性结肠炎模型
白细胞介素23
酪酸梭菌
降钙素基因相关肽
title Therapeutic effects of Clostridium butyricum on experimental colitis induced by oxazolone in rats
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