Enteral supplement enriched with glutamine, fiber, and oligosaccharide attenuates experimental colitis in mice

Ulcerative colitis is a chronic recurrent disease characterized by acute inflammation of the colonic mucosa. In Japan, a dietary supplementation product enriched with glutamine, dietary fiber, and oligosaccharide (GFO) is widely applied for enteral nutrition support. These three components have been...

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Published inNutrition (Burbank, Los Angeles County, Calif.) Vol. 29; no. 3; pp. 549 - 555
Main Authors Joo, Erina, Yamane, Shunsuke, Hamasaki, Akihiro, Harada, Norio, Matsunaga, Tetsuro, Muraoka, Atsushi, Suzuki, Kazuyo, Nasteska, Daniela, Fukushima, Toru, Hayashi, Tatsuya, Tsuji, Hidemi, Shide, Kenichiro, Tsuda, Kinsuke, Inagaki, Nobuya
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 01.03.2013
Elsevier
Elsevier Limited
Subjects
GFO
GFO
Online AccessGet full text
ISSN0899-9007
1873-1244
1873-1244
DOI10.1016/j.nut.2012.09.007

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Abstract Ulcerative colitis is a chronic recurrent disease characterized by acute inflammation of the colonic mucosa. In Japan, a dietary supplementation product enriched with glutamine, dietary fiber, and oligosaccharide (GFO) is widely applied for enteral nutrition support. These three components have been suggested to improve intestinal health. In this study, we investigated whether GFO has suppressive effects on mucosal damage in ulcerative colitis in an experimental mouse model. C57BL/6 mice received 2.5% dextran sulfate sodium in drinking water for 5 d to induce colitis. Then, they were given 0.25 mL of GFO or a 20% glucose solution twice daily for 10 d. Another set of mice receiving unaltered drinking water was used as the normal control group. The body weight loss and disease activity index were significantly lower in the GFO-treated mice compared with the glucose-treated mice (P < 0.05). The decrease in colon length induced by dextran sulfate sodium was significantly alleviated in GFO-treated mice compared with glucose-treated mice (P < 0.01). In addition, the histologic findings showed that intestinal inflammation was significantly attenuated in mice treated with GFO. Furthermore, treatment with GFO significantly inhibited the dextran sulfate sodium–induced increase in the mRNA expression of interleukin-1β. These results suggest that GFO has potential therapeutic value as an adjunct therapy for ulcerative colitis.
AbstractList Ulcerative colitis is a chronic recurrent disease characterized by acute inflammation of the colonic mucosa. In Japan, a dietary supplementation product enriched with glutamine, dietary fiber, and oligosaccharide (GFO) is widely applied for enteral nutrition support. These three components have been suggested to improve intestinal health. In this study, we investigated whether GFO has suppressive effects on mucosal damage in ulcerative colitis in an experimental mouse model. C57BL/6 mice received 2.5% dextran sulfate sodium in drinking water for 5 d to induce colitis. Then, they were given 0.25 mL of GFO or a 20% glucose solution twice daily for 10 d. Another set of mice receiving unaltered drinking water was used as the normal control group. The body weight loss and disease activity index were significantly lower in the GFO-treated mice compared with the glucose-treated mice (P < 0.05). The decrease in colon length induced by dextran sulfate sodium was significantly alleviated in GFO-treated mice compared with glucose-treated mice (P < 0.01). In addition, the histologic findings showed that intestinal inflammation was significantly attenuated in mice treated with GFO. Furthermore, treatment with GFO significantly inhibited the dextran sulfate sodium-induced increase in the mRNA expression of interleukin-1β. These results suggest that GFO has potential therapeutic value as an adjunct therapy for ulcerative colitis.
Abstract Objective Ulcerative colitis is a chronic recurrent disease characterized by acute inflammation of the colonic mucosa. In Japan, a dietary supplementation product enriched with glutamine, dietary fiber, and oligosaccharide (GFO) is widely applied for enteral nutrition support. These three components have been suggested to improve intestinal health. In this study, we investigated whether GFO has suppressive effects on mucosal damage in ulcerative colitis in an experimental mouse model. Methods C57BL/6 mice received 2.5% dextran sulfate sodium in drinking water for 5 d to induce colitis. Then, they were given 0.25 mL of GFO or a 20% glucose solution twice daily for 10 d. Another set of mice receiving unaltered drinking water was used as the normal control group. Results The body weight loss and disease activity index were significantly lower in the GFO-treated mice compared with the glucose-treated mice ( P < 0.05). The decrease in colon length induced by dextran sulfate sodium was significantly alleviated in GFO-treated mice compared with glucose-treated mice ( P < 0.01). In addition, the histologic findings showed that intestinal inflammation was significantly attenuated in mice treated with GFO. Furthermore, treatment with GFO significantly inhibited the dextran sulfate sodium–induced increase in the mRNA expression of interleukin-1β. Conclusion These results suggest that GFO has potential therapeutic value as an adjunct therapy for ulcerative colitis.
Ulcerative colitis is a chronic recurrent disease characterized by acute inflammation of the colonic mucosa. In Japan, a dietary supplementation product enriched with glutamine, dietary fiber, and oligosaccharide (GFO) is widely applied for enteral nutrition support. These three components have been suggested to improve intestinal health. In this study, we investigated whether GFO has suppressive effects on mucosal damage in ulcerative colitis in an experimental mouse model.OBJECTIVEUlcerative colitis is a chronic recurrent disease characterized by acute inflammation of the colonic mucosa. In Japan, a dietary supplementation product enriched with glutamine, dietary fiber, and oligosaccharide (GFO) is widely applied for enteral nutrition support. These three components have been suggested to improve intestinal health. In this study, we investigated whether GFO has suppressive effects on mucosal damage in ulcerative colitis in an experimental mouse model.C57BL/6 mice received 2.5% dextran sulfate sodium in drinking water for 5 d to induce colitis. Then, they were given 0.25 mL of GFO or a 20% glucose solution twice daily for 10 d. Another set of mice receiving unaltered drinking water was used as the normal control group.METHODSC57BL/6 mice received 2.5% dextran sulfate sodium in drinking water for 5 d to induce colitis. Then, they were given 0.25 mL of GFO or a 20% glucose solution twice daily for 10 d. Another set of mice receiving unaltered drinking water was used as the normal control group.The body weight loss and disease activity index were significantly lower in the GFO-treated mice compared with the glucose-treated mice (P < 0.05). The decrease in colon length induced by dextran sulfate sodium was significantly alleviated in GFO-treated mice compared with glucose-treated mice (P < 0.01). In addition, the histologic findings showed that intestinal inflammation was significantly attenuated in mice treated with GFO. Furthermore, treatment with GFO significantly inhibited the dextran sulfate sodium-induced increase in the mRNA expression of interleukin-1β.RESULTSThe body weight loss and disease activity index were significantly lower in the GFO-treated mice compared with the glucose-treated mice (P < 0.05). The decrease in colon length induced by dextran sulfate sodium was significantly alleviated in GFO-treated mice compared with glucose-treated mice (P < 0.01). In addition, the histologic findings showed that intestinal inflammation was significantly attenuated in mice treated with GFO. Furthermore, treatment with GFO significantly inhibited the dextran sulfate sodium-induced increase in the mRNA expression of interleukin-1β.These results suggest that GFO has potential therapeutic value as an adjunct therapy for ulcerative colitis.CONCLUSIONThese results suggest that GFO has potential therapeutic value as an adjunct therapy for ulcerative colitis.
OBJECTIVE: Ulcerative colitis is a chronic recurrent disease characterized by acute inflammation of the colonic mucosa. In Japan, a dietary supplementation product enriched with glutamine, dietary fiber, and oligosaccharide (GFO) is widely applied for enteral nutrition support. These three components have been suggested to improve intestinal health. In this study, we investigated whether GFO has suppressive effects on mucosal damage in ulcerative colitis in an experimental mouse model. METHODS: C57BL/6 mice received 2.5% dextran sulfate sodium in drinking water for 5 d to induce colitis. Then, they were given 0.25 mL of GFO or a 20% glucose solution twice daily for 10 d. Another set of mice receiving unaltered drinking water was used as the normal control group. RESULTS: The body weight loss and disease activity index were significantly lower in the GFO-treated mice compared with the glucose-treated mice (P < 0.05). The decrease in colon length induced by dextran sulfate sodium was significantly alleviated in GFO-treated mice compared with glucose-treated mice (P < 0.01). In addition, the histologic findings showed that intestinal inflammation was significantly attenuated in mice treated with GFO. Furthermore, treatment with GFO significantly inhibited the dextran sulfate sodium–induced increase in the mRNA expression of interleukin-1β. CONCLUSION: These results suggest that GFO has potential therapeutic value as an adjunct therapy for ulcerative colitis.
Ulcerative colitis is a chronic recurrent disease characterized by acute inflammation of the colonic mucosa. In Japan, a dietary supplementation product enriched with glutamine, dietary fiber, and oligosaccharide (GFO) is widely applied for enteral nutrition support. These three components have been suggested to improve intestinal health. In this study, we investigated whether GFO has suppressive effects on mucosal damage in ulcerative colitis in an experimental mouse model. C57BL/6 mice received 2.5% dextran sulfate sodium in drinking water for 5 d to induce colitis. Then, they were given 0.25 mL of GFO or a 20% glucose solution twice daily for 10 d. Another set of mice receiving unaltered drinking water was used as the normal control group. The body weight loss and disease activity index were significantly lower in the GFO-treated mice compared with the glucose-treated mice (P < 0.05). The decrease in colon length induced by dextran sulfate sodium was significantly alleviated in GFO-treated mice compared with glucose-treated mice (P < 0.01). In addition, the histologic findings showed that intestinal inflammation was significantly attenuated in mice treated with GFO. Furthermore, treatment with GFO significantly inhibited the dextran sulfate sodium-induced increase in the mRNA expression of interleukin-1β. These results suggest that GFO has potential therapeutic value as an adjunct therapy for ulcerative colitis.
Author Matsunaga, Tetsuro
Muraoka, Atsushi
Nasteska, Daniela
Hayashi, Tatsuya
Joo, Erina
Shide, Kenichiro
Tsuda, Kinsuke
Inagaki, Nobuya
Yamane, Shunsuke
Harada, Norio
Fukushima, Toru
Suzuki, Kazuyo
Tsuji, Hidemi
Hamasaki, Akihiro
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IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 3
Keywords GFO
Interleukin-1β
Glucagon-like peptide
Dextran sulfate sodium
Ulcerative colitis
Oligosaccharide
Cytokine
Rodentia
Interleukin 1β
Sulfates
Inflammatory disease
Vertebrata
Mammalia
Sodium
Mouse
Aminoacid
Animal
Digestive diseases
Intestinal disease
Colitis
Glutamine
Language English
License https://www.elsevier.com/tdm/userlicense/1.0
CC BY 4.0
Copyright © 2013 Elsevier Inc. All rights reserved.
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OpenAccessLink http://hdl.handle.net/2433/171237
PMID 23274091
PQID 1287045667
PQPubID 105601
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PublicationTitle Nutrition (Burbank, Los Angeles County, Calif.)
PublicationTitleAlternate Nutrition
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Snippet Ulcerative colitis is a chronic recurrent disease characterized by acute inflammation of the colonic mucosa. In Japan, a dietary supplementation product...
Abstract Objective Ulcerative colitis is a chronic recurrent disease characterized by acute inflammation of the colonic mucosa. In Japan, a dietary...
OBJECTIVE: Ulcerative colitis is a chronic recurrent disease characterized by acute inflammation of the colonic mucosa. In Japan, a dietary supplementation...
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SubjectTerms acute course
administration & dosage
analysis
Animals
Biological and medical sciences
Body weight
chemically induced
chemistry
chronic diseases
colitis
Colitis, Ulcerative
Colitis, Ulcerative - chemically induced
Colitis, Ulcerative - pathology
Colitis, Ulcerative - therapy
Colon
Colon - chemistry
Cytokines
Cytokines - genetics
Dextran Sulfate
Dextran sulfate sodium
Dietary fiber
Dietary Fiber - administration & dosage
Dietary Supplements
Disease Models, Animal
Drinking water
enteral feeding
Enteral Nutrition
Feeding. Feeding behavior
Fundamental and applied biological sciences. Psychology
Gastroenterology and Hepatology
Gastroenterology. Liver. Pancreas. Abdomen
gene expression
genetics
GFO
Glucagon-like peptide
Glucose
glutamine
Glutamine - administration & dosage
inflammation
Inflammatory bowel disease
Interleukin-1beta
Interleukin-1beta - genetics
Interleukin-1β
Intestinal Mucosa
Intestinal Mucosa - chemistry
Intestinal Mucosa - pathology
Japan
Male
Medical sciences
messenger RNA
Mice
Mice, Inbred C57BL
mucosa
Nutrition
Oligosaccharides
Oligosaccharides - administration & dosage
Other diseases. Semiology
pathology
Polymerase chain reaction
Receiving waters
RNA, Messenger
RNA, Messenger - analysis
Rodents
Sodium
sodium sulfate
Stomach. Duodenum. Small intestine. Colon. Rectum. Anus
Studies
Sulfates
therapy
Ulcerative colitis
Vertebrates: anatomy and physiology, studies on body, several organs or systems
weight loss
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Title Enteral supplement enriched with glutamine, fiber, and oligosaccharide attenuates experimental colitis in mice
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