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Hepatocyte growth factor, hepatocyte growth factor activator and arginine in a rat fulminant colitis model

INTRODUCTION: Dextran sodium sulfate (DSS) is commonly used to induce a murine fulminant colitis model. Hepatocyte growth factor (HGF) has been shown to decrease the symptoms of inflammatory bowel disease (IBD) but the effect of its activator, HGFA, is not well characterized. Arginine reduces effect...

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Autores principales: Zwintscher, Nathan P., Shah, Puja M., Salgar, Shashikumar K., Newton, Christopher R., Maykel, Justin A., Samy, Ahmed, Jabir, Murad, Steele, Scott R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4840393/
https://www.ncbi.nlm.nih.gov/pubmed/27144006
http://dx.doi.org/10.1016/j.amsu.2016.03.039
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author Zwintscher, Nathan P.
Shah, Puja M.
Salgar, Shashikumar K.
Newton, Christopher R.
Maykel, Justin A.
Samy, Ahmed
Jabir, Murad
Steele, Scott R.
author_facet Zwintscher, Nathan P.
Shah, Puja M.
Salgar, Shashikumar K.
Newton, Christopher R.
Maykel, Justin A.
Samy, Ahmed
Jabir, Murad
Steele, Scott R.
author_sort Zwintscher, Nathan P.
collection PubMed
description INTRODUCTION: Dextran sodium sulfate (DSS) is commonly used to induce a murine fulminant colitis model. Hepatocyte growth factor (HGF) has been shown to decrease the symptoms of inflammatory bowel disease (IBD) but the effect of its activator, HGFA, is not well characterized. Arginine reduces effects of oxidative stress but its effect on IBD is not well known. The primary aim is to determine whether HGF and HGFA, or arginine will decrease IBD symptoms such as pain and diarrhea in a DSS-induced fulminant colitis murine model. METHODS: A severe colitis was induced in young, male Fischer 344 rats with 4% (w/v) DSS oral solution for seven days; rats were sacrificed on day 10. Rats were divided into five groups of 8 animals: control, HGF (700 mcg/kg/dose), HGF and HGFA (10 mcg/dose), HGF and arginine, and high dose HGF (2800 mcg/kg/dose). Main clinical outcomes were pain, diarrhea and weight loss. Blinded pathologists scored the terminal ileum and distal colon. RESULTS: DSS reliably induced severe active colitis in 90% of animals (n = 36/40). There were no differences in injury scores between control and treatment animals. HGF led to 1.38 fewer days in pain (p = 0.036), while arginine led to 1.88 fewer days of diarrhea (P = 0.017) compared to controls. 88% of HGFA-treated rats started regaining weight (P < 0.001). DISCUSSION/CONCLUSION: Although treatment was unable to reverse fulminant disease, HGF and arginine were associated with decreased days of pain and diarrhea. These clinical interventions may reduce associated symptoms for severe IBD patients, even when urgent surgical intervention remains the only viable option.
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spelling pubmed-48403932016-05-03 Hepatocyte growth factor, hepatocyte growth factor activator and arginine in a rat fulminant colitis model Zwintscher, Nathan P. Shah, Puja M. Salgar, Shashikumar K. Newton, Christopher R. Maykel, Justin A. Samy, Ahmed Jabir, Murad Steele, Scott R. Ann Med Surg (Lond) Original Research INTRODUCTION: Dextran sodium sulfate (DSS) is commonly used to induce a murine fulminant colitis model. Hepatocyte growth factor (HGF) has been shown to decrease the symptoms of inflammatory bowel disease (IBD) but the effect of its activator, HGFA, is not well characterized. Arginine reduces effects of oxidative stress but its effect on IBD is not well known. The primary aim is to determine whether HGF and HGFA, or arginine will decrease IBD symptoms such as pain and diarrhea in a DSS-induced fulminant colitis murine model. METHODS: A severe colitis was induced in young, male Fischer 344 rats with 4% (w/v) DSS oral solution for seven days; rats were sacrificed on day 10. Rats were divided into five groups of 8 animals: control, HGF (700 mcg/kg/dose), HGF and HGFA (10 mcg/dose), HGF and arginine, and high dose HGF (2800 mcg/kg/dose). Main clinical outcomes were pain, diarrhea and weight loss. Blinded pathologists scored the terminal ileum and distal colon. RESULTS: DSS reliably induced severe active colitis in 90% of animals (n = 36/40). There were no differences in injury scores between control and treatment animals. HGF led to 1.38 fewer days in pain (p = 0.036), while arginine led to 1.88 fewer days of diarrhea (P = 0.017) compared to controls. 88% of HGFA-treated rats started regaining weight (P < 0.001). DISCUSSION/CONCLUSION: Although treatment was unable to reverse fulminant disease, HGF and arginine were associated with decreased days of pain and diarrhea. These clinical interventions may reduce associated symptoms for severe IBD patients, even when urgent surgical intervention remains the only viable option. Elsevier 2016-04-05 /pmc/articles/PMC4840393/ /pubmed/27144006 http://dx.doi.org/10.1016/j.amsu.2016.03.039 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Zwintscher, Nathan P.
Shah, Puja M.
Salgar, Shashikumar K.
Newton, Christopher R.
Maykel, Justin A.
Samy, Ahmed
Jabir, Murad
Steele, Scott R.
Hepatocyte growth factor, hepatocyte growth factor activator and arginine in a rat fulminant colitis model
title Hepatocyte growth factor, hepatocyte growth factor activator and arginine in a rat fulminant colitis model
title_full Hepatocyte growth factor, hepatocyte growth factor activator and arginine in a rat fulminant colitis model
title_fullStr Hepatocyte growth factor, hepatocyte growth factor activator and arginine in a rat fulminant colitis model
title_full_unstemmed Hepatocyte growth factor, hepatocyte growth factor activator and arginine in a rat fulminant colitis model
title_short Hepatocyte growth factor, hepatocyte growth factor activator and arginine in a rat fulminant colitis model
title_sort hepatocyte growth factor, hepatocyte growth factor activator and arginine in a rat fulminant colitis model
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4840393/
https://www.ncbi.nlm.nih.gov/pubmed/27144006
http://dx.doi.org/10.1016/j.amsu.2016.03.039
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