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Altered behavior and digestive outcomes in adult male rats primed with minimal colon pain as neonates

BACKGROUND: Neonatal colon irritation (CI; pain or inflammation) given for 2 weeks prior to postnatal day 22 (PND22), causes long-lasting functional disorders in rats that can be seen 6 months after the initial insult. This study looked at the effect of varying the frequency and duration of neonatal...

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Autores principales: Wang, Jing, Gu, Chunping, Al-Chaer, Elie D
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2518152/
https://www.ncbi.nlm.nih.gov/pubmed/18616817
http://dx.doi.org/10.1186/1744-9081-4-28
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author Wang, Jing
Gu, Chunping
Al-Chaer, Elie D
author_facet Wang, Jing
Gu, Chunping
Al-Chaer, Elie D
author_sort Wang, Jing
collection PubMed
description BACKGROUND: Neonatal colon irritation (CI; pain or inflammation) given for 2 weeks prior to postnatal day 22 (PND22), causes long-lasting functional disorders in rats that can be seen 6 months after the initial insult. This study looked at the effect of varying the frequency and duration of neonatal CI on the rate of growth, digestive outcomes, exploratory activity, and colon and skin sensitivity in adult rats. METHODS: Male Sprague-Dawley rats were given CI using repeated colorectal distension (CRD) at different time intervals and for varying durations starting at PND 8, 10 or 14. Control rats were handled by the investigator without any intracolonic insertion. Further experiments were done on adult rats. Digestive outcomes (food and water consumption, fecal and urinary outputs) were measured using metabolic cages. Exploratory behavior was measured using digital video tracking in an open field. Cutaneous sensitivity was assessed by measuring the responses to mechanical and heat stimuli applied to the shaved abdomen or hind paws. Visceral sensitivity was measured by recording electromyographic responses, under light isoflurane anesthesia, from the external oblique muscles in response to CRD. RESULTS: No significant weight differences were observed between CI and control rats. Exploratory behavior was reduced in rats with neonatal CI compared to control. Digestive outputs and somatic and visceral sensitivity changed between different treatment groups with earlier and more frequent insults yielding a higher deviation from normal. CONCLUSION: The diversity of behavioral and digestive symptoms in these rats parallels the diversity of symptoms in patients with functional gastrointestinal disorders and is consistent with global plastic changes affecting more than one system in the organism.
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spelling pubmed-25181522008-08-20 Altered behavior and digestive outcomes in adult male rats primed with minimal colon pain as neonates Wang, Jing Gu, Chunping Al-Chaer, Elie D Behav Brain Funct Research BACKGROUND: Neonatal colon irritation (CI; pain or inflammation) given for 2 weeks prior to postnatal day 22 (PND22), causes long-lasting functional disorders in rats that can be seen 6 months after the initial insult. This study looked at the effect of varying the frequency and duration of neonatal CI on the rate of growth, digestive outcomes, exploratory activity, and colon and skin sensitivity in adult rats. METHODS: Male Sprague-Dawley rats were given CI using repeated colorectal distension (CRD) at different time intervals and for varying durations starting at PND 8, 10 or 14. Control rats were handled by the investigator without any intracolonic insertion. Further experiments were done on adult rats. Digestive outcomes (food and water consumption, fecal and urinary outputs) were measured using metabolic cages. Exploratory behavior was measured using digital video tracking in an open field. Cutaneous sensitivity was assessed by measuring the responses to mechanical and heat stimuli applied to the shaved abdomen or hind paws. Visceral sensitivity was measured by recording electromyographic responses, under light isoflurane anesthesia, from the external oblique muscles in response to CRD. RESULTS: No significant weight differences were observed between CI and control rats. Exploratory behavior was reduced in rats with neonatal CI compared to control. Digestive outputs and somatic and visceral sensitivity changed between different treatment groups with earlier and more frequent insults yielding a higher deviation from normal. CONCLUSION: The diversity of behavioral and digestive symptoms in these rats parallels the diversity of symptoms in patients with functional gastrointestinal disorders and is consistent with global plastic changes affecting more than one system in the organism. BioMed Central 2008-07-10 /pmc/articles/PMC2518152/ /pubmed/18616817 http://dx.doi.org/10.1186/1744-9081-4-28 Text en Copyright © 2008 Wang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Wang, Jing
Gu, Chunping
Al-Chaer, Elie D
Altered behavior and digestive outcomes in adult male rats primed with minimal colon pain as neonates
title Altered behavior and digestive outcomes in adult male rats primed with minimal colon pain as neonates
title_full Altered behavior and digestive outcomes in adult male rats primed with minimal colon pain as neonates
title_fullStr Altered behavior and digestive outcomes in adult male rats primed with minimal colon pain as neonates
title_full_unstemmed Altered behavior and digestive outcomes in adult male rats primed with minimal colon pain as neonates
title_short Altered behavior and digestive outcomes in adult male rats primed with minimal colon pain as neonates
title_sort altered behavior and digestive outcomes in adult male rats primed with minimal colon pain as neonates
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2518152/
https://www.ncbi.nlm.nih.gov/pubmed/18616817
http://dx.doi.org/10.1186/1744-9081-4-28
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