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Vitamin E (α-tocopherol) supplementation in diabetic rats: effects on the proximal colon

BACKGROUND: Neuropathy is one of the complications caused by diabetes mellitus which is directly related to the gastrointestinal manifestations of the disease. Antioxidant substances, such as vitamin E, may play an important role in the reduction of the neurological damage caused by diabetes mellitu...

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Autores principales: Roldi, Luciana P, Pereira, Renata VF, Tronchini, Eleandro A, Rizo, Gabriela V, Scoaris, Célia R, Zanoni, Jacqueline N, Natali, Maria RM
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2788574/
https://www.ncbi.nlm.nih.gov/pubmed/19930636
http://dx.doi.org/10.1186/1471-230X-9-88
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author Roldi, Luciana P
Pereira, Renata VF
Tronchini, Eleandro A
Rizo, Gabriela V
Scoaris, Célia R
Zanoni, Jacqueline N
Natali, Maria RM
author_facet Roldi, Luciana P
Pereira, Renata VF
Tronchini, Eleandro A
Rizo, Gabriela V
Scoaris, Célia R
Zanoni, Jacqueline N
Natali, Maria RM
author_sort Roldi, Luciana P
collection PubMed
description BACKGROUND: Neuropathy is one of the complications caused by diabetes mellitus which is directly related to the gastrointestinal manifestations of the disease. Antioxidant substances, such as vitamin E, may play an important role in the reduction of the neurological damage caused by diabetes mellitus. The aim of the present study was to determine whether vitamin E (α-tocopherol) at different concentrations induces any effects on the morphology of the intestinal wall and intrinsic innervation in the proximal colon of diabetic rats. METHODS: Thirty rats (90-day-old) were assigned to the following groups: N (normoglycemic), NE1 (normoglycemic supplemented with vitamin E 0.1%), NE2 (normoglycemic supplemented with vitamin E 2%), D (diabetic), DE1 (diabetic supplemented with vitamin E 0.1%), and DE2 (diabetic supplemented with vitamin E 2%). Animals received vitamin E supplementation for 120 days and were sacrificed when they were 210 days old. The proximal colon of each animal was subjected to histology to study the intestinal wall and goblet cells and processed for whole-mount preparations to morphoquantitatively determine the total myenteric population. RESULTS: Supplementation with vitamin E significantly reduced glycemia and glycated hemoglobin values and preserved the number of myenteric neurons in group DE2, without affecting intestinal area or thickness of the intestinal wall or muscular tunic. CONCLUSION: Vitamin E (2%) influenced the glycemic parameters and had a neuroprotective effect on the total myenteric population, but the morphometric characteristics of the intestinal wall were unaffected.
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spelling pubmed-27885742009-12-04 Vitamin E (α-tocopherol) supplementation in diabetic rats: effects on the proximal colon Roldi, Luciana P Pereira, Renata VF Tronchini, Eleandro A Rizo, Gabriela V Scoaris, Célia R Zanoni, Jacqueline N Natali, Maria RM BMC Gastroenterol Research Article BACKGROUND: Neuropathy is one of the complications caused by diabetes mellitus which is directly related to the gastrointestinal manifestations of the disease. Antioxidant substances, such as vitamin E, may play an important role in the reduction of the neurological damage caused by diabetes mellitus. The aim of the present study was to determine whether vitamin E (α-tocopherol) at different concentrations induces any effects on the morphology of the intestinal wall and intrinsic innervation in the proximal colon of diabetic rats. METHODS: Thirty rats (90-day-old) were assigned to the following groups: N (normoglycemic), NE1 (normoglycemic supplemented with vitamin E 0.1%), NE2 (normoglycemic supplemented with vitamin E 2%), D (diabetic), DE1 (diabetic supplemented with vitamin E 0.1%), and DE2 (diabetic supplemented with vitamin E 2%). Animals received vitamin E supplementation for 120 days and were sacrificed when they were 210 days old. The proximal colon of each animal was subjected to histology to study the intestinal wall and goblet cells and processed for whole-mount preparations to morphoquantitatively determine the total myenteric population. RESULTS: Supplementation with vitamin E significantly reduced glycemia and glycated hemoglobin values and preserved the number of myenteric neurons in group DE2, without affecting intestinal area or thickness of the intestinal wall or muscular tunic. CONCLUSION: Vitamin E (2%) influenced the glycemic parameters and had a neuroprotective effect on the total myenteric population, but the morphometric characteristics of the intestinal wall were unaffected. BioMed Central 2009-11-23 /pmc/articles/PMC2788574/ /pubmed/19930636 http://dx.doi.org/10.1186/1471-230X-9-88 Text en Copyright ©2009 Roldi 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 Article
Roldi, Luciana P
Pereira, Renata VF
Tronchini, Eleandro A
Rizo, Gabriela V
Scoaris, Célia R
Zanoni, Jacqueline N
Natali, Maria RM
Vitamin E (α-tocopherol) supplementation in diabetic rats: effects on the proximal colon
title Vitamin E (α-tocopherol) supplementation in diabetic rats: effects on the proximal colon
title_full Vitamin E (α-tocopherol) supplementation in diabetic rats: effects on the proximal colon
title_fullStr Vitamin E (α-tocopherol) supplementation in diabetic rats: effects on the proximal colon
title_full_unstemmed Vitamin E (α-tocopherol) supplementation in diabetic rats: effects on the proximal colon
title_short Vitamin E (α-tocopherol) supplementation in diabetic rats: effects on the proximal colon
title_sort vitamin e (α-tocopherol) supplementation in diabetic rats: effects on the proximal colon
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2788574/
https://www.ncbi.nlm.nih.gov/pubmed/19930636
http://dx.doi.org/10.1186/1471-230X-9-88
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