Islet neogenesis: An apparent key component of long-term pancreas adaptation to increased insulin demand
- Autores
- Del Zotto, Héctor Herminio; Borelli, María Inés; Flores, Luis Emilio; García, María Elisa; Gómez Dumm, César Leandro Alberto; Chicco, A.; Lombardo, Y. B.; Gagliardino, Juan José
- Año de publicación
- 2004
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- This study aimed to determine the relative importance of different functional and morphological pancreatic changes induced by the chronic administration of a sucrose-rich diet (SRD) to maintain normal glucose homeostasis. Male Wistar rats were fed either sucrose (SRD) or starch (CD) for 6 and 12 months. At both periods, serum glucose and triacylglycerol levels were significantly higher (P<0.05; paired and unpaired Student's t-test) in SRD rats. Serum insulin levels were significantly lower in SRD only at 12 months. At 6 months, the insulin secretion dose-response curve in SRD rats showed a shift to the left that was no longer observed at 12 months, when SRD islets decreased their response to 16 mM glucose. At 6 months, SRD rats showed a significant increase in β-cell volume density (Vvi) and islet cell replication rate, together with a decrease in β-cell apoptotic rate. Changes were not detected in the percentage of PDX-1- and islet neogenesis associated protein (INGAP)-positive cells. Conversely, at 12 months, there was a significant decrease in β-cell Vvi and in the percentage of PDX-1-positive cells; the islet cell replication rate was not modified, and the number of apoptotic β-cells increased significantly. No signs of increased neogenesis or INGAP-positive cells were recorded at any period in SRD rats. Our results show that SRD rats are unable to develop functional and morphological pancreatic reactive changes sufficient to maintain normal glucose and triacylglycerol levels for a long period. Such failure could be ascribed to their inability to increase the rate of neogenesis and of INGAP production.
Centro de Endocrinología Experimental y Aplicada - Materia
-
Ciencias Médicas
Insulina
Páncreas - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by-nc-sa/4.0/
- Repositorio
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/84370
Ver los metadatos del registro completo
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Islet neogenesis: An apparent key component of long-term pancreas adaptation to increased insulin demandDel Zotto, Héctor HerminioBorelli, María InésFlores, Luis EmilioGarcía, María ElisaGómez Dumm, César Leandro AlbertoChicco, A.Lombardo, Y. B.Gagliardino, Juan JoséCiencias MédicasInsulinaPáncreasThis study aimed to determine the relative importance of different functional and morphological pancreatic changes induced by the chronic administration of a sucrose-rich diet (SRD) to maintain normal glucose homeostasis. Male Wistar rats were fed either sucrose (SRD) or starch (CD) for 6 and 12 months. At both periods, serum glucose and triacylglycerol levels were significantly higher (P<0.05; paired and unpaired Student's t-test) in SRD rats. Serum insulin levels were significantly lower in SRD only at 12 months. At 6 months, the insulin secretion dose-response curve in SRD rats showed a shift to the left that was no longer observed at 12 months, when SRD islets decreased their response to 16 mM glucose. At 6 months, SRD rats showed a significant increase in β-cell volume density (Vvi) and islet cell replication rate, together with a decrease in β-cell apoptotic rate. Changes were not detected in the percentage of PDX-1- and islet neogenesis associated protein (INGAP)-positive cells. Conversely, at 12 months, there was a significant decrease in β-cell Vvi and in the percentage of PDX-1-positive cells; the islet cell replication rate was not modified, and the number of apoptotic β-cells increased significantly. No signs of increased neogenesis or INGAP-positive cells were recorded at any period in SRD rats. Our results show that SRD rats are unable to develop functional and morphological pancreatic reactive changes sufficient to maintain normal glucose and triacylglycerol levels for a long period. Such failure could be ascribed to their inability to increase the rate of neogenesis and of INGAP production.Centro de Endocrinología Experimental y Aplicada2004info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf321-330http://sedici.unlp.edu.ar/handle/10915/84370enginfo:eu-repo/semantics/altIdentifier/issn/0022-0795info:eu-repo/semantics/altIdentifier/doi/10.1677/joe.1.05792info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-10-15T11:08:07Zoai:sedici.unlp.edu.ar:10915/84370Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-10-15 11:08:07.814SEDICI (UNLP) - Universidad Nacional de La Platafalse |
dc.title.none.fl_str_mv |
Islet neogenesis: An apparent key component of long-term pancreas adaptation to increased insulin demand |
title |
Islet neogenesis: An apparent key component of long-term pancreas adaptation to increased insulin demand |
spellingShingle |
Islet neogenesis: An apparent key component of long-term pancreas adaptation to increased insulin demand Del Zotto, Héctor Herminio Ciencias Médicas Insulina Páncreas |
title_short |
Islet neogenesis: An apparent key component of long-term pancreas adaptation to increased insulin demand |
title_full |
Islet neogenesis: An apparent key component of long-term pancreas adaptation to increased insulin demand |
title_fullStr |
Islet neogenesis: An apparent key component of long-term pancreas adaptation to increased insulin demand |
title_full_unstemmed |
Islet neogenesis: An apparent key component of long-term pancreas adaptation to increased insulin demand |
title_sort |
Islet neogenesis: An apparent key component of long-term pancreas adaptation to increased insulin demand |
dc.creator.none.fl_str_mv |
Del Zotto, Héctor Herminio Borelli, María Inés Flores, Luis Emilio García, María Elisa Gómez Dumm, César Leandro Alberto Chicco, A. Lombardo, Y. B. Gagliardino, Juan José |
author |
Del Zotto, Héctor Herminio |
author_facet |
Del Zotto, Héctor Herminio Borelli, María Inés Flores, Luis Emilio García, María Elisa Gómez Dumm, César Leandro Alberto Chicco, A. Lombardo, Y. B. Gagliardino, Juan José |
author_role |
author |
author2 |
Borelli, María Inés Flores, Luis Emilio García, María Elisa Gómez Dumm, César Leandro Alberto Chicco, A. Lombardo, Y. B. Gagliardino, Juan José |
author2_role |
author author author author author author author |
dc.subject.none.fl_str_mv |
Ciencias Médicas Insulina Páncreas |
topic |
Ciencias Médicas Insulina Páncreas |
dc.description.none.fl_txt_mv |
This study aimed to determine the relative importance of different functional and morphological pancreatic changes induced by the chronic administration of a sucrose-rich diet (SRD) to maintain normal glucose homeostasis. Male Wistar rats were fed either sucrose (SRD) or starch (CD) for 6 and 12 months. At both periods, serum glucose and triacylglycerol levels were significantly higher (P<0.05; paired and unpaired Student's t-test) in SRD rats. Serum insulin levels were significantly lower in SRD only at 12 months. At 6 months, the insulin secretion dose-response curve in SRD rats showed a shift to the left that was no longer observed at 12 months, when SRD islets decreased their response to 16 mM glucose. At 6 months, SRD rats showed a significant increase in β-cell volume density (Vvi) and islet cell replication rate, together with a decrease in β-cell apoptotic rate. Changes were not detected in the percentage of PDX-1- and islet neogenesis associated protein (INGAP)-positive cells. Conversely, at 12 months, there was a significant decrease in β-cell Vvi and in the percentage of PDX-1-positive cells; the islet cell replication rate was not modified, and the number of apoptotic β-cells increased significantly. No signs of increased neogenesis or INGAP-positive cells were recorded at any period in SRD rats. Our results show that SRD rats are unable to develop functional and morphological pancreatic reactive changes sufficient to maintain normal glucose and triacylglycerol levels for a long period. Such failure could be ascribed to their inability to increase the rate of neogenesis and of INGAP production. Centro de Endocrinología Experimental y Aplicada |
description |
This study aimed to determine the relative importance of different functional and morphological pancreatic changes induced by the chronic administration of a sucrose-rich diet (SRD) to maintain normal glucose homeostasis. Male Wistar rats were fed either sucrose (SRD) or starch (CD) for 6 and 12 months. At both periods, serum glucose and triacylglycerol levels were significantly higher (P<0.05; paired and unpaired Student's t-test) in SRD rats. Serum insulin levels were significantly lower in SRD only at 12 months. At 6 months, the insulin secretion dose-response curve in SRD rats showed a shift to the left that was no longer observed at 12 months, when SRD islets decreased their response to 16 mM glucose. At 6 months, SRD rats showed a significant increase in β-cell volume density (Vvi) and islet cell replication rate, together with a decrease in β-cell apoptotic rate. Changes were not detected in the percentage of PDX-1- and islet neogenesis associated protein (INGAP)-positive cells. Conversely, at 12 months, there was a significant decrease in β-cell Vvi and in the percentage of PDX-1-positive cells; the islet cell replication rate was not modified, and the number of apoptotic β-cells increased significantly. No signs of increased neogenesis or INGAP-positive cells were recorded at any period in SRD rats. Our results show that SRD rats are unable to develop functional and morphological pancreatic reactive changes sufficient to maintain normal glucose and triacylglycerol levels for a long period. Such failure could be ascribed to their inability to increase the rate of neogenesis and of INGAP production. |
publishDate |
2004 |
dc.date.none.fl_str_mv |
2004 |
dc.type.none.fl_str_mv |
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article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://sedici.unlp.edu.ar/handle/10915/84370 |
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http://sedici.unlp.edu.ar/handle/10915/84370 |
dc.language.none.fl_str_mv |
eng |
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eng |
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openAccess |
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http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) |
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