Morphological and metabolic adjustments in the small intestine to energy demands of growth, storage, and fasting in the first annual cycle of a hibernating lizard (Tupinambis merianae)

Detalhes bibliográficos
Autor(a) principal: Nascimento, Lucas Francisco R. do
Data de Publicação: 2016
Outros Autores: Silveira, Lilian Cristina da, Nisembaum, Laura Gabriela, Colquhoun, Alison, Abe, Agusto S. [UNESP], Mandarim-de-Lacerda, Carlos Alberto, Souza, Silvia Cristina R. de
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.cbpa.2016.02.002
http://hdl.handle.net/11449/161367
Resumo: Seasonal plasticity in the small intestine of neonatal tegu lizards was investigated using morphometry and analysis of enzymes involved in supplying energy to the intestinal tissue. In the autumn, the intestinal mass (Mi) was 1.0% of body mass and the scaling exponent b = 0.92 indicated that Mi was larger in smaller neonates. During arousal from dormancy Mi was 23% smaller; later in spring, Mi increased 60% in relation to the autumn and the exponent b = 0.14 indicated that the recovery was disproportionate in smaller tegus. During the autumn, the intestinal villi were greatly elongated; by midwinter, the Hv, SvEp, and VvEp were smaller than during the autumn (59%, 54%, 29%) and were restored to autumn levels during spring. In the active tegus, the maximum activity (Vmax) of enzymes indicated that the enterocytes can obtain energy from different sources, and possess gluconeogenic capacity. During winter, the Vmax of CS, HOAD, GDH, PEPCK was 40-50% lower in relation to the autumn and spring, while the Vmax of HK, PK, LDH, AST was unchanged. The hypoglycemia and the mucosal atrophy/ischemia during winter would prevent the enterocytes from using glucose, whereas they could slowly oxidize fatty acids released from body stores and amino acids from the tissue proteolysis to satisfy their needs of energy. Contrastingly, starvation during spring caused severe mass loss (50%); the tissue protein and the VvEp and VvLP did not change while the thickness of the muscular layer increased 51%, which suggested different effects along the length of the organ. In addition, the Vmax of the glycolytic enzymes was lower, indicating that a regulatory mechanism would spare blood glucose for vital organs during unanticipated food restriction. (C) 2016 Elsevier Inc. All rights reserved.
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spelling Morphological and metabolic adjustments in the small intestine to energy demands of growth, storage, and fasting in the first annual cycle of a hibernating lizard (Tupinambis merianae)Seasonal dormancyHibernationHypometabolismFastingStarvationIntestineScalingMetabolic enzymesTegu lizardTupinambis merianaeSeasonal plasticity in the small intestine of neonatal tegu lizards was investigated using morphometry and analysis of enzymes involved in supplying energy to the intestinal tissue. In the autumn, the intestinal mass (Mi) was 1.0% of body mass and the scaling exponent b = 0.92 indicated that Mi was larger in smaller neonates. During arousal from dormancy Mi was 23% smaller; later in spring, Mi increased 60% in relation to the autumn and the exponent b = 0.14 indicated that the recovery was disproportionate in smaller tegus. During the autumn, the intestinal villi were greatly elongated; by midwinter, the Hv, SvEp, and VvEp were smaller than during the autumn (59%, 54%, 29%) and were restored to autumn levels during spring. In the active tegus, the maximum activity (Vmax) of enzymes indicated that the enterocytes can obtain energy from different sources, and possess gluconeogenic capacity. During winter, the Vmax of CS, HOAD, GDH, PEPCK was 40-50% lower in relation to the autumn and spring, while the Vmax of HK, PK, LDH, AST was unchanged. The hypoglycemia and the mucosal atrophy/ischemia during winter would prevent the enterocytes from using glucose, whereas they could slowly oxidize fatty acids released from body stores and amino acids from the tissue proteolysis to satisfy their needs of energy. Contrastingly, starvation during spring caused severe mass loss (50%); the tissue protein and the VvEp and VvLP did not change while the thickness of the muscular layer increased 51%, which suggested different effects along the length of the organ. In addition, the Vmax of the glycolytic enzymes was lower, indicating that a regulatory mechanism would spare blood glucose for vital organs during unanticipated food restriction. (C) 2016 Elsevier Inc. All rights reserved.Univ Sao Paulo, Inst Biosci, Dept Physiol, BR-05508900 Sao Paulo, SP, BrazilUniv Sao Paulo, Inst Biomed Sci, Dept Cellular & Dev Biol, BR-05508900 Sao Paulo, SP, BrazilState Univ Sao Paulo, Inst Biosci, Dept Zool, POB 199, BR-13506900 Rio Claro, SP, BrazilUniv Estado Rio De Janeiro, Inst Biol, Dept Anat, BR-20551030 Rio De Janeiro, BrazilState Univ Sao Paulo, Inst Biosci, Dept Zool, POB 199, BR-13506900 Rio Claro, SP, BrazilElsevier B.V.Universidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)Universidade do Estado do Rio de Janeiro (UERJ)Nascimento, Lucas Francisco R. doSilveira, Lilian Cristina daNisembaum, Laura GabrielaColquhoun, AlisonAbe, Agusto S. [UNESP]Mandarim-de-Lacerda, Carlos AlbertoSouza, Silvia Cristina R. de2018-11-26T16:32:27Z2018-11-26T16:32:27Z2016-05-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article55-64application/pdfhttp://dx.doi.org/10.1016/j.cbpa.2016.02.002Comparative Biochemistry And Physiology A-molecular & Integrative Physiology. New York: Elsevier Science Inc, v. 195, p. 55-64, 2016.1095-6433http://hdl.handle.net/11449/16136710.1016/j.cbpa.2016.02.002WOS:000373410500008WOS000373410500008.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengComparative Biochemistry And Physiology A-molecular & Integrative Physiology0,836info:eu-repo/semantics/openAccess2023-10-29T06:09:00Zoai:repositorio.unesp.br:11449/161367Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T16:22:31.546786Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Morphological and metabolic adjustments in the small intestine to energy demands of growth, storage, and fasting in the first annual cycle of a hibernating lizard (Tupinambis merianae)
title Morphological and metabolic adjustments in the small intestine to energy demands of growth, storage, and fasting in the first annual cycle of a hibernating lizard (Tupinambis merianae)
spellingShingle Morphological and metabolic adjustments in the small intestine to energy demands of growth, storage, and fasting in the first annual cycle of a hibernating lizard (Tupinambis merianae)
Nascimento, Lucas Francisco R. do
Seasonal dormancy
Hibernation
Hypometabolism
Fasting
Starvation
Intestine
Scaling
Metabolic enzymes
Tegu lizard
Tupinambis merianae
title_short Morphological and metabolic adjustments in the small intestine to energy demands of growth, storage, and fasting in the first annual cycle of a hibernating lizard (Tupinambis merianae)
title_full Morphological and metabolic adjustments in the small intestine to energy demands of growth, storage, and fasting in the first annual cycle of a hibernating lizard (Tupinambis merianae)
title_fullStr Morphological and metabolic adjustments in the small intestine to energy demands of growth, storage, and fasting in the first annual cycle of a hibernating lizard (Tupinambis merianae)
title_full_unstemmed Morphological and metabolic adjustments in the small intestine to energy demands of growth, storage, and fasting in the first annual cycle of a hibernating lizard (Tupinambis merianae)
title_sort Morphological and metabolic adjustments in the small intestine to energy demands of growth, storage, and fasting in the first annual cycle of a hibernating lizard (Tupinambis merianae)
author Nascimento, Lucas Francisco R. do
author_facet Nascimento, Lucas Francisco R. do
Silveira, Lilian Cristina da
Nisembaum, Laura Gabriela
Colquhoun, Alison
Abe, Agusto S. [UNESP]
Mandarim-de-Lacerda, Carlos Alberto
Souza, Silvia Cristina R. de
author_role author
author2 Silveira, Lilian Cristina da
Nisembaum, Laura Gabriela
Colquhoun, Alison
Abe, Agusto S. [UNESP]
Mandarim-de-Lacerda, Carlos Alberto
Souza, Silvia Cristina R. de
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Universidade Estadual Paulista (Unesp)
Universidade do Estado do Rio de Janeiro (UERJ)
dc.contributor.author.fl_str_mv Nascimento, Lucas Francisco R. do
Silveira, Lilian Cristina da
Nisembaum, Laura Gabriela
Colquhoun, Alison
Abe, Agusto S. [UNESP]
Mandarim-de-Lacerda, Carlos Alberto
Souza, Silvia Cristina R. de
dc.subject.por.fl_str_mv Seasonal dormancy
Hibernation
Hypometabolism
Fasting
Starvation
Intestine
Scaling
Metabolic enzymes
Tegu lizard
Tupinambis merianae
topic Seasonal dormancy
Hibernation
Hypometabolism
Fasting
Starvation
Intestine
Scaling
Metabolic enzymes
Tegu lizard
Tupinambis merianae
description Seasonal plasticity in the small intestine of neonatal tegu lizards was investigated using morphometry and analysis of enzymes involved in supplying energy to the intestinal tissue. In the autumn, the intestinal mass (Mi) was 1.0% of body mass and the scaling exponent b = 0.92 indicated that Mi was larger in smaller neonates. During arousal from dormancy Mi was 23% smaller; later in spring, Mi increased 60% in relation to the autumn and the exponent b = 0.14 indicated that the recovery was disproportionate in smaller tegus. During the autumn, the intestinal villi were greatly elongated; by midwinter, the Hv, SvEp, and VvEp were smaller than during the autumn (59%, 54%, 29%) and were restored to autumn levels during spring. In the active tegus, the maximum activity (Vmax) of enzymes indicated that the enterocytes can obtain energy from different sources, and possess gluconeogenic capacity. During winter, the Vmax of CS, HOAD, GDH, PEPCK was 40-50% lower in relation to the autumn and spring, while the Vmax of HK, PK, LDH, AST was unchanged. The hypoglycemia and the mucosal atrophy/ischemia during winter would prevent the enterocytes from using glucose, whereas they could slowly oxidize fatty acids released from body stores and amino acids from the tissue proteolysis to satisfy their needs of energy. Contrastingly, starvation during spring caused severe mass loss (50%); the tissue protein and the VvEp and VvLP did not change while the thickness of the muscular layer increased 51%, which suggested different effects along the length of the organ. In addition, the Vmax of the glycolytic enzymes was lower, indicating that a regulatory mechanism would spare blood glucose for vital organs during unanticipated food restriction. (C) 2016 Elsevier Inc. All rights reserved.
publishDate 2016
dc.date.none.fl_str_mv 2016-05-01
2018-11-26T16:32:27Z
2018-11-26T16:32:27Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.cbpa.2016.02.002
Comparative Biochemistry And Physiology A-molecular & Integrative Physiology. New York: Elsevier Science Inc, v. 195, p. 55-64, 2016.
1095-6433
http://hdl.handle.net/11449/161367
10.1016/j.cbpa.2016.02.002
WOS:000373410500008
WOS000373410500008.pdf
url http://dx.doi.org/10.1016/j.cbpa.2016.02.002
http://hdl.handle.net/11449/161367
identifier_str_mv Comparative Biochemistry And Physiology A-molecular & Integrative Physiology. New York: Elsevier Science Inc, v. 195, p. 55-64, 2016.
1095-6433
10.1016/j.cbpa.2016.02.002
WOS:000373410500008
WOS000373410500008.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Comparative Biochemistry And Physiology A-molecular & Integrative Physiology
0,836
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 55-64
application/pdf
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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