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)
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , , , |
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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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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1808128639182569472 |