Supplementation of glycerol or fructose via drinking water to grazing lambs on tissue glycogen level and lipogenesis

Autores
Volpi Lagreca, Gabriela; Duckett, Susan K.
Año de publicación
2017
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Lambs (n = 18; 40.1 ± 7.4 kg BW) were used to assess supplementation of glycerol or fructose via drinking water on growth, tissue glycogen levels, postmortem glycolysis, and lipogenesis. Lambs were blocked by BW and allocated to alfalfa paddocks (2 lambs/paddock and 3 paddocks/treatment). Each paddock within a block was assigned randomly to drinking water treatments for 30 d: 1) control (CON), 2) 120 g fructose/L of drinking water (FRU), or 3) 120 g glycerol/L of drinking water (GLY). Lambs grazed alfalfa with free access to water treatments for 28 d and then were fasted in indoor pens for a final 2 d with access to only water treatments. Data were analyzed using the MIXED procedure of SAS with water treatment and time (when appropriate) in the model. During the 28-d grazing period, ADG was greater (P < 0.05) for GLY than for CON or FRU. During the 2-d fasting period, BW shrink was lower (P < 0.05) for GLY compared with CON or FRU. Hot carcass weight was greater (P < 0.05) for GLY than for FRU. The interaction for glycogen content × postmortem time was significant (P = 0.003) in LM and semitendinosus (ST) muscles. Glycogen content in the LM was greater (P <0.05) for GLY at 2 and 3 h and for FRU at 1 h postmortem compared with CON. Glycogen content in ST did not differ between treatments (P > 0.05). Liver glycogen content was over 14-fold greater (P < 0.05) for GLY compared with FRU or CON. Liver free glucose was greater (P < 0.05) for GLY than for CON, whereas liver lipid content was higher (P < 0.05) for CON than for GLY. Supplementation with GLY increased (P <0.05) odd-chain fatty acids in LM, subcutaneous fat (SQ), and the liver. Stearic acid (C18:0) concentrations were reduced in LM (P = 0.064) and subcutaneous adipose tissue (SQ; P = 0.018), whereas oleic acid (C18:1 cis-9) concentration tended to be increased (P = 0.066) in SQ with FRU and GLY. Linolenic acid (C18:3n-3) was reduced (P = 0.031) and all long-chain n-3 fatty acid (eicosapentaenoic acid, docosapentaenoic acid, and docosahexaenoic acid) concentrations were increased (P < 0.05) with FRU and GLY compared with CON. Glycerol supplementation upregulated (P < 0.05) stearoyl-CoA desaturate (SCD1) and fatty acid synthase (FASN) mRNA by over 40-fold in the SQ and 5-fold in the liver. Glycerol supplementation also upregulated (P < 0.05) glucose transporters and glycogen branching enzyme in the liver. Overall, glycerol supplementation improved growth, reduced BW shrink during fasting, increased glycogen content in muscle and the liver, and stimulated de novo lipogenesis.
EEA Anguil
Fil: Volpi Lagreca, Gabriela. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Anguil; Argentina. Clemson University; Estados Unidos
Fil: Duckett, Susan K. Clemson University; Estados Unidos
Fuente
Journal of animal scence 95 (6) : 2558–2575. (2017)
Materia
Producción animal
Cordero
Glicerol
Fructosa
Lipogénesis
Agua Potable
Supplements
Lambs
Glycerol
Drinking Water
Nivel de accesibilidad
acceso restringido
Condiciones de uso
Repositorio
INTA Digital (INTA)
Institución
Instituto Nacional de Tecnología Agropecuaria
OAI Identificador
oai:localhost:20.500.12123/634

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oai_identifier_str oai:localhost:20.500.12123/634
network_acronym_str INTADig
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network_name_str INTA Digital (INTA)
spelling Supplementation of glycerol or fructose via drinking water to grazing lambs on tissue glycogen level and lipogenesisVolpi Lagreca, GabrielaDuckett, Susan K.Producción animalCorderoGlicerolFructosaLipogénesisAgua PotableSupplementsLambsGlycerolDrinking WaterLambs (n = 18; 40.1 ± 7.4 kg BW) were used to assess supplementation of glycerol or fructose via drinking water on growth, tissue glycogen levels, postmortem glycolysis, and lipogenesis. Lambs were blocked by BW and allocated to alfalfa paddocks (2 lambs/paddock and 3 paddocks/treatment). Each paddock within a block was assigned randomly to drinking water treatments for 30 d: 1) control (CON), 2) 120 g fructose/L of drinking water (FRU), or 3) 120 g glycerol/L of drinking water (GLY). Lambs grazed alfalfa with free access to water treatments for 28 d and then were fasted in indoor pens for a final 2 d with access to only water treatments. Data were analyzed using the MIXED procedure of SAS with water treatment and time (when appropriate) in the model. During the 28-d grazing period, ADG was greater (P < 0.05) for GLY than for CON or FRU. During the 2-d fasting period, BW shrink was lower (P < 0.05) for GLY compared with CON or FRU. Hot carcass weight was greater (P < 0.05) for GLY than for FRU. The interaction for glycogen content × postmortem time was significant (P = 0.003) in LM and semitendinosus (ST) muscles. Glycogen content in the LM was greater (P <0.05) for GLY at 2 and 3 h and for FRU at 1 h postmortem compared with CON. Glycogen content in ST did not differ between treatments (P > 0.05). Liver glycogen content was over 14-fold greater (P < 0.05) for GLY compared with FRU or CON. Liver free glucose was greater (P < 0.05) for GLY than for CON, whereas liver lipid content was higher (P < 0.05) for CON than for GLY. Supplementation with GLY increased (P <0.05) odd-chain fatty acids in LM, subcutaneous fat (SQ), and the liver. Stearic acid (C18:0) concentrations were reduced in LM (P = 0.064) and subcutaneous adipose tissue (SQ; P = 0.018), whereas oleic acid (C18:1 cis-9) concentration tended to be increased (P = 0.066) in SQ with FRU and GLY. Linolenic acid (C18:3n-3) was reduced (P = 0.031) and all long-chain n-3 fatty acid (eicosapentaenoic acid, docosapentaenoic acid, and docosahexaenoic acid) concentrations were increased (P < 0.05) with FRU and GLY compared with CON. Glycerol supplementation upregulated (P < 0.05) stearoyl-CoA desaturate (SCD1) and fatty acid synthase (FASN) mRNA by over 40-fold in the SQ and 5-fold in the liver. Glycerol supplementation also upregulated (P < 0.05) glucose transporters and glycogen branching enzyme in the liver. Overall, glycerol supplementation improved growth, reduced BW shrink during fasting, increased glycogen content in muscle and the liver, and stimulated de novo lipogenesis.EEA AnguilFil: Volpi Lagreca, Gabriela. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Anguil; Argentina. Clemson University; Estados UnidosFil: Duckett, Susan K. Clemson University; Estados Unidos2017-07-11T13:37:47Z2017-07-11T13:37:47Z2017info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://hdl.handle.net/20.500.12123/634https://academic.oup.com/jas/article/95/6/2558/4702529Volpi-Lagreca, G., and S. K. Duckett. 2017. Supplementation of glycerol or fructose via drinking water to grazing lambs on tissue glycogen level and lipogenesis1. J. Anim. Sci. 95:2558-2575. doi:10.2527/jas.2017.14490021-881210.2527/jas 2017.1449Journal of animal scence 95 (6) : 2558–2575. (2017)reponame:INTA Digital (INTA)instname:Instituto Nacional de Tecnología Agropecuariaenginfo:eu-repo/semantics/restrictedAccess2025-09-04T09:46:53Zoai:localhost:20.500.12123/634instacron:INTAInstitucionalhttp://repositorio.inta.gob.ar/Organismo científico-tecnológicoNo correspondehttp://repositorio.inta.gob.ar/oai/requesttripaldi.nicolas@inta.gob.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:l2025-09-04 09:46:54.494INTA Digital (INTA) - Instituto Nacional de Tecnología Agropecuariafalse
dc.title.none.fl_str_mv Supplementation of glycerol or fructose via drinking water to grazing lambs on tissue glycogen level and lipogenesis
title Supplementation of glycerol or fructose via drinking water to grazing lambs on tissue glycogen level and lipogenesis
spellingShingle Supplementation of glycerol or fructose via drinking water to grazing lambs on tissue glycogen level and lipogenesis
Volpi Lagreca, Gabriela
Producción animal
Cordero
Glicerol
Fructosa
Lipogénesis
Agua Potable
Supplements
Lambs
Glycerol
Drinking Water
title_short Supplementation of glycerol or fructose via drinking water to grazing lambs on tissue glycogen level and lipogenesis
title_full Supplementation of glycerol or fructose via drinking water to grazing lambs on tissue glycogen level and lipogenesis
title_fullStr Supplementation of glycerol or fructose via drinking water to grazing lambs on tissue glycogen level and lipogenesis
title_full_unstemmed Supplementation of glycerol or fructose via drinking water to grazing lambs on tissue glycogen level and lipogenesis
title_sort Supplementation of glycerol or fructose via drinking water to grazing lambs on tissue glycogen level and lipogenesis
dc.creator.none.fl_str_mv Volpi Lagreca, Gabriela
Duckett, Susan K.
author Volpi Lagreca, Gabriela
author_facet Volpi Lagreca, Gabriela
Duckett, Susan K.
author_role author
author2 Duckett, Susan K.
author2_role author
dc.subject.none.fl_str_mv Producción animal
Cordero
Glicerol
Fructosa
Lipogénesis
Agua Potable
Supplements
Lambs
Glycerol
Drinking Water
topic Producción animal
Cordero
Glicerol
Fructosa
Lipogénesis
Agua Potable
Supplements
Lambs
Glycerol
Drinking Water
dc.description.none.fl_txt_mv Lambs (n = 18; 40.1 ± 7.4 kg BW) were used to assess supplementation of glycerol or fructose via drinking water on growth, tissue glycogen levels, postmortem glycolysis, and lipogenesis. Lambs were blocked by BW and allocated to alfalfa paddocks (2 lambs/paddock and 3 paddocks/treatment). Each paddock within a block was assigned randomly to drinking water treatments for 30 d: 1) control (CON), 2) 120 g fructose/L of drinking water (FRU), or 3) 120 g glycerol/L of drinking water (GLY). Lambs grazed alfalfa with free access to water treatments for 28 d and then were fasted in indoor pens for a final 2 d with access to only water treatments. Data were analyzed using the MIXED procedure of SAS with water treatment and time (when appropriate) in the model. During the 28-d grazing period, ADG was greater (P < 0.05) for GLY than for CON or FRU. During the 2-d fasting period, BW shrink was lower (P < 0.05) for GLY compared with CON or FRU. Hot carcass weight was greater (P < 0.05) for GLY than for FRU. The interaction for glycogen content × postmortem time was significant (P = 0.003) in LM and semitendinosus (ST) muscles. Glycogen content in the LM was greater (P <0.05) for GLY at 2 and 3 h and for FRU at 1 h postmortem compared with CON. Glycogen content in ST did not differ between treatments (P > 0.05). Liver glycogen content was over 14-fold greater (P < 0.05) for GLY compared with FRU or CON. Liver free glucose was greater (P < 0.05) for GLY than for CON, whereas liver lipid content was higher (P < 0.05) for CON than for GLY. Supplementation with GLY increased (P <0.05) odd-chain fatty acids in LM, subcutaneous fat (SQ), and the liver. Stearic acid (C18:0) concentrations were reduced in LM (P = 0.064) and subcutaneous adipose tissue (SQ; P = 0.018), whereas oleic acid (C18:1 cis-9) concentration tended to be increased (P = 0.066) in SQ with FRU and GLY. Linolenic acid (C18:3n-3) was reduced (P = 0.031) and all long-chain n-3 fatty acid (eicosapentaenoic acid, docosapentaenoic acid, and docosahexaenoic acid) concentrations were increased (P < 0.05) with FRU and GLY compared with CON. Glycerol supplementation upregulated (P < 0.05) stearoyl-CoA desaturate (SCD1) and fatty acid synthase (FASN) mRNA by over 40-fold in the SQ and 5-fold in the liver. Glycerol supplementation also upregulated (P < 0.05) glucose transporters and glycogen branching enzyme in the liver. Overall, glycerol supplementation improved growth, reduced BW shrink during fasting, increased glycogen content in muscle and the liver, and stimulated de novo lipogenesis.
EEA Anguil
Fil: Volpi Lagreca, Gabriela. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Anguil; Argentina. Clemson University; Estados Unidos
Fil: Duckett, Susan K. Clemson University; Estados Unidos
description Lambs (n = 18; 40.1 ± 7.4 kg BW) were used to assess supplementation of glycerol or fructose via drinking water on growth, tissue glycogen levels, postmortem glycolysis, and lipogenesis. Lambs were blocked by BW and allocated to alfalfa paddocks (2 lambs/paddock and 3 paddocks/treatment). Each paddock within a block was assigned randomly to drinking water treatments for 30 d: 1) control (CON), 2) 120 g fructose/L of drinking water (FRU), or 3) 120 g glycerol/L of drinking water (GLY). Lambs grazed alfalfa with free access to water treatments for 28 d and then were fasted in indoor pens for a final 2 d with access to only water treatments. Data were analyzed using the MIXED procedure of SAS with water treatment and time (when appropriate) in the model. During the 28-d grazing period, ADG was greater (P < 0.05) for GLY than for CON or FRU. During the 2-d fasting period, BW shrink was lower (P < 0.05) for GLY compared with CON or FRU. Hot carcass weight was greater (P < 0.05) for GLY than for FRU. The interaction for glycogen content × postmortem time was significant (P = 0.003) in LM and semitendinosus (ST) muscles. Glycogen content in the LM was greater (P <0.05) for GLY at 2 and 3 h and for FRU at 1 h postmortem compared with CON. Glycogen content in ST did not differ between treatments (P > 0.05). Liver glycogen content was over 14-fold greater (P < 0.05) for GLY compared with FRU or CON. Liver free glucose was greater (P < 0.05) for GLY than for CON, whereas liver lipid content was higher (P < 0.05) for CON than for GLY. Supplementation with GLY increased (P <0.05) odd-chain fatty acids in LM, subcutaneous fat (SQ), and the liver. Stearic acid (C18:0) concentrations were reduced in LM (P = 0.064) and subcutaneous adipose tissue (SQ; P = 0.018), whereas oleic acid (C18:1 cis-9) concentration tended to be increased (P = 0.066) in SQ with FRU and GLY. Linolenic acid (C18:3n-3) was reduced (P = 0.031) and all long-chain n-3 fatty acid (eicosapentaenoic acid, docosapentaenoic acid, and docosahexaenoic acid) concentrations were increased (P < 0.05) with FRU and GLY compared with CON. Glycerol supplementation upregulated (P < 0.05) stearoyl-CoA desaturate (SCD1) and fatty acid synthase (FASN) mRNA by over 40-fold in the SQ and 5-fold in the liver. Glycerol supplementation also upregulated (P < 0.05) glucose transporters and glycogen branching enzyme in the liver. Overall, glycerol supplementation improved growth, reduced BW shrink during fasting, increased glycogen content in muscle and the liver, and stimulated de novo lipogenesis.
publishDate 2017
dc.date.none.fl_str_mv 2017-07-11T13:37:47Z
2017-07-11T13:37:47Z
2017
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/20.500.12123/634
https://academic.oup.com/jas/article/95/6/2558/4702529
Volpi-Lagreca, G., and S. K. Duckett. 2017. Supplementation of glycerol or fructose via drinking water to grazing lambs on tissue glycogen level and lipogenesis1. J. Anim. Sci. 95:2558-2575. doi:10.2527/jas.2017.1449
0021-8812
10.2527/jas 2017.1449
url http://hdl.handle.net/20.500.12123/634
https://academic.oup.com/jas/article/95/6/2558/4702529
identifier_str_mv Volpi-Lagreca, G., and S. K. Duckett. 2017. Supplementation of glycerol or fructose via drinking water to grazing lambs on tissue glycogen level and lipogenesis1. J. Anim. Sci. 95:2558-2575. doi:10.2527/jas.2017.1449
0021-8812
10.2527/jas 2017.1449
dc.language.none.fl_str_mv eng
language eng
dc.rights.none.fl_str_mv info:eu-repo/semantics/restrictedAccess
eu_rights_str_mv restrictedAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv Journal of animal scence 95 (6) : 2558–2575. (2017)
reponame:INTA Digital (INTA)
instname:Instituto Nacional de Tecnología Agropecuaria
reponame_str INTA Digital (INTA)
collection INTA Digital (INTA)
instname_str Instituto Nacional de Tecnología Agropecuaria
repository.name.fl_str_mv INTA Digital (INTA) - Instituto Nacional de Tecnología Agropecuaria
repository.mail.fl_str_mv tripaldi.nicolas@inta.gob.ar
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