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A comparative study to determine the effects of breed and feed restriction on glucose metabolism of chickens

The glucose metabolism of poultry draws wide attention as they have nearly twice the fasting blood glucose than that of mammals. To define the relationship between glucose metabolism and breed of chicken, the outcomes from different growth rate chickens showed that Arbor Acres (AA) broilers, a well-...

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Autores principales: Du, Pengfei, Wang, Huanjie, Shi, Xiuwen, Zhang, Xiangli, Zhu, Yao, Chen, Wen, Zhang, Huaiyong, Huang, Yanqun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10164833/
https://www.ncbi.nlm.nih.gov/pubmed/37168446
http://dx.doi.org/10.1016/j.aninu.2023.02.005
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author Du, Pengfei
Wang, Huanjie
Shi, Xiuwen
Zhang, Xiangli
Zhu, Yao
Chen, Wen
Zhang, Huaiyong
Huang, Yanqun
author_facet Du, Pengfei
Wang, Huanjie
Shi, Xiuwen
Zhang, Xiangli
Zhu, Yao
Chen, Wen
Zhang, Huaiyong
Huang, Yanqun
author_sort Du, Pengfei
collection PubMed
description The glucose metabolism of poultry draws wide attention as they have nearly twice the fasting blood glucose than that of mammals. To define the relationship between glucose metabolism and breed of chicken, the outcomes from different growth rate chickens showed that Arbor Acres (AA) broilers, a well-known fast-growing breed, had a lower fasting blood glucose concentration and glucose clearance rate when compared to Silky chickens, a Chinese traditional medicinal chicken with black skin and a slow growth rate. Moreover, AA broilers had a relatively slow rise in blood glucose in response to oral glucose solution than the Silky chickens on 21 and 42 d (P < 0.05), which is probably attributed to downregulated expression of pancreatic insulin (INS), and upregulated transcription of phosphoenolpyruvate carboxy kinase 1 (PCK1) and glucose transporter 2 (GLUT2) in the liver of AA broilers (P < 0.05). In response to feeding restriction from 7 to 21 d, both the fasting blood glucose and the response speed of AA broilers to oral glucose were increased on d 21 (P < 0.05), and the serum glucose concentrations after 3 weeks compensatory growth were improved by early feed restriction in AA broilers. Feed restriction could also upregulate the mRNA level of pancreatic INS on d 21 and 42, as well as decrease the expressions of PCK1, glucose-6-phosphatase catalytic (G6PC), and GLUT2 in the liver on d 21 (P < 0.05) when compared to the free feeding group. These results revealed that Silky chickens have a stronger capability to regulate glucose homeostasis than AA broilers, and feed restriction could improve the fasting blood glucose and the response to oral glucose of AA broilers.
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spelling pubmed-101648332023-05-09 A comparative study to determine the effects of breed and feed restriction on glucose metabolism of chickens Du, Pengfei Wang, Huanjie Shi, Xiuwen Zhang, Xiangli Zhu, Yao Chen, Wen Zhang, Huaiyong Huang, Yanqun Anim Nutr Original Research Article The glucose metabolism of poultry draws wide attention as they have nearly twice the fasting blood glucose than that of mammals. To define the relationship between glucose metabolism and breed of chicken, the outcomes from different growth rate chickens showed that Arbor Acres (AA) broilers, a well-known fast-growing breed, had a lower fasting blood glucose concentration and glucose clearance rate when compared to Silky chickens, a Chinese traditional medicinal chicken with black skin and a slow growth rate. Moreover, AA broilers had a relatively slow rise in blood glucose in response to oral glucose solution than the Silky chickens on 21 and 42 d (P < 0.05), which is probably attributed to downregulated expression of pancreatic insulin (INS), and upregulated transcription of phosphoenolpyruvate carboxy kinase 1 (PCK1) and glucose transporter 2 (GLUT2) in the liver of AA broilers (P < 0.05). In response to feeding restriction from 7 to 21 d, both the fasting blood glucose and the response speed of AA broilers to oral glucose were increased on d 21 (P < 0.05), and the serum glucose concentrations after 3 weeks compensatory growth were improved by early feed restriction in AA broilers. Feed restriction could also upregulate the mRNA level of pancreatic INS on d 21 and 42, as well as decrease the expressions of PCK1, glucose-6-phosphatase catalytic (G6PC), and GLUT2 in the liver on d 21 (P < 0.05) when compared to the free feeding group. These results revealed that Silky chickens have a stronger capability to regulate glucose homeostasis than AA broilers, and feed restriction could improve the fasting blood glucose and the response to oral glucose of AA broilers. KeAi Publishing 2023-02-21 /pmc/articles/PMC10164833/ /pubmed/37168446 http://dx.doi.org/10.1016/j.aninu.2023.02.005 Text en © 2023 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co. Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research Article
Du, Pengfei
Wang, Huanjie
Shi, Xiuwen
Zhang, Xiangli
Zhu, Yao
Chen, Wen
Zhang, Huaiyong
Huang, Yanqun
A comparative study to determine the effects of breed and feed restriction on glucose metabolism of chickens
title A comparative study to determine the effects of breed and feed restriction on glucose metabolism of chickens
title_full A comparative study to determine the effects of breed and feed restriction on glucose metabolism of chickens
title_fullStr A comparative study to determine the effects of breed and feed restriction on glucose metabolism of chickens
title_full_unstemmed A comparative study to determine the effects of breed and feed restriction on glucose metabolism of chickens
title_short A comparative study to determine the effects of breed and feed restriction on glucose metabolism of chickens
title_sort comparative study to determine the effects of breed and feed restriction on glucose metabolism of chickens
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10164833/
https://www.ncbi.nlm.nih.gov/pubmed/37168446
http://dx.doi.org/10.1016/j.aninu.2023.02.005
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