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Analysis of Gastrointestinal Responses Revealed Both Shared and Specific Targets of Zinc Oxide and Carbadox in Weaned Pigs

Antibiotics and pharmacological zinc supplementation were commonly used as growth promoters for several decades in the swine industry before being limited because of public health and environmental concerns. Further, the physiological and metabolic responses associated with their growth promotion ef...

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Autores principales: Hung, Yuan-Tai, Hu, Qiong, Faris, Richard J., Guo, Juanjuan, Urriola, Pedro E., Shurson, Gerald C., Chen, Chi, Saqui-Salces, Milena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7460413/
https://www.ncbi.nlm.nih.gov/pubmed/32751572
http://dx.doi.org/10.3390/antibiotics9080463
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author Hung, Yuan-Tai
Hu, Qiong
Faris, Richard J.
Guo, Juanjuan
Urriola, Pedro E.
Shurson, Gerald C.
Chen, Chi
Saqui-Salces, Milena
author_facet Hung, Yuan-Tai
Hu, Qiong
Faris, Richard J.
Guo, Juanjuan
Urriola, Pedro E.
Shurson, Gerald C.
Chen, Chi
Saqui-Salces, Milena
author_sort Hung, Yuan-Tai
collection PubMed
description Antibiotics and pharmacological zinc supplementation were commonly used as growth promoters for several decades in the swine industry before being limited because of public health and environmental concerns. Further, the physiological and metabolic responses associated with their growth promotion effects are unclear. To characterize these responses induced by pharmacological zinc supplementation (2500 mg/kg) and carbadox (55 mg/kg), 192 post-weaning pigs were fed basal and test diets for 43 days. Compared with basal, pharmacological zinc and carbadox independently improved growth performance. Pharmacological zinc increased gastric mucosa thickness compared with basal zinc, while carbadox increased intestinal villus:crypt ratio compared with non-carbadox. Pharmacological zinc and carbadox independently reduced interleukin (IL)-1β concentration compared with basal zinc and non-carbadox. Pharmacological zinc increased IL-1RA:IL-1 ratio by 42% compared with basal zinc, while carbadox tended to increase the IL-10 and IL10:IL-12 ratio compared with non-carbadox. Carbadox increased fecal concentrations of histidine and lysine compared with non-carbadox. The independent effect of pharmacological zinc and carbadox on morphology and nutrient metabolism, and their shared effect on immunity may contribute to the additive effect on growth promotion. These results further confirmed the concept that growth promotion is multifactorial intervention. Therefore, elucidating growth-promoting effects and searching for alternatives should include wide-spectrum evaluation.
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spelling pubmed-74604132020-09-03 Analysis of Gastrointestinal Responses Revealed Both Shared and Specific Targets of Zinc Oxide and Carbadox in Weaned Pigs Hung, Yuan-Tai Hu, Qiong Faris, Richard J. Guo, Juanjuan Urriola, Pedro E. Shurson, Gerald C. Chen, Chi Saqui-Salces, Milena Antibiotics (Basel) Article Antibiotics and pharmacological zinc supplementation were commonly used as growth promoters for several decades in the swine industry before being limited because of public health and environmental concerns. Further, the physiological and metabolic responses associated with their growth promotion effects are unclear. To characterize these responses induced by pharmacological zinc supplementation (2500 mg/kg) and carbadox (55 mg/kg), 192 post-weaning pigs were fed basal and test diets for 43 days. Compared with basal, pharmacological zinc and carbadox independently improved growth performance. Pharmacological zinc increased gastric mucosa thickness compared with basal zinc, while carbadox increased intestinal villus:crypt ratio compared with non-carbadox. Pharmacological zinc and carbadox independently reduced interleukin (IL)-1β concentration compared with basal zinc and non-carbadox. Pharmacological zinc increased IL-1RA:IL-1 ratio by 42% compared with basal zinc, while carbadox tended to increase the IL-10 and IL10:IL-12 ratio compared with non-carbadox. Carbadox increased fecal concentrations of histidine and lysine compared with non-carbadox. The independent effect of pharmacological zinc and carbadox on morphology and nutrient metabolism, and their shared effect on immunity may contribute to the additive effect on growth promotion. These results further confirmed the concept that growth promotion is multifactorial intervention. Therefore, elucidating growth-promoting effects and searching for alternatives should include wide-spectrum evaluation. MDPI 2020-07-30 /pmc/articles/PMC7460413/ /pubmed/32751572 http://dx.doi.org/10.3390/antibiotics9080463 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hung, Yuan-Tai
Hu, Qiong
Faris, Richard J.
Guo, Juanjuan
Urriola, Pedro E.
Shurson, Gerald C.
Chen, Chi
Saqui-Salces, Milena
Analysis of Gastrointestinal Responses Revealed Both Shared and Specific Targets of Zinc Oxide and Carbadox in Weaned Pigs
title Analysis of Gastrointestinal Responses Revealed Both Shared and Specific Targets of Zinc Oxide and Carbadox in Weaned Pigs
title_full Analysis of Gastrointestinal Responses Revealed Both Shared and Specific Targets of Zinc Oxide and Carbadox in Weaned Pigs
title_fullStr Analysis of Gastrointestinal Responses Revealed Both Shared and Specific Targets of Zinc Oxide and Carbadox in Weaned Pigs
title_full_unstemmed Analysis of Gastrointestinal Responses Revealed Both Shared and Specific Targets of Zinc Oxide and Carbadox in Weaned Pigs
title_short Analysis of Gastrointestinal Responses Revealed Both Shared and Specific Targets of Zinc Oxide and Carbadox in Weaned Pigs
title_sort analysis of gastrointestinal responses revealed both shared and specific targets of zinc oxide and carbadox in weaned pigs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7460413/
https://www.ncbi.nlm.nih.gov/pubmed/32751572
http://dx.doi.org/10.3390/antibiotics9080463
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