Hostname: page-component-848d4c4894-8kt4b Total loading time: 0 Render date: 2024-06-16T17:57:18.547Z Has data issue: false hasContentIssue false

Dietary zinc oxide supplementation in weaner piglets does not cause differential expression of digestive enzymes

Published online by Cambridge University Press:  23 November 2017

H. Sargeant*
Affiliation:
University of Leeds, Leeds, United Kingdom
H.M. Miller
Affiliation:
University of Leeds, Leeds, United Kingdom
M.A. Shaw
Affiliation:
University of Leeds, Leeds, United Kingdom
Get access

Extract

Piglet weaner diets are often supplemented with the antimicrobial mineral zinc oxide (ZnO) to minimise the characteristic growth check post weaning in commercial systems. Zinc has been shown to decrease the incidence of scours, maintain gut morphology and feed intake, and increase growth rate, although the mechanism for these effects remains unclear. Weaning is often accompanied with a decrease in digestive enzyme production by enterocytes, decreasing digestive and absorptive capacity. Digestive enzyme requirements also alter with the dietary change from milk to a solid cereal-based diet, and improvements in enzymatic adaptations may increase digestion and absorption and improve feed utilisation. It is hypothesised in this study that the growth effects of ZnO are linked to improvement in digestion by altering digestive enzyme expression and activity. The aim of this study was to investigate whether the effects of ZnO are linked to expression of the digestive enzymes lactase phlorizin hydrolase (LPH) and aminopeptidase N (ANPEP) in the small intestine (S.I.).

Type
Poster Presentations
Copyright
Copyright © The British Society of Animal Science 2007

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Torp, N., Rossi, M., et al. (1993). “Lactase-phlorizin hydrolase and aminopeptidase N are differentially regulated in the small intestine of the pig.” The Biochemical Journal 295(1): 177-82.CrossRefGoogle Scholar