Effects of the lipid-coated zinc oxide dietary supplement on intestinal mucosal morphology and gene expression associated with the gut health in weanling pigs challenged with enterotoxigenic Escherichia coli K88
- Authors
- Han, Jeong Hee; Song, Mm Hye; Kim, Ha Na; Jang, Insurk; Lee, C. Young; Park, Byung-Chul
- Issue Date
- Sep-2018
- Publisher
- CANADIAN SCIENCE PUBLISHING
- Keywords
- pig; zinc oxide; diarrhea; morphology; gene expression
- Citation
- CANADIAN JOURNAL OF ANIMAL SCIENCE, v.98, no.3, pp 538 - 547
- Pages
- 10
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- CANADIAN JOURNAL OF ANIMAL SCIENCE
- Volume
- 98
- Number
- 3
- Start Page
- 538
- End Page
- 547
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/11286
- DOI
- 10.1139/cjas-2017-0127
- ISSN
- 0008-3984
1918-1825
- Abstract
- Effects of a lipid-coated zinc oxide (ZnO) Shield Zn (R) (SZ) vs. ZnO were evaluated. Forty 25-d-old weanling pigs were fed a nursery diet supplemented with 100 mg kg(-1) Zn with ZnO (ZnO-100), ZnO-2500, SZ-100, -200, or -400. All piglets were challenged orally with 5 x 10(8) colony-forming units of enterotoxigenic Escherichia coli K88 on day 7 and euthanized on day 14. The fecal consistency score (FCS) was less for the SZ group vs. ZnO-100 (P < 0.05). The intestinal villus height:crypt depth ratio and goblet cell density were greater for the SZ group vs. ZnO-100. By regression analyses, SZ-100 to -200 and SZ-300 to -400 were comparable to ZnO-2500 in the FCS and intestinal variables, respectively. The jejunal mucosal mRNA level did not differ between the SZ group and either ZnO group in insulin-like growth factor-I and multiple structural proteins and cytokines including zonula occludens protein (ZO) 1 and interleukin (IL) 10 except for lower ZO-1 and IL 10 mRNA levels for the SZ group than for ZnO-2500 and ZnO-100, respectively. The ZO-1 mRNA level regressed positively on the supplemental SZ concentration. Results suggest that SZ play a role in epithelial barrier function and inflammation by modulating the expression of ZO-1 and IL 10.
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