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1.
J Vet Med Sci ; 78(9): 1487-1494, 2016 Oct 01.
Article in English | MEDLINE | ID: mdl-27301842

ABSTRACT

This experiment was conducted to evaluate the effects of quercetin supplementation on intestinal integrity, intestinal reactive oxygen species (ROS) levels and intestinal inflammation in pigs under transport stress. A total of 170 finishing pigs were randomly assigned into two groups. Animals in the control group consumed a basal diet, while those in the treatment group consumed the same diet supplemented with 25 mg quercetin per kg feed. After a 4-week period, pigs were transported for 5 hr. The quercetin-supplemented pigs showed decreased serum levels of endotoxin (P<0.05), increased height of jejunum villi (P<0.05), and increased occludin and zonula occudens-1 (ZO-1) mRNA expression in the jejunum (P<0.05). These parameters are associated with intestinal health and were markedly improved by quercetin supplementation. Pigs consuming the quercetin-supplemented diet had lower intestinal levels of ROS and malondialdehyde (MDA) compared with the control group (P<0.05). This finding coincided with greater inhibition of the innate immune system (P<0.05), including mitogen-activated protein kinase (MAPK), protein kinase B (Akt) and nuclear factor κB (NF-κB) signaling pathways, as well as decreased expression of inflammatory cytokines in the jejunum. These results indicate that quercetin alleviates intestinal injury in pigs during transport, probably through modulation of intestinal oxidative status and inflammation.


Subject(s)
Antioxidants/therapeutic use , Inflammation/veterinary , Intestines/drug effects , Oxidative Stress/drug effects , Quercetin/therapeutic use , Swine Diseases/prevention & control , Animal Husbandry/methods , Animals , Dietary Supplements , Inflammation/prevention & control , Intestines/chemistry , Malondialdehyde/analysis , Occludin/analysis , Reactive Oxygen Species/analysis , Swine , Transportation , Zonula Occludens-1 Protein/analysis
2.
Vet Immunol Immunopathol ; 158(3-4): 182-8, 2014 Apr 15.
Article in English | MEDLINE | ID: mdl-24507560

ABSTRACT

Toll-like receptor 4 (TLR4) has been suggested to play a regulatory role in immune cell development; however, studies regarding the role of TLR4 in the development of the chick thymus are scarce. In this study, we investigated the distribution and expression pattern of TLR4 in normal chick thymi at different stages of development, in order to better understand the role of TLR4 in chick thymus development. We studied the thymi from 15 chicks, collected at days 7, 21 and 35 of age. The relative change in TLR4 mRNA expression in the chick thymus at different ages was determined by quantitative real-time PCR, and changes in protein expression were analyzed by immunohistochemistry and Western blotting. Furthermore, the distribution of TLR4 in the chick thymus was analyzed by immunohistochemistry, and compared with the distribution of TLR4 expression in juvenile female pigs (gilts). Our results indicated that TLR4 was constitutively expressed in the chick thymus. TLR4 was primarily expressed in the thymic cortico-medullary junction and the medulla, particularly in the epithelial cells of Hassall's corpuscles. The mRNA and protein expression level of TLR4 increased in the thymus with increasing age (p<0.05). Taken together, these results indicate that TLR4 is constitutively expressed by epithelial cells in the chick thymus, suggesting it may participate in thymic development by inducing factors affecting its development.


Subject(s)
Avian Proteins/immunology , Avian Proteins/metabolism , Thymus Gland/growth & development , Thymus Gland/immunology , Toll-Like Receptor 4/metabolism , Animals , Avian Proteins/genetics , Epithelial Cells/immunology , Epithelial Cells/metabolism , Female , Gene Expression Regulation, Developmental , Immunohistochemistry , Keratins/metabolism , RNA, Messenger/genetics , RNA, Messenger/metabolism , Real-Time Polymerase Chain Reaction , Species Specificity , Sus scrofa/genetics , Sus scrofa/immunology , Thymus Gland/cytology , Toll-Like Receptor 4/genetics
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