Protective Effects of Ferulic Acid against Heat Stress-Induced Intestinal Epithelial Barrier Dysfunction In Vitro and In Vivo

被引:63
作者
He, Shasha [1 ]
Liu, Fenghua [2 ]
Xu, Lei [2 ]
Yin, Peng [1 ]
Li, Deyin [2 ]
Mei, Chen [2 ]
Jiang, Linshu [2 ]
Ma, Yunfei [1 ]
Xu, Jianqin [1 ]
机构
[1] CAU, Coll Vet Med, CAU BUA TCVM Teaching & Researching Team, Beijing, Peoples R China
[2] BUA, Coll Anim Sci & Technol, Beijing Key Lab Dairy Cow Nutr, Beijing, Peoples R China
关键词
TIGHT JUNCTIONS; E-CADHERIN; PROTEIN EXPRESSION; INDUCED INJURY; OCCLUDIN; PERMEABILITY; PATHOGENESIS; HOMEOSTASIS; MECHANISMS; CLAUDIN-1;
D O I
10.1371/journal.pone.0145236
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Heat stress is important in the pathogenesis of intestinal epithelial barrier dysfunction. Ferulic acid (FA), a phenolic acid widely found in fruits and vegetables, can scavenge free radicals and activate cell stress responses. This study is aimed at investigating protective effects of FA on heat stress-induced dysfunction of the intestinal epithelial barrier in vitro and in vivo. Intestinal epithelial (IEC-6) cells were pretreated with FA for 4 h and then exposed to heat stress. Heat stress caused decreased transepithelial electrical resistance (TER) and increased permeability to 4-kDa fluorescein isothiocyanate (FITC)-dextran (FD4). Both effects were inhibited by FA in a dose-dependent manner. FA significantly attenuated the decrease in occludin, ZO-1 and E-cadherin expression observed with heat stress. The distortion and redistribution of occludin, ZO-1 and E-cadherin proteins were also effectively prevented by FA pretreatment. Moreover, heat stress diminished electron-dense material detected in tight junctions (TJs), an effect also alleviated by FA in a dose-dependent manner. In an in vivo heat stress model, FA (50 mg/kg) was administered to male Sprague- Dawley rats for 7 consecutive days prior to exposure to heat stress. FA pretreatment significantly attenuated the effects of heat stress on the small intestine, including the increased FD4 permeability, disrupted tight junctions and microvilli structure, and reduced occludin, ZO-1 and E-cadherin expression. Taken together, our results demonstrate that FA pretreatment is potentially protective against heat stress-induced intestinal epithelial barrier dysfunction.
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页数:15
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