Fang Tingting, Tian Gang, Chen Daiwen, He Jun, Zheng Ping, Mao Xiangbing, Yan Hui, Yu Bing
Key Laboratory of Animal Disease-Resistance Nutrition, Animal Nutrition Institute, Sichuan Agricultural University, Chengdu 611130, China.
Animals (Basel). 2024 Sep 14;14(18):2677. doi: 10.3390/ani14182677.
Intrauterine growth retardation (IUGR) in piglets is associated with a high rate of morbidity and mortality after birth due to gut dysfunction, and the underlying mechanisms remain poorly understood. This study selected six pairs of IUGR newborn male piglets and normal birth weight newborn piglets (Large White × Landrace) to investigate differences in intestinal structure and digestive functions, intestinal ERS and apoptosis, intestinal barrier function, and inflammatory response. The results showed that IUGR significantly reduced the jejunal villi height ( 0.05) and the ratio of villus-height-to-crypt-depth ( = 0.05) in neonatal piglets. Additionally, the microvilli in the jejunum of IUGR neonatal piglets were shorter than those in normal-weight piglets, and swelling of the mitochondria and expansion of the endoplasmic reticulum were observed. IUGR also significantly reduced serum glucose and lactase levels ( < 0.05) while significantly increasing mRNA levels of jejunal , , , , , , , , , , , and ( < 0.05), as well as GRP78 protein levels in neonatal piglets ( < 0.05). These findings suggest that IUGR impairs intestinal structure and barrier function in newborn piglets by enhancing intestinal inflammatory responses, activating intestinal ERS and the signaling pathways related to the unfolded protein response, thereby inducing ERS-related apoptosis.
仔猪宫内生长受限(IUGR)与出生后因肠道功能障碍导致的高发病率和死亡率相关,其潜在机制仍知之甚少。本研究选取了6对IUGR新生雄性仔猪和正常出生体重的新生仔猪(大白猪×长白猪),以研究肠道结构和消化功能、肠道内质网应激(ERS)和细胞凋亡、肠道屏障功能以及炎症反应的差异。结果表明,IUGR显著降低了新生仔猪空肠绒毛高度(P<0.05)和绒毛高度与隐窝深度之比(P = 0.05)。此外,IUGR新生仔猪空肠中的微绒毛比正常体重仔猪的短,并且观察到线粒体肿胀和内质网扩张。IUGR还显著降低了新生仔猪的血清葡萄糖和乳糖酶水平(P<0.05),同时显著增加了空肠中TLR2、TLR4、MyD88、NF-κB、IL-1β、IL-6、IL-8、TNF-α、IFN-γ、HMGB1、TGF-β和VEGF的mRNA水平(P<0.05),以及新生仔猪中的GRP78蛋白水平(P<0.05)。这些发现表明,IUGR通过增强肠道炎症反应、激活肠道ERS和与未折叠蛋白反应相关的信号通路,从而诱导ERS相关的细胞凋亡,损害新生仔猪的肠道结构和屏障功能。