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首页> 外文期刊>Journal of cellular and molecular medicine. >Postnatal growth retardation is associated with intestinal mucosa mitochondrial dysfunction and aberrant energy status in piglets
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Postnatal growth retardation is associated with intestinal mucosa mitochondrial dysfunction and aberrant energy status in piglets

机译:产后生长延迟与仔猪中的肠粘膜线粒体功能障碍和异常能量状态有关

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Individuals with postnatal growth retardation (PGR) are prone to developing chronic disease. Abnormal development in small intestine is casually implicated in impaired growth performance. However, the exact mechanism is still unknown. In this present study, PGR piglets (aged 42?days) were employed as a good model to analyse changes in nutrient absorption and energy metabolism in the intestinal mucosa. The results showed lower serum concentrations of free amino acids, and lipid metabolites in PGR piglets, which were in accordance with the down‐regulated mRNA expressions involved in fatty acid and amino acid transporters in the jejunal and ileal mucosa. The decreased activities of digestive enzymes and the marked swelling in mitochondria were also observed in the PGR piglets. In addition, it was found that lower ATP production, higher AMP/ATP ratio, deteriorated mitochondrial complex III and ATP synthase, and decreased manganese superoxide dismutase activity in the intestinal mucosa of PGR piglets. Furthermore, altered gene expression involved in energy metabolism, accompanied by decreases in the protein abundance of SIRT1, PGC‐1α and PPARγ, as well as phosphorylations of AMPKα, mTOR, P70S6K and 4E‐BP1 were observed in intestinal mucosa of PGR piglets. In conclusion, decreased capability of nutrient absorption, mitochondrial dysfunction, and aberrant energy status in the jejunal and ileal mucosa may contribute to PGR piglets.
机译:与出生后发育迟缓(PGR)的个体易于发展为慢性疾病。在小肠内发育异常生长性能受损被牵连随便。但是,确切的机制仍是未知数。在本研究中,PGR仔猪(42岁?天)作为一个很好的模型来分析肠黏膜中营养物质的吸收和能量代谢的变化。结果表明游离氨基酸降低血清浓度,和在PGR仔猪脂质代谢物,这是根据参与脂肪酸的下调mRNA表达和氨基酸转运在空肠和回肠黏膜。降低的消化酶的活性和在标记线粒体肿胀均在PGR仔猪也观察到。此外,已发现,较低的ATP产量,更高的AMP / ATP比,降低线粒体复合物III和ATP合成酶,和在PGR仔猪肠粘膜降低锰超氧化物歧化酶的活性。此外,在PGR仔猪肠粘膜中观察到改变的基因表达参与能量代谢,在蛋白质丰度SIRT1,PGC-1α和PPARγ,以及AMPKα,mTOR的,P70S6K和4E-BP1磷酸化的伴随着降低。总之,在空肠和回肠黏膜营养物质的吸收,线粒体功能障碍和异常的能量状态的能力下降可能有助于PGR仔猪。

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