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出生体重对新生仔猪皮下脂肪组织、肺和肌肉中内分泌谱及解偶联蛋白表达的影响。

Influence of size at birth on the endocrine profiles and expression of uncoupling proteins in subcutaneous adipose tissue, lung, and muscle of neonatal pigs.

作者信息

Mostyn Alison, Litten Jennie C, Perkins Katharine S, Euden Philippa J, Corson Anne M, Symonds Michael E, Clarke Lynne

机构信息

Centre for Reproduction and Early Life, Institute of Clinical Research, Academic Division of Child Health, School of Human Development, University Hospital, Nottingham, NG7 2UH United Kingdom.

出版信息

Am J Physiol Regul Integr Comp Physiol. 2005 Jun;288(6):R1536-42. doi: 10.1152/ajpregu.00423.2004. Epub 2005 Mar 3.

Abstract

Epidemiological studies suggest that infants of low birth weight show poor neonatal growth and increased susceptibility to adult diseases such as diabetes and lung disease. Uncoupling protein 2 and 3 (UCP2 and UCP3) have been implicated in the development of such diseases; pigs provide an ideal model to examine the influence of birth weight due to the natural variance in piglet weight within a litter. This study examined whether birth weight influences the expression of UCP2 and UCP3 in adipose tissue, skeletal muscle, and lung. Piglets from 11 litters were ranked according to birth weight and three from each litter assigned to small (SFD), normal (NFD), or large for dates (LFD) groups. Blood samples and morphometric measurements were taken over the first 14 days of life, and tissue samples were taken on day 7 or 14. Plasma hormone and metabolite concentrations and the expression of UCP2 and UCP3 mRNA in adipose tissue, skeletal muscle, and lung were measured. UCP2 and UCP3 expression in adipose tissue was lower in the SFD compared with the LFD group on day 7. UCP3 expression in skeletal muscle was higher than that of adipose tissue. Lung UCP2 and skeletal muscle UCP3 mRNA expression were unaffected by size at birth. Regression analysis indicated that UCP3 expression was differentially associated with IGF-1, leptin, and insulin. In conclusion, low birth weight is associated with tissue-specific effects on UCP expression. It remains to be established whether these subsequently contribute to pathological conditions such as diabetes.

摘要

流行病学研究表明,低出生体重的婴儿出生时生长发育较差,成年后患糖尿病和肺部疾病等疾病的易感性增加。解偶联蛋白2和3(UCP2和UCP3)与这些疾病的发生有关;由于一窝仔猪体重存在自然差异,猪提供了一个研究出生体重影响的理想模型。本研究调查了出生体重是否会影响脂肪组织、骨骼肌和肺中UCP2和UCP3的表达。将11窝仔猪按出生体重排序,每窝选取3只分别分配到小体重组(SFD)、正常体重组(NFD)或大于胎龄组(LFD)。在出生后的前14天采集血样并进行形态测量,在第7天或第14天采集组织样本。测量血浆激素和代谢物浓度以及脂肪组织、骨骼肌和肺中UCP2和UCP3 mRNA的表达。第7天,SFD组脂肪组织中UCP2和UCP3的表达低于LFD组。骨骼肌中UCP3的表达高于脂肪组织。肺UCP2和骨骼肌UCP3 mRNA的表达不受出生时体重大小的影响。回归分析表明,UCP3的表达与胰岛素样生长因子-1、瘦素和胰岛素存在差异相关。总之,低出生体重与UCP表达的组织特异性效应有关。这些是否随后会导致糖尿病等病理状况仍有待确定。

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