Shankar Kartik, Hidestrand Mats, Liu Xiaoli, Xiao Rijin, Skinner Charles M, Simmen Frank A, Badger Thomas M, Ronis Martin J J
Department of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Exp Biol Med (Maywood). 2006 Sep;231(8):1379-97. doi: 10.1177/153537020623100812.
Nutrition-ethanol (EtOH) interactions during gestation remain unclear primarily due to the lack of appropriate rodent models. In the present report we utilize total enteral nutrition (TEN) to specifically understand the roles of nutrition and caloric intake in EtOH-induced fetal toxicity. Time-impregnated rats were intragastrically fed either control or diets containing EtOH (8-14 g/kg/day) at a recommended caloric intake for pregnant rats or rats 30% undernourished, from gestation day (GD) 6-20. Decreased fetal weight and litter size (P < 0.05) and increased full litter resorptions (33% vs. 0%), were observed in undernourished dams compared to adequately fed rats given the same dose of EtOH, while undernutrition alone did not produce any fetal toxicity. Undernutrition led to impairment of EtOH metabolism, increased blood EtOH concentrations (160%), and decreased maternal hepatic ADH1 mRNA, protein, and activity. Microarray analyses of maternal hepatic gene expression on GD15 revealed that 369 genes were altered by EtOH in the presence of undernutrition, as compared to only 37 genes by EtOH per se (+/-2-fold, P < 0.05). Hierarchical clustering and gene ontology analysis revealed that stress and external stimulus responses, transcriptional regulation, cellular homeostasis, and protein metabolism were affected uniquely in the EtOH-under-nutrition group, but not by EtOH alone. Microarray data were confirmed using real-time RT-PCR. Undernourished EtOH-fed animals had 2-fold lower IGF-1 mRNA and 10-fold lower serum IGF-1 protein levels compared to undernourished controls (P < 0.0005). Examination of maternal GH signaling via STAT5a and -5b revealed significant reduction in both gene and protein expression produced by both EtOH and undernutrition. However, despite significantly elevated fetal BECs, fetal IGF-1 mRNA and protein were not affected by EtOH or EtOH-undernutrition combinations. Our data suggest that undernutrition potentiates the fetal toxicity of EtOH in part by disrupting maternal GH-IGF-1, signaling thereby decreasing maternal uterine capacity and placental growth.
孕期营养与乙醇(EtOH)的相互作用仍不清楚,主要原因是缺乏合适的啮齿动物模型。在本报告中,我们利用全肠内营养(TEN)来具体了解营养和热量摄入在乙醇诱导的胎儿毒性中的作用。从妊娠第6天至20天,对定时受孕的大鼠进行灌胃喂养,给予对照饮食或含乙醇(8 - 14克/千克/天)的饮食,热量摄入为推荐给妊娠大鼠的量或低于正常营养水平30%的量。与给予相同剂量乙醇的营养充足的大鼠相比,营养不良的母鼠所产胎儿体重和窝仔数降低(P < 0.05),全窝吸收增加(33%对0%),而单纯营养不良未产生任何胎儿毒性。营养不良导致乙醇代谢受损,血液乙醇浓度升高(160%),母鼠肝脏ADH1 mRNA、蛋白质和活性降低。对妊娠第15天母鼠肝脏基因表达进行微阵列分析显示,与乙醇单独作用相比(±2倍,P < 0.05),在营养不良情况下,有369个基因因乙醇而改变,而乙醇单独作用时只有37个基因改变。层次聚类和基因本体分析显示,应激和外部刺激反应、转录调控、细胞内稳态和蛋白质代谢在乙醇 - 营养不良组中受到独特影响,而乙醇单独作用时则未出现这种情况。微阵列数据通过实时RT - PCR得到证实。与营养不良的对照组相比,营养不良且摄入乙醇的动物IGF - 1 mRNA水平低2倍,血清IGF - 1蛋白水平低10倍(P < 0.0005)。通过STAT5a和 - 5b检测母鼠生长激素信号通路发现,乙醇和营养不良均导致基因和蛋白质表达显著降低。然而,尽管胎儿血乙醇浓度显著升高,但胎儿IGF - 1 mRNA和蛋白质不受乙醇或乙醇 - 营养不良组合的影响。我们的数据表明,营养不良通过破坏母鼠生长激素 - IGF - 1信号通路,部分增强了乙醇对胎儿的毒性,从而降低母鼠子宫容量和胎盘生长。