Department of Medicine, University of Texas Health Science Center, San Antonio, TX 78229, USA.
Reprod Sci. 2011 Apr;18(4):398-405. doi: 10.1177/1933719110386496. Epub 2010 Nov 15.
Hepatic β-adrenergic receptors (β-ARs) play a pivotal role in mobilization of reserves via gluconeogenesis and glycogenolysis to supply the animal with its energy needs during decreased nutrient availability. Using a unique nutrient-deprived baboon model, we have demonstrated for the first time that immunoreactive hepatic β(1)- and β(2)-AR subtypes are regionally distributed and localized on cells around the central lobular vein in 0.5 and 0.9 gestation (G) fetuses of ad libitum fed control (CTR) and maternal nutrient restricted (MNR) mothers. Furthermore, MNR decreased fetal liver immunoreactive β(1)-AR and increased immunoreactive β(2)-AR at 0.5G. However, at 0.9G, immunohistochemistry and Western blot analysis revealed a decrease in β(1)-AR and no change in β(2)-AR levels. Thus, MNR in a nonhuman primate species has effects on hepatic β(1)- and β(2)-ARs that are receptor- and gestation stage-specific and may represent compensatory systems whose effects would increase glucose availability in the presence of nutrient deprivation.
肝β-肾上腺素能受体(β-AR)在通过糖异生和糖原分解动员储备方面发挥着关键作用,以在营养物质供应减少时为动物提供能量需求。使用独特的营养剥夺狒狒模型,我们首次证明,在自由喂养的对照组(CTR)和母体营养受限(MNR)母亲的 0.5 和 0.9 孕(G)胎儿中,免疫反应性肝β(1)-和β(2)-AR 亚型呈区域性分布,并定位于中央小叶静脉周围的细胞上。此外,MNR 在 0.5G 时降低了胎儿肝脏免疫反应性β(1)-AR 并增加了免疫反应性β(2)-AR。然而,在 0.9G 时,免疫组织化学和 Western blot 分析显示β(1)-AR 减少,β(2)-AR 水平没有变化。因此,非人类灵长类动物中的 MNR 对肝β(1)-和β(2)-AR 具有受体和妊娠阶段特异性的影响,可能代表补偿系统,其作用将在存在营养剥夺时增加葡萄糖的可用性。