Pinheiro Ana Rita, Rodrigues Adriana Raquel, Matos Liliana, Costa José Júlio, Ricardo Sara, Guedes-Martins Luís, Almeida Henrique, Silva Elisabete
Unidade de Biologia Experimental, Departamento de Biomedicina, Faculdade de Medicina, Universidade do Porto, Rua Dr. Plácido da Costa, S/N, 4200 - 450, Porto, Portugal; Ageing and Stress Group, i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Rua Alfredo Allen, 208, 4200-135, Porto, Portugal.
Unidade de Biologia Experimental, Departamento de Biomedicina, Faculdade de Medicina, Universidade do Porto, Rua Dr. Plácido da Costa, S/N, 4200 - 450, Porto, Portugal; Ageing and Stress Group, i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Rua Alfredo Allen, 208, 4200-135, Porto, Portugal; Faculdade de Ciências da Nutrição e Alimentação, Universidade do Porto, Rua do Campo Alegre 823, 4150-180, Porto, Portugal.
Placenta. 2025 Feb;160:60-66. doi: 10.1016/j.placenta.2024.12.024. Epub 2024 Dec 30.
Pregnancy after the age of 35 is correlated with an increased risk of impaired placentation and the development of pregnancy-associated complications. Changes in uterine redox balance seem to play a role in these settings. In this work, we hypothesized that local redox dysregulation impacts the placenta metabolic profile. Thus, we aimed to study the expression of enzymes/transporters related to nutrient uptake during reproductive aging and the effect of antioxidant supplementation.
Placenta samples were collected from pregnant women aged between 22 and 41 years, and from mice of different reproductive ages (8-12 and 38-42 weeks). A subgroup of 38-42 weeks-old mice was treated with apocynin (5 mM) in the drinking water. Real-time PCR was carried out to assess gene expression, and immunohistochemistry or western blotting to assess protein expression.
A significant age-related decrease in the expression of glucose transporter type 1 (GLUT-1) was observed in both species. Regarding lipid metabolism, there was a strong negative and significant correlation between the gene expression of fatty-acid transporter type 4 and maternal age, in the human placenta. Perilipin isoform 2 (PLIN-2) decreased significantly with maternal age, in both models. Additionally, a significant age-related decrease in the gene expression of large neutral amino acid transporter type 4 with reproductive age was observed in the mice placenta. Supplementation with apocynin attenuated the observed alterations in GLUT-1 and PLIN-2. The observed changes suggest an age-related placenta metabolic dysfunction, likely associated with oxidative stress, that may negatively impact fetal and placental development.
35岁之后怀孕与胎盘形成受损及妊娠相关并发症发生风险增加相关。子宫氧化还原平衡的变化似乎在这些情况中发挥作用。在本研究中,我们假设局部氧化还原失调会影响胎盘代谢谱。因此,我们旨在研究生殖衰老过程中与营养物质摄取相关的酶/转运蛋白的表达以及抗氧化剂补充的作用。
收集年龄在22至41岁之间的孕妇以及不同生殖年龄(8 - 12周和38 - 42周)小鼠的胎盘样本。对38 - 42周龄小鼠的一个亚组给予饮用水中的载脂蛋白(5 mM)处理。进行实时PCR以评估基因表达,进行免疫组织化学或蛋白质印迹以评估蛋白质表达。
在两个物种中均观察到葡萄糖转运蛋白1(GLUT - 1)的表达随年龄显著下降。关于脂质代谢,在人胎盘中,脂肪酸转运蛋白4的基因表达与母亲年龄之间存在强烈的负相关且具有显著性。在两个模型中,脂滴包被蛋白亚型2(PLIN - 2)均随母亲年龄显著下降。此外,在小鼠胎盘中观察到大型中性氨基酸转运蛋白4的基因表达随生殖年龄显著下降。用载脂蛋白补充可减轻观察到的GLUT - 1和PLIN - 2的改变。观察到的变化表明与年龄相关的胎盘代谢功能障碍,可能与氧化应激有关,这可能对胎儿和胎盘发育产生负面影响。