Schavinski Aline Z, Reis Natany G, Morgan Henrique J N, Assis Ana Paula, Moro Matheus L, Valentim Rafael R, Seni-Silva Ana Carolina, Ramos Ester S, Kettelhut Isis C, Navegantes Luiz C C
Department of Physiology, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto 14049-900, SP, Brazil.
Department of Biochemistry/Immunology, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto 14049-900, SP, Brazil.
Int J Mol Sci. 2024 Apr 9;25(8):4136. doi: 10.3390/ijms25084136.
Recent studies have shown that maternal vitamin D deficiency (VDD) causes long-term metabolic changes in offspring. However, little is known about the impact of maternal VDD on offspring endocrine pancreas development and insulin secretion in the adult life of male and female animals. Female rats (Wistar Hannover) were fed either control (1000 IU Vitamin D3/kg), VDD (0 IU Vitamin D3/kg), or a Ca-enriched VDD diet (0 IU Vitamin D3/kg + Ca and P/kg) for 6 weeks and during gestation and lactation. At weaning, VDD status was confirmed based on low serum calcidiol levels in dams and pups. Next, male and female offspring were randomly separated and fed a standard diet for up to 90 days. At this age, serum calcidiol levels were restored to normal levels in all groups, but serum insulin levels were decreased in VDD males without affecting glucagon levels, glycemia, or glucose tolerance. Islets isolated from VDD males showed lower insulin secretion in response to different glucose concentrations, but this effect was not observed in VDD females. Furthermore, VDD males, but not females, showed a smaller total pancreatic islet area and lower β cell mass, an effect that was accompanied by reduced gene expression of , , , and . The decrease in expression was not related to the methylation profile of the promoter region of this gene. Most of these effects were observed in the male VDD+Ca group, indicating that the effects were not due to alterations in Ca metabolism. These data show that maternal VDD selectively impairs the morphology and function of β cells in adult male offspring rats and that female offspring are fully protected from these deleterious effects.
最近的研究表明,母体维生素D缺乏(VDD)会导致后代出现长期的代谢变化。然而,关于母体VDD对雄性和雌性动物成年期后代内分泌胰腺发育和胰岛素分泌的影响,我们知之甚少。将雌性大鼠(Wistar Hannover)分为三组,分别喂食对照饮食(1000 IU维生素D3/千克)、VDD饮食(0 IU维生素D3/千克)或富含钙的VDD饮食(0 IU维生素D3/千克 + 钙和磷/千克),为期6周,并持续整个妊娠期和哺乳期。断奶时,根据母鼠和幼鼠血清骨化二醇水平低来确认VDD状态。接下来,将雄性和雌性后代随机分开,喂食标准饮食长达90天。在这个年龄,所有组的血清骨化二醇水平都恢复到正常水平,但VDD雄性大鼠的血清胰岛素水平降低,而胰高血糖素水平、血糖或葡萄糖耐量不受影响。从VDD雄性大鼠分离的胰岛对不同葡萄糖浓度的反应显示胰岛素分泌较低,但在VDD雌性大鼠中未观察到这种效应。此外,VDD雄性大鼠而非雌性大鼠的胰腺胰岛总面积较小且β细胞质量较低,这一效应伴随着 、 、 和 的基因表达降低。 表达的降低与该基因启动子区域的甲基化谱无关。这些效应大多在雄性VDD+钙组中观察到,表明这些效应不是由于钙代谢改变所致。这些数据表明,母体VDD选择性地损害成年雄性后代大鼠β细胞的形态和功能,而雌性后代则完全免受这些有害影响。