Zhou Ling, Zhang Ruixue, Yang Shuangyan, Zhang Yaguang, Shi Dandan
Cangzhou Central Hospital, Cangzhou, Hebei, China.
Endocr Connect. 2020 Oct;9(9):939-945. doi: 10.1530/EC-20-0295.
Our previous study revealed that astragaloside IV (AS-IV) effectively improved gestational diabetes mellitus (GDM) by reducing hepatic gluconeogenesis. Due to the importance of placental oxidative stress, we further explored the protective role of AS-IV on placental oxidative stress in GDM.
First, non-pregnant mice were orally administrated with AS-IV to evaluate its safety and effect. Then GDM mice were orally administered with AS-IV for 20 days and its effect on the symptoms of GDM, placental oxidative stress, secretions of inflammatory cytokines, as well as toll-like receptor 4 (TLR4)/NF-κB signaling pathway, were evaluated.
AS-IV had no adverse effect on non-pregnant mice. On the other hand, AS-IV significantly attenuated the GDM-induced hyperglycemia, glucose intolerance, insulin resistance, placental oxidative stress, productions of inflammatory cytokines and the activation of TLR4/NF-κB pathway.
AS-IV effectively protected against GDM by alleviating placental oxidative stress and inflammation, in which TLR4/NF-κB might be involved.
我们之前的研究表明,黄芪甲苷IV(AS-IV)通过减少肝脏糖异生有效改善妊娠期糖尿病(GDM)。鉴于胎盘氧化应激的重要性,我们进一步探讨了AS-IV对GDM胎盘氧化应激的保护作用。
首先,对未怀孕小鼠口服给予AS-IV以评估其安全性和效果。然后对GDM小鼠口服给予AS-IV 20天,并评估其对GDM症状、胎盘氧化应激、炎性细胞因子分泌以及Toll样受体4(TLR4)/核因子κB(NF-κB)信号通路的影响。
AS-IV对未怀孕小鼠无不良影响。另一方面,AS-IV显著减轻了GDM诱导的高血糖、葡萄糖不耐受、胰岛素抵抗、胎盘氧化应激、炎性细胞因子产生以及TLR4/NF-κB通路的激活。
AS-IV通过减轻胎盘氧化应激和炎症有效预防GDM,其中可能涉及TLR4/NF-κB。