1 Department of Surgery Laboratory, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
2 Department of Neurology, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
J Cereb Blood Flow Metab. 2018 Nov;38(11):1954-1967. doi: 10.1177/0271678X17731956. Epub 2017 Sep 15.
Maternal environmental factors such as diet have consequences on later health of the offspring. We found that maternal high-fat diet (HFD) exposure renders adult offspring brain more susceptible to ischemic injury. The present study was further to investigate whether HFD consumption during rat pregnancy and lactation influences the cerebral vasculature in adult male offspring. Besides the endothelial damage observed in the transmission electron microscopy, the MCAs of offspring from fat-fed dams fed with control diet (HFD/C) also displayed increased wall thickness and media/lumen ratio, suggesting that cerebrovascular hypertrophy or hyperplasia occurs. Moreover, smaller lumen diameter and elevated myogenic tone of the MCAs over a range of intralumenal pressures indicate inward cerebrovascular remodeling in HFD/C rats, with a concomitant increase in vessel stiffness. More importantly, both wire and pressure myography demonstrated that maternal HFD intake also enhanced the MCAs contractility to ET-1, accompanied by increases in ET types A receptor (ETR) but not B (ETR) density in the arteries. Furthermore, ETR antagonism but not ETR antagonism restored maternal HFD-induced cerebrovascular dysfunction in adult offspring. Taken together, maternal diet can substantially influence adult offspring cerebrovascular health, through remodeling of both structure and function, at least partially in an ET-1 manner.
母体环境因素如饮食会对后代以后的健康产生影响。我们发现,母体高脂肪饮食(HFD)暴露会使成年后代的大脑更容易受到缺血性损伤。本研究进一步探讨了母体在妊娠和哺乳期内摄入高脂肪饮食是否会影响成年雄性后代的大脑血管。除了在透射电子显微镜下观察到的内皮损伤外,来自高脂肪饮食喂养的母鼠的 MCA 也显示出壁厚度增加和中膜/腔比增加,这表明脑血管发生了肥大或增生。此外,MCA 在一系列管腔内压力下的更小管腔直径和升高的肌源性张力表明 HFD/C 大鼠发生了内向性脑血管重塑,伴有血管硬度的增加。更重要的是,线描和压力描记术都表明,母体高脂肪饮食摄入还增强了 MCA 对 ET-1 的收缩性,同时动脉中 ET 类型 A 受体(ETR)而不是 B(ETR)密度增加。此外,ETR 拮抗作用而非 ETR 拮抗作用恢复了成年后代中由母体高脂肪饮食引起的脑血管功能障碍。总之,母体饮食可以通过结构和功能的重塑,对成年后代的脑血管健康产生重大影响,至少部分是通过 ET-1 方式。