Department of Pharmacology, Basic Medical School of Wuhan University, Wuhan, 430071, China.
Department of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Sci Rep. 2017 Nov 1;7(1):14825. doi: 10.1038/s41598-017-14881-0.
We previously demonstrated thatprenatal caffeine exposure (PCE) suppressed fetal adrenal steroidogenesis and resulted in developmental programming changes in offspring rats. However, whether these changes play a role in adrenal corticosterone synthesis under high-fat diet (HFD) and unpredictable chronic stress (UCS) remains unknown. In present study, rat model was established by PCE (120 mg/kg.d), and male offspring were provided normal diet or HFD after weaning. At postnatal week 21, several rats fed HFD were exposed to UCS for 3 weeks and sacrificed. The results showed that compared with the corresponding control group, the serum corticosterone levels and adrenal steroid synthetase expression of the PCE offspring without UCS were reduced. Moreover, the glucocorticoid (GC)-activation system was inhibited, and insulin-like growth factor 1 (IGF1) signaling pathway expression was increased. With UCS exposure in the PCE offspring, serum corticosterone levels and adrenal steroid synthetase expression were increased, the activity of GC-activation system was enhanced, and adrenal IGF1 signaling pathway expression was decreased. Based on these findings, PCE induced adrenal hypersensitivity in adult male offspring rats, as shown by the reduced corticosterone levels under HFD conditions but significantly enhanced corticosterone levels with UCS, in which GC-IGF1 axis programming alteration may play an important role.
我们之前的研究表明,产前咖啡因暴露(PCE)抑制胎儿肾上腺类固醇生成,并导致后代大鼠发育编程改变。然而,这些变化在高脂肪饮食(HFD)和不可预测的慢性应激(UCS)下是否对肾上腺皮质酮合成起作用尚不清楚。在本研究中,通过 PCE(120mg/kg.d)建立大鼠模型,并在断奶后为雄性后代提供正常饮食或 HFD。在出生后第 21 周,一些 HFD 喂养的大鼠接受 UCS 暴露 3 周后处死。结果表明,与相应的对照组相比,未接受 UCS 的 PCE 后代的血清皮质酮水平和肾上腺类固醇合成酶表达降低。此外,糖皮质激素(GC)激活系统受到抑制,胰岛素样生长因子 1(IGF1)信号通路表达增加。在 PCE 后代中暴露于 UCS 后,血清皮质酮水平和肾上腺类固醇合成酶表达增加,GC-激活系统的活性增强,而肾上腺 IGF1 信号通路表达减少。基于这些发现,PCE 导致成年雄性后代大鼠的肾上腺超敏反应,表现为 HFD 条件下皮质酮水平降低,但 UCS 后皮质酮水平显著升高,其中 GC-IGF1 轴编程改变可能发挥重要作用。