Department of Physiology, Faculty of Medicine, Tabriz University of Medical Sciences, PO Box: 5166614756, Tabriz, Iran.
Department of Physiology, School of Medicine, Shahid Beheshti University of Medical Sciences, PO Box: 19615-1178, Tehran, Iran.
Sci Rep. 2022 Jul 22;12(1):12552. doi: 10.1038/s41598-022-16621-5.
Exposure to perinatal (prenatal and/or postnatal) stress is considered as a risk factor for metabolic disorders in later life. Accordingly, this study aimed to investigate the perinatal stress effects on the pancreatic endoplasmic reticulum (ER) stress induction, insulin secretion impairment and WFS1 (wolframin ER transmembrane Glycoprotein, which is involved in ER homeostasis and insulin secretion) expression changes, in rat offspring. According to the dams' period of exposure to variable stress, their male offspring were divided into, control (CTRL); pre-pregnancy, pregnancy, lactation stress (PPPLS); pre-pregnancy stress (PPS); pregnancy stress (PS); lactation stress (LS); pre-pregnancy, pregnancy stress (PPPS); pregnancy, lactation stress (PLS); pre-pregnancy, lactation stress (PPLS) groups. Offspring pancreases were removed for ER extraction and the assessment of ER stress biomarkers, WFS1 gene DNA methylation, and isolated islets' insulin secretion. Glucose tolerance was also tested. In the stressed groups, maternal stress significantly increased plasma corticosterone levels. In PPS, PS, and PPPS groups, maternal stress increased Bip (Hsp70; heat shock protein family A member 4), Chop (Ddit3; DNA- damage inducible transcript3), and WFS1 protein levels in pancreatic extracted ER. Moreover, the islets' insulin secretion and content along with glucose tolerance were impaired in these groups. In PPS, PS, LS and PPPS groups, the pancreatic glucocorticoid receptor (GR) expression increased. Maternal stress did not affect pancreatic WFS1 DNA methylation. Thus, maternal stress, during prenatal period, impaired the islets' insulin secretion and glucose homeostasis in adult male offspring, possibly through the induction of ER stress and GR expression in the pancreas, in this regard the role of WFS1 protein alteration in pancreatic ER should also be considered.
围产期(产前和/或产后)应激被认为是晚年代谢紊乱的一个风险因素。因此,本研究旨在探讨围产期应激对胰腺内质网(ER)应激诱导、胰岛素分泌障碍和 WFS1(一种参与 ER 稳态和胰岛素分泌的 Wolframin ER 跨膜糖蛋白)表达变化的影响,研究对象为雄性仔鼠。根据母鼠暴露于不同应激的时期,将其雄性仔鼠分为对照组(CTRL)、孕前、孕期、哺乳期应激组(PPPLS)、孕前应激组(PPS)、孕期应激组(PS)、哺乳期应激组(LS)、孕前、孕期应激组(PPPS)、孕期、哺乳期应激组(PLS)、孕前、哺乳期应激组(PPLS)。分离胰腺提取 ER,评估 ER 应激生物标志物、WFS1 基因 DNA 甲基化和分离胰岛的胰岛素分泌情况,并检测葡萄糖耐量。应激组母鼠的血浆皮质酮水平显著升高。在 PPS、PS 和 PPPS 组中,母鼠应激增加了胰腺提取 ER 中的 Bip(Hsp70;热休克蛋白家族 A 成员 4)、Chop(DDIT3;DNA 损伤诱导转录 3)和 WFS1 蛋白水平。此外,这些组的胰岛胰岛素分泌和含量以及葡萄糖耐量受损。在 PPS、PS、LS 和 PPPS 组中,胰腺糖皮质激素受体(GR)表达增加。母鼠应激不影响胰腺 WFS1 DNA 甲基化。因此,孕期母鼠应激可通过诱导胰腺内质网应激和 GR 表达,损害成年雄性仔鼠胰岛的胰岛素分泌和葡萄糖稳态,在这方面,还应考虑 WFS1 蛋白在胰腺 ER 中的改变作用。