Trigiani Lianne J, Lecrux Clotilde, Royea Jessika, Lavoie Julie L, Lesage Frédéric, Pilote Louise, Hamel Edith
Laboratory of Cerebrovascular Research, Montreal Neurological Institute, McGill University, Montréal, QC, Canada.
Centre de Recherche du Centre Hospitalier de l'Universite de Montreal and School of Kinesiology and physical activity sciences, Université de Montréal, Montréal, QC, Canada.
Front Physiol. 2021 Feb 1;12:611984. doi: 10.3389/fphys.2021.611984. eCollection 2021.
Preeclampsia is a common hypertensive disorder in pregnant women and whose causes and consequences have focused primarily on cardiovascular outcomes on the mother and offspring, often without taking into consideration the possible effects on the brain. One possible cause of preeclampsia has been attributed to alterations in the renin-angiotensin system, which has also been linked to cognitive decline. In this pilot study, we use a transgenic mouse model that chronically overexpresses human angiotensinogen and renin (RA mice) that displayed characteristics of preeclampsia such as proteinuria during gestation. Offspring of these mothers as well as from control mothers were also examined. We were primarily interested in detecting whether cognitive deficits were present in the mothers and offspring in the long term and used a spatial learning and memory task as well as an object recognition task at three timepoints: 3, 8, and 12 months post-partum or post-natal, while measuring blood pressure and performing urine analysis after each timepoint. While we did not find significant deficits in preeclamptic mothers at the later timepoints, we did observe negative consequences in the pups of RA mice that coincided with hemodynamic alterations whereby pups had higher whisker-evoked oxygenated hemoglobin levels and increased cerebral blood flow responses compared to control pups. Our study provides validation of this preeclampsia mouse model for future studies to decipher the underlying mechanisms of long-term cognitive deficits found in offspring.
子痫前期是妊娠期常见的高血压疾病,其病因和后果主要集中在对母亲和后代心血管系统的影响上,常常未考虑对大脑可能产生的影响。子痫前期的一个可能病因被认为与肾素-血管紧张素系统的改变有关,而这也与认知功能下降相关。在这项初步研究中,我们使用了一种转基因小鼠模型,该模型长期过度表达人血管紧张素原和肾素(RA小鼠),这些小鼠在妊娠期表现出子痫前期的特征,如蛋白尿。我们还检查了这些母亲以及对照母亲的后代。我们主要关注长期检测母亲和后代是否存在认知缺陷,并在产后或出生后的3个月、8个月和12个月这三个时间点使用空间学习和记忆任务以及物体识别任务,同时在每个时间点测量血压并进行尿液分析。虽然我们在后期时间点未发现子痫前期母亲存在明显缺陷,但我们确实观察到RA小鼠的幼崽出现了负面后果,这与血流动力学改变相一致,即与对照幼崽相比,幼崽的触须诱发的氧合血红蛋白水平更高,脑血流反应增加。我们的研究为未来研究解读后代中发现的长期认知缺陷的潜在机制验证了这种子痫前期小鼠模型。