Department of Neurology, Univ. of Vermont, 89 Beaumont Ave., Given C454, Burlington, VT 05405, USA.
J Appl Physiol (1985). 2011 Feb;110(2):329-39. doi: 10.1152/japplphysiol.01159.2010. Epub 2010 Nov 11.
The cerebral circulation has a central role in mediating the neurological complications of eclampsia, yet our understanding of how pregnancy and preeclampsia affect this circulation is severely limited. Here, we show that pregnancy causes outward remodeling of penetrating arterioles and increased capillary density in the brain due to activation of peroxisome proliferator-activated receptor-γ (PPARγ), a transcription factor involved in cerebrovascular remodeling and highly activated in pregnancy. Pregnancy-induced PPARγ activation also significantly affected cerebral hemodynamics, decreasing vascular resistance and increasing cerebral blood flow by ∼40% in response to acute hypertension that caused breakthrough of autoregulation. These structural and hemodynamic changes in the brain during pregnancy were associated with substantially increased blood-brain barrier permeability, an effect that could promote passage of damaging proteins into the brain and cause the neurological complications of eclampsia, including seizure.
脑循环在介导子痫的神经并发症方面起着核心作用,但我们对妊娠和子痫如何影响这一循环的理解非常有限。在这里,我们表明,妊娠导致穿透性小动脉的外向重塑和脑内毛细血管密度增加,这是由于过氧化物酶体增殖物激活受体-γ(PPARγ)的激活所致,PPARγ 是一种参与脑血管重塑的转录因子,在妊娠中高度激活。妊娠诱导的 PPARγ 激活也显著影响脑血流动力学,在急性高血压导致自动调节突破时,血管阻力降低约 40%,脑血流量增加。这些妊娠期间大脑的结构和血流动力学变化与血脑屏障通透性的显著增加有关,这种效应可能促进有害蛋白进入大脑,并导致子痫的神经并发症,包括癫痫发作。