Fatimah M Al Darwish, Caren M van Kammen, Fieke Terstappen, Lindy K Alles, Raymond M Schiffelers, A Titia Lely, Gustav J Strijkers, Bram F Coolen
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引用次数: 0
Abstract
Placental insufficiency is a major cause of preeclampsia and fetal growth restriction. The reduced uterine perfusion pressure (RUPP) rat model reproduces cardinal features of these disorders, but longitudinal changes in placental perfusion after RUPP are poorly documented. This study aimed to assess the acute and late effects of RUPP on placental perfusion between gestational day (GD) 14 and GD18 using 3D dynamic contrast-enhanced magnetic resonance imaging (3D-DCE MRI). Pregnant Sprague Dawley rats (n = 31) were randomized to RUPP or normal pregnant (NP) groups on GD14. 3D-DCE MRI scans were performed on GD14, GD15, and GD16 or GD18. Perfusion parameters, including time to peak (TTP), maximum enhancement (ME), wash-out percentage (WO%), initial area under the curve (iAUC), and total area under the curve (AUC), were derived from fitted signal-time curves. In addition, exploratory voxel-wise histogram analysis was performed to assess intralitter variability. At GD14, RUPP placentas showed delayed TTP (p < 0.0001), reduced ME (p = 0.03), reduced WO% (p < 0.0001), and elevated iAUC (p = 0.02). Differences persisted for TTP (p = 0.02) and WO% (p = 0.01) at GD15 but resolved by GD16-GD18. Voxel-wise analysis revealed intralitter heterogeneity, with 20% of analyzed RUPP placentas deviating from the NP template. These findings indicate that RUPP induces an acute but transient impairment of placental perfusion, with recovery by late gestation. GD14-GD15 emerge as a critical window for detecting acute perfusion impairment and evaluating interventions targeting acute injury.
期刊介绍:
NMR in Biomedicine is a journal devoted to the publication of original full-length papers, rapid communications and review articles describing the development of magnetic resonance spectroscopy or imaging methods or their use to investigate physiological, biochemical, biophysical or medical problems. Topics for submitted papers should be in one of the following general categories: (a) development of methods and instrumentation for MR of biological systems; (b) studies of normal or diseased organs, tissues or cells; (c) diagnosis or treatment of disease. Reports may cover work on patients or healthy human subjects, in vivo animal experiments, studies of isolated organs or cultured cells, analysis of tissue extracts, NMR theory, experimental techniques, or instrumentation.