Deruyver Yves, Rietjens Roma, Franken Jan, Pinto Silvia, Van Santvoort Ann, Casteels Cindy, Voets Thomas, De Ridder Dirk
Laboratory of Experimental Urology, Department of Development and Regeneration, KU Leuven, Herestraat 49, 3000, Leuven, Belgium.
Laboratory of Ion Channel Research, Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium.
EJNMMI Res. 2015 Dec;5(1):55. doi: 10.1186/s13550-015-0132-0. Epub 2015 Oct 15.
This feasibility study established an experimental protocol to evaluate brain activation patterns using fluorodeoxyglucose positron emission tomography ((18F)FDG-PET) during volume-induced voiding and isovolumetric bladder contractions in rats.
Female Sprague-Dawley rats were anaesthetized with urethane and underwent either volume-induced voiding cystometry or isovolumetric cystometry and simultaneous functional PET brain imaging after injection of (18F)FDG in the tail vein. Brain glucose metabolism in both groups was compared to their respective control conditions (empty bladder). Relative glucose metabolism images were anatomically standardized to Paxinos space and analysed voxel-wise using Statistical Parametric Mapping 12 (SPM12).
During volume-induced voiding, glucose hypermetabolism was observed in the insular cortex while uptake was decreased in a cerebellar cluster and the dorsal midbrain. Relative glucose metabolism during isovolumetric bladder contractions increased in the insular and cingulate cortices and decreased in the cerebellum.
Our findings demonstrate that volume-induced voiding as well as isovolumetric bladder contractions in rats provokes changes in brain metabolism, including activation of the insular and cingulate cortices, which is consistent with their role in the mapping of bladder afferent activity. These findings are in line with human studies. Our results provide a basis for further research into the brain control of the lower urinary tract in small laboratory animals.
本可行性研究建立了一个实验方案,以评估大鼠在容量诱导排尿和膀胱等容收缩期间使用氟脱氧葡萄糖正电子发射断层扫描((18F)FDG-PET)时的脑激活模式。
雌性Sprague-Dawley大鼠用乌拉坦麻醉,在尾静脉注射(18F)FDG后,进行容量诱导排尿膀胱测压或等容膀胱测压以及同步功能性PET脑成像。将两组的脑葡萄糖代谢与其各自的对照条件(膀胱空虚)进行比较。相对葡萄糖代谢图像在解剖学上标准化到帕西诺斯空间,并使用统计参数映射12(SPM12)进行逐体素分析。
在容量诱导排尿期间,岛叶皮质观察到葡萄糖代谢亢进,而小脑簇和中脑背侧的摄取减少。膀胱等容收缩期间,岛叶和扣带回皮质的相对葡萄糖代谢增加,小脑的相对葡萄糖代谢减少。
我们的研究结果表明,大鼠的容量诱导排尿以及膀胱等容收缩会引起脑代谢变化,包括岛叶和扣带回皮质的激活,这与其在膀胱传入活动映射中的作用一致。这些发现与人体研究一致。我们的结果为进一步研究小型实验动物下尿路的脑控制提供了基础。