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Molecular Mechanisms of Neurogenic Lower Urinary Tract Dysfunction after Spinal Cord Injury.脊髓损伤后神经原性下尿路功能障碍的分子机制。
Int J Mol Sci. 2023 Apr 26;24(9):7885. doi: 10.3390/ijms24097885.
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Current Knowledge and Novel Frontiers in Lower Urinary Tract Dysfunction after Spinal Cord Injury: Basic Research Perspectives.脊髓损伤后下尿路功能障碍的当前知识与新前沿:基础研究视角
Urol Sci. 2022 Jul-Sep;33(3):101-113. doi: 10.4103/uros.uros_31_22. Epub 2022 Aug 25.
4
Animal models of compression spinal cord injury.压迫性脊髓损伤的动物模型。
J Neurosci Res. 2022 Dec;100(12):2201-2212. doi: 10.1002/jnr.25120. Epub 2022 Sep 19.
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Analysis of gene expression profiles in two spinal cord injury models.两种脊髓损伤模型中的基因表达谱分析。
Eur J Med Res. 2022 Aug 23;27(1):156. doi: 10.1186/s40001-022-00785-x.
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The Time Sequence of Gene Expression Changes after Spinal Cord Injury.脊髓损伤后基因表达变化的时间序列。
Cells. 2022 Jul 18;11(14):2236. doi: 10.3390/cells11142236.
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Temporal and spatial cellular and molecular pathological alterations with single-cell resolution in the adult spinal cord after injury.成年脊髓损伤后以单细胞分辨率显示的时空细胞和分子病理改变。
Signal Transduct Target Ther. 2022 Mar 2;7(1):65. doi: 10.1038/s41392-022-00885-4.
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Exploring propriospinal neuron-mediated neural circuit plasticity using recombinant viruses after spinal cord injury.探索脊髓损伤后使用重组病毒介导的 propriospinal 神经元神经回路可塑性。
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Inflammation after spinal cord injury: a review of the critical timeline of signaling cues and cellular infiltration.脊髓损伤后的炎症反应:信号通路和细胞浸润的关键时间进程综述。
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控制有无脊髓损伤的小鼠尿道外括约肌的脊髓神经回路的性别二态性。

Sexual Dimorphism of Spinal Neural Circuits Controlling the Mouse External Urethral Sphincter With and Without Spinal Cord Injury.

机构信息

Department of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

Department of Urology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

出版信息

J Comp Neurol. 2024 Jul;532(7):e25658. doi: 10.1002/cne.25658.

DOI:10.1002/cne.25658
PMID:38987904
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11260501/
Abstract

Spinal cord injury (SCI) disrupts coordination between the bladder and the external urinary sphincter (EUS), leading to transient or permanent voiding impairment, which is more severe in males. Male versus female differences in spinal circuits related to the EUS as well as post-SCI rewiring are essential for understanding of sex-/gender-specific impairments and possible recovery mechanisms. To quantitatively assess differences between EUS circuits in males versus females and in spinal intact (SI) versus SCI animals, we retrogradely traced and counted EUS-related neurons. In transgenic ChAT-GFP mice, motoneurons (MNs), interneurons (INs), and propriospinal neurons (PPNs) were retrogradely trans-synaptically traced with PRV614-red fluorescent protein (RFP) injected into EUS. EUS-MNs in dorsolateral nucleus (DLN) were separated from other GFP MNs by tracing them with FluoroGold (FG). We found two morphologically distinct cell types in DLN: FG spindle-shaped bipolar (SB-MNs) and FG rounded multipolar (RM-MNs) cholinergic cells. Number of MNs of both types in males was twice as large as in females. SCI caused a partial loss of MNs in all spinal nuclei. After SCI, males showed a fourfold rise in the number of RFP-labeled cells in retro-DLN (RDLN) innervating hind limbs. This suggests (a) an existence of direct synaptic interactions between spinal nuclei and (b) a post-SCI increase of non-specific inputs to EUS-MNs from other motor nuclei. Number of INs and PPNs deferred between males and females: In SI males, the numbers of INs and PPNs were ∼10 times larger than in SI females. SCI caused a twofold decrease of INs and PPNs in males but not in females.

摘要

脊髓损伤 (SCI) 破坏了膀胱和外部尿道括约肌 (EUS) 之间的协调性,导致暂时性或永久性排尿功能障碍,男性更为严重。了解与 EUS 相关的脊髓回路以及 SCI 后的重新布线中的雄性与雌性之间的差异,对于理解性别/性别特异性损伤和可能的恢复机制至关重要。为了定量评估雄性与雌性之间以及脊髓完整 (SI) 与 SCI 动物之间 EUS 回路之间的差异,我们逆行追踪和计数了与 EUS 相关的神经元。在 ChAT-GFP 转基因小鼠中,通过将 PRV614-红色荧光蛋白 (RFP) 注射到 EUS 中,对运动神经元 (MNs)、中间神经元 (INs) 和 propriospinal 神经元 (PPNs) 进行逆行跨突触追踪。通过用 FluoroGold (FG) 追踪 EUS-MNs 来分离背外侧核 (DLN) 中的 MNs。我们在 DLN 中发现了两种形态不同的细胞类型:FG 纺锤形双极 (SB-MNs) 和 FG 圆形多极 (RM-MNs) 胆碱能细胞。两种类型的 MNs 在雄性中的数量是雌性的两倍。SCI 导致所有脊髓核中的 MN 部分丢失。SCI 后,雄性中支配后肢的逆行 DLN (RDLN) 中的 RFP 标记细胞数量增加了四倍。这表明 (a) 脊髓核与 (b) 其他运动核之间存在直接的突触相互作用,以及 SCI 后 EUS-MNs 的非特异性输入增加。INs 和 PPNs 的数量在雄性和雌性之间存在差异:在 SI 雄性中,INs 和 PPNs 的数量是 SI 雌性的 10 倍左右。SCI 导致雄性的 INs 和 PPNs 减少了两倍,但在雌性中没有。