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创伤性脑损伤后代谢和结构的大脑进行性紊乱:大鼠体内成像研究。

Progressive metabolic and structural cerebral perturbations after traumatic brain injury: an in vivo imaging study in the rat.

机构信息

Department of Medicine, The Royal Melbourne Hospital, University of Melbourne, Victoria, Australia.

出版信息

J Nucl Med. 2010 Nov;51(11):1788-95. doi: 10.2967/jnumed.110.078626.

Abstract

UNLABELLED

Traumatic brain injury (TBI) has a high incidence of long-term neurologic and neuropsychiatric morbidity. Metabolic and structural changes in rat brains were assessed after TBI using serial (18)F-FDG PET and 3-dimensional MRI in vivo.

METHODS

Rats underwent lateral fluid percussion injury (FPI; n = 16) or a sham procedure (n = 11). PET and MR images were acquired at 1 wk and at 1, 3, and 6 mo after injury. Morphologic changes were assessed using MRI-based regions of interest, and hippocampal shape changes were assessed with large-deformation high-dimensional mapping. Metabolic changes were assessed using region-of-interest analysis and statistical parametric mapping with the flexible factorial analysis. Anxiety-like behavior and learning were assessed at 1, 3, and 6 mo after injury.

RESULTS

PET analyses showed widespread hypometabolism in injured rats, in particular involving the ipsilateral cortex, hippocampus, and amygdalae, present at 1 wk after FPI, most prominent at 1 mo, and then decreasing. Compared with the sham group, rats in the FPI group had decreased structural volume which progressively increased over 3-6 mo, occurring in the ipsilateral cortex, hippocampus, and ventricles after FPI (P < 0.05). Large-deformation high-dimensional mapping showed evolving hippocampal shape changes across the 6 mo after FPI. Injured rats displayed increased anxiety-like behavior (P < 0.05), but there were no direct correlations between the severity of the behavior abnormalities and functional or structural imaging changes.

CONCLUSION

In selected brain structures, FPI induces early hypometabolism and delayed progressive atrophic changes that are dynamic and continue to evolve for months. These findings have implications for the understanding of the pathophysiology and evolution of long-term neurologic morbidity following TBI, and indicate an extended window for targeted neuroprotective interventions.

摘要

未加说明

创伤性脑损伤(TBI)具有较高的长期神经和神经精神发病率。使用连续(18)F-FDG PET 和三维 MRI 在体内评估 TBI 后大鼠大脑的代谢和结构变化。

方法

大鼠接受侧方液体冲击伤(FPI;n = 16)或假手术(n = 11)。在损伤后 1 周以及 1、3 和 6 个月时采集 PET 和 MRI 图像。使用基于 MRI 的感兴趣区域评估形态变化,使用大变形高维映射评估海马形状变化。使用感兴趣区域分析和基于柔性因子分析的统计参数映射评估代谢变化。在损伤后 1、3 和 6 个月时评估焦虑样行为和学习。

结果

PET 分析显示受伤大鼠广泛存在代谢低下,特别是损伤侧皮质、海马和杏仁核,在 FPI 后 1 周即可见到,1 个月时最为明显,然后逐渐减少。与假手术组相比,FPI 组大鼠的结构体积减少,在 3-6 个月内逐渐增加,在 FPI 后发生在损伤侧皮质、海马和脑室(P < 0.05)。大变形高维映射显示 FPI 后 6 个月内海马形状不断变化。受伤大鼠表现出焦虑样行为增加(P < 0.05),但行为异常的严重程度与功能或结构成像变化之间没有直接相关性。

结论

在选定的脑结构中,FPI 会引起早期代谢低下和延迟的进行性萎缩变化,这些变化是动态的,并持续数月演变。这些发现对理解 TBI 后长期神经发病率的病理生理学和演变具有重要意义,并表明有机会进行靶向神经保护干预。

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