Bai Yingnan, Yuan Mingyuan, Mi Honglan, Zhang Fengchen, Liu Xiangyu, Lu Chen, Bao Yinghui, Li Yuehua, Lu Qing
Department of Cardiology, Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital and Institute of Biomedical Sciences, Fudan University, Shanghai, China.
Department of Radiology, Affiliated Zhoupu Hospital, Shanghai University of Medicine and Health Sciences, Shanghai, China.
Front Neurol. 2022 Oct 20;13:957055. doi: 10.3389/fneur.2022.957055. eCollection 2022.
The glymphatic system has recently been shown to clear brain extracellular solutes and can be extensively impaired after traumatic brain injury (TBI). Despite hypothermia being identified as a protective method for the injured brain via minimizing the formation of edema in the animal study, little is known about how hypothermia affects the glymphatic system following TBI. We use dynamic contrast-enhanced MRI (DCE-MRI) following cisterna magna infusion with a low molecular weight contrast agent to track glymphatic transport in male Sprague-Dawley rats following TBI with hypothermia treatment and use diffusion-weighted imaging (DWI) sequence to identify edema after TBI, and further distinguish between vasogenic and cytotoxic edema. We found that hypothermia could attenuate brain edema, as demonstrated by smaller injured lesions and less vasogenic edema in most brain subregions. However, in contrast to reducing cerebral edema, hypothermia exacerbated the reduction of efficiency of glymphatic transportation after TBI. This deterioration of glymphatic drainage was present brain-wide and showed hemispherical asymmetry and regional heterogeneity across the brain, associated with vasogenic edema. Moreover, our data show that glymphatic transport reduction and vasogenic edema are closely related to reducing perivascular aquaporin-4 (AQP) expression. The suppression of glymphatic transportation might eliminate the benefits of brain edema reduction induced by hypothermia and provide an alternative pathophysiological factor indicating injury to the brain after TBI. Thus, this study poses a novel emphasis on the potential role of hypothermia in managing severe TBI.
最近研究表明,类淋巴系统可清除脑内细胞外溶质,且在创伤性脑损伤(TBI)后会受到广泛损害。尽管在动物研究中,低温被确定为一种通过减少水肿形成来保护受损大脑的方法,但关于低温如何影响TBI后的类淋巴系统,人们知之甚少。我们在雄性Sprague-Dawley大鼠TBI并接受低温治疗后,通过在小脑延髓池注入低分子量造影剂后进行动态对比增强磁共振成像(DCE-MRI)来追踪类淋巴转运,并使用扩散加权成像(DWI)序列来识别TBI后的水肿,并进一步区分血管源性水肿和细胞毒性水肿。我们发现,低温可减轻脑水肿,大多数脑区的损伤灶较小且血管源性水肿较少即证明了这一点。然而,与减轻脑水肿相反,低温加剧了TBI后类淋巴转运效率的降低。这种类淋巴引流的恶化在全脑均存在,并表现出半球不对称性和全脑区域异质性,与血管源性水肿相关。此外,我们的数据表明,类淋巴转运减少和血管源性水肿与血管周围水通道蛋白-4(AQP)表达降低密切相关。类淋巴转运的抑制可能会消除低温诱导的减轻脑水肿的益处,并提供一个表明TBI后脑损伤的替代病理生理因素。因此,本研究对低温在严重TBI治疗中的潜在作用提出了新的强调。