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创伤性脑损伤大鼠模型中脑水肿的动态特征

Dynamic features of brain edema in rat models of traumatic brain injury.

作者信息

Ren Huanhuan, Lu Hong

机构信息

Department of Radiology, Chongqing Seventh People's Hospital, Chongqing, China.

出版信息

Neuroreport. 2019 Jun 12;30(9):605-611. doi: 10.1097/WNR.0000000000001213.

DOI:10.1097/WNR.0000000000001213
PMID:30969247
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6530974/
Abstract

We explored the dynamic features of brain edema after traumatic brain injury (TBI) using healthy adult male Wistar rats. After inducing moderate brain injuries in the rats, we divided them randomly among seven groups on the basis of the time elapsed between TBI and examination: 1, 6, 12, 24, 48, 72, and 168 h. All rats were scanned using diffusion-weighted imaging (DWI) to observe tissue changes in the contusion penumbra (CP) after TBI. Immunoglobulin G expression was also detected. At 1 h after TBI, there was an annular light-colored region in the CP where the intercellular space was enlarged, suggesting vasogenic edema. At 6 h, the cells expanded, their nuclei shrank, and the cytoplasm was replaced by vacuoles, indicating intracellular edema. Vasogenic edema and intracellular edema increased 12 h after TBI, but decreased 24 h after TBI, with vasogenic edema increasing 48 h after TBI. By 72 h after TBI, intracellular edema dominated until resolution of all edema by 168 h after TBI. DWI indicated that the relative apparent diffusion coefficient increased markedly at 1 h after TBI, but was reduced at 6 and 12 h after TBI. At 48 h, relative apparent diffusion coefficient increased gradually and then declined at 72 h. In rats, TBI-related changes include dynamic variations in intracellular and vasogenic edema severity. Routine MRI and DWI examinations do not distinguish between the center of trauma and CP; however, the apparent diffusion coefficient diagram can portray variations in CP edema type and degree at different time-points following TBI.

摘要

我们使用健康成年雄性Wistar大鼠探究了创伤性脑损伤(TBI)后脑水肿的动态特征。在诱导大鼠发生中度脑损伤后,根据TBI与检查之间的时间间隔,将它们随机分为七组:1、6、12、24、48、72和168小时。使用扩散加权成像(DWI)对所有大鼠进行扫描,以观察TBI后挫伤半暗带(CP)的组织变化。还检测了免疫球蛋白G的表达。TBI后1小时,CP中出现环形浅色区域,细胞间隙增大,提示血管源性水肿。6小时时,细胞肿胀,细胞核缩小,细胞质被空泡取代,提示细胞内水肿。血管源性水肿和细胞内水肿在TBI后12小时增加,但在TBI后24小时减少,血管源性水肿在TBI后48小时增加。到TBI后72小时,细胞内水肿占主导,直到TBI后168小时所有水肿消退。DWI显示,相对表观扩散系数在TBI后1小时显著增加,但在TBI后6小时和12小时降低。在48小时时,相对表观扩散系数逐渐增加,然后在72小时下降。在大鼠中,TBI相关变化包括细胞内和血管源性水肿严重程度的动态变化。常规MRI和DWI检查无法区分创伤中心和CP;然而,表观扩散系数图可以描绘TBI后不同时间点CP水肿类型和程度的变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6c4/6530974/42362f269912/wnr-30-605-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6c4/6530974/8d16f96233ef/wnr-30-605-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6c4/6530974/a478a9edc681/wnr-30-605-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6c4/6530974/19fb918e3b78/wnr-30-605-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6c4/6530974/42362f269912/wnr-30-605-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6c4/6530974/8d16f96233ef/wnr-30-605-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6c4/6530974/32b1ddf066c1/wnr-30-605-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6c4/6530974/a478a9edc681/wnr-30-605-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6c4/6530974/19fb918e3b78/wnr-30-605-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6c4/6530974/42362f269912/wnr-30-605-g005.jpg

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