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实验性蛛网膜下腔出血后高血糖作用的多模态成像

Multimodal imaging of the role of hyperglycemia following experimental subarachnoid hemorrhage.

作者信息

Joya Ana, Plaza-García Sandra, Padro Daniel, Aguado Laura, Iglesias Leyre, Garbizu Maider, Gómez-Vallejo Vanessa, Laredo Carlos, Cossío Unai, Torné Ramon, Amaro Sergio, Planas Anna M, Llop Jordi, Ramos-Cabrer Pedro, Justicia Carles, Martín Abraham

机构信息

Achucarro Basque Center for Neuroscience, Leioa, Spain.

CIC biomaGUNE, Basque Research and Technology Alliance, San Sebastian, Spain.

出版信息

J Cereb Blood Flow Metab. 2024 May;44(5):726-741. doi: 10.1177/0271678X231197946. Epub 2023 Sep 20.

DOI:10.1177/0271678X231197946
PMID:37728631
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11197138/
Abstract

Hyperglycemia has been linked to worsening outcomes after subarachnoid hemorrhage (SAH). Nevertheless, the mechanisms involved in the pathogenesis of SAH have been scarcely evaluated so far. The role of hyperglycemia was assessed in an experimental model of SAH by T weighted, dynamic contrast-enhanced magnetic resonance imaging (TW and DCE-MRI), [F]BR-351 PET imaging and immunohistochemistry. Measures included the volume of bleeding, the extent of cerebral infarction and brain edema, blood brain barrier disruption (BBBd), neutrophil infiltration and matrix metalloprotease (MMP) activation. The neurofunctional outcome, neurodegeneration and myelinization were also investigated. The induction of hyperglycemia increased mortality, the size of the ischemic lesion, brain edema, neurodegeneration and worsened neurological outcome during the first 3 days after SAH in rats. In addition, these results show for the first time the exacerbating effect of hyperglycemia on MMP activation, Intercellular Adhesion Molecule 1 (ICAM-1) expression and neutrophil infiltration together with increased BBBd, bleeding volume and fibrinogen accumulation at days 1 and 3 after SAH. Notably, these data provide valuable insight into the detrimental effect of hyperglycemia on early BBB damage mediated by neutrophil infiltration and MMP activation that could explain the worse prognosis in SAH.

摘要

高血糖与蛛网膜下腔出血(SAH)后病情恶化有关。然而,迄今为止,SAH发病机制中涉及的机制很少得到评估。通过T加权、动态对比增强磁共振成像(TW和DCE-MRI)、[F]BR-351正电子发射断层显像(PET)成像和免疫组化,在SAH实验模型中评估了高血糖的作用。测量指标包括出血量、脑梗死和脑水肿的范围、血脑屏障破坏(BBBd)、中性粒细胞浸润和基质金属蛋白酶(MMP)激活。还研究了神经功能结局、神经变性和髓鞘形成。高血糖的诱导增加了大鼠SAH后前3天的死亡率、缺血性病变大小、脑水肿、神经变性,并使神经功能结局恶化。此外,这些结果首次显示了高血糖对SAH后第1天和第3天MMP激活、细胞间黏附分子1(ICAM-1)表达和中性粒细胞浸润的加剧作用,同时伴有BBBd增加、出血量和纤维蛋白原积累。值得注意的是,这些数据为高血糖对由中性粒细胞浸润和MMP激活介导的早期血脑屏障损伤的有害作用提供了有价值的见解,这可以解释SAH中更差的预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a563/11197138/58c09f67da09/10.1177_0271678X231197946-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a563/11197138/b7ce5da258f0/10.1177_0271678X231197946-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a563/11197138/ecc2f1c478d1/10.1177_0271678X231197946-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a563/11197138/3aacda2ae5ec/10.1177_0271678X231197946-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a563/11197138/87c577db913e/10.1177_0271678X231197946-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a563/11197138/5d4123006cfc/10.1177_0271678X231197946-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a563/11197138/58c09f67da09/10.1177_0271678X231197946-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a563/11197138/b7ce5da258f0/10.1177_0271678X231197946-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a563/11197138/ecc2f1c478d1/10.1177_0271678X231197946-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a563/11197138/3aacda2ae5ec/10.1177_0271678X231197946-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a563/11197138/87c577db913e/10.1177_0271678X231197946-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a563/11197138/5d4123006cfc/10.1177_0271678X231197946-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a563/11197138/58c09f67da09/10.1177_0271678X231197946-fig6.jpg

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