Puy Laurent, Kuchcinski Gregory, Leboullenger Clémence, Auger Florent, Cordonnier Charlotte, Bérézowski Vincent
Univ. Lille, Inserm, CHU Lille, U1172 - LilNCog - Lille Neuroscience & Cognition, Lille, France.
Univ. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, Lille, France.
J Cereb Blood Flow Metab. 2025 Jan;45(1):140-152. doi: 10.1177/0271678X241270198. Epub 2024 Aug 7.
The peri-hematomal area (PHA) emerges as a key but puzzling interface where edematous and neuroinflammatory events co-occur after intracerebral hemorrhage (ICH), while being considered either as deleterious or protective. We aimed at unraveling the pathogeny and natural history of PHA over time after experimental ICH. Male and female rats were longitudinally followed up to day 7 using multimodal brain MRI. MRI measures were compared to neuropathological and behavioural results. While the peak of PHA volume at day 3 was predictive for spontaneous locomotor deficit without sex-effect, its drop at day 7 fitted with locomotor recovery and hematoma resorption. The PHA highest water density was observed at onset despite microvascular hypoperfusion, taken over by blood-brain barrier (BBB) leakage at day 3. Water density dropped at day 7, when vascular integrity was normalized, and the highest number of reactive astrocytes, microglial cells, and siderophages found. This study shows that the PHA with edematous component is hematoma-driven at onset and BBB-driven at day 3, but this excess neuroinflammation enabled PHA volume reduction and significant hematoma resorption as soon as day 7. Therapeutic interventions should consider this pathogeny, and be monitored by multimodal MRI in preclinical ICH models.
血肿周围区域(PHA)是脑出血(ICH)后水肿和神经炎症事件共同发生的关键但令人费解的界面,其作用被认为既有有害的一面,也有保护的一面。我们旨在揭示实验性脑出血后PHA随时间变化的发病机制和自然病程。使用多模态脑MRI对雄性和雌性大鼠进行长达7天的纵向随访。将MRI测量结果与神经病理学和行为学结果进行比较。虽然第3天PHA体积峰值可预测无性别效应的自发运动功能障碍,但其在第7天的下降与运动功能恢复和血肿吸收相吻合。尽管存在微血管灌注不足,但在发病时观察到PHA的水密度最高,在第3天被血脑屏障(BBB)渗漏所取代。当血管完整性恢复正常且发现反应性星形胶质细胞、小胶质细胞和含铁血黄素吞噬细胞数量最多时,水密度在第7天下降。这项研究表明,具有水肿成分的PHA在发病时由血肿驱动,在第3天由BBB驱动,但这种过度的神经炎症在第7天就使PHA体积减小并显著促进血肿吸收。治疗干预应考虑这种发病机制,并在临床前ICH模型中通过多模态MRI进行监测。