Intestinal flora influences the progression of subarachnoid hemorrhage by affecting peripheral and central inflammatory pathways

•The study used an endovascular perforation model to simulate brain haemorrhage.•Altered intestinal flora in rats after subarachnoid haemorrhage.•Increased damage after cerebral haemorrhage in rats following altered gut flora. Subarachnoid hemorrhage (SAH) is a debilitating condition that leaves sur...

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Veröffentlicht in:Brain research 2024-10, Vol.1840, p.149032, Article 149032
Hauptverfasser: Zhang, Ming, Gan, Xiaokui, Fang, Yiming, Song, Xiaowei, Li, Qingquan, Huang, Baosheng
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Sprache:eng
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Zusammenfassung:•The study used an endovascular perforation model to simulate brain haemorrhage.•Altered intestinal flora in rats after subarachnoid haemorrhage.•Increased damage after cerebral haemorrhage in rats following altered gut flora. Subarachnoid hemorrhage (SAH) is a debilitating condition that leaves survivors with neurological disability for the rest of their lives. No effective treatment for early brain injury (EBI) has been developed. Gut microbiome (GM) impact the host immune system and can influence disease processes in several organs, including the brain. However, it remains unclear whether the GM has an impact on the outcome of SAH brain injury. Here, we wondered whether microbiota could relieve the injury. We changed the microbiota of 8-week-old male rats by administering antibiotic-containing water for 2 weeks. Composition of the GM was profiled by using 16S rRNA. We induced SAH by puncture the internal carotid artery of control rats and rats with altered GM. Additionally, we studied inflammatory cells using HE stains, Intestinal lymphocyte flow cytometry, and Neuroinflammatory factor WB. SAH was significantly averted by alterations in GM using antibiotics. The altered GM significantly increased the intestinal and intracranial inflammation after SAH. This was manifested by Mosin (MSN) inflammatory cytokines. Our findings demonstrated that the brain injury following SAH is associated with GM.
ISSN:0006-8993
1872-6240
1872-6240
DOI:10.1016/j.brainres.2024.149032