2. Academic Validation
  3. Osteopontin inhibitor alleviates neuroinflammation after subarachnoid hemorrhage in rats via TLR4/NF-κB pathway

Osteopontin inhibitor alleviates neuroinflammation after subarachnoid hemorrhage in rats via TLR4/NF-κB pathway

  • Brain Res Bull. 2025 Oct 27:232:111607. doi: 10.1016/j.brainresbull.2025.111607.
Dexun Kong 1,  Jing Guo 2,  Sha Yang 2,  Xiang Wang 3,  Qihui Guo 4,  Xiangqian Ren 4,  Jiqin Zhang 5,  Hao Yin 6,  Xin Xiang 7,  Ying Tan 8
Affiliations

Affiliations

  • 1 Guizhou Medical University, Guiyang, China; Department of Respiratory Medicine, Weining County People's Hospital, Bijie, China.
  • 2 GuiZhou University Medical College, Guiyang, Guizhou, China.
  • 3 Department of Neurosurgery, The Third Affiliated Hospital of Guizhou Medical University, China.
  • 4 Guizhou Medical University, Guiyang, China.
  • 5 Department of Anesthesiology, Guizhou Provincial People's Hospital, Guiyang, China.
  • 6 Department of Neurosurgery, Guizhou Provincial People's Hospital, Guiyang, China.
  • 7 Department of Neurosurgery, the Affiliated Hospital of Guizhou Medical University, Guiyang, China. Electronic address: xiangxin828@163.com.
  • 8 Department of Neurosurgery, Guizhou Provincial People's Hospital, Guiyang, China. Electronic address: tanyinggz5055@163.com.
PMID: 41161421 DOI: 10.1016/j.brainresbull.2025.111607
Abstract

Subarachnoid haemorrhage (SAH) has a high mortality and morbidity rate. In the early stages of subarachnoid haemorrhage, neuroinflammation is one of the important mechanisms leading to brain damage.The aim of this study was to investigate the protective effect of Osteobridging protein (OPN) inhibitors against subarachnoid haemorrhage in rats. The temporal lobe tissues of rats showed a significant increase in SPP1 (OPN) in the SAH group by single-cell RNA Sequencing, differential gene expression. Brain stereotactic ventricular injection of 250 umol/L OPN inhibitor was used to observe cognition 24 h after SAH rat model. The permeability of the blood-brain barrier was detected and the activation degree of microglia was observed by immunofluorescence. The results showed that OPN inhibitor improved cognitive impairment and reduced the permeability of the blood-brain barrier in rats, as well as reduced microglia activation while inhibiting the expression of inflammatory factors, which may be related to the inhibition of the TLR4/NF-κB pathway. These findings suggest that OPN inhibitors may be promising agents for the treatment of SAH by modulating blood-brain barrier permeability and inhibiting neuroinflammation.

Keywords

Blood-brain barrier; Early brain injury; Neuroinflammation; Subarachnoid hemorrhage.

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