Background: The inflammatory pathway in cerebrospinal fluid (CSF) leads to delayed cerebral vasospasm (DCVS) and delayed cerebral ischemia (DCI) after subarachnoid hemorrhage (SAH). The role of IL-1α has never been evaluated in a rabbit SAH model. The aim of our study is to analyze systemic and CSF changes of IL-1α, and to evaluate potential associations with the onset of DCVS in a rabbit closed cranium SAH model. Methods 17 New Zealand white rabbits were randomized into two groups, SAH ( = 12) and sham ( = 5). In the first group, SAH was induced by extracranial-intracranial shunting from the subclavian artery into the cerebral cistern of magna under intracranial pressure (ICP) monitoring. The sham group served as a control. The CSF and blood samples for IL-1α measurement were taken at day zero before SAH induction and at day three.
Results: There was a significant increase of ICP ( = 0.00009) and a decrease of cerebral perfusion pressure (CPP) ( = 0.00089) during SAH induction. At follow up, there was a significant increase of systemic IL-1α in the SAH as compared with the sham group ( = 0.042) There was no statistically significant difference in the CSF values in both groups. The CSF IL-1α values showed a correlation trend of DCVS.
Conclusions: Systemic IL-1α levels are elevated after SAH induction in a rabbit SAH model.
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http://dx.doi.org/10.3390/brainsci9100249 | DOI Listing |
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Faculty of Medicine, University of Cyberjaya, Cyberjaya, Malaysia.
Background: The rapid rise of non-communicable diseases, particularly type 2 diabetes mellitus (T2DM), poses a significant global public health challenge, with South Asia experiencing an increasingly severe burden. This study aimed to analyse historical trends of T2DM across South Asia from 1990 to 2021 and forecast incidence through 2031.
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Department of Sociology, Virginia Tech, Blacksburg, VA, USA.
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Ferroptosis, a recently identified form of regulated cell death, is characterized by lipid peroxidation and iron accumulation, plays a critical role in early brain injury after subarachnoid hemorrhage. Ginsenoside Rd, an active compound isolated from ginseng, is known for its neuroprotective properties. However, its influence on SAH-induced ferroptosis remains unclear.
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