British journal of pharmacology · 2026
The histone deacetylase inhibitor, suberoylanilide hydroxamic acid, restores blood-brain barrier integrity in a human stem cell-based model of ischaemic stroke.
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Szecskó Anikó, Párdi Koppány, Cui Zuhao, Porkoláb Gergő, Hoyk Zsófia, Kovács Csilla, Adegbite Janet F, Fodor Virág, Cser Nárcisz M, Dér László, Nagy Krisztina, Sajben Csilla, Tengölics Roland, Deli Mária A, Veszelka Szilvia
Аннотация
BACKGROUND AND PURPOSE: Ischaemic stroke is characterised by acute cerebrovascular occlusion, blood-brain barrier (BBB) breakdown and a narrow therapeutic window for recovery. Its treatment is a clinical challenge due to the risk of reperfusion injury and the limited efficacy of thrombolytic therapies; therefore, novel therapeutic approaches are needed. Histone deacetylase inhibitors (HDACi) have emerged as neuroprotective agents in stroke models, but their effect on preserving BBB integrity is unexplored. Our aim was to investigate the effects of the HDACi, suberoylanilide hydroxamic acid (SAHA), on BBB changes in a cell culture model of ischaemic stroke.
EXPERIMENTAL APPROACH: The effects of SAHA were tested on a human BBB co-culture model following a 6-h oxygen-glucose deprivation (OGD) under normoxia and during a 24 h reoxygenation (OGD/R).
KEY RESULTS: SAHA treatment ameliorated the OGD/R-induced loss of BBB integrity, as shown by an increase in transendothelial electrical resistance and reduced BBB permeability. The expression of genes involved in cell proliferation decreased, whereas an increase was measured for basement membrane protein, glycocalyx-synthesis enzyme and Wnt signalling-related genes. SAHA treatment elevated the claudin-5 protein expression and a metabolic shift from glycolysis to aerobic respiration was observed.
CONCLUSION AND IMPLICATIONS: Our results suggest that SAHA could be a potential adjunctive therapeutic drug for the treatment of ischaemia-reperfusion injury via BBB protection. Because SAHA has already been approved for human use as the anticancer drug vorinostat, its repurposing to restore BBB functions and prevent poststroke damages may be greatly facilitated.
EXPERIMENTAL APPROACH: The effects of SAHA were tested on a human BBB co-culture model following a 6-h oxygen-glucose deprivation (OGD) under normoxia and during a 24 h reoxygenation (OGD/R).
KEY RESULTS: SAHA treatment ameliorated the OGD/R-induced loss of BBB integrity, as shown by an increase in transendothelial electrical resistance and reduced BBB permeability. The expression of genes involved in cell proliferation decreased, whereas an increase was measured for basement membrane protein, glycocalyx-synthesis enzyme and Wnt signalling-related genes. SAHA treatment elevated the claudin-5 protein expression and a metabolic shift from glycolysis to aerobic respiration was observed.
CONCLUSION AND IMPLICATIONS: Our results suggest that SAHA could be a potential adjunctive therapeutic drug for the treatment of ischaemia-reperfusion injury via BBB protection. Because SAHA has already been approved for human use as the anticancer drug vorinostat, its repurposing to restore BBB functions and prevent poststroke damages may be greatly facilitated.