Work

CS-NO releasing hydrogel protects against neuron apoptosis and inflammation through suppressing the HIF-1α and MAPK pathway in stroke

Year: 2026

Type: article

Abstract: Stroke remains a leading cause of global mortality and long-term disability. Chitosan-based nitric oxide nanoparticles (CS-NO), a novel injectable hydrogel, demonstrate protective effects in ischemia/reperfusion injury. However, the therapeutic efficacy and underlying mechanisms of CS-NO in stroke remain unclear. Here, we found that CS-NO exerted significant neuroprotective effects, as evidenced by neurofunctional assessments, along with marked reductions in neuronal apoptosis and inflammatory responses in stroke male mice models. Mechanistically, RNA-seq analysis combined with functional studies using an AAV9 delivery system revealed that the pathological interaction between HIF-1α and the MAPK pathway serves as a key driver in stroke development, which could be effectively inhibited by CS-NO administration. Notably, combination therapy involving CS-NO with either HIF-1α or TLR4 inhibitors showed superior neurological outcomes compared to monotherapy in stroke male mice. Collectively, CS-NO’s neuroprotection may stem from disrupting HIF-1α-MAPK crosstalk following stroke, suggesting the need for translational studies to further validate its clinical potential. This study introduces a novel chitosan-based nitric oxide (NO)-releasing hydrogel (CS-NO) designed for responsive release in the ischemic microenvironment, offering a targeted and sustained therapeutic approach distinct from bolus NO donors. Therapeutic Mechanism of Nitric Oxide-Releasing Hydrogel (CS-NO) in Ischemic Stroke. Ischemic stroke activates MAPK signaling and stabilizes HIF-1α, leading to neuroinflammation and neuronal apoptosis. CS-NO exerts its therapeutic effects by coordinately inhibiting both MAPK and HIF-1α signaling pathways, thereby disrupting this detrimental cascade. This dual-pathway inhibition represents the key molecular mechanism underlying CS-NO's neuroprotective action in ischemic stroke treatment. • Novel CS-NO hydrogel demonstrates potent neuroprotection by reducing neuronal apoptosis and inflammation in ischemic stroke models. • CS-NO disrupts pathological crosstalk between HIF-1α and MAPK pathways, identified as a key driver of post-stroke damage. • Combination therapy (CS-NO + HIF-1α/TLR4 inhibitors) outperforms monotherapy, enhancing functional recovery in stroke mice. • HIF-1α overexpression negates CS-NO benefits, confirming HIF-1α/MAPK suppression as central to CS-NO’s mechanism. • CS-NO restores cerebral blood flow, neuronal ultrastructure, and motor function via ROS-responsive nitric oxide release.

Source: Materials Today Bio

DOI: 10.1016/j.mtbio.2026.102805