Transcranial photobiomodulation ameliorates hypobaric hypoxia-induced spatial cognitive dysfunction by enhancing...

High-altitude environments are characterized by hypobaric hypoxia (HH), which disrupts cerebral homeostasis and precipitates cognitive dysfunction. Transcranial photobiomodulation (tPBM), a non-invasive neuromodulatory intervention for neuroprotection and functional restoration, has emerged as a promising therapeutic strategy. This study aimed to evaluate the therapeutic efficacy of tPBM against HH-induced spatial cognitive dysfunction and elucidate the underlying neurobiological mechanisms. Spatial learning and memory were assessed using the Barnes maze. Regional cerebral blood flow dynamics were evaluated using diffuse reflectance spectroscopy and laser Doppler flowmetry. Additionally, histological examination, transcriptome sequencing, and molecular biology analyses, were integrated to delineate the biological mechanisms and identify candidate signaling pathways and molecular targets. Barnes maze performance demonstrated that tPBM significantly ameliorated HH-induced deficits in spatial learning and memory. Mechanistically, tPBM modulated hemodynamic responses and enhanced cerebral oxygen-binding efficiency within the lateral parietal association cortex (LPtA). Furthermore, tPBM improved mitochondrial function by elevating cytochrome c oxidase activity and promoting ATP synthesis. Concurrently, tPBM suppressed hypoxia-inducible factor-1α overexpression and microglial reactivity, reduced oxidative stress biomarkers, and augmented antioxidant enzyme activity. These molecular alterations were associated with preservation of synaptic structure, including reversal of dendritic spine loss. Transcriptome analysis further indicated that tPBM may preserves synaptic plasticity homeostasis by modulating the PI3K-Akt, cAMP-PKA, and calcium signaling pathways, with Adora2a identified as a potential therapeutic target. Collectively, these findings demonstrate that tPBM exerts neuroprotective effects against HH-induced spatial cognitive dysfunction by improving cerebral hemodynamics, enhancing mitochondrial function, attenuating neuroinflammation and oxidative stress, and preserving structural synaptic plasticity.