Journal of Cerebral Blood Flow & Metabolism · 2023 · 11 citations · 42 references
MedicineNeurologyNeuroscienceClinical NeuroscienceEpilepsyEpileptologyBlood-brain Barrier BiologyBlood-brain Barrier DysfunctionCerebrovascular AnatomyEpilepsy PathologyEpilepsy SurgeryNeurovascular DysfunctionBlood-brain Barrier PermeabilityCerebral MicrocirculationCerebrovascular Endothelial InjuryEpilepsy-associated Barrier DysfunctionGlycocalyx DamageGlycocalyx IntegrityMicrocirculationMicrovascular Permeability
Temporal lobe epilepsy (TLE) is increasingly associated with blood-brain barrier dysfunction and microvascular alterations, yet the pathophysiological link is missing. An important barrier function is exerted by the glycocalyx, a gel-like layer coating the endothelium. To explore such associations, we used intraoperative videomicroscopy to quantify glycocalyx and microcirculation properties of the neocortex and hippocampus of 15 patients undergoing resective brain surgery as treatment for drug-resistant TLE, and 15 non-epileptic controls. Fluorescent lectin staining of neocortex and hippocampal tissue was used for blood vessel surface area quantification. Neocortical perfused boundary region, the thickness of the glycocalyx’ impaired layer, was higher in patients (2.64 ± 0.52 µm) compared to controls (1.31 ± 0.29 µm), P < 0.01, indicative of reduced glycocalyx integrity in patients. Moreover, erythrocyte flow velocity analysis revealed an impaired ability of TLE patients to (de-)recruit capillaries in response to changing metabolic demands ( R 2 = 0.75, P < 0.01), indicating failure of neurovascular coupling mechanisms. Blood vessel quantification comparison between intraoperative measurements and resected tissue showed strong correlation ( R 2 = 0.94, P < 0.01). This is the first report on in vivo assessment of glycocalyx and microcirculation properties in TLE patients, confirming the pivotal role of cerebrovascular changes. Further assessment of the cerebral microcirculation in relation to epileptogenesis might open avenues for new therapeutic targets for drug-resistant epilepsy.
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