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DOI 10.1089/neu.2024.0070

Медицинская библиотека · Journal of neurotrauma · 2025

Mitigation of Acute Seizures and Neuropathology after Traumatic Brain Injury by Structure-Based Discovery-Identified Drugs.

Kajevu Natallie, Banuelos Ivette, Andrade Pedro, Hämäläinen Elina, Sabatier Laureano, Couyoupetrou Manuel, Villalba María Luisa, Gavernet Luciana, Lipponen Anssi, Natunen Teemu, Puhakka Noora, Hiltunen Mikko, Talevi Alan, Pitkänen Asla

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Аннотация

Our objective was to test the hypothesis that structure-based identified or designed compounds exhibiting neuroprotective, antioxidant, and anti-inflammatory properties in vitro will mitigate early seizures and neuropathology after traumatic brain injury (TBI) in vivo. The neuroprotective and anti-inflammatory effects of 11 compounds identified by computer-assisted approximations were tested in vitro in neuronal microglial co-cultures. Among these, compound FBA exhibited the best neuroprotective (MAP-2, microtubule-associated-protein 2, a neuronal damage biomarker), antioxidative (nitrite production), and anti-inflammatory effects in vitro (all p < 0.01). Consequently, its neuroprotective and antiseizure effects were assessed in vivo in adult male Sprague-Dawley rats exposed to severe lateral fluid-percussion-induced TBI. Rats under continuous video-electroencephalogram monitoring received prophylactic treatment with an intraperitoneal (i.p.) injection of FBA (FBApro, 30 mg/kg) or vehicle (VEH, 48% PEG in 0.9% saline, 3 mL/kg) at 2 and 24 h post-TBI. Rats that developed status epilepticus received 1-2 additional on-demand FBA doses (FBApro+, 100 mg/kg, i.p.) to stop epileptiform activity. FBApro treatment reduced the cortical lesion area (18.9 ± 4.1 mm2, n = 7) compared with VEH treatment (24.8 ± 5.7 mm2, n = 10, p < 0.05). FBApro treatment also showed a favorable effect on the white matter by reducing plasma levels of pNF-H, a biomarker of axonal injury, compared with VEH treatment (Cohen's delta 0.657). Both FBApro (368 ± 407 s) and FBApro+ (256 ± 327 s) treatments reduced the average cumulative seizure duration compared with VEH (896 ± 703 s, both p < 0.05). The FBApro+ treatment regimen also reduced the mean relative theta and alpha power and increased the mean relative gamma power in the electroencephalogram (p < 0.05). Our data identified FBA as a novel structure-based discovered compound with promising favorable effects on structural and functional recovery after TBI.

Для цитирования: Kajevu Natallie, Banuelos Ivette, Andrade Pedro, Hämäläinen Elina, Sabatier Laureano, Couyoupetrou Manuel, Villalba María Luisa, Gavernet Luciana, Lipponen Anssi, Natunen Teemu, Puhakka Noora, Hiltunen Mikko, Talevi Alan, Pitkänen Asla. Mitigation of Acute Seizures and Neuropathology after Traumatic Brain Injury by Structure-Based Discovery-Identified Drugs.. Journal of neurotrauma. 2025. DOI: 10.1089/neu.2024.0070.

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