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Acta Pharmacol Sin ; 45(7): 1381-1392, 2024 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-38514863

RESUMO

Status epilepticus (SE), a serious and often life-threatening medical emergency, is characterized by abnormally prolonged seizures. It is not effectively managed by present first-line anti-seizure medications and could readily develop into drug resistance without timely treatment. In this study, we highlight the therapeutic potential of CZL80, a small molecule that inhibits caspase-1, in SE termination and its related mechanisms. We found that delayed treatment of diazepam (0.5 h) easily induces resistance in kainic acid (KA)-induced SE. CZL80 dose-dependently terminated diazepam-resistant SE, extending the therapeutic time window to 3 h following SE, and also protected against neuronal damage. Interestingly, the effect of CZL80 on SE termination was model-dependent, as evidenced by ineffectiveness in the pilocarpine-induced SE. Further, we found that CZL80 did not terminate KA-induced SE in Caspase-1-/- mice but partially terminated SE in IL1R1-/- mice, suggesting the SE termination effect of CZL80 was dependent on the caspase-1, but not entirely through the downstream IL-1ß pathway. Furthermore, in vivo calcium fiber photometry revealed that CZL80 completely reversed the neuroinflammation-augmented glutamatergic transmission in SE. Together, our results demonstrate that caspase-1 inhibitor CZL80 terminates diazepam-resistant SE by blocking glutamatergic transmission. This may be of great therapeutic significance for the clinical treatment of refractory SE.


Assuntos
Anticonvulsivantes , Caspase 1 , Camundongos Endogâmicos C57BL , Estado Epiléptico , Animais , Estado Epiléptico/tratamento farmacológico , Caspase 1/metabolismo , Camundongos , Masculino , Anticonvulsivantes/farmacologia , Anticonvulsivantes/uso terapêutico , Ácido Caínico/farmacologia , Camundongos Knockout , Ácido Glutâmico/metabolismo , Inibidores de Caspase/farmacologia , Inibidores de Caspase/uso terapêutico , Diazepam/farmacologia , Diazepam/uso terapêutico , Transmissão Sináptica/efeitos dos fármacos
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