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J Stroke Cerebrovasc Dis ; 33(7): 107728, 2024 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-38643942

RESUMO

OBJECTIVES: Subarachnoid haemorrhage (SAH) carries a high burden of morbidity and mortality. One in three patients develop vasospasm, which is associated with Delayed Cerebral Ischemia. The pathophysiology includes vasoconstrictor receptor upregulation in cerebral arteries. The protein kinase C - inhibitor RO-31-7549 reduces the expression of several vasoconstrictor receptors and normalizes cerebral blood flow in experimental SAH but functional and behavioural effects are unknown. This study was undertaken to analyse functional outcomes up to 14 days after experimental SAH. MATERIALS AND METHODS: 54 male rats were randomised to experimental SAH or sham, using the pre-chiasmatic, single injection model, and subsequent treatment or vehicle. 42 remained for final analysis. The animals were euthanized on day 14 or when reaching a humane endpoint. The primary endpoint was overall survival, defined as either spontaneous mortality or when reaching a predefined humane endpoint. The secondary outcomes were differences in the rotating pole test, weight, open field test, novel object recognition and qPCR of selected inflammatory markers. RESULTS: In the vehicle group 6/15 rats reached the humane endpoint of >20 % weight loss compared to 1/14 in the treatment group. This resulted in a significant reduced risk of early euthanasia due to >20 % weight loss of HR 0.15 (0.03-0.66, p = 0.04). Furthermore, the treatment group did significantly better on the rotating pole test, RR 0.64 (0.47-0.91, p = 0.02). CONCLUSION: RO-31-7549 improved outcomes in terms >20 % weight loss and rotating pole performance after experimental SAH and could be investigated.


Assuntos
Comportamento Animal , Modelos Animais de Doenças , Proteína Quinase C , Inibidores de Proteínas Quinases , Ratos Sprague-Dawley , Hemorragia Subaracnóidea , Redução de Peso , Animais , Hemorragia Subaracnóidea/fisiopatologia , Hemorragia Subaracnóidea/tratamento farmacológico , Masculino , Inibidores de Proteínas Quinases/farmacologia , Fatores de Tempo , Redução de Peso/efeitos dos fármacos , Proteína Quinase C/metabolismo , Proteína Quinase C/antagonistas & inibidores , Comportamento Animal/efeitos dos fármacos , Recuperação de Função Fisiológica , Estado Funcional , Mediadores da Inflamação/metabolismo , Atividade Motora/efeitos dos fármacos , Indóis/farmacologia , Pirazóis/farmacologia , Transdução de Sinais
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