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Impact of calcineurin inhibitors on rat glioma cells viability / 영남의대학술지
Yeungnam University Journal of Medicine ; : 105-108, 2019.
Artigo em Inglês | WPRIM | ID: wpr-785313
ABSTRACT

BACKGROUND:

Although kidney transplantation outcomes have improved dramatically after using calcineurin inhibitors (CNIs), CNI toxicity continues to be reported and the mechanism remains uncertain. Here, we investigated the neurotoxicity of CNIs by focusing on the viability of glioma cells.

METHODS:

Glioma cells were treated with several concentrations of CNIs for 24 hours at 37℃ and their cell viability was evaluated using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay.

RESULTS:

Exposure to 0, 0.25, 0.5, 2.5, 5.0, and 10.0 mM concentrations respectively showed 100%, 64.3%, 61.3%, 68.1%, 62.4%, and 68.6% cell viability for cyclosporine and 100%, 38.6%, 40.8%, 43.7%, 37.8%, and 43.0% for tacrolimus. The direct toxic effect of tacrolimus on glioma cell viability was stronger than that of cyclosporine at the same concentration.

CONCLUSION:

CNIs can cause neurological side effects by directly exerting cytotoxic effects on brain cells. Therefore, we should carefully monitor the neurologic symptoms and level of CNIs in kidney transplant patients.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Encéfalo / Sobrevivência Celular / Transplante de Rim / Tacrolimo / Ciclosporina / Calcineurina / Inibidores de Calcineurina / Glioma / Rim / Manifestações Neurológicas Limite: Animais / Humanos Idioma: Inglês Revista: Yeungnam University Journal of Medicine Ano de publicação: 2019 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Encéfalo / Sobrevivência Celular / Transplante de Rim / Tacrolimo / Ciclosporina / Calcineurina / Inibidores de Calcineurina / Glioma / Rim / Manifestações Neurológicas Limite: Animais / Humanos Idioma: Inglês Revista: Yeungnam University Journal of Medicine Ano de publicação: 2019 Tipo de documento: Artigo