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Effect of zolpidem on functional recovery in a rat model of ischemic stroke

OBJECTIVE: To evaluate the effects of zolpidem on functional recovery in a rat model of acute ischemic stroke. METHODS: Following ischemic stroke procedures, 42 rats (six in each group) were randomly assigned to receive zolpidem (0.1, 0.25, 0.5, 1.0, 2.0 or 4.0 mg/kg) or normal saline administer int...

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Detalles Bibliográficos
Autores principales: Oh, Min-Kyun, Yoon, Kyung Jae, Lee, Yong-Taek, Chae, Seoung Wan, Choi, Hye Young, Shin, Hee Suk, Park, Yun Hee, Chun, Se-Woong, Park, Young Sook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6011331/
https://www.ncbi.nlm.nih.gov/pubmed/28831822
http://dx.doi.org/10.1177/0300060517723799
Descripción
Sumario:OBJECTIVE: To evaluate the effects of zolpidem on functional recovery in a rat model of acute ischemic stroke. METHODS: Following ischemic stroke procedures, 42 rats (six in each group) were randomly assigned to receive zolpidem (0.1, 0.25, 0.5, 1.0, 2.0 or 4.0 mg/kg) or normal saline administer intraperitoneally once daily for two weeks. Motor behavioural index (MBI) scores, radial 8-arm maze (RAM) test times and brain MRI scans were obtained 24 hours (Day 1) and two weeks (Day 14) post-procedure. Immunohistochemistry was performed on Day 14. RESULTS: By comparison with the normal saline group, the 0.5 and 1.0 mg/kg zolpidem groups showed statistically significant improvements in MBI scores and increased numbers of brain-derived neurotrophic factor (BDNF) stained cells over the two week dosing period. By contrast, the 4.0 mg/kg zolpidem group had statistically significantly impaired MBI scores compared with the control group. No differences among groups were found in RAM times or infarction volumes. CONCLUSIONS: This study in a rat model showed that 0.5–1.0 mg/kg of zolpidem had beneficial effects on behavioural recovery by enhancing neural plasticity without causing any memory impairment in acute ischemic stroke.