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Exposure to propofol down-regulates myelin basic protein expression in zebrafish embryos: its neurotoxicity on oligodendrocytes and the molecular mechanisms / 南方医科大学学报
Journal of Southern Medical University ; (12): 1115-1120, 2018.
Artículo en Chino | WPRIM | ID: wpr-691205
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the mechanism underlying propofol- induced down-regulation of myelin basic protein (MBP) in zebrafish embryos.</p><p><b>METHODS</b>Zebrafish embryos (6-48 h post-fertilization [hpf]) were randomized into 4 equal groups for exposure to dimethyl sulfoxide (DMSO), 20 μg/mL propofol, 30 μg/mL propofol, or no particular treatment (control group). The larvae were collected at 48 or 72 hpf for detecting the mRNA levels of MBP, Olig1, Olig2, and Sox10 using qRT-PCR (=80). The protein expression of MBP was quantitatively detected using Western blotting (=80), and the apoptosis of the oligodendrocytes was investigated using TUNEL staining (=6).</p><p><b>RESULTS</b>Exposure to 20 and 30 μg/mL propofol caused significant reductions in the mRNA expressions of Olig1, Olig2, and Sox10 at 48 and 72 hpf ( < 0.05) and also in MBP mRNA and protein levels at 72 hpf ( < 0.05). Exposure to 30 μg/mL propofol induced more obvious reduction in MBP protein expression than 20 μg/mL propofol at 72 hpf ( < 0.05), and the exposures resulted in a significant increase of oligodendrocyte apoptosis at 72 hpf ( < 0.05).</p><p><b>CONCLUSIONS</b>Propofol exposure reduces MBP expression at both the mRNA and protein levels in zebrafish embryos by down-regulating the expressions of Olig1, Olig2 and Sox10 mRNA levels and increasing apoptosis of the oligodendrocytes.</p>

Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Tipo de estudio: Ensayo Clínico Controlado Idioma: Chino Revista: Journal of Southern Medical University Año: 2018 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Tipo de estudio: Ensayo Clínico Controlado Idioma: Chino Revista: Journal of Southern Medical University Año: 2018 Tipo del documento: Artículo