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Effects of neuroactive steroid allopregnanolone on the damage of cortical neurons / 中国应用生理学杂志
Article de Zh | WPRIM | ID: wpr-351207
Bibliothèque responsable: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the protective mechanism of neuroactive steroid allopregnanolone on N-methyl-D-aspartate (NMDA) induced toxicity in primary mouse cortical neurons.</p><p><b>METHODS</b>Primary cultured mouse cortical neurons were subjected to allopregnanolone, the expression of beta-aminobutyric acid receptor beta2 subunit (beta2-GABA-R) mRNAs was detected by RT-PCR and Akt phosphorylation was assayed by Western blot using Akt-phosphoserine 473-specific antibody. After the cultured mouse cortical neurons were pretreated with or without allopregnanolone prior to treatment with NMDA , DNA isolated was analyzed by agarose gel electrophoresis and proteins collected were analyzed by Western blot with anti-cleaved-PARP, anti-cleaved caspase-3, and anti-cleaved caspase-9 antibodies.</p><p><b>RESULTS</b>When cultured mouse cortical neurons were exposed to allopregnanolone both the expression of beta2-GABA-R mRNAs and Akt phosphorylation increased. Allopregnanolone inhibited the NMDA-induced apoptosis and decreased the level of active-PARP, active-caspase-3 and active-caspase-9 notably at a final concentration of 5 x 10(6) mol/L.</p><p><b>CONCLUSION</b>Pretreatment with allopregnanolone may be neuroprotective on NMDA-induced neuronal cells apoptosis by increasing beta2-GABA-R expression and Akt phosphorylation.</p>
Sujet(s)
Texte intégral: 1 Indice: WPRIM Sujet Principal: Pharmacologie / Prégnanolone / ARN messager / Cortex cérébral / N-Méthyl-aspartate / Poly(ADP-ribose) polymerases / Apoptose / Récepteurs GABA-B / Neuroprotecteurs / Biologie cellulaire Limites du sujet: Animals langue: Zh Texte intégral: Chinese Journal of Applied Physiology Année: 2011 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Pharmacologie / Prégnanolone / ARN messager / Cortex cérébral / N-Méthyl-aspartate / Poly(ADP-ribose) polymerases / Apoptose / Récepteurs GABA-B / Neuroprotecteurs / Biologie cellulaire Limites du sujet: Animals langue: Zh Texte intégral: Chinese Journal of Applied Physiology Année: 2011 Type: Article