General anesthesia activates BDNF-dependent neuroapoptosis in the developing rat brain

被引:223
作者
Lu, Lucy X.
Yon, Jun-Heum
Carter, Lisa B.
Jevtovic-Todorovic, Vesna
机构
[1] Univ Virginia Hlth Syst, Dept Anesthesiol, Charlottesville, VA 22908 USA
[2] Inje Univ, Dept Anesthesiol, Sanggye Paik Hosp, Seoul, South Korea
关键词
Akt; caspase; ceramide; neurotoxicity; neurotrophins; p75(NTR); synaptogenesis; beta estradiol;
D O I
10.1007/s10495-006-8762-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Brain-derived neurotrophic factor (BDNF) is important in supporting neuronal development. BDNF imbalance due to excessive neuronal inhibition can result in the apoptotic degeneration of developing neurons. Since general anesthetics cause profound depression of neuronal activity and are known to induce widespread degeneration in the developing brain, we studied their potential to activate BDNF-mediated developmental neuroapoptosis. When P7 rats (at the peak of brain development) were exposed to a commonly-used and highly pro-apoptotic anesthesia protocol (midazolam, isoflurane, nitrous oxide) for a period of 2, 4 or 6 h, we found that anesthesia modulates the key steps in BDNF-activated apoptotic cascade in two of the most vulnerable brain regions-cerebral cortex and thalamus in time-dependent fashion by activating both Trk-dependent (in thalamus) and Trk-independent p75(NTR) dependent (in cerebral cortex) neurotrophic pathways. beta-estradiol, a sex hormone that upregulates the protein levels of the activated Akt, protects against anesthesia-induced neuroapoptosis.
引用
收藏
页码:1603 / 1615
页数:13
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