Sall Jeffrey W, Stratmann Greg, Leong Jason, McKleroy William, Mason Daniel, Shenoy Shanti, Pleasure Samuel J, Bickler Phillip E
Department of Anesthesia and Perioperative Care, University of California, San Francisco, USA.
Anesthesiology. 2009 Apr;110(4):826-33. doi: 10.1097/ALN.0b013e31819b62e2.
Isoflurane causes long-term hippocampal-dependent learning deficits in rats despite limited isoflurane-induced hippocampal cell death, raising questions about the causality between isoflurane-induced cell death and isoflurane-induced cognitive function. Neurogenesis in the dentate gyrus is required for hippocampal-dependent learning and thus constitutes a potential alternative mechanism by which cognition can be altered after neonatal anesthesia. The authors tested the hypothesis that isoflurane alters proliferation and differentiation of hippocampal neural progenitor cells.
Multipotent neural progenitor cells were isolated from pooled rat hippocampi (postnatal day 2) and grown in culture. These cells were exposed to isoflurane and evaluated for cell death using lactate dehydrogenase release, caspase activity, and immunocytochemistry for nuclear localization of cleaved caspase 3. Growth was assessed by cell counting and BrdU incorporation. Expression of markers of stemness (Sox2) and cell division (Ki67) were determined by quantitative polymerase chain reaction. Cell fate selection was assessed using immunocytochemistry to stain for neuronal and glial markers.
Isoflurane did not change lactate dehydrogenase release, activity of caspase 3/7, or the amount of nuclear cleaved caspase 3. Isoflurane decreased caspase 9 activity, inhibited proliferation, and decreased the proportion of cells in s-phase. messenger ribonucleic acid expression of Sox2 (stem cells) and Ki67 (proliferation) were decreased. Differentiating neural progenitor cells more often select a neuronal fate after isoflurane exposure.
The authors conclude that isoflurane does not cause cell death, but it does act directly on neural progenitor cells independently of effects on the surrounding brain to decrease proliferation and increase neuronal fate selection. These changes could adversely affect cognition after isoflurane anesthesia.
异氟烷可导致大鼠出现长期的海马体依赖性学习缺陷,尽管异氟烷诱导的海马体细胞死亡有限,这引发了关于异氟烷诱导的细胞死亡与异氟烷诱导的认知功能之间因果关系的疑问。海马体依赖性学习需要齿状回中的神经发生,因此构成了新生儿麻醉后认知功能改变的一种潜在替代机制。作者测试了异氟烷会改变海马神经祖细胞增殖和分化的假设。
从新生大鼠(出生后第2天)的合并海马体中分离出多能神经祖细胞,并在培养中生长。将这些细胞暴露于异氟烷中,并使用乳酸脱氢酶释放、半胱天冬酶活性以及裂解的半胱天冬酶3核定位的免疫细胞化学方法评估细胞死亡情况。通过细胞计数和BrdU掺入评估细胞生长。通过定量聚合酶链反应测定干性标志物(Sox2)和细胞分裂标志物(Ki67)的表达。使用免疫细胞化学对神经元和胶质细胞标志物进行染色来评估细胞命运选择。
异氟烷未改变乳酸脱氢酶释放、半胱天冬酶3/7的活性或核裂解的半胱天冬酶3的量。异氟烷降低了半胱天冬酶9的活性,抑制了增殖,并降低了处于S期的细胞比例。Sox2(干细胞)和Ki67(增殖)的信使核糖核酸表达降低。异氟烷暴露后,分化中的神经祖细胞更常选择神经元命运。
作者得出结论,异氟烷不会导致细胞死亡,但它确实直接作用于神经祖细胞,独立于对周围脑组织的影响,以减少增殖并增加神经元命运选择。这些变化可能会对异氟烷麻醉后的认知产生不利影响。