首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >The general anesthetic sevoflurane affects the expression of clock gene mPer2 accompanying the change of NAD+ level in the suprachiasmatic nucleus of mice.
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The general anesthetic sevoflurane affects the expression of clock gene mPer2 accompanying the change of NAD+ level in the suprachiasmatic nucleus of mice.

机译:全身麻醉性七氟醚伴随着小鼠视交叉上核NAD +水平的变化而影响时钟基因mPer2的表达。

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摘要

Sevoflurane is an anesthetic for the general anesthesia. In this study, we showed that sevoflurane anesthesia affects the expression of mouse Per2 (mPer2), which is a clock gene in the brain which is considered the organ where the anesthetics act in. 64.5% of mPer2 circadian expression was repressed under anesthesia in the suprachiasmatic nucleus (SCN) of the brain. After recovering from the anesthesia, the repressed mPer2 expression was restored to the same level as in non anesthesia-treated mice. This repression pattern was also observed in the subsequent phases of diurnal mPer2 expression. However, obvious phase-shift in the mPer2 expression was not showed in this study. On the other hand, the behavior analysis in this experiment exhibited that the phases in the circadian behavioral rhythm were shifted backwards. We also measured the NAD(+) level in the SCN, which was a mediator regulating the mPer2 expression. Then, significant increase of NAD(+) was detected under the anesthesia. These results indicate that the anesthesia induces the increase of NAD(+), and consequently leads to the repression of mPer2 expression and modifies the circadian expression pattern and diurnal behavioral rhythm of mice. Furthermore, the modification of mPer2 expression by the anesthesia is considered to affect various gene expressions.
机译:七氟醚是用于全身麻醉的麻醉剂。在这项研究中,我们显示七氟醚麻醉会影响小鼠Per2(mPer2)的表达,mPer2是大脑中的时钟基因,被认为是麻醉药在其中起作用。在麻醉下,mPer2昼夜节律的表达被抑制了64.5%。大脑上裂眼上核(SCN)。从麻醉中恢复后,抑制的mPer2表达恢复到与未麻醉处理的小鼠相同的水平。在每日mPer2表达的后续阶段中也观察到了这种抑制模式。但是,在这项研究中未显示mPer2表达的明显相移。另一方面,该实验中的行为分析表明,昼夜节律行为节奏的相位向后移动。我们还测量了SCN中的NAD(+)水平,SCN是调节mPer2表达的介体。然后,在麻醉下检测到NAD(+)明显增加。这些结果表明,麻醉诱导了NAD(+)的增加,并因此导致mPer2表达的抑制,并改变了小鼠的昼夜节律表达模式和昼夜行为节律。此外,认为通过麻醉对mPer2表达的修饰会影响各种基因表达。

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