首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Effect of propofol on the levels of neurotransmitters in normal human brain: A magnetic resonance spectroscopy study
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Effect of propofol on the levels of neurotransmitters in normal human brain: A magnetic resonance spectroscopy study

机译:丙泊酚对正常人脑神经递质水平的影响:磁共振波谱研究

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Though widely used in anesthesia for many years, the mechanism underlying propofol anesthesia on human is not clear. Animal studies have already demonstrated that propofol functioned mainly by affecting neurotransmitters release. In our study, 10 healthy volunteers ranging from 20 to 40 years old were enrolled. With the help of target-controlled infusion pump, propofol was delivered intravenously. The target-controlled concentration (TCC) of propofol was gradually elevated from 0.5 to 3.0 μg/ml (for 6 steps with an increment of 0.5 μg/ml). During each step the Observer's Assessment of Alertness/Sedation Scale (OAA/S) was performed to evaluate asleep to awake/alert status. Magnetic resonance spectroscopy (MRS) was performed to evaluate neurotransmitters (choline compounds (Cho), creatine (Cr), glutamate (GLU), γ-aminobutyric acid (GABA) and N-acetyl aspartate (NAA)) changes in brains following propofol anesthesia. OAA/S scoring showed that when the TCCs of propofol were 0, 1.5 and 3.0 μg/ml, the volunteers were in awake, sedative and unconscious, respectively. Significantly down-regulated Cho and GLU, but up-regulated GABA was observed in unconscious state in all the detected regions. NAA was decreased in unconscious status only in the hippocampus and thalamus. There was no obvious change in Cr levels in any statuses or brain regions. Our results indicate that propofol has an impact on the levels of neurotransmitters such as NAA, GLU, GABA and Cho in normal human brain. During propofol anesthesia, enhancement of inhibition or suppression of excitation may each play key roles in different brain regions.
机译:尽管异丙酚麻醉多年来在麻醉中广泛使用,但其机制尚不清楚。动物研究已经表明,丙泊酚主要通过影响神经递质的释放而起作用。在我们的研究中,招募了10名20至40岁的健康志愿者。借助于靶标控制的输液泵,静脉注射丙泊酚。丙泊酚的目标控制浓度(TCC)从0.5逐渐增加到3.0μg/ ml(6步,增量为0.5μg/ ml)。在每个步骤中,执行观察员的警报/镇静评估量表(OAA / S)来评估从睡眠到清醒/警报状态。进行了磁共振波谱(MRS)评估丙泊酚麻醉后大脑中神经递质(胆碱化合物(Cho),肌酸(Cr),谷氨酸(GLU),γ-氨基丁酸(GABA)和N-乙酰天门冬氨酸(NAA))的变化。 OAA / S评分显示,当丙泊酚的TCC为0、1.5和3.0μg/ ml时,志愿者分别处于清醒状态,镇静状态和无意识状态。 Cho和GLU明显下调,但在所有检测到的区域中,在无意识状态下观察到GABA上调。 NAA仅在海马和丘脑的无意识状态下降低。在任何状态或大脑区域,Cr水平均无明显变化。我们的结果表明,丙泊酚对正常人脑中神经递质(如NAA,GLU,GABA和Cho)的水平有影响。在异丙酚麻醉期间,抑制作用的增强或兴奋的抑制可能在不同的大脑区域各自发挥关键作用。

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