Department of Biomedical Sciences, School of Medicine, University of Missouri-Kansas City, Kansas City, MO 64108, USA.
Department of Biomedical Sciences, School of Medicine, University of Missouri-Kansas City, Kansas City, MO 64108, USA; Department of Anesthesiology, School of Medicine, University of Missouri-Kansas City, Kansas City, MO 64108, USA.
Brain Res. 2024 Jan 15;1823:148671. doi: 10.1016/j.brainres.2023.148671. Epub 2023 Nov 10.
The commonly used general anesthetic propofol can enhance the γ-aminobutyric acid-mediated inhibitory synaptic transmission and depress the glutamatergic excitatory synaptic transmission to achieve general anesthesia and other outcomes. In addition to the actions at postsynaptic sites, the modulation of presynaptic activity by propofol is thought to contribute to neurophysiological effects of the anesthetic, although potential targets of propofol within presynaptic nerve terminals are incompletely studied at present. In this study, we explored the possible linkage of propofol to synapsins, a family of neuron-specific phosphoproteins which are the most abundant proteins on presynaptic vesicles, in the adult mouse brain in vivo. We found that an intraperitoneal injection of propofol at a dose that caused loss of righting reflex increased basal levels of synapsin phosphorylation at the major representative phosphorylation sites (serine 9, serine 62/67, and serine 603) in the prefrontal cortex (PFC) of male and female mice. Propofol also elevated synapsin phosphorylation at these sites in the striatum and S9 and S62/67 phosphorylation in the hippocampus, while propofol had no effect on tyrosine hydroxylase phosphorylation in striatal nerve terminals. Total synapsin protein expression in the PFC, hippocampus, and striatum was not altered by propofol. These results reveal that synapsin could be a novel substrate of propofol in the presynaptic neurotransmitter release machinery. Propofol possesses the ability to upregulate synapsin phosphorylation in broad mouse brain regions.
常用的全身麻醉药异丙酚可以增强γ-氨基丁酸介导的抑制性突触传递,抑制谷氨酸能兴奋性突触传递,从而达到全身麻醉等效果。除了在后突触部位的作用外,异丙酚对突触前活动的调节被认为有助于麻醉的神经生理效应,尽管目前对突触前神经末梢内异丙酚的潜在靶点研究还不完全。在这项研究中,我们在体内探索了异丙酚与突触相关蛋白(synapsin)的可能联系,突触相关蛋白是一种神经元特异性磷酸蛋白,是突触小泡上最丰富的蛋白质,在成年小鼠大脑中。我们发现,腹腔注射异丙酚的剂量导致翻正反射丧失,会增加雄性和雌性小鼠前额叶皮质(prefrontal cortex,PFC)中突触相关蛋白磷酸化的基础水平,在主要代表磷酸化位点(丝氨酸 9、丝氨酸 62/67 和丝氨酸 603)。异丙酚还增加了纹状体和海马中的突触相关蛋白在这些位点的磷酸化,而异丙酚对纹状体神经末梢中酪氨酸羟化酶的磷酸化没有影响。异丙酚对 PFC、海马和纹状体中的总突触相关蛋白表达没有影响。这些结果表明,突触相关蛋白可能是突触前神经递质释放机制中异丙酚的一个新的底物。异丙酚具有在广泛的小鼠脑区上调突触相关蛋白磷酸化的能力。