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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >ANALYZING THE EFFECTS OF A SINGLE EPISODE OF NEONATAL MATERNAL DEPRIVATION ON METABOLITE PROFILES IN RAT BRAIN: A PROTON NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY STUDY
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ANALYZING THE EFFECTS OF A SINGLE EPISODE OF NEONATAL MATERNAL DEPRIVATION ON METABOLITE PROFILES IN RAT BRAIN: A PROTON NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY STUDY

机译:分析新生儿母体剥夺的单一情节对大鼠脑中代谢物谱的影响:质子核磁共振光谱研究

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摘要

Animal models have greatly contributed to the understanding of neuropsychiatric disorders and have provided extensive evidence for the "neurodevelopmental hypothesis." In this regard, a single and prolonged episode (24 h) of early matemal deprivation early in life, on postnatal day 9, has been proposed as an animal model for the investigation of certain neuropsychiatric disorders, including schizophrenia. Since metabolic changes in hippocampus (HIP) and prefrontal cortex (PFC) have been described among schizophrenic patients by using ex vivo high-resolution magic angle spinning (HR-MAS) proton (~1H) nuclear magnetic resonance spectros-copy, in the present study we aimed to investigate the effects of maternal deprivation (MD) on the metabolite profiles of the developing brain by using the HR-MAS technique. MD significantly altered the hippocampal and cortical metabolic profile of neonatal rats (PND 13) in a sex-dependent manner. Glutamine and glutamate (Glx) and taurine of male and female rat pups were altered in both brain areas analyzed. Differences in hippocampai phosphorylethanolamine have also been found as a function of the MD protocol. In addition, MD induced some other region- and sex-dependent effects, including changes in N-acetyl aspartate and total choline signals in the hippocampi of male pups. Present findings indicate a different brain metabolic profile in our animal model of early life stress suggesting its potential utility in the implementation of translational neuropsychiatric research.
机译:动物模型极大地促进了对神经精神疾病的理解,并为“神经发育假设”提供了广泛的证据。在这方面,已经提出了在生命期间早期的早期未剥夺的单一和延长的发作(24小时),作为对某些神经精神疾病调查的动物模型,包括精神分裂症。由于在本发明的前体内高分辨率魔角旋转(HR-MAS)质子(〜1H)核磁共振谱 - 拷贝,因此精神分裂症患者中描述了海马(HIP)和前额叶皮质(PFC)的代谢变化。研究我们旨在通过使用HR-MAS技术来研究母体剥夺(MD)对发展大脑的代谢物谱的影响。 MD以性别依赖性方式显着改变新生大鼠(PND 13)的海马和皮质代谢谱。在分析的两种脑区,谷氨酰胺和谷氨酸(Glx)和牛磺酸幼兔子被改变。还发现了海马磷酸乙醇胺的差异作为MD方案的函数。此外,MD诱导了一些其他区域和性依赖性的作用,包括在雄性幼崽的海马中的N-乙酰基天冬氨酸和总胆碱信号的变化。目前的研究结果表明我们的早期生命压力的动物模型中的不同脑代谢型材,表明其在平移神经精神科研究中实施的潜在效用。

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