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Experimentally-induced maternal hypothyroidism alters crucial enzyme activities in the frontal cortex and hippocampus of the offspring rat

机译:实验性母体甲状腺功能减退症改变后代大鼠额叶皮层和海马中的关键酶活性

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Thyroid hormone insufficiency during neurodevelopment can result into significant structural and functional changes within the developing central nervous system (CNS), and is associated with the establishment of serious cognitive impairment and neuropsychiatric symptomatology. The aim of the present study was to shed more light on the effects of gestational and/or lactational maternal exposure to propylthiouracil (PTU)-induced hypothyroidism as a multilevel experimental approach to the study of hypothyroidism-induced changes on crucial brain enzyme activities of 21-day-old Wistar rat offspring in a brain region-specific manner. This experimental approach has been recently developed and characterized by the authors based on neurochemical analyses performed on newborn and 21-day-old rat offspring whole brain homogenates; as a continuum to this effort, the current study focused on two CNS regions of major significance for cognitive development: the frontal cortex and the hippocampus. Maternal exposure to PTU in the drinking water during gestation and/or lactation resulted into changes in the activities of acetylcholinesterase and two important adenosinetriphosphatases (Na+,K+- and Mg2+-ATPase), that seemed to take place in a CNS-region-specific manner and that were dependent upon the PTU-exposure timeframe followed. As these findings are analyzed and compared to the available literature, they: (i) highlight the variability involved in the changes of the aforementioned enzymatic parameters in the studied CNS regions (attributed to both the different neuroanatomical composition and the thyroid-hormone-dependent neurodevelopmental growth/differentiation patterns of the latter), (ii) reveal important information with regards to the neurochemical mechanisms that could be involved in the way clinical hypothyroidism could affect optimal neurodevelopment and, ultimately, cognitive function, as well as (iii) underline the need for the adoption of more consistent approaches towards the experimental simulation of congenital and early-age-occurring hypothyroidism.
机译:在神经发育过程中,甲状腺激素功能不足会导致发育中的中枢神经系统(CNS)发生明显的结构和功能变化,并与严重的认知障碍和神经精神症状有关。本研究的目的是进一步阐明妊娠和/或哺乳期母亲暴露于丙硫氧嘧啶(PTU)诱发的甲状腺功能减退的影响,作为研究甲状腺功能减退症引起的对关键性脑酶活性的改变的多层次实验方法21日龄的Wistar大鼠后代以大脑区域特定的方式运行。作者基于对新生和21日龄大鼠后代全脑匀浆进行的神经化学分析,开发了这种实验方法并对其进行了表征。作为这项工作的延续,当前的研究集中在两个对认知发育具有重要意义的中枢神经系统区域:额叶皮层和海马体。孕妇在妊娠和/或哺乳期间暴露于饮用水中的PTU导致乙酰胆碱酯酶和两种重要的腺苷三磷酸酶(Na +,K +-和Mg2 + -ATPase)的活性发生变化,这似乎是以CNS区域特定的方式发生的而这取决于随后的PTU暴露时间范围。由于对这些发现进行了分析并与现有文献进行了比较,因此:(i)在研究的中枢神经系统区域(既归因于不同的神经解剖成分,又依赖甲状腺激素依赖性神经发育)突显了上述酶学参数变化所涉及的变异性。 (ii)揭示了有关神经化学机制的重要信息,这些信息可能涉及临床甲状腺功能减退症可能影响最佳神经发育并最终影响认知功能的方式,以及(iii)强调了这种需求为采用更一致的方法进行先天性和早期甲状腺功能减退的实验模拟。

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