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首页> 外文期刊>Frontiers in Veterinary Science >Brain plasticity in mammals: An example for the role of comparative medicine in the Neurosciences
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Brain plasticity in mammals: An example for the role of comparative medicine in the Neurosciences

机译:哺乳动物的大脑可塑性:神经科学中比较医学的作用的一个例子

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Comparative medicine deals with similarities and differences between veterinary and human medicine. All mammals share most basic cellular and molecular mechanisms, thus justifying murine animal models in a translational perspective; yet “mice are not men”, thus some biases can emerge when complex biological processes are concerned. Brain plasticity is a cutting-edge, expanding topic in the field of Neurosciences with important translational implications, yet, with remarkable differences among mammals, as emerging from comparative studies. In particular, adult neurogenesis (the genesis of new neurons from brain stem cell niches) is a life-long process in laboratory rodents but a vestigial, mostly postnatal remnant in humans and dolphins. Another form of “whole cell” plasticity consisting of a population of “immature” neurons which are generated prenatally but continue to express markers of immaturity during adulthood has gained interest more recently, as a reservoir of young neurons in the adult brain. The distribution of the immature neurons also seems quite heterogeneous among different animal species, being confined within the paleocortex in rodents while extending into neocortex in other mammals. A recent study carried out in sheep, definitely showed that gyrencephalic, large-sized brains do host higher amounts of immature neurons, also involving subcortical, white and gray matter regions. Hence, “whole cell” plasticity such as adult neurogenesis and immature neurons are biological processes which, as a whole, cannot be studied exclusively in laboratory rodents, but require investigation in comparative medicine, involving large-sized, long-living mammals, in order to gain insights for translational pourposes.
机译:比较医学涉及兽医学和人类医学之间的异同。所有哺乳动物都拥有最基本的细胞和分子机制,因此从翻译的角度证明了鼠类动物模型的合理性。然而“老鼠不是人”,因此,当涉及复杂的生物过程时,可能会出现一些偏见。脑可塑性是神经科学领域中一个前沿的,不断扩展的话题,具有重要的翻译意义,但随着比较研究的出现,哺乳动物之间存在显着差异。特别是,成年神经发生(来自脑干细胞壁new的新神经元的产生)在实验室啮齿动物中是一生的过程,但在人类和海豚中却是残留物,大部分是产后残留物。另一种形式的“全细胞”可塑性,是由成年前的“未成熟”神经元群体组成的,但在成年期仍继续表达未成熟标记,作为成年大脑中年轻神经元的储备,这种形式已引起人们越来越多的关注。未成熟神经元的分布在不同动物物种之间似乎也很不均一,被限制在啮齿动物的古大脑皮层中,而在其他哺乳动物中则延伸到新皮层中。最近在绵羊上进行的一项研究明确表明,脑脊髓大的大脑确实容纳大量未成熟神经元,还涉及皮层下,白质和灰质区域。因此,诸如成人神经发生和未成熟神经元之类的“全细胞”可塑性是整体上不能专门在实验室啮齿动物中研究的生物学过程,而是需要在涉及大而长寿哺乳动物的比较医学中进行研究。获得有关翻译目的的见解。

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