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甲状腺激素影响成年大鼠齿状回中的神经发生。

Thyroid hormones affect neurogenesis in the dentate gyrus of adult rat.

作者信息

Ambrogini Patrizia, Cuppini Riccardo, Ferri Paola, Mancini Cecilia, Ciaroni Sandra, Voci Adriana, Gerdoni Ezio, Gallo Gabriella

机构信息

Istituto di Scienze Fisiologiche, Università di Urbino Carlo Bo, Italia.

出版信息

Neuroendocrinology. 2005;81(4):244-53. doi: 10.1159/000087648. Epub 2005 Aug 18.

Abstract

Thyroid hormones play a crucial role in new neuron production and maturation during brain development. However, the knowledge about the involvement of these hormones on adult neurogenesis is still incomplete. Hippocampus is an anatomical region where neurogenesis occurs throughout adulthood and where high levels of thyroid hormone receptors have been found. In this work the possible involvement of thyroid hormones in the regulation of adult neurogenesis in the granule cell layer of rat hippocampus dentate gyrus was investigated using an experimental model of adult-onset pharmacologically-induced hypothyroidism. Neurogenesis was assessed by means of the thymidine analogue 5-bromo-2'-deoxyuridine 24 h and 30 days after its last administration in order to study neural precursor proliferation and newborn cell survival, respectively. Mitotic activity of the neural precursors was not affected by thyroid hormone deficiency; on the contrary, newborn cell survival dramatically decreased under these conditions when compared with controls, leading to a lower number of immature neurons being added to the granule cell layer. Moreover, in conditions of hypothyroidism, new neurons exhibit a delay in neuronal differentiation showing a prolonged expression of the neuritogenesis-associated immature neuron marker TUC-4 and a very immature morphology. Finally, the total number and size of granule cells, and granule cell layer volume decreased in hypothyroid rats. These results suggest that thyroid hormones play a role in regulating new neuron production during adult life in dentate gyrus of rat hippocampus.

摘要

甲状腺激素在大脑发育过程中的新神经元生成和成熟中起着至关重要的作用。然而,关于这些激素参与成年神经发生的知识仍不完整。海马体是一个在成年期全程都发生神经发生的解剖区域,并且已发现其中存在高水平的甲状腺激素受体。在这项研究中,使用成年期药理学诱导的甲状腺功能减退实验模型,研究了甲状腺激素在大鼠海马齿状回颗粒细胞层成年神经发生调节中的可能作用。通过在最后一次给药后24小时和30天使用胸腺嘧啶类似物5-溴-2'-脱氧尿苷来评估神经发生,以便分别研究神经前体细胞增殖和新生细胞存活情况。神经前体细胞的有丝分裂活性不受甲状腺激素缺乏的影响;相反,与对照组相比,在这些条件下新生细胞存活率显著降低,导致添加到颗粒细胞层的未成熟神经元数量减少。此外,在甲状腺功能减退的情况下,新神经元在神经元分化方面表现出延迟,表现为神经突发生相关的未成熟神经元标志物TUC-4的表达延长以及形态非常不成熟。最后,甲状腺功能减退大鼠的颗粒细胞总数和大小以及颗粒细胞层体积均减小。这些结果表明,甲状腺激素在调节成年大鼠海马齿状回成年期新神经元生成中发挥作用。

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