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促甲状腺激素受体信号缺陷可损害小鼠的空间学习和记忆能力。

Thyrotropin receptor signaling deficiency impairs spatial learning and memory in mice.

机构信息

Department of Endocrinology, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, China.

Shandong Provincial Key Laboratory of Endocrinology and Lipid Metabolism, Jinan, Shandong, China.

出版信息

J Endocrinol. 2020 Jul;246(1):41-55. doi: 10.1530/JOE-20-0026.

Abstract

Subclinical hyperthyroidism, a condition characterized by decreased thyroid-stimulating hormone (TSH) and normal concentration of thyroid hormone, is associated with an elevated risk for cognitive impairment. TSH is the major endogenous ligand of the TSH receptor (TSHR) and its role is dependent on signal transduction of TSHR. It has not, however, been established whether TSHR signaling is involved in the regulation of cognition. Here, we utilized Tshr knockout mice and found that Tshr deletion led to significantly compromised performance in learning and memory tests. Reduced dendritic spine density and excitatory synaptic density as well as altered synaptic structure in CA1 subfield of the hippocampus were also noted. Furthermore, the synapse-related gene expression was altered in the hippocampus of Tshr -/- mice. These findings suggest that TSHR signaling deficiency impairs spatial learning and memory, which discloses a novel role of TSHR signaling in brain function.

摘要

亚临床甲状腺功能亢进症,一种以促甲状腺激素(TSH)降低和甲状腺激素浓度正常为特征的疾病,与认知障碍的风险增加有关。TSH 是 TSH 受体(TSHR)的主要内源性配体,其作用取决于 TSHR 的信号转导。然而,尚未确定 TSHR 信号是否参与认知调节。在这里,我们利用 Tshr 敲除小鼠发现,Tshr 缺失导致学习和记忆测试的表现明显受损。海马 CA1 亚区的树突棘密度和兴奋性突触密度降低以及突触结构改变也被注意到。此外,Tshr-/-小鼠海马中的突触相关基因表达发生改变。这些发现表明,TSHR 信号缺失会损害空间学习和记忆,这揭示了 TSHR 信号在大脑功能中的新作用。

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