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SAT-285 TSH/TSHR Signaling Deficiency Impairs Spatial Learning and Memory

Background: Subclinical hyperthyroidism is associated with cognitive impairment, but the mechanism has remained unclear. As subclinical hyperthyroidism is characterized by significantly decreased TSH levels, this study aimed to investigate whether TSH regulates cognitive function. Methods: The corre...

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Autores principales: Luan, Sisi, Zhao, He, Zhao, Jiajun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208007/
http://dx.doi.org/10.1210/jendso/bvaa046.023
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author Luan, Sisi
Zhao, He
Zhao, Jiajun
author_facet Luan, Sisi
Zhao, He
Zhao, Jiajun
author_sort Luan, Sisi
collection PubMed
description Background: Subclinical hyperthyroidism is associated with cognitive impairment, but the mechanism has remained unclear. As subclinical hyperthyroidism is characterized by significantly decreased TSH levels, this study aimed to investigate whether TSH regulates cognitive function. Methods: The correlation between TSH and cognitive impairment was investigated in a cross-sectional population study. The role of TSH/TSH receptor (TSHR) signaling in spatial learning and memory was further examined by behavior tests in Tshr(-/-) mice. Dendritic spine, synaptic density and structure of hippocampal CA1 pyramidal neurons were detected by Golgi’s method and electron microscopy. The mRNA and protein expression levels of learning and memory-related genes were assessed by RNA sequencing, real-time PCR, immunoblotting and immunofluorescence approaches. Results: Serum TSH level correlated negatively with cognitive impairment in the current population. Consistently, Tshr deletion in mice led to significantly compromised performance in hippocampus-dependent tasks, reduced dendritic spine density and excitatory synaptic density as well as altered synaptic structure in CA1 subfield of the hippocampus. Furthermore, the mRNA levels of learning and memory-related genes were altered, and protein levels of CREB-regulated genes were downregulated in the hippocampus of Tshr(-/-) mice. Conclusions: These findings reveal that TSH/TSHR signaling ablation impairs spatial learning and memory, indicating a decline in TSH level might contribute to the increased prevalence of cognitive impairment in subclinical hyperthyroidism patients.
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spelling pubmed-72080072020-05-13 SAT-285 TSH/TSHR Signaling Deficiency Impairs Spatial Learning and Memory Luan, Sisi Zhao, He Zhao, Jiajun J Endocr Soc Neuroendocrinology and Pituitary Background: Subclinical hyperthyroidism is associated with cognitive impairment, but the mechanism has remained unclear. As subclinical hyperthyroidism is characterized by significantly decreased TSH levels, this study aimed to investigate whether TSH regulates cognitive function. Methods: The correlation between TSH and cognitive impairment was investigated in a cross-sectional population study. The role of TSH/TSH receptor (TSHR) signaling in spatial learning and memory was further examined by behavior tests in Tshr(-/-) mice. Dendritic spine, synaptic density and structure of hippocampal CA1 pyramidal neurons were detected by Golgi’s method and electron microscopy. The mRNA and protein expression levels of learning and memory-related genes were assessed by RNA sequencing, real-time PCR, immunoblotting and immunofluorescence approaches. Results: Serum TSH level correlated negatively with cognitive impairment in the current population. Consistently, Tshr deletion in mice led to significantly compromised performance in hippocampus-dependent tasks, reduced dendritic spine density and excitatory synaptic density as well as altered synaptic structure in CA1 subfield of the hippocampus. Furthermore, the mRNA levels of learning and memory-related genes were altered, and protein levels of CREB-regulated genes were downregulated in the hippocampus of Tshr(-/-) mice. Conclusions: These findings reveal that TSH/TSHR signaling ablation impairs spatial learning and memory, indicating a decline in TSH level might contribute to the increased prevalence of cognitive impairment in subclinical hyperthyroidism patients. Oxford University Press 2020-05-08 /pmc/articles/PMC7208007/ http://dx.doi.org/10.1210/jendso/bvaa046.023 Text en © Endocrine Society 2020. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Neuroendocrinology and Pituitary
Luan, Sisi
Zhao, He
Zhao, Jiajun
SAT-285 TSH/TSHR Signaling Deficiency Impairs Spatial Learning and Memory
title SAT-285 TSH/TSHR Signaling Deficiency Impairs Spatial Learning and Memory
title_full SAT-285 TSH/TSHR Signaling Deficiency Impairs Spatial Learning and Memory
title_fullStr SAT-285 TSH/TSHR Signaling Deficiency Impairs Spatial Learning and Memory
title_full_unstemmed SAT-285 TSH/TSHR Signaling Deficiency Impairs Spatial Learning and Memory
title_short SAT-285 TSH/TSHR Signaling Deficiency Impairs Spatial Learning and Memory
title_sort sat-285 tsh/tshr signaling deficiency impairs spatial learning and memory
topic Neuroendocrinology and Pituitary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208007/
http://dx.doi.org/10.1210/jendso/bvaa046.023
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