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Transcriptomic responses of hypothalamus to acute exercise in type 2 diabetic Goto-Kakizaki rats

The hypothalamus has an integral role in energy homeostasis regulation, and its dysfunctions lead to the development of type 2 diabetes (T2D). Physical activity positively affects the prevention and treatment of T2D. However, there is not much information on the adaptive mechanisms of the hypothalam...

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Autores principales: Fu, Shuying, Meng, Yuhuan, Lin, Shudai, Zhang, Wenlu, He, Yuting, Huang, Lizhen, Du, Hongli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764357/
https://www.ncbi.nlm.nih.gov/pubmed/31579613
http://dx.doi.org/10.7717/peerj.7743
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author Fu, Shuying
Meng, Yuhuan
Lin, Shudai
Zhang, Wenlu
He, Yuting
Huang, Lizhen
Du, Hongli
author_facet Fu, Shuying
Meng, Yuhuan
Lin, Shudai
Zhang, Wenlu
He, Yuting
Huang, Lizhen
Du, Hongli
author_sort Fu, Shuying
collection PubMed
description The hypothalamus has an integral role in energy homeostasis regulation, and its dysfunctions lead to the development of type 2 diabetes (T2D). Physical activity positively affects the prevention and treatment of T2D. However, there is not much information on the adaptive mechanisms of the hypothalamus. In this study, RNA sequencing was used to determine how acute exercise affects hypothalamic transcriptome from both type 2 diabetic Goto-Kakizaki (GK) and control Wistar rats with or without a single session of running (15 m/min for 60 min). Through pairwise comparisons, we identified 957 differentially expressed genes (DEGs), of which 726, 197, and 98 genes were found between GK and Wistar, exercised GK and GK, and exercised Wistar and Wistar, respectively. The results of Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway enrichment revealed that lipid metabolism-related terms and pathways were enriched in GK and exercised GK rats, and nervous system related terms and pathways were enriched in exercised GK and Wistar rats. Furthermore, 45 DEGs were associated with T2D and related phenotypes according to the annotations in the Rat Genome Database. Among these 45 DEGs, several genes (Plin2, Cd36, Lpl, Wfs1, Cck) related to lipid metabolism or the nervous system are associated with the exercise-induced benefits in the hypothalamus of GK rats. Our findings might assist in identifying potential therapeutic targets for T2D prevention and treatment.
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spelling pubmed-67643572019-10-02 Transcriptomic responses of hypothalamus to acute exercise in type 2 diabetic Goto-Kakizaki rats Fu, Shuying Meng, Yuhuan Lin, Shudai Zhang, Wenlu He, Yuting Huang, Lizhen Du, Hongli PeerJ Genomics The hypothalamus has an integral role in energy homeostasis regulation, and its dysfunctions lead to the development of type 2 diabetes (T2D). Physical activity positively affects the prevention and treatment of T2D. However, there is not much information on the adaptive mechanisms of the hypothalamus. In this study, RNA sequencing was used to determine how acute exercise affects hypothalamic transcriptome from both type 2 diabetic Goto-Kakizaki (GK) and control Wistar rats with or without a single session of running (15 m/min for 60 min). Through pairwise comparisons, we identified 957 differentially expressed genes (DEGs), of which 726, 197, and 98 genes were found between GK and Wistar, exercised GK and GK, and exercised Wistar and Wistar, respectively. The results of Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway enrichment revealed that lipid metabolism-related terms and pathways were enriched in GK and exercised GK rats, and nervous system related terms and pathways were enriched in exercised GK and Wistar rats. Furthermore, 45 DEGs were associated with T2D and related phenotypes according to the annotations in the Rat Genome Database. Among these 45 DEGs, several genes (Plin2, Cd36, Lpl, Wfs1, Cck) related to lipid metabolism or the nervous system are associated with the exercise-induced benefits in the hypothalamus of GK rats. Our findings might assist in identifying potential therapeutic targets for T2D prevention and treatment. PeerJ Inc. 2019-09-24 /pmc/articles/PMC6764357/ /pubmed/31579613 http://dx.doi.org/10.7717/peerj.7743 Text en ©2019 Fu et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Genomics
Fu, Shuying
Meng, Yuhuan
Lin, Shudai
Zhang, Wenlu
He, Yuting
Huang, Lizhen
Du, Hongli
Transcriptomic responses of hypothalamus to acute exercise in type 2 diabetic Goto-Kakizaki rats
title Transcriptomic responses of hypothalamus to acute exercise in type 2 diabetic Goto-Kakizaki rats
title_full Transcriptomic responses of hypothalamus to acute exercise in type 2 diabetic Goto-Kakizaki rats
title_fullStr Transcriptomic responses of hypothalamus to acute exercise in type 2 diabetic Goto-Kakizaki rats
title_full_unstemmed Transcriptomic responses of hypothalamus to acute exercise in type 2 diabetic Goto-Kakizaki rats
title_short Transcriptomic responses of hypothalamus to acute exercise in type 2 diabetic Goto-Kakizaki rats
title_sort transcriptomic responses of hypothalamus to acute exercise in type 2 diabetic goto-kakizaki rats
topic Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764357/
https://www.ncbi.nlm.nih.gov/pubmed/31579613
http://dx.doi.org/10.7717/peerj.7743
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