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FGF21 ameliorates the neurocontrol of blood pressure in the high fructose-drinking rats

Fibroblast growth factor-21 (FGF21) is closely related to various metabolic and cardiovascular disorders. However, the direct targets and mechanisms linking FGF21 to blood pressure control and hypertension are still elusive. Here we demonstrated a novel regulatory function of FGF21 in the baroreflex...

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Autores principales: He, Jian-Li, Zhao, Miao, Xia, Jing-Jun, Guan, Jian, Liu, Yang, Wang, Lu-Qi, Song, Dong-Xue, Qu, Mei-Yu, Zuo, Meng, Wen, Xin, Yu, Xue, Huo, Rong, Pan, Zhen-Wei, Ban, Tao, Zhang, Yan, Zhu, Jiu-Xin, Shou, Weinian, Qiao, Guo-Fen, Li, Bai-Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937430/
https://www.ncbi.nlm.nih.gov/pubmed/27387420
http://dx.doi.org/10.1038/srep29582
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author He, Jian-Li
Zhao, Miao
Xia, Jing-Jun
Guan, Jian
Liu, Yang
Wang, Lu-Qi
Song, Dong-Xue
Qu, Mei-Yu
Zuo, Meng
Wen, Xin
Yu, Xue
Huo, Rong
Pan, Zhen-Wei
Ban, Tao
Zhang, Yan
Zhu, Jiu-Xin
Shou, Weinian
Qiao, Guo-Fen
Li, Bai-Yan
author_facet He, Jian-Li
Zhao, Miao
Xia, Jing-Jun
Guan, Jian
Liu, Yang
Wang, Lu-Qi
Song, Dong-Xue
Qu, Mei-Yu
Zuo, Meng
Wen, Xin
Yu, Xue
Huo, Rong
Pan, Zhen-Wei
Ban, Tao
Zhang, Yan
Zhu, Jiu-Xin
Shou, Weinian
Qiao, Guo-Fen
Li, Bai-Yan
author_sort He, Jian-Li
collection PubMed
description Fibroblast growth factor-21 (FGF21) is closely related to various metabolic and cardiovascular disorders. However, the direct targets and mechanisms linking FGF21 to blood pressure control and hypertension are still elusive. Here we demonstrated a novel regulatory function of FGF21 in the baroreflex afferent pathway (the nucleus tractus solitarii, NTS; nodose ganglion, NG). As the critical co-receptor of FGF21, β-klotho (klb) significantly expressed on the NTS and NG. Furthermore, we evaluated the beneficial effects of chronic intraperitoneal infusion of recombinant human FGF21 (rhFGF21) on the dysregulated systolic blood pressure, cardiac parameters, baroreflex sensitivity (BRS) and hyperinsulinemia in the high fructose-drinking (HFD) rats. The BRS up-regulation is associated with Akt-eNOS-NO signaling activation in the NTS and NG induced by acute intravenous rhFGF21 administration in HFD and control rats. Moreover, the expressions of FGF21 receptors were aberrantly down-regulated in HFD rats. In addition, the up-regulated peroxisome proliferator-activated receptor-γ and -α (PPAR-γ/-α) in the NTS and NG in HFD rats were markedly reversed by chronic rhFGF21 infusion. Our study extends the work of the FGF21 actions on the neurocontrol of blood pressure regulations through baroreflex afferent pathway in HFD rats.
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spelling pubmed-49374302016-07-13 FGF21 ameliorates the neurocontrol of blood pressure in the high fructose-drinking rats He, Jian-Li Zhao, Miao Xia, Jing-Jun Guan, Jian Liu, Yang Wang, Lu-Qi Song, Dong-Xue Qu, Mei-Yu Zuo, Meng Wen, Xin Yu, Xue Huo, Rong Pan, Zhen-Wei Ban, Tao Zhang, Yan Zhu, Jiu-Xin Shou, Weinian Qiao, Guo-Fen Li, Bai-Yan Sci Rep Article Fibroblast growth factor-21 (FGF21) is closely related to various metabolic and cardiovascular disorders. However, the direct targets and mechanisms linking FGF21 to blood pressure control and hypertension are still elusive. Here we demonstrated a novel regulatory function of FGF21 in the baroreflex afferent pathway (the nucleus tractus solitarii, NTS; nodose ganglion, NG). As the critical co-receptor of FGF21, β-klotho (klb) significantly expressed on the NTS and NG. Furthermore, we evaluated the beneficial effects of chronic intraperitoneal infusion of recombinant human FGF21 (rhFGF21) on the dysregulated systolic blood pressure, cardiac parameters, baroreflex sensitivity (BRS) and hyperinsulinemia in the high fructose-drinking (HFD) rats. The BRS up-regulation is associated with Akt-eNOS-NO signaling activation in the NTS and NG induced by acute intravenous rhFGF21 administration in HFD and control rats. Moreover, the expressions of FGF21 receptors were aberrantly down-regulated in HFD rats. In addition, the up-regulated peroxisome proliferator-activated receptor-γ and -α (PPAR-γ/-α) in the NTS and NG in HFD rats were markedly reversed by chronic rhFGF21 infusion. Our study extends the work of the FGF21 actions on the neurocontrol of blood pressure regulations through baroreflex afferent pathway in HFD rats. Nature Publishing Group 2016-07-08 /pmc/articles/PMC4937430/ /pubmed/27387420 http://dx.doi.org/10.1038/srep29582 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
He, Jian-Li
Zhao, Miao
Xia, Jing-Jun
Guan, Jian
Liu, Yang
Wang, Lu-Qi
Song, Dong-Xue
Qu, Mei-Yu
Zuo, Meng
Wen, Xin
Yu, Xue
Huo, Rong
Pan, Zhen-Wei
Ban, Tao
Zhang, Yan
Zhu, Jiu-Xin
Shou, Weinian
Qiao, Guo-Fen
Li, Bai-Yan
FGF21 ameliorates the neurocontrol of blood pressure in the high fructose-drinking rats
title FGF21 ameliorates the neurocontrol of blood pressure in the high fructose-drinking rats
title_full FGF21 ameliorates the neurocontrol of blood pressure in the high fructose-drinking rats
title_fullStr FGF21 ameliorates the neurocontrol of blood pressure in the high fructose-drinking rats
title_full_unstemmed FGF21 ameliorates the neurocontrol of blood pressure in the high fructose-drinking rats
title_short FGF21 ameliorates the neurocontrol of blood pressure in the high fructose-drinking rats
title_sort fgf21 ameliorates the neurocontrol of blood pressure in the high fructose-drinking rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937430/
https://www.ncbi.nlm.nih.gov/pubmed/27387420
http://dx.doi.org/10.1038/srep29582
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