Increased fibroblast growth factor-21 in chronic kidney disease is a trade-off between survival benefit and blood pressure dysregulation.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
17 12 2019
Historique:
received: 29 08 2019
accepted: 27 11 2019
entrez: 19 12 2019
pubmed: 19 12 2019
medline: 5 11 2020
Statut: epublish

Résumé

Circulating levels of fibroblast growth factor-21 (FGF21) start increasing in patients with chronic kidney disease (CKD) since early stages during the cause of disease progression. FGF21 is a liver-derived hormone that induces responses to stress through acting on hypothalamus to activate the sympathetic nervous system and the hypothalamus-pituitary-adrenal endocrine axis. However, roles that FGF21 plays in pathophysiology of CKD remains elusive. Here we show in mice that FGF21 is required to survive CKD but responsible for blood pressure dysregulation. When introduced with CKD, Fgf21

Identifiants

pubmed: 31848393
doi: 10.1038/s41598-019-55643-4
pii: 10.1038/s41598-019-55643-4
pmc: PMC6917750
doi:

Substances chimiques

fibroblast growth factor 21 0
Fibroblast Growth Factors 62031-54-3

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

19247

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Auteurs

Toshihiro Nakano (T)

Division of Anti-aging Medicine, Center for Molecular Medicine, Jichi Medical University, Tochigi, Japan.
Department of Medicine IV, Tokyo Women's Medical University, Tokyo, Japan.

Kazuhiro Shiizaki (K)

Division of Anti-aging Medicine, Center for Molecular Medicine, Jichi Medical University, Tochigi, Japan.

Yutaka Miura (Y)

Division of Anti-aging Medicine, Center for Molecular Medicine, Jichi Medical University, Tochigi, Japan.

Masahiro Matsui (M)

Graduate School of Comprehensive Human Sciences, University of Tsukuba, Ibaraki, Japan.

Keisei Kosaki (K)

Faculty of Sport Sciences, Waseda University, Saitama, Japan.
Faculty of Health and Sport Sciences, University of Tsukuba, Ibaraki, Japan.
Japan Society for the Promotion of Science, Tokyo, Japan.

Shoya Mori (S)

Graduate School of Comprehensive Human Sciences, University of Tsukuba, Ibaraki, Japan.

Kunihiro Yamagata (K)

Department of Nephrology, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan.

Seiji Maeda (S)

Faculty of Health and Sport Sciences, University of Tsukuba, Ibaraki, Japan.

Takuya Kishi (T)

Faculty of Health and Welfare Sciences in Fukuoka, International University of Health and Welfare, Fukuoka, Japan.

Naoki Usui (N)

Division of Brain and Neurophysiology, Department of Physiology, Jichi Medical University, Tochigi, Japan.

Masahide Yoshida (M)

Division of Brain and Neurophysiology, Department of Physiology, Jichi Medical University, Tochigi, Japan.

Tatsushi Onaka (T)

Division of Brain and Neurophysiology, Department of Physiology, Jichi Medical University, Tochigi, Japan.

Hiroaki Mizukami (H)

Division of Genetic Therapeutics, Center for Molecular Medicine, Jichi Medical University, Tochigi, Japan.

Ruri Kaneda (R)

Division of Anti-aging Medicine, Center for Molecular Medicine, Jichi Medical University, Tochigi, Japan.

Kazunori Karasawa (K)

Department of Medicine IV, Tokyo Women's Medical University, Tokyo, Japan.

Kosaku Nitta (K)

Department of Medicine IV, Tokyo Women's Medical University, Tokyo, Japan.

Hiroshi Kurosu (H)

Division of Anti-aging Medicine, Center for Molecular Medicine, Jichi Medical University, Tochigi, Japan.

Makoto Kuro-O (M)

Division of Anti-aging Medicine, Center for Molecular Medicine, Jichi Medical University, Tochigi, Japan. mkuroo@jichi.ac.jp.
Charles and Jane Pak Center for Mineral Metabolism and Clinical Research, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas, USA. mkuroo@jichi.ac.jp.
AMED-CREST, Japan Agency for Medical Research and Development, Tokyo, Japan. mkuroo@jichi.ac.jp.

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Classifications MeSH