Systemic treatment with a novel basic fibroblast growth factor mimic small-molecule compound boosts functional recovery after spinal cord injury.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 17 03 2020
accepted: 26 06 2020
entrez: 18 7 2020
pubmed: 18 7 2020
medline: 23 9 2020
Statut: epublish

Résumé

Neurotrophic factors have been regarded having promising potentials for neuronal protection and regeneration, and thus promoting beneficial effects of kinesiological functions. They can be suspected to play important roles in cell/tissue grafting for various neural diseases. The clinical applications of such trophic factors to the central nervous system (CNS), however, have caused problematic side effects on account of the distinctive bioactive properties. In the course of developing synthetic compounds reflecting beneficial properties of basic fibroblast growth factor (bFGF), we conducted screening candidates that stimulate to trigger the intracellular tyrosine phosphorylation of FGF receptor and lead to the subsequent intracellular signaling in neurons. A small synthetic molecule SUN13837 was characterized by mimicking the beneficial properties of bFGF, which have been known as its specific activities when applied to CNS. What is more remarkable is that SUN13837 is eliminated the bioactivity to induce cell proliferation of non-neuronal somatic cells. On the bases of studies of pharmacology, behavior, physiology and histology, the present study reports that SUN13837 is characterized as a promising synthetic compound for treatment of devastating damages onto the rat spinal cord.

Identifiants

pubmed: 32678832
doi: 10.1371/journal.pone.0236050
pii: PONE-D-20-07741
pmc: PMC7367485
doi:

Substances chimiques

Small Molecule Libraries 0
Fibroblast Growth Factor 2 103107-01-3

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0236050

Déclaration de conflit d'intérêts

The authors have read the journal's policy and the authors of this manuscript have the following competing interests: S.I., K.K., Y.Ma. and Y.Mo. received research funding from Asubio Pharma Co. Ltd. R.O., S.U., N.M., N.T., Y.S., T.K., S.T.,M.K. and T.I. are employed by Asubio Pharma Co., Ltd. N.M. and N.T. are inventors on a patent granted (“Nitrogenated aromatic 6-membered ring derivative, and pharmaceutical agent comprising the same” Publication of US9139559B2). This does not alter our adherence to PLOS ONE policies on sharing data and materials

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Auteurs

Shiro Imagama (S)

Department of Orthopaedic Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Ryoko Ogino (R)

Asubio Pharma Co., Ltd., Kobe, Japan.

Shinya Ueno (S)

Asubio Pharma Co., Ltd., Kobe, Japan.

Norihito Murayama (N)

Asubio Pharma Co., Ltd., Kobe, Japan.

Naohiro Takemoto (N)

Asubio Pharma Co., Ltd., Kobe, Japan.

Yoshiari Shimmyo (Y)

Asubio Pharma Co., Ltd., Kobe, Japan.

Taisuke Kadoshima (T)

Asubio Pharma Co., Ltd., Kobe, Japan.

Shigeki Tamura (S)

Asubio Pharma Co., Ltd., Kobe, Japan.

Mariko Kuroda (M)

Asubio Pharma Co., Ltd., Kobe, Japan.

Yukihiro Matsuyama (Y)

Department of Orthopaedic Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan.

Kenji Kadomatsu (K)

Department of Biochemistry, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Yasuhiro Morita (Y)

Faculty of Pharmacy, Laboratory of Physiology and Morphology, Yasuda Women's University, Hiroshima, Japan.

Teruyoshi Inoue (T)

Asubio Pharma Co., Ltd., Kobe, Japan.

Naoki Ishiguro (N)

Department of Orthopaedic Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

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