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A novel neurotrophic pyrimidine compound MS‐818 enhances neurotrophic effects of basic fibroblast growth factor
Author(s) -
Sanjo Nobuo,
Owada Kiyoshi,
Kobayashi Takayoshi,
Mizusawa Hidehiro,
Awaya Akira,
Michikawa Makoto
Publication year - 1998
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/(sici)1097-4547(19981201)54:5<604::aid-jnr5>3.0.co;2-w
Subject(s) - mapk/erk pathway , basic fibroblast growth factor , neurotrophic factors , neurite , neurotrophin , kinase , nerve growth factor , chemistry , fibroblast growth factor , growth factor , protein kinase a , brain derived neurotrophic factor , pharmacology , microbiology and biotechnology , biology , receptor , biochemistry , in vitro
MS‐818 (2‐piperadino‐6‐methyl‐5‐oxo‐5, 6‐dihydro (7H) pyrrolo [2,3‐d]pyrimidine maleate), a newly synthesized heterocyclic pyrimidine derivative, promotes neurite outgrowth in neuronal cell lines. The survival‐promoting effect of MS‐818 on cultured neurons isolated from mouse cortices was examined. MS‐818 promoted neuronal survival by inhibiting apoptosis in a dose‐dependent manner. MS‐818 treatment also activated mitogen‐activated protein kinase (MAPK) of the extracellular signal regulation kinase 2, as demonstrated by Western blot analysis. The MAPK activation level in the cultures treated with MS‐818 was almost equivalent to that in cultures treated with nerve growth factor but was less than that in cultures treated with epidermal growth factor and basic fibroblast growth factor (bFGF). MAPK was activated within 3 min after the addition of MS‐818, and its activity level returned to baseline within 120 min. Its activation was protein kinase C independent. We further investigated the effect of concurrent treatment with MS‐818 and bFGF on neuronal survival. MS‐818 enhanced the neuronal survival‐promoting effect of bFGF in shifting the half‐maximally effective dose from 2.1 ng/ml to 0.036 ng/ml in the sigmoidal dose effect of bFGF and permitted nearly maximum MAPK activation. The enhancement by MS‐818 of the neuronal survival‐promoting effect of bFGF was accompanied by sustained activation of MAPK to a degree that far exceeded, in magnitude and duration, the cooperative effect of MS‐818 and bFGF. These results indicate that MS‐818 promotes neuronal survival and enhances the neurotrophic actions of bFGF through stimulation of synchronous signals that may elevate MAPK levels within neurons. J. Neurosci. Res. 54:604–612, 1998. © 1998 Wiley‐Liss, Inc.