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Wiley InterScience

Journal of Neurochemistry

Journal of Neurochemistry

Volume 64 Issue 5, Pages 1954 - 1964

Published Online: 23 Nov 2002

Journal compilation © 2010 International Society for Neurochemistry



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Evidence for Nerve Growth Factor-Potentiating Activities of the Nonpeptidic Compound SR 57746A in PC12 Cells
Anne Pradines, Marilyn Magazin, Pascal Schiltz, Gérard Le Fur, Daniel Caput, and Pascual Ferrara
  Sanofi Recherche, Labège, France
Address correspondence and reprint requests to Dr. P. Ferrara at Sanofi Recherche, Voie 1, Labège Innopole, B.P. 137, 31676 Labège Cédex, France.
Copyright Blackwell Science Inc
KEYWORDS
SR 57746A • Nerve growth factor • Neuritogenesis • F-actin redistribution • Phosphorylation • PC12 cells

ABSTRACT

Abstract: SR 57746A {1-[2-(naphth-2-yl)ethyl]-4-(3-trifluoromethylphenyl)-1,2,5,6-tetrahydropyridine hydrochloride} exhibits neurotrophic activities in vivo and in vitro. We used the rat pheochromocytoma PC12 cell line to investigate in vitro cellular changes induced by SR 57746A. A significant increase in the percentage of cells bearing neurite-like processes was obtained in cells treated by SR 57746A and nerve growth factor (NGF) compared with NGF treatment alone. SR 57746A added alone, however, had no effect on morphogenesis or on survival of cells in serum-free medium. In contrast, SR 57746A induced a "priming" effect on PC12 cells for neurite outgrowth within 6 h of addition of the protein tyrosine kinase inhibitor genistein. An increase in α-actinin content resulted from treatment with SR 57746A. Expression of NGF-mediated acetylcholinesterase and choline acetyltransferase was enhanced within 5 days by SR 57746A. The molecule also induced rapid F-actin redistribution. Within 2 min of incubation, outgrowth of F-actin-containing filopodia was clearly visible at the cell periphery, as previously shown with NGF. It is interesting that this effect of SR 57746A could be mimicked by protein tyrosine kinase inhibitors and abolished by preincubation with sodium orthovanadate, a protein tyrosine phosphatase inhibitor.


Received June 30, 1994; revised manuscript received October 19, 1994; accepted October 19, 1994.

DIGITAL OBJECT IDENTIFIER (DOI)
10.1046/j.1471-4159.1995.64051954.x About DOI

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