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“The effect of DHEA was reversed by the selective sigma antagonist N-dipropyl-2-(4-methoxy-3- (2-phenylethoxy)phenyl)- ethylamine monohydrochloride (NE-100) and by haloperidol , but not by spiperone.”
The Journal of neuroscience : the official journal of the Society for Neuroscience • 1996 | View Paper
“The sigma antagonists haloperidol and 1-[2-(3,4-dichlorophenyl)-ethyl]-4-methylpiperazine, although inactive by themselves, completely prevented the effects of DHEA S , PREG S, and 1,3-di(2-tolyl)guanidine on NMDA-evoked [3H]NE release.”