Naloxone potentiates the inotropic effect of circulating catecholamine
s in the isolated canine heart. The stereospecificity of this response
was evaluated with the aid of the less active (+)enantiomer of naloxo
ne. The more common (-)isomer of naloxone increased the contractile re
sponse to epinephrine only at the higher dose tested (4 mg). This eff
ect of naloxone was not observed at a tentold lower dose (0.4 mg), ind
icating a very narrow dose-response range. (+)Naloxone was effective a
t the lower dose and was, therefore, equal to or better than (-)naloxo
ne in potentiating the inotropic eff ect of epinephrine. When introduc
ed afterward, (-)naloxone did not add to the effect of (+)naloxone. Th
ese data suggest that naloxone modifies cellular responsiveness to cat
echolamines through a nontraditional opiate receptor, through a nonopi
ate receptor, or through a nonreceptor mechanism. (C) 1993 Wiley-Liss,
Inc.