Naloxone is generally considered to be a pure antagonist, but it may produc
e several behavioral effects, such as hyperalgesia or stimulation of respir
ation. We studied the effect of naloxone on gastric emptying and gastrointe
stinal transit in rats. Six to eight Wistar rats (200 - 250 g) were used fo
r each experiment. Either saline or naloxone (0.01-10 mg/kg) was injected i
ntraperitoneally at 0 min. At 30 min, radiolabeled saline or milk 1 mi, was
infused into the stomach. At 60 min, gastric emptying and gastrointestinal
transit were calculated by measuring the radioactivity in the gastrointest
inal tract. Naloxone significantly inhibited gastric emptying of saline (P
= 0.002) and of milk (P < 0.05), but not the gastrointestinal transit of ei
ther (P > 0.05). Gastric emptying of saline showed a significant peak (P <
0.05) in the dose-response curve at 0.7 mg/kg. Therefore, naloxone signific
antly inhibits gastric emptying of saline and milk, but not the gastrointes
tinal transit of either. Implications: Although naloxone is generally consi
dered to be a pure opioid receptor antagonist, it delays gastric emptying o
f saline or milk, as does morphine in the rat. However, it is uncertain fro
m our results whether naloxone inhibited gastric emptying by antagonizing t
he effects of endogenous opioids.