The effect of narcotic analgesics on the uptake of 5‐hydroxytryptamine and (—)‐metaraminol by blood platelets

Abstract

1 The effects of narcotic analgesic and related drugs were studied on the uptake of 5-hydroxytryptamine (5-HT) and (—)-metaraminol by blood platelets. 2 The most potent drug in inhibiting the uptake of 5-HT (10 μm) by human platelets was methadone, followed by pentazocine>piminodine ˜ pethidine ˜ anileridine ˜ cyclazocine ˜ thebaine > dextropropoxyphene. Alphaprodine, papaverine, apomorphine, nalorphine, codeine, and morphine were almost without effect. Methadone was slightly less active than desipramine, and had 10% of the activity of imipramine under similar conditions. Naloxone did not antagonize the effect of methadone on 5-HT uptake. 3 The most potent inhibitor of metaraminol (3 μm) uptake by human platelets was piminodine, followed by pentazocine>anileridine>cyclazocine=methadone > dextropropoxyphene ˜ thebaine > papaverine ˜ alphaprodine >pethidine>morphine. The activity of morphine was 1% of that of piminodine. Piminodine was more potent than desipramine and protriptyline under similar conditions. The order of potency of drugs studied in inhibiting the uptake of metaraminol by rabbit platelets was similar to that obtained with human platelets. 4 The effects of the analgesics studied on inhibiting uptake of monoamines did not correlate with their pain-relieving properties.