Quinacrine resistance has been induced in 3 Giardia duodenalis laborat
ory stocks and 4 lines resistant to other drugs. The quinacrine-resist
ant lines were maintained in normally lethal levels of 5 mu M quinacri
ne and some lines are viable in 20 mu M levels of the drug. Fluorescen
ce studies indicated that quinacrine was taken up by sensitive cells b
ut was actively excluded from resistant trophozoites. The nuclei were
not a site of drug accumulation and no specific fluorescence in the tr
ophozoite could be attributed to any structure. Blebs of concentrated
drug appeared prior to disintegration of the membrane of drug-sensitiv
e trophozoites exposed to drug overnight. Parasite lines already resis
tant to furazolidone adapted more readily to quinacrine exposure than
drug-sensitive stocks. This multiple drug resistant phenotype was not
as marked with metronidazole-resistant lines.