Search Results

You are looking at 1 - 1 of 1 items for

  • Author or Editor: J. Roger Easley x
  • Refine by Access: All Content x
Clear All Modify Search


During earlier investigations of the hepatic effects in dogs of long-term administration of phenytoin alone or in combination with primidone, erythrocytic macrocytosis, neutropenia, neutrophilic hypersegmentation, and thrombocytopenia were observed. Such abnormalities were observed most often in dogs given phenytoin and resembled those known to be attributable to folate deficiency in human beings with epilepsy treated with phenytoin. To pursue the theory that these hematologic aberrations were caused by drug-induced folate deficiency, 12 dogs were given a diet specifically formulated to contain a minimally adequate concentration of folate. After 2 weeks, phenytoin was administered daily (400 mg, po, q 8 h) to 8 of the 12 dogs for 54 weeks. A cbc, bone marrow aspiration biopsy, and measurement of plasma and rbc folate concentrations were done every 3 weeks. Bone marrow aspirates were examined by transmission electron microscopy after 24 and 36 weeks, and at the end of the treatment period. Hepatic folate concentration was also determined in all dogs before and after treatment. Excretion of formiminoglutamic acid, as a marker of folate deficiency, was measured in all dogs at the end of the study.

All dogs remained healthy throughout the treatment phase. Consistent abnormalities were not observed in the blood or bone marrow of treated dogs. Plasma and RBC folate concentrations decreased in control and treated dogs as a result of dietary restriction (P < 0.02), and remained stable until the end of the study. The rbc folate content decreased further in treated dogs (P < 0.02), although the hepatic folate content was similar in control and treated dogs. Treated dogs did not excrete formiminoglutamic acid more rapidly than did control dogs. Gross necropsy or histologic abnormalities were not identified in control or treated dogs. We concluded that long-term administration of phenytoin was not associated with clinical, hematologic, or biochemical evidence of folate deficiency in dogs.

Free access
in American Journal of Veterinary Research