© 1986 Oxford University Press
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Preliminary Toxicity Findings in Dogs and Rodents Given the Iron Chelator Ethylenediamine-N,N'-bis(2-hydroxyphenylacetic acid) (EDHPA)1
Department of Biochemical Pharmacology. EG & G Mason Research Institute Worcester, Massachusetts 01608
Preliminary Toxicity Findings in Dogs and Rodents Given the Iron Chelator Ethylenediamine N,N'-bis(2-hydroxyphenylacetic acid) (EDHPA). ROSENKRANTZ, H., METTERVILLE, J. J., AND FLEISCHMAN, R. W. (1986). Fundam. Appl. Toxicol 6, 292–298. Because of a projected pilot study with EDHPA in Cooley's anemia patients, animal studies with emphasis on reversibility of potential toxic signs were performed. Young dogs were treated iv with 6–18 mg/kg or orally with 30–240 mg/kg for 14 days followed by a 16-day recovery period. Drug-induced emesis, elevated BUN changes in kidney, spleen, and thymus weights diminished during recovery. One deceased dog exhibited nephrotoxicity consisting of tubular necrosis and deposition of the iron—EDHPA complex. The latter was observed in the excreta of survivors but kidney damage was not evident. Atrophy of the spleen and thymus in the deceased dog was consistent with less intense organ weight changes in recovered survivors. In the absence of morphologic changes after recovery, the precise effect on the immune system is unknown. The iv LD50 was 53 mg/kg for rats and mice. No rodent deaths occurred at an oral dose of 6000 mg/kg An elevated BUN and changes in kidney, spleen, and thymus weights were confirmed in rodents given iv doses of 5–20 mg/kg or oral doses of 150–600 mg/kg for 5 days. It is cautioned that during the use of EDHPA derivatives that the functions of the renal and immune systems be monitored.