Comparison of the effectiveness of (±)-1,2-bis(3,5-dioxopiperazinyl-1-yl)propane (ICRF-187) and N-acetylcysteine in preventing chronic doxorubicin cardiotoxicity in beagles

• Published in: Cancer research (Chicago, Ill.) Vol. 45; no. 1; pp. 276 - 281
• Main Authors: HERMAN, E. H, FERRANS, V. J, VAN VLEET, J. F
• Format: Journal Article
• Language: English
• Published: Philadelphia, PA American Association for Cancer Research 1985
• Subjects: Acetylcysteine - pharmacology; Animals; Biological and medical sciences; Dogs; Doxorubicin - antagonists & inhibitors; Doxorubicin - toxicity; Drug toxicity and drugs side effects treatment; Female; Heart - drug effects; Heart Ventricles - pathology; Hematocrit; Hemoglobins - analysis; Leukocyte Count; Male; Medical sciences; Myocardium - pathology; Pharmacology. Drug treatments; Piperazines - pharmacology; Razoxane - pharmacology; Stereoisomerism; Toxicity: cardiovascular system; Antineoplastic agent; Heart; Fissipedia; Carnivora; Toxicity; Prevention; Vertebrata; Antibiotic; Mammalia; Animal; Racemate; Anthracyclins; Drug interaction; Dog
• ISSN: 0008-5472; 1538-7445

This investigation examined the potential of N-acetylcysteine (NAC) and ICRF-187, alone and in combination, to protect against chronic doxorubicin cardiotoxicity. Adult beagles of either sex (7.3 to 12.5 kg) were given doxorubicin (1.75 mg/kg i.v.) either alone or 30 min after either ICRF-187 (25 mg/kg i.p.), NAC (200 mg/kg i.p.), or ICRF-187 (25 mg/kg i.p.) and NAC (200 mg/kg i.p.) at 3-week intervals. Control dogs received ICRF-187 (25 mg/kg i.p.), NAC (200 mg/kg i.p.), ICRF-187 (25 mg/kg i.p.) and NAC (200 mg/kg i.p.), or 0.9% NaCl solution without doxorubicin. The experiment was terminated 3 weeks after the seventh injection (total doxorubicin dose, 12.25 mg/kg). Three animals pretreated with NAC and one pretreated with ICRF-187 before receiving doxorubicin died or were in poor condition and were killed before the end of the study. The frequency and extent of myocardial lesions (vacuolization and myofibrillar loss) were assessed on a scale of 0 to 4+. Such lesions were present in all six dogs given doxorubicin alone and were marked to severe (3+ to 4+) in five of these dogs and moderate (2+) in one. Lesions of comparable severity (2+ to 4+) were also apparent in the hearts of dogs given the combination of NAC and doxorubicin. In contrast, no abnormalities (lesion score 0) were found in the hearts of three of six dogs given doxorubicin and ICRF-187 and in four of six dogs given doxorubicin following the combination of ICRF-187 and NAC; the remaining animals in these two groups had minimal lesions. At the dosage regimen used in the present experiments, doxorubicin, NAC, or ICRF-187 alone or in combination did not cause alterations in lungs, liver, kidney, or small intestine. Decreases in WBC count, RBC count, and hemoglobin occurred in dogs given doxorubicin with or without the various pretreatments. Thus, pretreatment with ICRF-187 was effective and pretreatment with NAC was ineffective in reducing chronic doxorubicin cardiotoxicity.