Key result
Imatinib treatment in adult male rats resulted in a higher mean cardiac injury score (2.1 vs 0.6) and histological alterations including myofibrillar loss, necrosis, and mild fibrosis.
Why the study?
Conflicting results exist regarding imatinib-induced cardiac toxicity.
Does imatinib induce histopathological cardiotoxicity in adult male rats?
Does imatinib induce histopathological cardiotoxicity in adult male rats?
Absolute Event Rate: 2.1% vs 0.6%
Imatinib administration in adult male rats induces significant histopathological cardiac injury, including myofibrillar loss and necrosis, suggesting a potential for clinical cardiotoxicity.
Suggests possible human cardiotoxicity risk with imatinib; hypothesis-generating and requires clinical confirmation.
BACKGROUND: Cardiotoxicity is an unanticipated adverse effect associated with some chemotherapeutic agents. There are conflicting results about imatinib-induced cardiac toxicity. AIM: This study aims at investigating the possible cardiotoxic effects of imatinib in rat model through assessing the possible histopathological alterations that might develop. MATERIALS AND METHODS: This is a case–control and experimental study conducted over a period of 3 months at laboratory of postgraduate studies, Department of Anatomy, College of Medicine, University of Mosul, Mosul, Northern Iraq. Sixteen adult male Albino rats were randomly assigned to either “control group” or “imatinib-treated group.” The control group was gavaged with distilled water daily for 4 weeks while the second group was given oral imatinib (200 mg/kg/day) for the same duration. Animals were sacrificed by euthanization after 24 h of the last dose. Hearts were obtained and cardiac specimens were immersed in paraffin. Sections’ staining by hematoxylin (Harris)-eosin (H&E) and Massons’ Thrichrom. RESULTS: Rats treated with imatinib showed decreased physical activity and food intake. Regular arrangements of myofilaments were noticed during light microscopic examination of cardiac sections of control rats. However, sections from imatinib group showed several histological alterations (mainly myofibrillar loss in myocardium with vacuolated cytoplasm). Necrosis of cardiac muscle fibers was also noticed in some sections. Appearance of deeply staining cells with pyknotic nucleus, in addition to shrinkage of cardiac muscle fibers, was also noticed in some sections. The mean score of cardiac injury in the treated group was 2.1 (vs. 0.6 in controls). Some sections of treated group showed an increment (mild) in collagen fibers in-between cardiac myocytes. CONCLUSIONS: The observations concluded that imatinib has targeted action on cardiomyocytes. Oncologists should be cautious regarding imatinib dose and duration besides the close cardiac monitoring throughout and beyond therapy duration.
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Al-Allaf et al. (2023) studied Cardiotoxicity (n=16). Imatinib vs. Distilled water was evaluated on Total cardiac injury score. Imatinib treatment in adult male rats resulted in a higher mean cardiac injury score (2.1 vs 0.6) and histological alterations including myofibrillar loss, necrosis, and mild fibrosis.
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