Key result
Lycopene-Cub-NPs mitigate cisplatin-induced cardiotoxicity in rats, cutting serum LDH by ~57%.
Why the study?
To explore the novel application of a lycopene nanoformulation to reduce cisplatin-induced cardiotoxicity and determine the underlying cardioprotective mechanisms.
Does Lycopene-Cub-NPs prevent cisplatin-induced cardiotoxicity in a rat model?
Population
Rats
Comparison
Lycopene-Cub-NPs + Cis vs Lycopene Free + Cis, Cis alone, and control groups
Design
Animal study with seven allocated groups
Authors
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Hypothesis-generating in rat cardiotoxicity models; leaves open translation to cisplatin-treated patients.
Does Lycopene-Cub-NPs prevent cisplatin-induced cardiotoxicity in a rat model?
Effect estimate: 57.36% reduction
p-value: p=<0.05
Lycopene cubosomal nanoparticles mitigate cisplatin-induced cardiotoxicity in rats more effectively than free lycopene via antioxidant, anti-inflammatory, and anti-apoptotic pathways.
Alotaibi et al. (2025) studied Cisplatin-induced cardiotoxicity (n=42). Lycopene-Cub-NPs vs. Cisplatin alone was evaluated on Serum LDH level (57.36% reduction, p=<0.05). Lycopene-Cub-NPs mitigated cisplatin-induced cardiotoxicity in rats by significantly reducing serum LDH and CK-MB levels by 57.36% and 62.49%, respectively, compared to cisplatin alone.
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