Why the study?
Does S-Allylcysteine reduce mortality and cardiotoxicity in mice treated with doxorubicin?
Population
Mice with severe doxorubicin toxicity induced by a single intraperitoneal injection (15 mg/kg body weight)
Comparison
S-Allylcysteine 30 mg/kg injected… vs Doxorubicin only (no SAC treatment)
Design
Preclinical
Follow-up
6 days after doxorubicin administration
Authors
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Hypothesis-generating for S-allylcysteine cardioprotection in mice; leaves open translation to human chemotherapy.
Does S-Allylcysteine reduce mortality and cardiotoxicity in mice treated with doxorubicin?
S-Allylcysteine attenuates doxorubicin-induced mortality, cardiotoxicity, and hepatotoxicity in a mouse model, suggesting potential as a protective agent during cancer chemotherapy.
Mostafa et al. (2000) studied this question.
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