Key result
Farnesol treatment reduced doxorubicin-induced cardiac injuries in rats by reversing oxidative stress, proinflammatory and proapoptotic markers, and histopathological aberrations.
Why the study?
Doxorubicin-induced cardiotoxicity limits its clinical use, prompting investigation into the potential cardioprotective effects of farnesol.
Does Farnesol prevent doxorubicin-induced cardiotoxicity in male Wistar rats?
Does Farnesol prevent doxorubicin-induced cardiotoxicity in male Wistar rats?
Farnesol demonstrates cardioprotective effects against doxorubicin-induced cardiotoxicity in a rat model by reducing oxidative stress, inflammation, and apoptosis.
Farnesol attenuates doxorubicin cardiotoxicity in rats; hypothesis-generating only, with clinical translation untested.
Doxorubicin (DOXO) is an antineoplastic drug that is used extensively in managing multiple cancer types. However, DOXO-induced cardiotoxicity is a limiting factor for its widespread use and considerably affects patients’ quality of life. Farnesol (FSN) is a sesquiterpene with antioxidant, anti-inflammatory, and anti-tumor properties. Thus, the current study explored the cardioprotective effect of FSN against DOXO-induced cardiotoxicity. In this study, male Wistar rats were randomly divided into five groups (n = 7) and treated for 14 days. Group I (Control): normal saline, p.o. daily for 14 days; Group II (TOXIC): DOXO 2.4 mg/kg, i.p, thrice weekly for 14 days; Group III: FSN 100 mg/kg, p.o. daily for 14 days + DOXO similar to Group II; Group IV: FSN 200 mg/kg, p.o. daily for 14 days + DOXO similar to Group II; Group V (Standard): nifedipine 10 mg/kg, p.o. daily for 14 days + DOXO similar to Group II. At the end of the study, animals were weighed, blood was collected, and heart-weight was measured. The cardiac tissue was used to estimate biochemical markers and for histopathological studies. The observed results revealed that the FSN-treated group rats showed decrease in heart weight and heart weight/body weight ratio, reversed the oxidative stress, cardiac-specific injury markers, proinflammatory and proapoptotic markers and histopathological aberrations towards normal, and showed cardioprotection. In summary, the FSN reduces cardiac injuries caused by DOXO via its antioxidant, anti-inflammatory, and anti-apoptotic potential. However, more detailed mechanism-based studies are needed to bring this drug into clinical use.
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Alkhanjaf et al. (2022) studied Doxorubicin-induced cardiotoxicity (n=35). Farnesol vs. Doxorubicin alone or normal saline was evaluated on Cardiac injuries (heart weight, oxidative stress, injury markers, histopathological aberrations). Farnesol treatment reduced doxorubicin-induced cardiac injuries in rats by reversing oxidative stress, proinflammatory and proapoptotic markers, and histopathological aberrations.
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