Doxorubicin Therapy is Associated with Atherosclerotic Vascular Injury in Rats: Attenuating Role of Lutein, a Non-Provitamin-A Carotenoid
摘要
Lutein, a natural carotenoid with potent antioxidant and anti-inflammatory properties, has shown protective effects in various oxidative stress-related disorders. However, its potential to mitigate doxorubicin, an anthracycline chemotherapeutic agent known to induce atherosclerotic vascular injury, remains poorly understood. This study therefore investigated the protective role of lutein against doxorubicin-induced vascular injury in male Wistar rats.
MethodsAtherosclerotic vascular injury was induced by intraperitoneal administration of doxorubicin (15 mg/kg) for three consecutive days, followed by treatment with lutein (40 mg/kg) for 25 days. After day 28, animals were euthanized and aorta removed for biochemical and histological studies. Meanwhile, blood was collected and centrifuged for lipid profile.
ResultsDoxorubicin administration led to increased vascular oxidative stress, inflammation, apoptosis, hyperlipidemia, impaired vascular tone, and loss of endothelial integrity, hallmarks of atherosclerotic injury. Lutein treatment markedly ameliorated these effects by exerting antioxidant, anti-inflammatory, anti-apoptotic, and anti-atherogenic actions. Additionally, lutein enhanced cell adhesion and improved vascular tone, suggesting a role in promoting angiogenesis and endothelial recovery.
ConclusionLutein effectively attenuates doxorubicin-induced atherosclerotic vascular injury in male Wistar rats, likely through modulation of oxidative stress, inflammation, and endothelial repair mechanisms.