Key result
Halofuginone reduced radiation-induced endocardial thickening in rats at 16 weeks compared to radiotherapy alone.
Why the study?
Does halofuginone improve radiation-induced cardiovascular injury in a rat model?
Does halofuginone improve radiation-induced cardiovascular injury in a rat model?
In a rat model, halofuginone significantly ameliorated radiation-induced cardiovascular injury and fibrosis, particularly at a higher dose over long-term follow-up.
Answers are grounded in this paper and cite their sources.
Halofuginone may attenuate radiation-induced CV injury in rats; leaves open translation to clinical radiotherapy.
Purpose: The main purpose of this study was to evaluate the effects of Halofuginone on radiation-induced cardiovascular injury in a rat model. Methods : Sixty Wistar-Albino rats were divided into six groups (the control group, radiotherapy (RT) only group Irradiation (IR), 2.5 and 5 μg Halofuginone groups (Hal (2.5)/C and Hal (5.0)/C), and RT plus 2.5 and 5 μg Halofuginone groups (Hal (2.5)/IR and Hal (5.0)/IR). Rats were exposed to a single dose of 12 Gy irradiation generated by a linear accelerator. Halofuginone was applied intraperitoneally with daily doses. At the 6 th and 16 th weeks of RT, 5 rats from each group sacrificed and; heart and thoracic aorta tissues removed for both light microscopic and electron microscopic examinations. Results : Light microscopic examinations revealed that the endocardial thickness of all study groups was significantly different at 6 th and 16 th week of RT ( p < 0.001 for both). Pair-wise comparisons showed that the differences were significant in IR- Hal (2.5)/IR ( p < 0.001); IR-Hal (5.0)/IR ( p < 0.001); and Hal (2.5)/IR-Hal (5.0)/IR ( p = 0.001) at 16 th week of RT. There were significant differences within the study groups regarding to the thoracic aorta fibrosis scores only at 16 th week of RT ( p = 0.002). Electron microscopic examinations demonstrated that there were significant differences between all the groups with respect to heart mitochondria scores at both 6 th week and 16 th weeks of RT ( p < 0.001 for both). The differences between Hal (2.5)/IR and Hal (5.0)/IR with respect to the heart mitochondria scores were significant only at 16 th week of RT ( p = 0.001). Conclusion : These data demonstrated that Halofuginone may improve radiation-induced cardiovascular injury. The most prominent improvement was observed in higher dose of Halofuginone group after long term follow-up.
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Yavaş et al. (2015) studied Radiation-induced cardiovascular injury (n=60). Halofuginone vs. Radiotherapy alone was evaluated on Endocardial thickness at 16th week of RT (microns) (p=<0.001). Halofuginone reduced radiation-induced endocardial thickening in rats at 16 weeks compared to radiotherapy alone.
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