首页> 外文期刊>International Journal of Radiation Oncology, Biology, Physics >Prevention and treatment of functional and structural radiation injury in the rat heart by pentoxifylline and alpha-tocopherol.
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Prevention and treatment of functional and structural radiation injury in the rat heart by pentoxifylline and alpha-tocopherol.

机译:己酮可可碱和α-生育酚预防和治疗大鼠心脏的功能性和结构性放射损伤。

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PURPOSE: Radiation-induced heart disease (RIHD) is a severe side effect of thoracic radiotherapy. This study examined the effects of pentoxifylline (PTX) and alpha-tocopherol on cardiac injury in a rat model of RIHD. METHODS AND MATERIALS: Male Sprague-Dawley rats received fractionated local heart irradiation with a daily dose of 9 Gy for 5 days and were observed for 6 months after irradiation. Rats were treated with a combination of PTX, 100 mg/kg/day, and alpha-tocopherol (20 IU/kg/day) and received these compounds either from 1 week before until 6 months after irradiation or starting 3 months after irradiation, a time point at which histopathologic changes become apparent in our model of RIHD. RESULTS: Radiation-induced increases in left ventricular diastolic pressure (in mm Hg: 35 +/- 6 after sham-irradiation, 82 +/- 11 after irradiation) were significantly reduced by PTX and alpha-tocopherol (early treatment: 48 +/- 7; late treatment: 53 +/- 6). PTX and alpha-tocopherol significantly reduced deposition of collagen types I (radiation only: 3.5 +/- 0.2 mum(2) per 100 mum(2); early treatment: 2.7 +/- 0.8; late treatment: 2.2 +/- 0.2) and III (radiation only: 13.9 +/- 0.8; early treatment: 11.0 +/- 1.2; late treatment: 10.6 +/- 0.8). On the other hand, radiation-induced alterations in heart/body weight ratios, myocardial degeneration, left ventricular mast cell densities, and most echocardiographic parameters were not significantly altered by PTX and alpha-tocopherol. CONCLUSIONS: Treatment with PTX and alpha-tocopherol may have beneficial effects on radiation-induced myocardial fibrosis and left ventricular function, both when started before irradiation and when started later during the process of RIHD.
机译:目的:放射诱发性心脏病(RIHD)是胸腔放疗的严重副作用。这项研究检查了己酮可可碱(PTX)和α-生育酚对RIHD大鼠模型心脏损伤的影响。方法和材料:雄性Sprague-Dawley大鼠接受局部局部放射治疗,每天9 Gy剂量辐照5天,并在辐照后观察6个月。用PTX,100 mg / kg /天和α-生育酚(20 IU / kg /天)的组合对大鼠进行治疗,从照射前1周至照射后6个月或照射后3个月开始接受这些化合物,在我们的RIHD模型中组织病理学改变变得明显的时间点。结果:PTX和α-生育酚显着降低了辐射诱发的左心室舒张压增加(以毫米汞柱表示:假照射后为35 +/- 6,放射后为82 +/- 11)(早期治疗:48 + / -7;后期治疗:53 +/- 6)。 PTX和α-生育酚显着降低了I型胶原蛋白的沉积(仅放射:每100毫米(2)辐射3.5 +/- 0.2毫米(2);早期治疗:2.7 +/- 0.8;晚期治疗:2.2 +/- 0.2)和III(仅辐射:13.9 +/- 0.8;早期治疗:11.0 +/- 1.2;晚期治疗:10.6 +/- 0.8)。另一方面,PTX和α-生育酚并未明显改变辐射引起的心脏/体重比,心肌变性,左室肥大细胞密度和大多数超声心动图参数的改变。结论:无论是在放射线照射之前还是在RIHD过程的后期开始使用PTX和α-生育酚治疗都可能对辐射诱发的心肌纤维化和左心室功能产生有益的影响。

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