Caloglu Murat, Caloglu Vuslat Yurut, Yalta Tulin, Yalcin Omer, Uzal Cem
Department of Radiation Oncology, Trakya University, Edirne, Turkey.
J Cancer Res Ther. 2012 Apr-Jun;8(2):260-5. doi: 10.4103/0973-1482.98982.
The aim of the study was to compare the protective efficacy of l-carnitine (LC) to amifostine on radiation-induced acute small intestine damage.
Thirty, 4-week-old Wistar albino rats were randomly assigned to four groups - Group 1: control (CONT, n = 6), Group 2: irradiation alone (RT, n = 8), Group 3: amifostine plus irradiation (AMI+RT, n = 8), and Group 4: l-Carnitine plus irradiation (LC+RT, n = 8). The rats in all groups were irradiated individually with a single dose of 20 Gy to the total abdomen, except those in CONT. LC (300 mg/kg) or amifostine (200 mg/kg) was used 30 min before irradiation. Histopathological analysis of small intestine was carried out after euthanasia.
Pretreatment with amifostine reduced the radiation-induced acute degenerative damage (P = 0.009) compared to the RT group. Pretreatment with LC did not obtain any significant difference compared to the RT group. The vascular damage significantly reduced in both of the AMI+RT (P = 0.003) and LC+RT group (P = 0.029) compared to the RT group. The overall damage score was significantly lower in the AMI+RT group than the RT group (P = 0.009). There was not any significant difference between the LC+RT and RT group.
Amifostine has a marked radioprotective effect against all histopathological changes on small intestinal tissue while LC has limited effects which are mainly on vascular structure.
本研究旨在比较左旋肉碱(LC)与氨磷汀对辐射诱导的急性小肠损伤的保护效果。
30只4周龄的Wistar白化大鼠被随机分为四组——第1组:对照组(CONT,n = 6),第2组:单纯照射组(RT,n = 8),第3组:氨磷汀加照射组(AMI+RT,n = 8),第4组:左旋肉碱加照射组(LC+RT,n = 8)。除CONT组外,所有组的大鼠均接受单次20 Gy全腹部照射。在照射前30分钟使用LC(300 mg/kg)或氨磷汀(200 mg/kg)。安乐死后对小肠进行组织病理学分析。
与RT组相比,氨磷汀预处理可减轻辐射诱导的急性退行性损伤(P = 0.009)。与RT组相比,LC预处理未获得任何显著差异。与RT组相比,AMI+RT组(P = 0.003)和LC+RT组(P = 0.029)的血管损伤均显著减轻。AMI+RT组的总体损伤评分显著低于RT组(P = 0.009)。LC+RT组与RT组之间无显著差异。
氨磷汀对小肠组织的所有组织病理学变化均具有显著的辐射防护作用,而LC的作用有限,主要作用于血管结构。