Mitryayeva N A, Grebinyk L V, Uzlenkova N E
State Institution «Grigoriev Institute for medical Radiology NAMS of Ukraine», 82 Pushkinska St.,Kharkiv, 61024, Ukraine.
Probl Radiac Med Radiobiol. 2019 Dec;24:261-269. doi: 10.33145/2304-8336-2019-24-261-269.
The objective of this work was to study the effect of the combined action of X-radiation and the cyclooxygenase-2 (COX-2) inhibitor on the level of vascular endothelial growth factor (VEGF) and prostaglandin E2 (PGE-2) in blood serum of rat-tumor carriers at irradiation in different doses.
20 tumor-bearing rats of the Wistar population weighing 160-180 g, with transplanted Guerin carcinoma, fractionated irradiation (5 Gy + 5 Gy) and (0.5 Gy + 0.5 Gy) of the tumor growth zone on the RUM- 17 was carried out, with an interval between sessions of 24 hours. The drug «Meloxivet» - a selective inhibitor of cyclooxygenase-2 was administered 24 hours before irradiation and 2 hours before the second exposure (0.2 mg per 1 kg body weight). Blood sampling was performed by the method of life-time decapitation after 24 hours after the last fraction of irradiation. The content of VEGF in blood serum was determined by the method of enzyme immunoas- say using standardResults. After fractionated irradiation in a total dose of 1 Gy (0.5 Gy + 0.5 Gy), the level of VEGF was increased by 1.5 times compared with intact control, and in animals that were irradiated in a total dose of 10 Gy (5 Gy + 5 Gy ), the VEGF level was reduced by 1.92 times. That is, there was a difference in the content of VEGF in blood serum of rat tumor carriers, depending on the dose of irradiation: in a total dose of 1 Gy - stimulation of angiogenesis, and in the total dose of 10 Gy - a significant slowdown in this process. In the case of combined exposure to radiation (10 Gy) and the COX-2 inhibitor, meloxivet, the potential decrease in VEGF levels was 3.49 times compared to con- trol and 1.8 times with isolated exposure. At the same time, the level of PGE-2 also decreased with respect to iso- lated exposure by 1.5 times, indicating COX-2 inhibition. With a combined low dose (1 Gy) irradiation and COX-2- meloxivet inhibitor, VEGF levels were reduced by 1.1 times compared to control and 1.7 times relative to isolated exposure. At the same time, the level of PGE-2 also decreased in comparison with isolated radiation in 1,1 times. The obtained results indicate the influence of the combined act of irradiation and meloxivet on the level of VEGF and PGE-2, which causes the antiangiogenic effect.Сonclusions. It has been shown that low doses of ionizing radiation (1 Gy) and high doses (10 Gy) have a different effect on VEGF expression, and thus on angiogenesis processes. The combined effect of ionizing radiation and the COX-2 inhibitor (meloxivet) affects the level of PGE-2, VEGF, ie, the slowing of angiogenesis. In the case of large doses of exposure, this effect is even more expressed.
本研究旨在探讨不同剂量X射线辐射与环氧化酶-2(COX-2)抑制剂联合作用对荷瘤大鼠血清中血管内皮生长因子(VEGF)和前列腺素E2(PGE-2)水平的影响。
选取20只体重160 - 180 g的Wistar荷瘤大鼠,移植了格林癌,对肿瘤生长区域进行分次照射(5 Gy + 5 Gy)和(0.5 Gy + 0.5 Gy),照射在RUM - 17上进行,两次照射间隔24小时。在照射前24小时及第二次照射前2小时给予药物“美洛昔韦”(一种COX-2选择性抑制剂,每1 kg体重0.2 mg)。在最后一次照射分次后的24小时,采用断头取血法采集血液。血清中VEGF的含量采用酶联免疫吸附测定法测定。结果显示,在总剂量为1 Gy(0.5 Gy + 0.5 Gy)的分次照射后,VEGF水平相较于完整对照组升高了1.5倍;而在总剂量为10 Gy(5 Gy + 5 Gy)照射的动物中,VEGF水平降低了1.92倍。即荷瘤大鼠血清中VEGF的含量因照射剂量而异:总剂量为1 Gy时促进血管生成,总剂量为10 Gy时显著减缓这一过程。在联合暴露于辐射(10 Gy)和COX-2抑制剂美洛昔韦的情况下,VEGF水平相较于对照组潜在降低了3.49倍,相较于单独暴露降低了1.8倍。同时,PGE-2水平相较于单独暴露也降低了1.5倍,表明COX-2受到抑制。在低剂量(1 Gy)照射与COX-2抑制剂美洛昔韦联合作用时,VEGF水平相较于对照组降低了1.1倍,相较于单独暴露降低了1.7倍。同时,PGE-2水平相较于单独辐射也降低了1.1倍。所得结果表明照射与美洛昔韦的联合作用对VEGF和PGE-2水平有影响,从而产生抗血管生成作用。结论:已表明低剂量(1 Gy)和高剂量(10 Gy)的电离辐射对VEGF表达有不同影响,进而对血管生成过程产生不同影响。电离辐射与COX-2抑制剂(美洛昔韦)的联合作用影响PGE-2、VEGF水平,即减缓血管生成。在大剂量暴露情况下,这种作用更为明显。