Kaplan Metin, Kılınç Ahmet, Ozturk Sait, Ilhan Nevin, Gurocak Simay, Gonen Murat
Department of Neurosurgery, Firat University, Elazig, Turkey.
Department of Biochemistry, Firat University, Elazig, Turkey.
Asian J Neurosurg. 2017 Apr-Jun;12(2):185-188. doi: 10.4103/1793-5482.145575.
Radiotherapy causes injury in the endothelial cells of blood vessels and the production of vasoactive amines such as endothelin-1 (ET-1). ET-1 is an important peptide in cancer development. In this study, the effects of radiation on brain tissue ET-1 level were evaluated. Is it possible to suggest a mechanism using ET-1 level in the production of this adverse effect? In this paper, the relationship between the development of brain tumors and the ET-1 level has been discussed.
Twenty-eight adult Sprague Dawley rats were used in the experiments. The rats were divided into four groups ( = 7) as follows: control group: radiation was not applied during the experiment; Group 1: Decapitated on the 1 day following radiation; Group 2: Decapitated on the 7 day following radiation; and Group 3: Decapitated on the 30 day following radiation. ET-1 levels were measured with enzyme-linked immunosorbent assay (ELISA) method. The -test, variance analysis, and Tukey honestly significant difference (HSD) tests were used in the statistical analysis. A value of < 0.05 was accepted as significant.
No statistical differences were observed in the tissue ET-1 levels between the control group and other groups. According to the variance analysis and Tukey test, the differences between the groups were not significant.
We observed in this study that the effects of radiation on brain tumor development or malignant transformation are not mediated by ET-1 levels. In addition, these results support the hypothesis of the fact that medical treatment with ET-1 antagonists in clinical cases receiving radiotheraphy is unnecessary.
放射治疗会导致血管内皮细胞损伤,并产生诸如内皮素 -1(ET-1)等血管活性胺。ET-1是癌症发展过程中的一种重要肽类。在本研究中,评估了辐射对脑组织ET-1水平的影响。是否有可能利用ET-1水平来提示产生这种不良反应的机制呢?本文讨论了脑肿瘤发展与ET-1水平之间的关系。
实验使用了28只成年Sprague Dawley大鼠。将大鼠分为四组(每组n = 7)如下:对照组:实验期间未进行放射治疗;第1组:放射治疗后第1天断头处死;第2组:放射治疗后第7天断头处死;第3组:放射治疗后第30天断头处死。采用酶联免疫吸附测定(ELISA)法测量ET-1水平。统计分析采用t检验、方差分析和Tukey真实显著差异(HSD)检验。P < 0.05的值被认为具有显著性。
对照组与其他组之间的组织ET-1水平未观察到统计学差异。根据方差分析和Tukey检验,各组之间的差异不显著。
我们在本研究中观察到,辐射对脑肿瘤发展或恶性转化的影响并非由ET-1水平介导。此外,这些结果支持了在接受放射治疗的临床病例中使用ET-1拮抗剂进行医学治疗没有必要这一假设。