Protective effects of boron on radiation-induced intestinal injury and associated microRNA changes.

IF 2.4
Yasin Korucu, Eren Cetin, Seda Ekici, Yasin Ozkabadayi
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Abstract

Purpose: Radiation-induced intestinal injury (RIII) remains a significant dose-limiting toxicity despite advances in radiotherapy techniques. Boron has been suggested to exert beneficial effects on intestinal structure and oxidative stress; however, its potential radioprotective effects have not been fully characterized. This study investigated the effects of boron on histological, immunohistochemical, and circulating miRNA changes in an experimental model of RIII.

Materials and methods: A single fraction of 8 Gy whole-body irradiation was delivered, and animals were evaluated on days 2 and 6 post-irradiation. Intestinal injury was assessed by histopathological scoring, villus height (VH), crypt-depth (CD), and VH/CD ratio. Immuno-histochemical expression of transforming growth factor beta 1 (TGF-β1) and matrix metalloproteinase-1 (MMP-1) was evaluated using H-score analysis. Circulating miRNA expression profiles were analyzed by quantitative real-time PCR using the 2-ΔΔCt method.

Results: Irradiation caused marked intestinal damage, particularly in the acute phase, characterized by villus shortening, crypt injury, and increased histopathological scores. Boron administration partially preserved intestinal architecture, with significant protection of VH and CD, especially at day 2. TGF-β1 and MMP-1 expression was reduced following irradiation but was partially preserved in boron-treated irradiated groups, particularly within the crypt compartment. Irradiation induced significant, time-dependent alterations in circulating miR-150-5p, miR-320a-5p, miR-30a-5p, and miR-200b-5p, while boron administration modulated these radiation-associated miRNA changes.

Conclusion: Boron mitigates RIII and is associated with partial preservation of epithelial structure, modulation of TGF-β1 and MMP-1 expression, and regulation of radiation-responsive circulating miRNAs. These findings support further investigation of boron-based approaches in intestinal radioprotection.

硼对辐射诱导肠道损伤的保护作用及相关的microRNA变化。
目的:尽管放射治疗技术有所进步,但辐射诱导的肠道损伤(RIII)仍然是一种显著的剂量限制性毒性。硼被认为对肠道结构和氧化应激有有益作用;然而,其潜在的辐射防护作用尚未得到充分的描述。本研究研究了硼对RIII实验模型的组织学、免疫组织化学和循环miRNA变化的影响。材料和方法:给予单次8 Gy的全身照射,并在照射后第2天和第6天对动物进行评价。采用组织病理学评分、绒毛高度(VH)、隐窝深度(CD)和VH/CD比值评估肠损伤。采用H-score法评价转化生长因子β1 (TGF-β1)和基质金属蛋白酶-1 (MMP-1)的免疫组化表达。采用2-ΔΔCt方法,实时荧光定量PCR分析循环miRNA表达谱。结果:辐照引起明显的肠道损伤,特别是在急性期,以绒毛缩短、隐窝损伤和组织病理学评分升高为特征。硼能部分保护肠道结构,对VH和CD有显著保护作用,尤其是在第2天。TGF-β1和MMP-1的表达在照射后降低,但在硼处理组中部分保留,特别是在隐窝腔内。辐照诱导了循环miR-150-5p、miR-320a-5p、miR-30a-5p和miR-200b-5p显著的时间依赖性改变,而硼处理调节了这些与辐射相关的miRNA变化。结论:硼可减轻RIII,并与部分保存上皮结构、调节TGF-β1和MMP-1表达以及调节辐射响应性循环mirna有关。这些发现支持进一步研究以硼为基础的肠道放射防护方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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