Characteristics of proliferation and apoptosis of hepatocytes after administration of ascorbic acid in a model of radiation hepatitis

Morphology Pub Date : 2024-03-25 DOI:10.17816/morph.624714
G. Demyashkin, D. Atyakshin, Vladislav A. Yakimenko, Dali Ugurchieva, M. Vadyukhin, Alikhan Abuev
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Abstract

BACKGROUND: Radiation hepatitis with the development of radiation-induced acute liver failure is considered one of the most serious complications of radiotherapy for malignant neoplasms of the liver, abdominal organs, or whole body irradiation. However, the exact mechanisms of radiation-induced liver cell death have not been fully elucidated, and therefore the study of changes in the proliferative-apoptotic ratio in liver structures remains relevant, and pre-irradiation administration of ascorbic acid can potentially protect them from the effects of electron irradiation. AIM: assessment of proliferation and apoptosis of hepatocytes after administration of ascorbic acid in a model of radiation hepatitis. METHODS: Wistar rats (Rattus Wistar; n=40) were divided into four experimental groups: I – control (n=10); II (n=10) – fractional irradiation with electrons in a total irradiation dose of 30 Gy; III (n=10) – administration of ascorbic acid before electron irradiation; IV (n=10) – administration of ascorbic acid. Animals of all groups (I – IV) were removed from the experiment a week after the last fraction. Morphological and immunohistochemical (with antibodies to Ki-67 and caspase-3) studies were carried out. RESULTS: A week after electron irradiation, a sharp decrease in the proportion of Ki-67-positive hepatocytes in combination with an increase in immunolabeling with antibodies to caspase-3 was observed in group II. During the administration of ascorbic acid in group III, less pronounced depth and range of liver damage was noted, confirmed by morphological and immunohistochemical methods (less pronounced decrease in the level of Ki-67 expression and an increase in the proportion of caspase-positive hepatocytes compared to the control) methods. CONCLUSION: An immunohistochemical study of proliferation and apoptosis of hepatocytes revealed that a week after fractional electron irradiation in SOD 30 Gy, there is a decrease in mitotic activity and an increase in cell death, and pre-irradiation administration of ascorbic acid helped level out the detected changes, which indicates its protective effect.
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在放射性肝炎模型中服用抗坏血酸后肝细胞增殖和凋亡的特点
背景:肝脏、腹部器官恶性肿瘤放疗或全身照射引起的放射性肝炎是最严重的并发症之一。然而,辐射诱导肝细胞死亡的确切机制尚未完全阐明,因此,研究肝脏结构中增殖-凋亡比率的变化仍具有现实意义,辐照前服用抗坏血酸有可能使其免受电子辐照的影响。目的:在放射性肝炎模型中评估服用抗坏血酸后肝细胞的增殖和凋亡情况。方法:将 Wistar 大鼠(Rattus Wistar;n=40)分为四个实验组:I组--对照组(n=10);II组(n=10)--用电子进行部分辐照,总辐照剂量为30 Gy;III组(n=10)--在电子辐照前服用抗坏血酸;IV组(n=10)--服用抗坏血酸。所有组别(I - IV)的动物在最后一部分照射一周后退出实验。进行形态学和免疫组化(Ki-67和Caspase-3抗体)研究。结果:电子辐照一周后,观察到第二组中 Ki-67 阳性肝细胞的比例急剧下降,同时 Caspase-3 抗体的免疫标记增加。通过形态学和免疫组化方法(与对照组相比,Ki-67 表达水平下降不明显,而 Caspase 阳性肝细胞比例增加)证实,第三组在服用抗坏血酸期间,肝损伤的深度和范围较小。结论:对肝细胞增殖和凋亡的免疫组化研究表明,在 SOD 30 Gy 分次电子辐照一周后,有丝分裂活性下降,细胞死亡增加,而辐照前服用抗坏血酸有助于平复检测到的变化,这表明抗坏血酸具有保护作用。
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