实验性肝纤维化大鼠视黄醇和α-生育酚的含量

I. A. Kondratovich, Y. Novogrodskaya, V. Andreev, R. Kravchuk, A. Ostrovskaya, I. E. Gulyai, S. Shalesnaya, M. Kurbat, V. Tsyrkunov
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引用次数: 0

摘要

背景。人体内视黄醇和α-生育酚的含量影响慢性肝病的发生进展,并与肝周脂细胞(HSC)功能和生物膜状态有关。目的:探讨大鼠实验性肝纤维化过程中血浆和肝组织中视黄醇和α-生育酚含量的变化。材料和方法。性成熟雄性大鼠以200 mg / kg /隔日腹腔注射硫乙酰胺(TAA)溶液,连续4周和12周建立肝纤维化/肝硬化模型。对照组动物给予等量生理盐水。采用泰勒法测定α-生育酚和视黄醇的含量。结果。在大鼠肝脏制剂中,TAA溶液给予动物4周后,观察到FII-III期纤维化迹象。电镜观察,造血干细胞处于过渡状态,呈细长状;细胞质中脂质包涵体的数量减少。TAA给药12周导致大鼠肝硬化的形成,并出现特征性的宏观和微观变化。光镜下,TAA给药3个月后,大鼠肝脏制剂中hsc数量减少;遇到活化的hsc,其获得拉长的形状并失去脂质内含物。第二组(肝纤维化II-III期)动物的视黄醇含量是对照组的2.2倍,是肝硬化第三组的1.8倍(p < 0.05)。TAA给药4周后肝组织中视黄醇含量下降11.7%,12周后下降1.5倍。FII-III期肝脏α-生育酚水平较对照组下降21%,肝硬化期α-生育酚水平较对照组下降2倍。结论。大鼠使用硫代乙酰胺1和3个月可导致肝纤维化和肝硬化。随着肝纤维化/肝硬化的进展,肝脏中视黄醇和α-生育酚含量降低。肝纤维化FII-III期血浆中视黄醇和α-生育酚含量高是由于HSC的脱颗粒(活化)所致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
THE CONTENT OF RETINOL AND α-TOCOPHEROL IN EXPERIMENTAL LIVER FIBROSIS IN RATS
Background. The content of retinol and α-tocopherol in the human body affects the development and progression of chronic liver diseases and is associated with the functioning of perisinusoidal lipocytes (HSC) and the state of biological membranes. Objective – to evaluate the content of retinol and α-tocopherol in blood plasma and liver tissue in the dynamics of experimental liver fbrosis in rats. Material and methods. Modeling of liver fbrosis / cirrhosis was carried out on sexually mature male rats by intraperitoneal administration of thioacetamide (TAA) solution at a dose of 200 mg / kg every other day for 4 and 12 weeks. The control group of animals received an equal volume of saline. The concentration of α-tocopherol and retinol was determined by S.L. Taylor’s method. Results. In rat liver preparations, 4 weeks after administration of TAA solution to animals, signs of FII-III stage of fbrosis were observed. According to electron microscopy, HSCs were in a transitional state and acquired a more elongated shape; the number of lipid inclusions in their cytoplasm decreased. The administration of TAA for 12 weeks led to the formation of liver cirrhosis in rats, with characteristic macro- and microscopic changes. On light microscopy, the number of HSCs decreased in rat liver preparations 3 months after administration of TAA; activated HSCs were encountered, which acquired an elongated shape and lost lipid inclusions. The content of retinol in the 2nd group of animals (with liver fbrosis stage II-III) was 2.2 times higher than in the control group, and 1.8 times higher than in the 3rd group with liver cirrhosis (p < 0.05). The content of retinol in the liver tissue after 4 weeks of TAA administration decreased by 11.7%, after 12 weeks - by 1.5 times. The level of α-tocopherol in the liver at the stage of fbrosis FII-III decreased by 21% compared with the control group, at the stage of cirrhosis - by 2 times. Conclusion. The use of thioacetamide in rats for 1 and 3 months leads to the development of liver fbrosis and cirrhosis. A decrease in the content of retinol and α-tocopherol in the liver occurs with the progression of liver fbrosis /cirrhosis. The high content of retinol and α-tocopherol in plasma at the stage of liver fbrosis FII-III is due to degranulation (activation) of HSC.
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