慢性低动力大鼠心脏生化形态学变化的特点及肾上腺素损伤的发生。

Q3 Medicine
Olha V Denefil, Roman B Druzіuk, Volodymyr Ye Pelykh, Olena O Kulianda, Larysa Ya Fedoniuk, Zoya M Nebesna, Oleh B Yasinovskyi
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引用次数: 0

摘要

目的:探讨慢性低动力大鼠肾上腺素性心脏损伤(EHD)发生过程中心脏氧化过程状态及形态学变化。对象与方法:材料与方法:以雄性Wistar大鼠144只为实验对象。实验动物分为两组:1组为对照组,2组为低动力组。对于EHD,大鼠腹腔注射0.18%的水酒石酸肾上腺素溶液一次,剂量为0.5 mg/kg体重。对2.5 ~ 4.0月龄大鼠进行应激诱导。在1.5个月的时间里,这些动物一直被关在生活空间有限的笼子里。测定心脏中二烯和三烯偶联物(DC、TC)、希夫碱(SB)、tba活性产物(TBA-ap)、氧化修饰蛋白(OMP)、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)活性。用azan三色染色进行了形态学研究。所有研究均在肾上腺素注射后的对照、1、3、7、14和28天进行。结果:ⅰ组患者在EHD 1 d后DC和TC升高,3 d后降至对照值,14 d后呈波浪形(最高),SB降低,TBA-ap升高(14 d后最大)。1、3 d后OMP370升高,14 d后高于对照组,28 d后下降。除28 d外,其余各指标的OMP430均高于对照组。抗氧化酶活性在各时间点均低于对照组。低动力引起脂质过氧化增加和OMP降低。低动力导致CAT升高,SOD降低。SOD、CAT各项指标均高于II组动物EHD时抗氧化指标的升高水平。生化变化与形态学一致。注射肾上腺素后,观察到严重的血管病变,水肿,内皮细胞损伤,微循环障碍,周围组织出血,动、小静脉壁硬化。形态学研究证实II组有较高的扰动。结论:运动不足导致大鼠心脏脂质过氧化产物和过氧化氢酶活性升高,而氧化修饰蛋白含量和超氧化物歧化酶活性降低。肾上腺素注射引起脂质过氧化的激活,特别是次级形式,并且在氧化修饰的蛋白质含量中积累较少。在肾上腺素心脏损伤的发展过程中,慢性低动力动物的抗氧化剂活性明显升高。生化变化与形态学变化一致,表明ⅰ组动物在肾上腺素心脏损伤的发展过程中心肌受到了更大的损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The peculiarities of biochemical and morphological changes in the heart of the rats under chronic hypodynamia in the development of adrenalin damage of heart.

Objective: Aim: To evaluate the state of oxidation processes and morphological changes in the heart of rats with chronic hypodynamia during the development of epinephrine heart damage (EHD)..

Patients and methods: Materials and Methods: The study was performed on 144 white male Wistar rats. The animals were divided into two groups: 1 - control, 2 - hypodynamia. For EHD, rats were injected once intraperitoneally with a 0.18% solution of adrenaline hydrotartrate at the rate of 0.5 mg/kg of weight. Stress was induced in rats from 2.5 to 4.0 months of age. The animals were constantly kept in cages with limited living space for 1.5 months. The concentration of diene and triene conjugates (DC, TC), Schiff's bases (SB), TBA-active products (TBA-ap), oxidatively modified proteins (OMP), activity of superoxide dismutase (SOD) and catalase (CAT) were determined in the heart. A morphological study of preparations stained with Azan-trichrome was carried out. All studies were performed in control, 1, 3, 7, 14 and 28 days after adrenaline injection.

Results: Results: In the I series DC and TC increased after 1 day of EHD, fell to control values after 3 days, and then had wave-like character (highest - after 14 days), SB decreased, TBA-ap increase (maximal after 14 days). OMP370 increased after 1 and 3 days, after 14 days they were higher than in control, and after 28 days they decreased. OMP430 were greater than the control in all terms, except 28 days. The activity of antioxidant enzymes was lower than the control at all times. Hypodynamia caused an increase of lipid peroxidation and a decrease in OMP. Hypodynamia leads to increase of CAT, and decrase of SOD. All indicators of SOD and CAT exceeded hihger level of the antioxidant indicators of animals of the II group at EHD. Biochemical changes are consistent with morphological. After injection of epinephrine, severe vascular disorders, edema, endothelial cell damage, microcirculatory disorders, hemorrhages in the surrounding tissues, and sclerosing of the walls of arteries and venules were observed. Morphological studies established higher disturbances in the II group.

Conclusion: Conclusions: Hypodynamia in rats causes an increase of lipid peroxidation products and catalase activity in the heart, but a decrease in the content of oxidatively modified proteins and superoxide dismutase activity. Adrenaline injection causes activation of lipid peroxidation, especially secondary forms, and an less accumulation in the content of oxidatively modified proteins. During the development of epinephrine heart damage, the activity of antioxidants is significantly higher in animals with chronic hypodynamia. Biochemical changes are consistent with morphological changes, and indicate more damage to the myocardium in the process of development of epinephrine heart damage in animals of the I group.

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Polski Merkuriusz Lekarski
Polski Merkuriusz Lekarski Medicine-Medicine (all)
CiteScore
1.90
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