Effect of hyperhomocysteinemia on proteolytic activity in the spleen

IF 1 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
N. Raksha, O. Kostyuk, T. Synelnyk, O. Kharchenko, Serhii Shchypanskyi, I. Gunas, O. Nazarova, A. Gritsenko, T. Andriichuk, O. Maievskyi
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Abstract

Background: The aim of the study was to investigate the effect of hyperhomocysteinemia (HC) on proteolytic activity in the spleen of rats. Methods: Albino nonlinear male rats of different ages (young, adults, and old) were involved in the study. HC was induced by intragastric administration of DL-homocysteine thiolactone. The total proteolytic activity was evaluated using casein as a substrate. The activity of metal-dependent and serine proteases was determined using proteases inhibitors ethylenediaminetetraacetic acid and phenylmethylsulfonyl. The levels of matrix metalloproteinases (MMPs), tissue inhibitors of metalloproteinases (TIMPs), and cytokines were measured by enzyme-linked immunosorbent assay. The fraction of serine proteases was isolated by affinity chromatography. Results: HC causes an increase in the total proteolytic activity, which is due to an increase in the activity of proteases of various catalytic types (serine, cysteine, aspartic proteases, and metal-dependent enzymes). The levels of MMP-2, MMP-3, MMP-8, and MMP-10 were significantly reduced in the spleen of adult and old rats and were at the control level in young rats. A disorder of the balance between MMP-1 and TIMP-1 in the spleen of rats with HC in favor of the active form of MMP-1 was revealed. At the same time, the level of serine proteases was increased in the spleen of rats of all groups. A decrease in the level of some pro-inflammatory cytokines was also revealed. Conclusions: HC causes disturbances in the proteolytic balance, manifested by an increase in proteolytic activity. The pathogenesis of this disease is not associated with the development of inflammation in the spleen.
高同型半胱氨酸血症对脾脏蛋白水解活性的影响
背景:本研究旨在探讨高同型半胱氨酸血症(HC)对大鼠脾脏蛋白水解活性的影响。方法:采用不同年龄的白化非线性雄性大鼠(青年、成年、老年)为研究对象。通过灌胃dl -同型半胱氨酸硫内酯诱导HC。以酪蛋白为底物评价总蛋白水解活性。用蛋白酶抑制剂乙二胺四乙酸和苯基甲基磺酰基测定金属依赖性蛋白酶和丝氨酸蛋白酶的活性。采用酶联免疫吸附法测定基质金属蛋白酶(MMPs)、组织金属蛋白酶抑制剂(TIMPs)和细胞因子水平。亲和层析法分离丝氨酸蛋白酶。结果:HC引起总蛋白水解活性的增加,这是由于各种催化类型的蛋白酶(丝氨酸、半胱氨酸、天冬氨酸蛋白酶和金属依赖性酶)的活性增加。成年大鼠和老年大鼠脾脏中MMP-2、MMP-3、MMP-8、MMP-10水平均显著降低,幼龄大鼠脾脏中MMP-2、MMP-3、MMP-8、MMP-10水平与对照水平持平。HC大鼠脾脏中MMP-1和TIMP-1之间的平衡紊乱,有利于MMP-1的活性形式。同时,各组大鼠脾脏丝氨酸蛋白酶水平均升高。一些促炎细胞因子的水平也有所下降。结论:HC引起蛋白水解平衡紊乱,表现为蛋白水解活性增加。本病的发病机制与脾炎的发展无关。
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来源期刊
Biomedical and Biotechnology Research Journal
Biomedical and Biotechnology Research Journal Biochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
2.20
自引率
42.90%
发文量
24
审稿时长
11 weeks
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