Popazova Olena, Belenichev Igor, Yadlovskyi Oleh, Oksenych Valentyn, Kamyshnyi Aleksandr
Department of Histology, Cytology and Embryology, Zaporizhzhia State Medical and Pharmaceutical University, 69000 Zaporizhzhia, Ukraine.
Department of Pharmacology and Medical Formulation with Course of Normal Physiology, Zaporizhzhia State Medical and Pharmaceutical University, 69000 Zaporizhzhia, Ukraine.
Curr Issues Mol Biol. 2023 Oct 30;45(11):8704-8715. doi: 10.3390/cimb45110547.
Many children and adults who have suffered prenatal hypoxia at an early age develop many serious diseases. This disease is an actual problem of pediatric cardiology and little studied. The aim was to analyze the cardioprotective effect of L-arginine, Thiotriazoline, Angioline, and Mildronate on the cardiovascular system of rats after prenatal hypoxia. Methods: The experiments were carried out on 50 female white rats; intraperitoneal sodium nitrite solution was administered daily to pregnant female rats after 16 days at a dose of 50 mg/kg. Control pregnant rats received saline. The offspring were divided into groups: 1-intact; 2-the control group of rat pups after PH, treated daily with physiological saline; 3-six groups of rat pups after PH, treated daily from the 1st to the 30th day after birth. Heat shock protein HSP70 was determined by enzyme immunoassay, ST2 Nitrotyrosine, and eNOS was observed by ELISA. Results: Angiolin showed a high cardioprotective effect even a month after discontinuation of the drug, and after introduction, the highest decrease in ST2 nitrotyrosine was revealed. Thiotriazoline and L-arginine have an antioxidant effect and a positive effect on eNOS expression, increasing the concentration of HSP70. Mildronate increased the expression of eNOS and the concentration of HSP70 in the blood of experimental rats after a course of administration, but did not show an antioxidant effect and did not reduce the concentration of nitrotyrosine. The results obtained indicate the cardioprotective effect of modulators of the NO system with different mechanisms of action of drugs after prenatal hypoxia.
许多在幼年时遭受过产前缺氧的儿童和成人会患上许多严重疾病。这种疾病是小儿心脏病学的一个实际问题,且研究较少。目的是分析L-精氨酸、硫代三唑啉、血管生成素和米多君对产前缺氧后大鼠心血管系统的心脏保护作用。方法:对50只雌性白色大鼠进行实验;怀孕雌性大鼠在第16天后每天腹腔注射剂量为50mg/kg的亚硝酸钠溶液。对照怀孕大鼠接受生理盐水。后代分为几组:1-完整组;2-产前缺氧后大鼠幼崽的对照组,每天用生理盐水治疗;3-产前缺氧后大鼠幼崽的六组,在出生后第1天至第30天每天进行治疗。通过酶免疫测定法测定热休克蛋白HSP70,通过酶联免疫吸附测定法观察ST2硝基酪氨酸和内皮型一氧化氮合酶(eNOS)。结果:血管生成素即使在停药一个月后仍显示出高心脏保护作用,给药后ST2硝基酪氨酸的下降最为明显。硫代三唑啉和L-精氨酸具有抗氧化作用,并对eNOS表达有积极影响,增加HSP70的浓度。米多君在给药一个疗程后增加了实验大鼠血液中eNOS的表达和HSP70的浓度,但未显示出抗氧化作用,也未降低硝基酪氨酸的浓度。所得结果表明,产前缺氧后具有不同作用机制的一氧化氮系统调节剂具有心脏保护作用。