Aliyeva Olena, Belenichev Igor F, Bilai Ivan, Duiun Iryna, Makyeyeva Lyudmyla, Oksenych Valentyn, Kamyshnyi Oleksandr
Department of Histology, Cytology and Embryology, Zaporizhzhia State Medical and Pharmaceutical University, 69035 Zaporizhzhia, Ukraine.
Department of Pharmacology and Medical Formulation with Course of Normal Physiology, Zaporizhzhia State Medical and Pharmaceutical University, 69035 Zaporizhzhia, Ukraine.
Biomedicines. 2025 Apr 17;13(4):982. doi: 10.3390/biomedicines13040982.
Prenatal hypoxia (PH) is a leading cause of nervous system disorders in early childhood and subsequently leads to a decline in the cognitive and mnemonic functions of the central nervous system (such as memory impairment, reduced learning ability, and information processing). It also increases anxiety and the risk of brain disorders in adulthood. Compensatory-adaptive mechanisms of the mother-placenta-fetus system, which enhance the fetus's CNS resilience, are known, including the activation of endogenous neuroprotection in response to hypoxic brain injury through the pharmacological modulation of HSP. To evaluate the effect of HSP modulators-Cerebrocurin, Angiolin, Tamoxifen, Glutaredoxin, Thiotriazoline, and HSF-1 (heat shock factor 1 protein), as well as Mildronate and Mexidol-on the motor skills, exploratory behaviors, psycho-emotional activities, learning, and memories of offspring after PH. Experimental PH was induced by daily intraperitoneal injections of sodium nitrite solution into pregnant female rats from the 16th to the 21st day of pregnancy at a dose of 50 mg/kg. The newborns received intraperitoneal injections of Angiolin (50 mg/kg), Thiotriazoline (50 mg/kg), Mexidol (100 mg/kg), Cerebrocurin (150 µL/kg), L-arginine (200 mg/kg), Glutaredoxin (200 µg/kg), HSF-1 (50 mg/kg), or Mildronate (50 mg/kg) for 30 days. At 1 month, the rats were tested in the open field test, and at 2 months, they were trained and tested for working and spatial memory in the radial maze. Modeling PH led to persistent impairments in exploratory activity, psycho-emotional behavior, and a decrease in the cognitive-mnestic functions of the CNS. It was found that Angiolin and Cerebrocurin had the most pronounced effects on the indicators of exploratory activity and psycho-emotional status in 1-month-old animals after PH. They also exhibited the most significant cognitive-enhancing and memory-supporting effects during the training and evaluation of skill retention in the maze in 2-month-old offspring after PH. for the first time, we obtained experimental data on the effects of HSP modulators on exploratory activity, psycho-emotional behavior, and cognitive-mnestic functions of the central nervous system in offspring following intrauterine hypoxia. Based on the results of this study, we identified the pharmacological agents Angiolin and Cerebrocurin as promising neuroprotective agents after perinatal hypoxia.
产前缺氧(PH)是幼儿期神经系统疾病的主要原因,随后会导致中枢神经系统的认知和记忆功能下降(如记忆障碍、学习能力降低和信息处理能力下降)。它还会增加成年后患焦虑症和脑部疾病的风险。已知母-胎-胎盘系统的代偿适应机制可增强胎儿中枢神经系统的恢复力,包括通过对热休克蛋白(HSP)进行药理调节来激活内源性神经保护,以应对缺氧性脑损伤。为了评估HSP调节剂——脑苷肌肽、血管生成素、他莫昔芬、谷氧还蛋白、硫代三唑啉和热休克因子1蛋白(HSF-1),以及米屈肼和甲磺酸倍他司汀——对产前缺氧后代的运动技能、探索行为、心理情绪活动、学习和记忆的影响。通过从怀孕第16天到第21天每天给怀孕的雌性大鼠腹腔注射剂量为50 mg/kg的亚硝酸钠溶液来诱导实验性产前缺氧。新生大鼠腹腔注射血管生成素(50 mg/kg)、硫代三唑啉(50 mg/kg)、甲磺酸倍他司汀(100 mg/kg)、脑苷肌肽(150 μL/kg)、L-精氨酸(200 mg/kg)、谷氧还蛋白(200 μg/kg)、HSF-1(50 mg/kg)或米屈肼(50 mg/kg),持续30天。在1个月时,对大鼠进行旷场试验测试,在2个月时,对它们进行放射状迷宫工作记忆和空间记忆的训练和测试。产前缺氧模型导致探索活动、心理情绪行为持续受损,以及中枢神经系统的认知记忆功能下降。研究发现,血管生成素和脑苷肌肽对产前缺氧后1个月大动物的探索活动指标和心理情绪状态影响最为显著。在对产前缺氧后2个月大的后代进行迷宫技能保持训练和评估期间,它们还表现出最显著的认知增强和记忆支持作用。我们首次获得了关于HSP调节剂对子宫内缺氧后代中枢神经系统的探索活动、心理情绪行为和认知记忆功能影响的实验数据。基于这项研究的结果,我们确定血管生成素和脑苷肌肽这两种药物是围产期缺氧后有前景的神经保护剂。