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Published on: September 30, 2011
HSP70 Modulators for the Correction of Cognitive, Mnemonic, and Behavioral Disorders After Prenatal Hypoxia
Olena Aliyeva1, Igor F Belenichev2, Ivan Bilai3
1Department of Histology, Cytology and Embryology, Zaporizhzhia State Medical and Pharmaceutical University, 69035 Zaporizhzhia, Ukraine.
Insights
Prenatal hypoxia impairs offspring
Area of Science:
- Neuroscience
- Pharmacology
- Developmental Biology
Background:
- Prenatal hypoxia (PH) is a significant cause of early childhood nervous system disorders.
- PH can lead to cognitive deficits, memory impairment, and increased anxiety.
- The mother-placenta-fetus system has compensatory mechanisms, including endogenous neuroprotection via HSP70 modulation.
Purpose of the Study:
- To evaluate the effects of HSP70 modulators on offspring exposed to PH.
- To assess the impact on motor skills, behavior, learning, and memory.
- To identify potential neuroprotective agents for perinatal hypoxia.
Main Methods:
- Experimental prenatal hypoxia induced in pregnant rats using sodium nitrite.
- Offspring treated with various HSP70 modulators (Angiolin, Cerebrocurin, etc.).
- Behavioral and cognitive assessments including open field test and radial maze at 1 and 2 months.
Main Results:
- PH induced lasting impairments in exploratory activity, behavior, and cognitive functions.
- Angiolin and Cerebrocurin showed the most significant positive effects on behavior and cognition.
- These agents demonstrated notable cognitive-enhancing and memory-supporting effects in offspring.
Conclusions:
- First experimental data on HSP70 modulators' effects on offspring CNS functions post-intrauterine hypoxia.
- Angiolin and Cerebrocurin identified as promising neuroprotective agents.
- Further research into these agents for perinatal hypoxia is warranted.
Abstract:
Background/Objectives: 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 HSP70. Methods: To evaluate the effect of HSP70 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. Results: 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. Conclusions: for the first time, we obtained experimental data on the effects of HSP70 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.
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