Effect of Prenatal Hypoxia on Activity of the Soluble Forms of Cholinesterases in Rat Brain Structures during Early Postnatal Ontogenesis
Autor: | A. Yu. Morozova, L. S. Kozina, A. V. Arutyunyan, N. N. Nalivaeva, Igor A. Zhuravin, P. Yu. Morozova |
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Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
medicine.medical_specialty Cerebellum Physiology Aché Embryogenesis Neurogenesis Biology Hypoxia (medical) Biochemistry language.human_language 03 medical and health sciences 030104 developmental biology 0302 clinical medicine Endocrinology medicine.anatomical_structure Blood serum Internal medicine medicine language Cholinergic medicine.symptom 030217 neurology & neurosurgery Ecology Evolution Behavior and Systematics Homeostasis |
Zdroj: | Journal of Evolutionary Biochemistry and Physiology. 56:531-540 |
ISSN: | 1608-3202 0022-0930 |
DOI: | 10.1134/s002209302006006x |
Popis: | The dynamics of soluble AChE and BChE (EC 3.1.1.7; EC 3.1.1.8) in the hippocampus, cortex, cerebellum and blood serum of control rats and rats exposed to prenatal hypoxia was studied on days 5, 10 and 30 of postnatal development. The activity of soluble AChE in all brain structures was found to reach its maximum on postnatal day 10, and then either persisted at this level (in the cerebellum and cortex) or decreased by day 30 (in the hippocampus). Similar changes were found in the activity of BChE, which was roughly one level of magnitude lower than of AChE in all the brain structures studied in this work. Prenatal hypoxic exposure on day 14 of embryonic development led to statistically significant changes in the activity of soluble AChE and BChE in all the brain structures studied, as well as in blood serum. In rats exposed to prenatal hypoxia, serum AChE and BChE activities on postnatal days 5 and 10 were significantly lower while, on day 30, they were indistinguishable from the control values. Thus, oxygen deficit in the maternal organism during pregnancy significantly affects the activity of soluble forms of the key enzymes of the central and peripheral cholinergic systems, indicating possible changes in the formation of these systems in early ontogenesis. This may lead both to impaired neurogenesis and malformation of the motor and cognitive functions and general homeostatic imbalance during animal and human development. |
Databáze: | OpenAIRE |
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