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- W4366595104 abstract "The brain myelin and neurons destruction in multiple sclerosis may be associated with the production of neuroinflammatory cells (macrophages, astrocytes, T-lymphocytes) of pro-inflammatory cytokines and free radicals. The age-associated changes of the above cells can influence on the response of nervous system cells to toxic damaging and regulatory factors of humoral/endocrine nature, in particular pineal hormone melatonin. The study aim was (1) to evaluate changes of the brain macrophages, astrocytes, T-cells, neural stem cells, neurons, and central nervous system (CNS) functioning in the neurotoxin cuprizone-treated mice of different age; and (2) to assess in such mice the effects of exogenous melatonin and possible courses of its action.A toxic demyelination and neurodegeneration model was induced in 129/Sv mice aged 3-5 and 13-15 months by adding cuprizone neurotoxin to their food for 3 weeks. From the 8th day of the cuprizone treatment, melatonin was injected intraperitoneally at 6 p.m. daily, at a dose of 1 mg/kg. The brain GFPA + -cells were evaluated by immunohistochemical method, the proportion of CD11b+, CD3+CD11b+, CD3+, CD3+CD4+, CD3+CD8+, Nestin+-cells was determined via flow cytometry. Macrophage activity was evaluated by their ability to phagocytose latex beads Morphometric analysis of the brain neurons and the behavioral reactions (open field and rotarod tests) were performed. To assess the involvement of the bone marrow and thymus in the action of melatonin, the amount of granulocyte/macrophage colony-forming cells (GM-CFC), and blood monocytes and thymic hormone thymulin were evaluated.The numbers of the GFAP+-, CD3+-, CD3+CD4+, CD3+CD8+, CD11b+, CD3+CD11b+, Nestin+-cells and macrophages phagocytic latex beads and malondialdehyde (MDA) content were increased in the brain of young and aging mice under cuprizone influence. The proportion of undamaged neurons within the brain, motor, affective, and exploratory activities, and muscle tone decreased in mice of both ages. Introducing melatonin to mice of any age reduced the number of GFAP+-, CD3+- cells and their subpopulations, macrophage activation, and MDA content. At the same time, the percentage of brain neurons that were unchanged increased as the number of Nestin+ cells decreased. The behavioral responses were also improved. Besides, the number of bone marrow GM-CFC and the blood level of monocytes and thymulin increased. The effects of both neurotoxin and melatonin on the brain astrocytes, macrophages T-cells, and immune system organs as well as the structure and functioning of neurons were more pronounced in the young mice.We have observed the involvement of the astrocytes, macrophages, T-cells, neural stem cells, and neurons in the brain reaction of mice different age after administration of neurotoxin cuprizone and melatonin. The brain cell composition reaction has the age features. The neuroprotective effects of melatonin in cuprizone-treated mice have been realized through an improvement of the brain cell composition and oxidative stress factors and functioning of bone marrow and thymus." @default.
- W4366595104 created "2023-04-23" @default.
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- W4366595104 date "2023-04-20" @default.
- W4366595104 modified "2023-10-17" @default.
- W4366595104 title "Reaction of different cell types of the brain on neurotoxin cuprizone and hormone melatonin treatment in young and aging mice" @default.
- W4366595104 cites W1194272897 @default.
- W4366595104 cites W1545082774 @default.
- W4366595104 cites W169600661 @default.
- W4366595104 cites W1754595315 @default.
- W4366595104 cites W1914347682 @default.
- W4366595104 cites W1949446280 @default.
- W4366595104 cites W1962579791 @default.
- W4366595104 cites W1971230000 @default.
- W4366595104 cites W1971874355 @default.
- W4366595104 cites W1987145582 @default.
- W4366595104 cites W1991883207 @default.
- W4366595104 cites W1993509899 @default.
- W4366595104 cites W1994646052 @default.
- W4366595104 cites W2002287505 @default.
- W4366595104 cites W2006178657 @default.
- W4366595104 cites W2016753814 @default.
- W4366595104 cites W2019399727 @default.
- W4366595104 cites W2047585900 @default.
- W4366595104 cites W2050540506 @default.
- W4366595104 cites W2053054955 @default.
- W4366595104 cites W2053383237 @default.
- W4366595104 cites W2055693317 @default.
- W4366595104 cites W2057242248 @default.
- W4366595104 cites W2067668823 @default.
- W4366595104 cites W2073078340 @default.
- W4366595104 cites W2075367242 @default.
- W4366595104 cites W2077013720 @default.
- W4366595104 cites W2077198366 @default.
- W4366595104 cites W2091617675 @default.
- W4366595104 cites W2097417855 @default.
- W4366595104 cites W2102952096 @default.
- W4366595104 cites W2132579719 @default.
- W4366595104 cites W2136879071 @default.
- W4366595104 cites W2156446986 @default.
- W4366595104 cites W2164058704 @default.
- W4366595104 cites W2165386666 @default.
- W4366595104 cites W2170038614 @default.
- W4366595104 cites W2236165509 @default.
- W4366595104 cites W2540362227 @default.
- W4366595104 cites W2565712892 @default.
- W4366595104 cites W2582993274 @default.
- W4366595104 cites W2623385207 @default.
- W4366595104 cites W2735866967 @default.
- W4366595104 cites W2737622125 @default.
- W4366595104 cites W2742430687 @default.
- W4366595104 cites W2757161456 @default.
- W4366595104 cites W2761098718 @default.
- W4366595104 cites W2766910441 @default.
- W4366595104 cites W2769071992 @default.
- W4366595104 cites W2783258630 @default.
- W4366595104 cites W2797384836 @default.
- W4366595104 cites W2897827110 @default.
- W4366595104 cites W2907263930 @default.
- W4366595104 cites W2907839520 @default.
- W4366595104 cites W2907975539 @default.
- W4366595104 cites W2919471794 @default.
- W4366595104 cites W2935777701 @default.
- W4366595104 cites W2949370138 @default.
- W4366595104 cites W2969825959 @default.
- W4366595104 cites W2986625735 @default.
- W4366595104 cites W2988340250 @default.
- W4366595104 cites W2989558653 @default.
- W4366595104 cites W2990737501 @default.
- W4366595104 cites W3004780218 @default.
- W4366595104 cites W3011848199 @default.
- W4366595104 cites W3014214236 @default.
- W4366595104 cites W3014521573 @default.
- W4366595104 cites W3025636420 @default.
- W4366595104 cites W3033104124 @default.
- W4366595104 cites W3033713180 @default.
- W4366595104 cites W3047661272 @default.
- W4366595104 cites W3197136220 @default.
- W4366595104 cites W4200420063 @default.
- W4366595104 cites W4205899571 @default.
- W4366595104 cites W4210299272 @default.
- W4366595104 cites W4229064788 @default.
- W4366595104 cites W4252257621 @default.
- W4366595104 cites W4281855432 @default.
- W4366595104 cites W4281878587 @default.
- W4366595104 cites W780581045 @default.
- W4366595104 doi "https://doi.org/10.3389/fncel.2023.1131130" @default.
- W4366595104 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/37153635" @default.
- W4366595104 hasPublicationYear "2023" @default.
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