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1.
Bull Exp Biol Med ; 150(1): 131-6, 2010 Dec.
Article in English | MEDLINE | ID: mdl-21161071

ABSTRACT

Mesenchymal stem cells enzymatically isolated from human placenta were labeled with magnetic fluorescent microparticles (d=0.96 µ). We showed that microparticles in high doses (>10 µl stock suspension per 1 ml culture medium) significantly inhibited cell proliferation in culture. In our work we determined the optimal concentration of particles not affecting physiological properties of mesenchymal stem cells: it does not change cell proliferation, does not induce apoptosis, and does not modulate their transdifferentiation into neuronal cells. In vivo experiments showed that the chosen particles allow easy visualization of transplanted cells ex vivo on sections of different tissues.


Subject(s)
Magnetics , Mesenchymal Stem Cell Transplantation , Mesenchymal Stem Cells/cytology , Mesenchymal Stem Cells/drug effects , Nanoparticles/adverse effects , Animals , Apoptosis/drug effects , Cell Differentiation/drug effects , Cell Proliferation/drug effects , Cells, Cultured , Female , Humans , Male , Nanoparticles/chemistry , Pregnancy , Rats , Rats, Wistar
3.
Vestn Ross Akad Med Nauk ; (4): 60-2, 1997.
Article in Russian | MEDLINE | ID: mdl-9213487

ABSTRACT

Lifestyle, environmental factors, genetics, and medical care are the main factors that determine the health status of man. Of particular attention are biological mechanisms ensuring the body's adaptation to constantly changing environmental conditions. The noradrenergic neuronal populations, the sympathetic nervous system in particular, modulate metabolic processes and supports a variety of activities, making them relevant to changing living conditions. There is a clear correlation between the life span and the number of sympathetic nerve cells functioning during postnatal ontogenesis. The exposures that reduce the activity of peripheral and central noradrenergic neurons and slow down aging processes in them loosen the relationships between the inner and outer world to prevent hyperactivity and to prolong life.


Subject(s)
Adaptation, Physiological , Aging , Catecholamines/metabolism , Health Status , Neurons/metabolism , Sympathetic Nervous System/physiology , Adolescent , Adult , Animals , Female , Humans , Hydroxydopamines/administration & dosage , Hydroxydopamines/pharmacology , Life Expectancy , Locus Coeruleus/drug effects , Male , Meclofenoxate/administration & dosage , Meclofenoxate/pharmacology , Middle Aged , Neuroprotective Agents/administration & dosage , Neuroprotective Agents/pharmacology , Nootropic Agents/administration & dosage , Nootropic Agents/pharmacology , Rats
6.
Vestn Akad Med Nauk SSSR ; (2): 46-8, 1990.
Article in Russian | MEDLINE | ID: mdl-2356656

ABSTRACT

Age-related changes in the transcriptional activities of Purkinje cells chromatin and sympathetic cranial cervical ganglion under the influence of morphine and some natural and synthetic peptide compounds were found. It was shown that at different stages of the ontogenesis, morphine was capable of increasing the template activity of nucleolar and/or extranucleolar chromatin, and that this process was inhibited by antipain. The findings suggest the presence of DNA sites in the eucaryotic genome, that are induced by the protease mechanism and are likely to be similar to the SOS-genes of procaryotes. The SOS-genes of procaryotes are activated under unfavourable conditions and promote the survival of the microbial population, while in eucaryotes these genes are believed to provide the formation of definite cell populations whose composition is the most adequate for the living conditions of an adult organism.


Subject(s)
Antipain/pharmacology , Cell Nucleolus/ultrastructure , DNA/drug effects , Ganglia, Sympathetic/ultrastructure , Liver/ultrastructure , Oligopeptides/pharmacology , Purkinje Cells/ultrastructure , Transcription, Genetic/drug effects , Animals , Culture Media , DNA/genetics , Depression, Chemical , In Vitro Techniques , Morphine/pharmacology , Rats , Stimulation, Chemical , Transcription, Genetic/physiology
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