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1.
Bull Exp Biol Med ; 149(2): 226-32, 2010 Aug.
Artículo en Inglés, Ruso | MEDLINE | ID: mdl-21113497

RESUMEN

Changes in the functional status under the effect of intense mental exercise were studied in carriers of different variants of DAT1, DRD2, and COMT genes. The volunteers (n=140) performed 3-h monotonous mental work (information processing and logical problem solving). The degree of fatigue was evaluated before and after exercise by the HAM (Health status-Activity-Moods) and AMF (Acute Mental Fatigue) questionnaires. A significant relationship between the DAT1, DRD2, and COMT gene polymorphism and changes in the mental sphere status were revealed. The effects of these polymorphisms were the most pronounced in girls. The results are discussed within the framework of hypothesis on the effects of changes in the phasic/tonic dopamine proportion on the studied functions.


Asunto(s)
Catecol O-Metiltransferasa/genética , Proteínas de Transporte de Dopamina a través de la Membrana Plasmática/genética , Variación Genética , Fatiga Mental/fisiopatología , Receptores de Dopamina D2/genética , Cartilla de ADN/genética , Femenino , Humanos , Masculino , Fatiga Mental/genética , Reacción en Cadena de la Polimerasa , Factores Sexuales , Encuestas y Cuestionarios , Adulto Joven
2.
Fiziol Cheloveka ; 36(1): 48-55, 2010.
Artículo en Ruso | MEDLINE | ID: mdl-20196447

RESUMEN

The association of 5-HTTLPR gene polymorthism and aggression was studied in control group of males and females and in the athletes. The sport activities were found to decrease the aggression: the effect persist for the synchronized swimmers and for the wrestlers. Control group of males were characterized by higher aggression scores (Assault, Negativism, Suspicion and Verbal aggression scales of Buss-Durkee Hostility Inventory) compared to females. For all female-subjects irrespective of sport activities and age, the association between the variants of 5-HTTLPR gene and the Indirect Aggression and Negativism scores were found: carries of SS genotype has higher scores on Indirect Aggression and lower scores on Negativism. For the males the association was different: The averaged Hostility scores were higher for the carriers of LL-genotype. The brain processes, presumably underlying the association between aggression and 5-HTLPR gene, were studied in male control group. The increased MMN component of ERP, which responsible for the automatic change detection, and decreased P3a component, related to involuntary attention and cognitive control were found in LL-carries. It might be considered as a sign that SS-carries process the information with more cognitive resources. Probably they perceive the stimulus as more complicated, which lead to activation the additional resources of frontal cortex. It might be also suggested that the carries of SS-genotype tend to deeper processing of the incoming information. Probably, it is this more "serious" analysis of external information, which underlies the rejection of impulsive aggressive actions.


Asunto(s)
Cognición , Lóbulo Frontal/fisiopatología , Polimorfismo Genético , Proteínas de Transporte de Serotonina en la Membrana Plasmática/genética , Medio Social , Adolescente , Adulto , Agresión , Niño , Femenino , Genotipo , Humanos , Masculino , Factores Socioeconómicos
3.
Bull Exp Biol Med ; 147(4): 462-5, 2009 Apr.
Artículo en Inglés, Ruso | MEDLINE | ID: mdl-19704949

RESUMEN

In order to test the "serotonin" hypothesis of the genesis of central fatigue, we studied association between genotype and fatigue (3-hour mental workload consisting of information processing and logical task solution) using analysis of variance for different indices (well-being, activity, mood, mental fatigue index). It was concluded that young men with serotonin deficit (LL genotype) and girls with serotonin excess (S genotype) were less tolerant to long-lasting mental workload. Thus, we confirmed that the degree of central fatigue depends on the function of the serotonin system and revealed gender differences in adaptive capacities of carriers of different variants of serotonin transporter.


Asunto(s)
Fatiga/genética , Procesos Mentales , Polimorfismo Genético , Proteínas de Transporte de Serotonina en la Membrana Plasmática/genética , Caracteres Sexuales , Afecto , Alelos , Análisis de Varianza , Femenino , Humanos , Masculino , Pruebas Neuropsicológicas , Pruebas Psicológicas , Encuestas y Cuestionarios , Adulto Joven
4.
Bull Exp Biol Med ; 146(6): 774-8, 2008 Dec.
Artículo en Inglés, Ruso | MEDLINE | ID: mdl-19513381

RESUMEN

Associations of functional polymorphism in genes of dopamine receptor DRD2, dopamine transporter DAT, and dopamine degrading enzyme COMT with variations in anxiety sensitivity threshold were studied. On the basis of genetic and psychological analysis, an attempt was undertaken to evaluate the relationship of DRD2, DAT and COMT genotypes with values obtained using different anxiety scales. It was found that carriers of VA1(+)9(+) genotype exhibit increased anxiety and significantly differed from individuals with other genotypes. The results were illustrated with model of dopamine diffusion in the extracellular space of the striatum in carriers of different genotypes.


Asunto(s)
Ansiedad/genética , Predisposición Genética a la Enfermedad/genética , Adolescente , Adulto , Catecol O-Metiltransferasa/genética , Dopamina/metabolismo , Proteínas de Transporte de Dopamina a través de la Membrana Plasmática/genética , Femenino , Marcadores Genéticos , Genotipo , Humanos , Masculino , Modelos Biológicos , Modelos Teóricos , Receptores de Dopamina D2/genética , Adulto Joven
5.
Artículo en Ruso | MEDLINE | ID: mdl-17944104

RESUMEN

The association between the subjective time perception and polymorphism of some genes, regulating activity of serotonin and dopamine, was studied in 89 synchronized swimmers. COMT gene, responsible for dopamine destruction, influences on reproduction of short time intervals (1-2 s). 5-HT2A and MAOA genes, regulating activity of serotonin, influence on subjective time flow. 5-HTT and COMT genes, regulating activity of serotonin and dopamine respectively, are related with accuracy of orientation in time. Association of time perception with different genes and mediators suggests different perception mechanisms, in different time ranges, in concordance with the previous physiological studies. The current study reveals that these physiological mechanisms have different molecular-neurochemical basis that helps to overcome the gap between the investigation on systemic and molecular levels.


Asunto(s)
Catecol O-Metiltransferasa/genética , Monoaminooxidasa/genética , Receptor de Serotonina 5-HT2A/genética , Proteínas de Transporte de Serotonina en la Membrana Plasmática/genética , Natación , Percepción del Tiempo , Adolescente , Adulto , Anciano , Niño , Dopamina/metabolismo , Femenino , Humanos , Persona de Mediana Edad , Polimorfismo Genético , Serotonina/metabolismo
6.
Artículo en Ruso | MEDLINE | ID: mdl-10923379

RESUMEN

Nonlinear dependence between the emotion intensity and main emotion components: the value of need and probability of its satisfaction is confirmed by the analysis of subjective and objective indices during mental reproduction of emotional situations. The dependence suggests a possibility of application of some its linear analogs in a certain range of changes in the intensity of need and possibility of its satisfaction.


Asunto(s)
Emociones/fisiología , Humanos , Modelos Psicológicos , Psicofisiología
7.
Klin Med (Mosk) ; 75(10): 59-63, 1997.
Artículo en Ruso | MEDLINE | ID: mdl-9490344

RESUMEN

12 cardiologists trained as experts in assessment of medical care quality (MCQ) made a computer-assisted expertise of the care rendered to 110 anginal patients. Of these 68 patients had angina of effort (AE) and 42 had unstable angina (UA). This made up 10% of annual number of anginal patients treated in the cardiological clinic in 1996. Medical errors were of the same type in both the groups. Inadequate collection of information, erroneous diagnosis, treatment, continuity occurred in 50, 30, 15 and 5% of all the errors, respectively. Negative effects of the errors were mild (less seriously suffered AE patients), but led to waste of health service resources.


Asunto(s)
Angina de Pecho/diagnóstico , Angina de Pecho/terapia , Errores Médicos , Interpretación Estadística de Datos , Procesamiento Automatizado de Datos , Humanos , Errores Médicos/estadística & datos numéricos , Garantía de la Calidad de Atención de Salud/estadística & datos numéricos , Estudios Retrospectivos
13.
Bull Exp Biol Med ; 145(4): 391-4, 2008 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-19110575

RESUMEN

We studied the effect of angiotensin-converting enzyme gene polymorphism on human emotional state in humans (189 athletes and 212 volunteers not engaged in sport activity). The distribution of angiotensin-converting enzyme genotypes was estimated. The dependence of aggression on age, sex, and professional activity was evaluated. This polymorphism was associated with physical aggression in female synchronized swimmers. Physical aggression in II genotype carriers was lower than in D allele carriers. Our results indicate that individual differences in aggression depend on professional activity and are genetically determined.


Asunto(s)
Emociones/fisiología , Sistema Renina-Angiotensina/fisiología , Adolescente , Adulto , Agresión/fisiología , Estudios de Casos y Controles , Niño , Femenino , Genotipo , Humanos , Masculino , Peptidil-Dipeptidasa A/genética , Polimorfismo Genético/fisiología , Sistema Renina-Angiotensina/genética , Deportes/fisiología , Adulto Joven
14.
Bull Exp Biol Med ; 145(1): 62-4, 2008 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-19024004

RESUMEN

Genetic and psychological analysis of the relationships between catechol-O-methyltransferase Val158Met polymorphism and various types of aggressiveness was performed in 114 women. Dispersion analysis revealed significant association of ValVal genotype with elevated physical aggression.


Asunto(s)
Agresión , Catecol O-Metiltransferasa/genética , Polimorfismo de Nucleótido Simple , Adolescente , Niño , Femenino , Predisposición Genética a la Enfermedad , Humanos , Masculino , Metionina/genética , Personalidad/genética , Valina/genética , Adulto Joven
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