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BACKGROUND: Stress exposure at an early age can have serious long-term consequences for the development of the human body, leading to adaptive disorders, increased anxiety, depression and other mental disorders in people. The effect of stressors in the first weeks after birth affects the proliferation, differentiation and migration of neurons, in particular, the neurogenesis of hippocampal cells. Repetitive stress can lead to changes in the structure and function of the brain, including deterioration of memory and skill acquisition, reduced resistance to stress in the future, decreased immune system function and increased risk of depression and other mental illnesses. AIM: The aim was to study the effect of social isolation weaning on the level of ghrelin receptor mRNA expression in the brain structures of Wistar rats. MATERIALS AND METHODS: 60 male rats (8 litters) with a body weight of 230250 g were used in the work and three experimental groups were formed: control (n = 20); maternal deprivation (n = 20); social isolation (n = 20). On the 90th day of life, the animals were decapitated, the brain was quickly extracted, placed in the cold and brain structures (hypothalamus, amygdala, prefrontal cortex) were isolated, immediately frozen in liquid nitrogen and stored at a temperature of 80C until PCR analysis was performed. The data obtained were normalized to the expression level of the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene and calculated in relative units with respect to the expression value of the GRLN-R gene for each structure separately by method 2 (-DeltaDelta C(T)). RESULTS: In rats raised in conditions of social isolation, compared with the indicators of the control group and the group of animals with maternal deprivation (p 0.05), an increase in the expression of the GHSR1A gene was noted in the hypothalamus. Whereas in rats after the stress of maternal deprivation in the amygdala there was an increase in the expression of the GHSR1A gene compared with the indicators in the control group of rats. CONCLUSIONS: 1. In rats that survived weaning from the mother from the 2nd to the 12th postnatal day, a significant statistically significant increase in the expression of the GHSR1A gene was revealed in the hypothalamus in comparison with the control group and the social isolation group. 2. In rats raised in conditions of social isolation from their relatives, a significant statistically significant increase in the expression of the GHSR1A gene in the amygdala was revealed in comparison with the control group and the weaning group.
BACKGROUND: Stress exposure at an early age can have serious long-term consequences for the development of the human body, leading to adaptive disorders, increased anxiety, depression and other mental disorders in people. The effect of stressors in the first weeks after birth affects the proliferation, differentiation and migration of neurons, in particular, the neurogenesis of hippocampal cells. Repetitive stress can lead to changes in the structure and function of the brain, including deterioration of memory and skill acquisition, reduced resistance to stress in the future, decreased immune system function and increased risk of depression and other mental illnesses. AIM: The aim was to study the effect of social isolation weaning on the level of ghrelin receptor mRNA expression in the brain structures of Wistar rats. MATERIALS AND METHODS: 60 male rats (8 litters) with a body weight of 230250 g were used in the work and three experimental groups were formed: control (n = 20); maternal deprivation (n = 20); social isolation (n = 20). On the 90th day of life, the animals were decapitated, the brain was quickly extracted, placed in the cold and brain structures (hypothalamus, amygdala, prefrontal cortex) were isolated, immediately frozen in liquid nitrogen and stored at a temperature of 80C until PCR analysis was performed. The data obtained were normalized to the expression level of the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene and calculated in relative units with respect to the expression value of the GRLN-R gene for each structure separately by method 2 (-DeltaDelta C(T)). RESULTS: In rats raised in conditions of social isolation, compared with the indicators of the control group and the group of animals with maternal deprivation (p 0.05), an increase in the expression of the GHSR1A gene was noted in the hypothalamus. Whereas in rats after the stress of maternal deprivation in the amygdala there was an increase in the expression of the GHSR1A gene compared with the indicators in the control group of rats. CONCLUSIONS: 1. In rats that survived weaning from the mother from the 2nd to the 12th postnatal day, a significant statistically significant increase in the expression of the GHSR1A gene was revealed in the hypothalamus in comparison with the control group and the social isolation group. 2. In rats raised in conditions of social isolation from their relatives, a significant statistically significant increase in the expression of the GHSR1A gene in the amygdala was revealed in comparison with the control group and the weaning group.
Background. Compulsive overeating (bulimia nervosa, binge eating disorder) is the basis of eating disorders and is included in ICD-11 and DSM-5 as a manifestation of a non-chemical form of addiction. It is a behavioral disorder of impulsivity and compulsivity. Obesity and eating disorders are characterized by compulsive food consumption, similar to the compulsive drug use of substance use disorders. Aim. Study of the effect of the OX1 receptor antagonist anthorex on compulsive overeating in animals in a model of maternal deprivation. Materials and methods. Sexually mature male rats, which were separated from their mother for 3 hours after birth from days 2 to 12, were fed a high-carbohydrate diet every third day for 1 hour for 45 days. In this case, high-calorie food was placed within 5 cm of reach with visual contact 15 minutes before feeding. Orexin receptor antagonist Anthorex was administered intranasally for 7 days at a dose of 1 µg/1 µl, 20 µl. Results. Intermittent consumption of high-calorie foods caused compulsive overeating in rats. Sexually mature animals that experienced deprivation from their mother in early ontogenesis showed increased signs of compulsive overeating of high-carbohydrate foods in our model relative to the control (p 0.001). At the same time, the consumption of standard briquetted feed did not change. Intranasal administration of the OX1 receptor antagonist anthorex reduced the manifestations of compulsive overeating in rats after weaning under conditions of intermittent consumption of high-calorie food compared to the control group (p 0.05). Consumption of standard food did not differ relative to the control group, both before and after the course of administration of the orexin antagonist. Conclusion. The work suggest new ways of studying and synthesizing peptide drugs based on orexin and its antagonists for the correction of compulsive overeating caused by chronic stress in ontogenesis.
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