BDNF-MEDIATED MECHANISM OF ANTI-STRESS EFFECT OF MELANOCORTINS

A. Yasenyavskaya, L. Andreeva, N. Myasoedov, O. Bashkina, M. Samotrueva
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Despite the formation of adaptive mechanisms under stress in the form of generalized activation of the body, focusing of attention and memory, stress-induced analgesia, under conditions of intense and prolonged influence of a negative factor, the central nervous system loses its ability to adapt and the processes of neurogenesis are often disturbed as a result of distress. This fact explains the development of stress-induced pathological processes in the central nervous system, which emphasizes the relevance of the search and study of the mechanisms of action of pharmacological agents exhibiting stress-protective and neurotropic properties. Melanocortins (N-terminal fragments of adrenocorticotropic hormone, fragments of proopiomelanocortin and their synthetic analogs) are characterized by pronounced neurometabolic, neuroregenerative and antistress activity. One of the possible mechanisms of action of melanocortins is the influence on the levels of expression in the central nervous system of neurotrophic factors that provide the main processes of regulation of homeostasis of the body. Brain Derived Neurotrophic Factor (BDNF) which is able to reduce the negative effects of hypoxic, toxic and stressful damage to brain cells, which is due to binding to tyrosine kinase B receptor and activation of the main metabolic cascades, is one of the effective regulatory proteins. Taking into account the fact that the question of the mechanisms of the stress-protective action of substances capable of protecting brain cells from the damaging effect of stress factors is relevant, the study of the effect of melanocortins on the level of neurotrophic factors is of scientific interest. The study was carried out on 70 male white rats of 6 months of age. 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Abstract

In recent years studies devoted to the study of the mechanisms of regulation of physiological and pathophysiological processes are of particular interest in connection with the active development of molecular medicine. Stress caused by various biological, social and technogenic factors is an integral part of modern human life and is a non-specific reaction of the body to various extreme influences. Despite the formation of adaptive mechanisms under stress in the form of generalized activation of the body, focusing of attention and memory, stress-induced analgesia, under conditions of intense and prolonged influence of a negative factor, the central nervous system loses its ability to adapt and the processes of neurogenesis are often disturbed as a result of distress. This fact explains the development of stress-induced pathological processes in the central nervous system, which emphasizes the relevance of the search and study of the mechanisms of action of pharmacological agents exhibiting stress-protective and neurotropic properties. Melanocortins (N-terminal fragments of adrenocorticotropic hormone, fragments of proopiomelanocortin and their synthetic analogs) are characterized by pronounced neurometabolic, neuroregenerative and antistress activity. One of the possible mechanisms of action of melanocortins is the influence on the levels of expression in the central nervous system of neurotrophic factors that provide the main processes of regulation of homeostasis of the body. Brain Derived Neurotrophic Factor (BDNF) which is able to reduce the negative effects of hypoxic, toxic and stressful damage to brain cells, which is due to binding to tyrosine kinase B receptor and activation of the main metabolic cascades, is one of the effective regulatory proteins. Taking into account the fact that the question of the mechanisms of the stress-protective action of substances capable of protecting brain cells from the damaging effect of stress factors is relevant, the study of the effect of melanocortins on the level of neurotrophic factors is of scientific interest. The study was carried out on 70 male white rats of 6 months of age. Sensory contact in the absence of physical contact with the subsequent formation of aggressive and submissive types of behavior was used as an experimental model of «social» stress. Laboratory animals, taking into account the gradation by types of behavior, were divided into groups: a group of control / intact animals; a group of rats exposed to «social» stress for 20 days; a group of individuals who received Semax (ACTH(4-7)-Pro-Gly-Pro) at a dose of 100 μg / kg / day intraperitoneally from the 1st day of stress exposure for a course of 20 days; a group of animals that received ACTH(6-9)-Pro-Gly-Pro at a dose of 100 μg/kg/day intraperitoneally from day 1 of stress exposure for a course of 20 days. The BDNF level in the blood serum of white rats was assessed by the enzyme-linked immunosorbent assay using ELISA Kit for Brain Derived Neurotrophic Factor (BDNF) (USA). It was found that under conditions of «social» stress, a decrease in the level of BDNF was observed. The introduction of the studied melanocortins (ACTH(4-7)-Pro-Gly-Pro (Semax) and ACTH(6-9)-Pro-Gly-Pro) under conditions of induced «social» stress increases the concentration of BDNF in the blood serum of experimental animals. The study of the mechanisms of disturbances induced by experimental stress in various models showed that stress provokes the development of a depression-like state in rodents, which is accompanied by neuroplastic changes, including inhibition of neurogenesis in the hippocampus. Currently a large amount of experimental data has been accumulated, indicating that a pathological stress response contributes to a decrease in the level of BDNF. Deficiency of BDNF plays an important role in the pathophysiology of stress, inducing impairments of neurogenesis associated with impaired neuroplasticity, as well as dysfunction of the hypothalamic-pituitary-adrenal and neurotransmitter serotonergic systems. The effectiveness of therapy with stress protectors and antidepressants is due to their effect on neurogenesis and neuronal plasticity. Thus the fact of a decrease of BDNF under conditions of «social» stress established in the work and the positive effect of melanocortins (ACTH(4-7)-Pro-Gly-Pro (Semax) and ACTH(6-9)-Pro-Gly-Pro), contributing to the restoration of these parameters, indicates the effect of neuropeptides on the expression of BDNF and allows us to suggest a possible mechanism of the antistress effect. It should be noted that the serum level of brain neurotrophic factor can be considered as a biomarker of stress-induced disorders and affective disorders, as well as an indicator of the effectiveness of therapy with stress protectors. In addition, the level of BDNF in the blood serum can be considered as indicators of prognosis and evaluation of the effectiveness of therapy.
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bdnf介导的黑素皮质素抗应激作用机制
近年来,随着分子医学的积极发展,对生理和病理生理过程的调节机制的研究引起了人们的特别关注。由各种生物、社会和技术因素引起的压力是现代人类生活的一个组成部分,是身体对各种极端影响的一种非特异性反应。尽管在压力下形成了适应机制,表现为身体的全面激活、注意力和记忆的集中、应激性镇痛,但在负面因素的强烈和长期影响下,中枢神经系统失去了适应能力,神经发生过程往往因压力而受到干扰。这一事实解释了应激诱导中枢神经系统病理过程的发展,这强调了寻找和研究具有应激保护和神经营养特性的药理作用机制的相关性。黑素皮质激素(促肾上腺皮质激素的n端片段,原黑素皮质素片段及其合成类似物)具有显著的神经代谢,神经再生和抗应激活性。黑素皮质素可能的作用机制之一是影响中枢神经系统中神经营养因子的表达水平,而神经营养因子是调节机体内稳态的主要过程。脑源性神经营养因子(Brain Derived Neurotrophic Factor, BDNF)是脑源性神经营养因子的有效调控蛋白之一,它通过与酪氨酸激酶B受体结合,激活主要代谢级联反应,能够减轻缺氧、毒性和应激性损伤对脑细胞的负面影响。考虑到能够保护脑细胞免受应激因素破坏作用的物质的应激保护作用机制的问题是相关的,研究黑素皮质素对神经营养因子水平的影响具有科学意义。这项研究是在70只6个月大的雄性白鼠身上进行的。在缺乏身体接触的情况下,感官接触与随后形成的攻击性和顺从性行为类型被用作“社会”压力的实验模型。考虑到行为类型的分级,实验动物被分为两组:一组是对照组/完整的动物;一组大鼠暴露在“社会”压力下20天;一组从应激暴露第1天开始腹腔注射100 μg / kg /天的Semax (ACTH(4-7)-Pro-Gly-Pro),连续20天;一组动物从应激暴露第1天开始腹腔注射ACTH(6-9)-Pro-Gly-Pro,剂量为100 μg/kg/天,疗程为20天。采用美国脑源性神经营养因子(BDNF) ELISA试剂盒,采用酶联免疫吸附法测定大鼠血清BDNF水平。研究发现,在“社会”压力条件下,BDNF水平下降。在诱导的“社会”应激条件下引入所研究的黑素皮质素(ACTH(4-7)-Pro-Gly-Pro (Semax)和ACTH(6-9)-Pro-Gly-Pro)可增加实验动物血清中BDNF的浓度。对各种模型实验应激引起的干扰机制的研究表明,应激可引起啮齿动物出现抑郁样状态,并伴有神经可塑性改变,包括海马神经发生受到抑制。目前已经积累了大量的实验数据,表明病理性应激反应导致BDNF水平下降。BDNF缺乏在应激的病理生理中起着重要作用,诱导与神经可塑性受损相关的神经发生障碍,以及下丘脑-垂体-肾上腺和神经递质5 -羟色胺能系统的功能障碍。应激保护剂和抗抑郁药治疗的有效性是由于它们对神经发生和神经元可塑性的影响。因此,在工作中建立的“社会”压力条件下BDNF减少的事实以及黑素皮质素(ACTH(4-7)-Pro-Gly-Pro (Semax)和ACTH(6-9)-Pro-Gly-Pro)的积极作用有助于这些参数的恢复,表明神经肽对BDNF表达的影响,并允许我们提出抗应激作用的可能机制。值得注意的是,血清中脑神经营养因子的水平可以被认为是应激性疾病和情感性疾病的生物标志物,也是应激保护剂治疗效果的指标。此外,血清BDNF水平可作为预后和评价治疗效果的指标。
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