利用肽和核苷酸制剂纠正应激性免疫和神经内分泌系统功能障碍

Q4 Immunology and Microbiology
E. Rybakina, S. N. Shanin, E. Fomicheva, E. Dmitrienko, T. A. Filatenkova, E. Korneva
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引用次数: 0

摘要

作者分析了短肽和天然DNA制剂在不同应激条件下对免疫和神经内分泌系统功能的影响。这些多肽和核苷酸的制剂被认为是免疫和神经内分泌系统的有效调节剂。在这里,我们讨论了一个新的概念,即内源性短肽及其合成类似物结合到DNA链中的特定核苷酸序列。这些位点特异性肽- DNA相互作用调节细胞遗传功能,并形成了应激保护短合成肽的分子遗传学基础。研究表明,核苷酸制剂对免疫和神经内分泌系统功能受损有保护作用。这些作用似乎是基于核苷酸穿透细胞并随后分裂成核苷酸的能力,这些核苷酸在从细胞中释放出来后,与嘌呤能P2受体结合。结果表明,短合成肽和天然DNA制剂能够纠正应激引起的神经免疫功能损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Correction of Stress-induced Dysfunctions of the Immune and Neuroendocrine Systems by Peptide and Nucleotide Preparations
The authors analyzed the effects of short synthetic peptides and native DNA preparations on the function of the immune and neuroendocrine systems under various stress conditions. These preparations of peptides and nucleotides are known to be effective modulators of the immune and neuroendocrine systems. Here we discuss a new concept, which suggests that endogenous short peptides and their synthetic analogs bind to specific sequences of nucleotides in DNA strands. These site-specific peptide- DNA interactions modulate cellular genetic functions and form the basis of molecular-genetics of stress-protective short synthetic peptides. Protective action of nucleotide preparations on impaired functions of the immune and neuroendocrine systems was shown. It seems that these effects are based on the ability of nucleotides to penetrate cells and subsequently splitting into nucleotides, which, after releasing from the cell, bind to purinergic P2 receptors. The results indicate that short synthetic peptides and native DNA preparations are capable of correcting stress induced impairment of neuroimmune function.
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来源期刊
Advances in Neuroimmune Biology
Advances in Neuroimmune Biology Immunology and Microbiology-Immunology
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