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Epigenetic Alterations in DNA and Histone Modifications Caused by Depression and Antidepressant Drugs: Lessons from the Rodent Models

机译:抑郁症和抗抑郁药引起的DNA和组蛋白修饰中的表观遗传改变:啮齿动物模型的课程

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摘要

Epigenetic modifications regulate chromatin folding and function. Epigenetic mechanisms regulate transcription mediating effects of various stimuli on gene expression. These mechanisms are involved in transcriptional control in various physiological and pathological conditions including neuropsychiatric disorders and behavioral abnormalities such as depression. In rodents, exposure to chronic social stress was shown to induce behavioral impairments and memory/learning deficits that resemble depressive-like phenotype in humans. The rodent models of chronic stress were widely used to study molecular mechanisms of depression. In these models, early exposure to chronic stress such as prenatal or postnatal stress induces long-term hyperactive stress responses, behavioral abnormalities, and functional impairments in brain function that persist in adulthood. Furthermore, these alterations can be transmitted to offspring of chronically stressed animals across several generations. Molecular studies in animal models showed that chronic stress induces stable epigenetic changes in specific brain regions, primarily in the limbic system. These changes lead to long-lasting abnormalities in behavior that persist in adulthood and can be transmitted to offspring. Treatment with epigenetically active antidepressants disrupts the abnormal stress-induced epigenetic programming and provides epigenetic patterns that resemble epigenetic background of stress resilient individuals.
机译:表观遗传修饰调节染色质折叠和功能。表观遗传机制调节各种刺激对基因表达的转录介质作用。这些机制参与各种生理和病理病症的转录控制,包括神经精神病症和行为异常,如抑郁症。在啮齿动物中,显示出暴露于慢性社会压力,诱导类似于人类的抑郁样表型的行为障碍和记忆/学习缺陷。慢性胁迫的啮齿动物模型被广泛用于研究抑郁的分子机制。在这些模型中,早期暴露于产前或产前应激等慢性应激诱导长期过度应激应答,行为异常和在成年期坚持的脑功能中的功能损伤。此外,这些改变可以传递到跨越几代慢性应激动物的后代。动物模型中的分子研究表明,慢性应激在主要在肢体系统中诱导特定脑区的稳定表观遗传变化。这些变化导致在成年期持续存在的行为的长期异常,并且可以传递给后代。用外形活性抗抑郁药治疗破坏了异常应激诱导的表观遗传编程,并提供了类似于应力弹性个体的表观遗传背景的表观遗传模式。

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