Use of Antisense Oligodeoxynucleotides in the Study of Neuroendocrine Aging

Scarbrough Kathryn
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引用次数: 1

Abstract

One of the difficulties in the field of the neurobiology of aging is that many of the studies are necessarily correlative in nature. Investigators interested in the neurotransmitter or neuropeptide control of a given brain function often describe the situation in young animals and compare these observations with findings for groups of aged animals. However, ascribing causation with such studies is difficult at best. The use of antisense oligodeoxynucleotides described in this article allows the investigator to target one or more neuropeptides expressed in a confined area of the brain for selective abiation. The assessment of cause and effect on the physiological endpoint of Interest then becomes more tractable. Having previously identified age-related changes in neuropeptide dynamics that may underlie certain aspects of endocrine aging, we used this method to determine whether specific antisense oligodeoxynucleotide treatment of young animals mimicked the effect of age on the endocrine system. The theoretical background and practical aspects of the method are presented in sufficient detail to allow investigators not familiar with the technique to design appropriate oligodeoxynucleotides and use them in their research.

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反义寡核苷酸在神经内分泌衰老研究中的应用
衰老神经生物学领域的难点之一是,许多研究在本质上必然是相关的。对特定大脑功能的神经递质或神经肽控制感兴趣的研究人员经常描述年轻动物的情况,并将这些观察结果与老年动物组的研究结果进行比较。然而,用这样的研究来确定因果关系充其量是很困难的。本文中所述的反义寡核苷酸的使用使研究者能够靶向在大脑的受限区域中表达的一种或多种神经肽进行选择性abiation。然后,对感兴趣的生理终点的因果关系的评估变得更加容易处理。先前已经确定了可能是内分泌衰老某些方面的神经肽动力学的年龄相关变化,我们使用这种方法来确定幼兽的特异性反义寡核苷酸治疗是否模拟了年龄对内分泌系统的影响。详细介绍了该方法的理论背景和实践方面,使不熟悉该技术的研究人员能够设计合适的寡核苷酸并将其用于研究。
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Editorial Use of Antisense Oligodeoxynucleotides in the Study of Neuroendocrine Aging Delivery of Peptides into the Central Nervous System by Molecular Packaging and Sequential Metabolism as a Method of Altering Neuropeptide Activity during Aging Author Index for Volume 4 Electron Microscopic Methods for Determining Changes in the Density of Synaptic Input to Neurons in the Aging Brain
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