过氧化物酶体增殖激活受体-γ 激动剂:胎儿酒精中毒谱系障碍相关神经病理学的潜在疗法。

IF 4.8 4区 物理与天体物理 Q2 PHYSICS, CONDENSED MATTER
Journal of Semiconductors Pub Date : 2016-12-01 Epub Date: 2016-11-14 DOI:10.4172/2155-9899.1000469
Paul D Drew, Cynthia J M Kane
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引用次数: 0

摘要

胎儿酒精谱系障碍(FASD)是胎儿在怀孕期间接触酒精所致。这些疾病会带来各种后遗症,包括中枢神经系统(CNS)受累,对认知功能和行为产生持久影响。FASD 的发病率惊人,对个人和社会都有重大影响。对于 FASD,目前还没有有效的治疗方法。最新研究表明,乙醇会在发育中大脑的许多区域诱发强烈的神经炎症。此外,抗炎药物(如过氧化物酶体增殖激活受体(PPAR)-γ 激动剂)可抑制乙醇诱导的神经炎症和神经退行性变。这表明抗炎药物对治疗 FASD 可能有效。未来的研究旨在确定酒精在发育中的中枢神经系统中诱导神经炎症的具体机制,这可能会导致针对 FASD 的靶向疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Peroxisome Proliferator-Activated Receptor-γ Agonists: Potential Therapeutics for Neuropathology Associated with Fetal Alcohol Spectrum Disorders.

Fetal alcohol spectrum disorders (FASD) result from fetal exposure to alcohol during pregnancy. These disorders present a variety of sequelae including involvement of the central nervous system (CNS) with lasting impact on cognitive function and behavior. FASD occur at an alarming rate and have significant personal and societal impact. There are currently no effective treatments for FASD. Recent studies demonstrate that ethanol induces potent neuroinflammation in many regions of the developing brain. Furthermore, anti-inflammatory agents such as peroxisome proliferator-activated receptor (PPAR)-γ agonists suppress ethanol-induced neuroinflammation and neurodegeneration. This suggests that anti-inflammatory agents may be effective in treatment of FASD. Future studies designed to determine the specific mechanisms by which alcohol induces neuroinflammation in the developing CNS may lead to targeted therapies for FASD.

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来源期刊
Journal of Semiconductors
Journal of Semiconductors PHYSICS, CONDENSED MATTER-
CiteScore
6.70
自引率
9.80%
发文量
119
期刊介绍: Journal of Semiconductors publishes articles that emphasize semiconductor physics, materials, devices, circuits, and related technology.
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