低浓度二甲基亚砜(dmso)可调节 4-氨基吡啶体外模型中的癫痫同步化。

IF 2.7 4区 医学 Q2 BIOCHEMICAL RESEARCH METHODS
Fei Ran Li , Mia Gemayel , Maxime Lévesque , Siyan Wang , Camila Franco Suarez , Massimo Avoli
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引用次数: 0

摘要

二甲基亚砜(DMSO)具有双极性和钝化性,常用于溶解不溶于水的药物。它也是许多药理学研究的载体。然而,有报道称二甲基亚砜可诱导人类患者癫痫发作、降低体内癫痫发作阈值以及调节体外离子受体的活性。因此,我们在此研究了 0.03% 和 0.06% 的二甲基亚砜对雄性小鼠脑片癫痫样同步化模型的影响,它们比以往研究中通常使用的二甲基亚砜低 10 到 50 倍。我们发现,0.03% 和 0.06% DMSO 会增加 4AP 诱导的发作性放电率,而 0.06% DMSO 会减少发作性放电持续时间。我们的结果表明,DMSO 对神经元兴奋性的影响值得进一步分析,研究人员需要注意其作为溶剂的混杂效应,即使浓度很低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low concentration dimethyl sulfoxide (DMSO) modulates epileptiform synchronization in the 4-aminopyridine in vitro model

Dimethyl sulfoxide (DMSO) is commonly used to dissolve water-insoluble drugs due to its dipolar and aprotic properties. It also serves as a vehicle in many pharmacological studies. However, it has been reported that DMSO can induce seizures in human patients, lower seizure threshold in vivo, and modulate ion receptors activities in vitro. Therefore, we investigated here the effect of 0.03 % and 0.06 % DMSO, which are 10–50 times lower than what usually employed in previous studies, in the 4-aminopyridine (4AP) model of epileptiform synchronization in male mouse brain slices. We found that 0.03 % and 0.06 % DMSO increase 4AP-induced ictal discharge rate, while 0.06 % DMSO decreases ictal discharge duration. Our results suggest that the effects of DMSO on neuronal excitability deserve further analysis and that investigators need to be aware of its confounding effect as a solvent, even at very low concentrations.

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来源期刊
Journal of Neuroscience Methods
Journal of Neuroscience Methods 医学-神经科学
CiteScore
7.10
自引率
3.30%
发文量
226
审稿时长
52 days
期刊介绍: The Journal of Neuroscience Methods publishes papers that describe new methods that are specifically for neuroscience research conducted in invertebrates, vertebrates or in man. Major methodological improvements or important refinements of established neuroscience methods are also considered for publication. The Journal''s Scope includes all aspects of contemporary neuroscience research, including anatomical, behavioural, biochemical, cellular, computational, molecular, invasive and non-invasive imaging, optogenetic, and physiological research investigations.
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