MA-5改善了出生前接触丙戊酸的小鼠的自闭症样行为。

IF 1.6 4区 心理学 Q3 BEHAVIORAL SCIENCES Behavioural Pharmacology Pub Date : 2023-12-01 Epub Date: 2023-10-01 DOI:10.1097/FBP.0000000000000758
Yasuhiro Nakagami, Mina Nishi
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引用次数: 0

摘要

吲哚-3-乙酸是植物中常见的天然生长素。该化合物的合成衍生物,4-(2,4-二氟苯基)-2-(1H-吲哚-3-基)-4-氧代丁酸,也称为线粒体酸5(MA-5),已显示在应激诱导条件下可提高线粒体疾病患者成纤维细胞的存活率。进一步的研究证实了其在病理模型中的疗效,如缺血再灌注模型,可能通过增加ATP的产生。然而,MA-5对焦虑、精神分裂症和自闭症谱系障碍(ASD)等精神障碍的疗效尚未得到研究。我们的研究重点是在产前暴露于丙戊酸(VPA)诱导的ASD小鼠模型中检测MA-5的作用。VPA暴露显著降低了开放场地测试中的焦虑和探索行为水平。我们给小鼠喂食含MA-5的饮食5周,并观察到MA-5喂养组的上述行为有所改善。MA-5的疗效也在高架+迷宫和三腔试验中观察到。这些发现表明,MA-5可能用于治疗ASD,尤其是在线粒体功能障碍的患者中。
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MA-5 ameliorates autism-like behavior in mice prenatally exposed to valproic acid.

Indole-3-acetic acid is a common naturally occurring auxin in plants. A synthesized derivative of this compound, 4-(2,4-difluorophenyl)-2-(1H-indol-3-yl)-4-oxobutanoic acid also called mitochonic acid 5 (MA-5), has shown to increase the survival ratio of fibroblasts from patients with mitochondrial disease under stress-induced conditions. Further studies verified its efficacy in pathological models, such as an ischemia-reperfusion model, possibly by increasing ATP production. However, the efficacy of MA-5 in mental disorders, such as anxiety, schizophrenia, and autism spectrum disorders (ASD), has not been investigated. Our study focused on examining the effect of MA-5 in a mouse model of ASD induced by prenatal exposure to valproic acid (VPA). VPA exposure significantly deteriorated the level of anxiety and exploratory behavior in an open field test. We fed mice an MA-5-containing diet for 5 weeks and observed an improvement in the above behavior in the MA-5-fed groups. The efficacy of MA-5 was also observed in the elevated plus maze and three-chambered tests. These findings suggest that MA-5 could potentially be used to treat ASD, especially in patients with mitochondrial dysfunction.

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来源期刊
Behavioural Pharmacology
Behavioural Pharmacology 医学-行为科学
CiteScore
3.40
自引率
0.00%
发文量
84
审稿时长
6-12 weeks
期刊介绍: Behavioural Pharmacology accepts original full and short research reports in diverse areas ranging from ethopharmacology to the pharmacology of schedule-controlled operant behaviour, provided that their primary focus is behavioural. Suitable topics include drug, chemical and hormonal effects on behaviour, the neurochemical mechanisms under-lying behaviour, and behavioural methods for the study of drug action. Both animal and human studies are welcome; however, studies reporting neurochemical data should have a predominantly behavioural focus, and human studies should not consist exclusively of clinical trials or case reports. Preference is given to studies that demonstrate and develop the potential of behavioural methods, and to papers reporting findings of direct relevance to clinical problems. Papers making a significant theoretical contribution are particularly welcome and, where possible and merited, space is made available for authors to explore fully the theoretical implications of their findings. Reviews of an area of the literature or at an appropriate stage in the development of an author’s own work are welcome. Commentaries in areas of current interest are also considered for publication, as are Reviews and Commentaries in areas outside behavioural pharmacology, but of importance and interest to behavioural pharmacologists. Behavioural Pharmacology publishes frequent Special Issues on current hot topics. The editors welcome correspondence about whether a paper in preparation might be suitable for inclusion in a Special Issue.
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