Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, ON M5S 3E1, Canada.
Department of Pharmaceutical Sciences, University of Toronto, Toronto, ON M5S 3M2, Canada.
Sci Signal. 2022 Jul 5;15(741):eabo1857. doi: 10.1126/scisignal.abo1857.
The nuclear receptor peroxisome proliferator-activated receptor alpha (PPARα) is emerging as an important target in the brain for the treatment or prevention of cognitive disorders. The identification of high-affinity ligands for brain PPARα may reveal the mechanisms underlying the synaptic effects of this receptor and facilitate drug development. Here, using an affinity purification-untargeted mass spectrometry (AP-UMS) approach, we identified an endogenous, selective PPARα ligand, 7()-hydroxy-docosahexaenoic acid [7()-HDHA]. Results from mass spectrometric detection of 7()-HDHA in mouse and rat brain tissues, time-resolved FRET analyses, and thermal shift assays collectively revealed that 7()-HDHA potently activated PPARα with an affinity greater than that of other ligands identified to date. We also found that 7()-HDHA activation of PPARα in cultured mouse cortical neurons stimulated neuronal growth and arborization, as well as the expression of genes associated with synaptic plasticity. The findings suggest that this DHA derivative supports and enhances neuronal synaptic capacity in the brain.
过氧化物酶体增殖物激活受体α(PPARα)是一种核受体,它作为治疗或预防认知障碍的大脑靶点正在兴起。鉴定脑 PPARα 的高亲和力配体可以揭示该受体的突触作用的机制,并促进药物的开发。在这里,我们使用亲和纯化非靶向质谱(AP-UMS)方法,鉴定了一种内源性、选择性的 PPARα 配体,7()-羟基二十二碳六烯酸[7()-HDHA]。在小鼠和大鼠脑组织中对 7()-HDHA 的质谱检测、时间分辨荧光共振能量转移分析和热移位测定的结果共同表明,7()-HDHA 以比迄今鉴定的其他配体更高的亲和力强烈激活 PPARα。我们还发现,7()-HDHA 在培养的小鼠皮质神经元中激活 PPARα,刺激神经元的生长和分支,以及与突触可塑性相关的基因的表达。这些发现表明,这种 DHA 衍生物支持和增强大脑中的神经元突触容量。