Makinde Emmanuel, Ma Linlin, Mellick George D, Feng Yunjiang
Griffith Institute for Drug Discovery, Griffith University, Brisbane, QLD 4111, Australia.
School of Environment and Science, Griffith University, Brisbane, QLD 4111, Australia.
Biomolecules. 2024 Apr 4;14(4):440. doi: 10.3390/biom14040440.
Mitochondria, the energy hubs of the cell, are progressively becoming attractive targets in the search for potent therapeutics against neurodegenerative diseases. The pivotal role of mitochondrial dysfunction in the pathogenesis of various diseases, including Parkinson's disease (PD), underscores the urgency of discovering novel therapeutic strategies. Given the limitations associated with available treatments for mitochondrial dysfunction-associated diseases, the search for new potent alternatives has become imperative. In this report, we embarked on an extensive screening of 4224 fractions from 384 Australian marine organisms and plant samples to identify natural products with protective effects on mitochondria. Our initial screening using PD patient-sourced olfactory neurosphere-derived (hONS) cells with rotenone as a mitochondria stressor resulted in 108 promising fractions from 11 different biota. To further assess the potency and efficacy of these hits, the 11 biotas were subjected to a subsequent round of screening on human neuroblastoma (SH-SY5Y) cells, using 6-hydroxydopamine to induce mitochondrial stress, complemented by a mitochondrial membrane potential assay. This rigorous process yielded 35 active fractions from eight biotas. Advanced analysis using an orbit trap mass spectrophotometer facilitated the identification of the molecular constituents of the most active fraction from each of the eight biotas. This meticulous approach led to the discovery of 57 unique compounds, among which 12 were previously recognized for their mitoprotective effects. Our findings highlight the vast potential of natural products derived from Australian marine organisms and plants in the quest for innovative treatments targeting mitochondrial dysfunction in neurodegenerative diseases.
线粒体作为细胞的能量枢纽,在寻找针对神经退行性疾病的有效治疗方法的过程中,正逐渐成为具有吸引力的靶点。线粒体功能障碍在包括帕金森病(PD)在内的各种疾病的发病机制中起着关键作用,这凸显了发现新治疗策略的紧迫性。鉴于与线粒体功能障碍相关疾病的现有治疗方法存在局限性,寻找新的有效替代方法已势在必行。在本报告中,我们对来自384种澳大利亚海洋生物和植物样本的4224个组分进行了广泛筛选,以鉴定对线粒体具有保护作用的天然产物。我们最初使用来自帕金森病患者的嗅觉神经球衍生(hONS)细胞,并以鱼藤酮作为线粒体应激源进行筛选,从11种不同的生物群中得到了108个有前景的组分。为了进一步评估这些命中组分的效力和功效,对这11种生物群在人神经母细胞瘤(SH-SY5Y)细胞上进行了第二轮筛选,使用6-羟基多巴胺诱导线粒体应激,并辅以线粒体膜电位测定。这个严格的过程从8种生物群中产生了35个活性组分。使用轨道阱质谱仪进行的高级分析有助于鉴定来自这8种生物群中每种生物群最活跃组分的分子成分。这种细致的方法导致发现了57种独特的化合物,其中12种以前因其对线粒体的保护作用而被认可。我们的研究结果突出了源自澳大利亚海洋生物和植物的天然产物在寻求针对神经退行性疾病中线粒体功能障碍的创新治疗方法方面的巨大潜力。