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A High-Throughput Screening of a Natural Products Library for Mitochondria Modulators

Overview
Journal Biomolecules
Publisher MDPI
Date 2024 Apr 27
PMID 38672457
Authors
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Abstract

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.

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References
1.
Abate M, Festa A, Falco M, Lombardi A, Luce A, Grimaldi A . Mitochondria as playmakers of apoptosis, autophagy and senescence. Semin Cell Dev Biol. 2019; 98:139-153. DOI: 10.1016/j.semcdb.2019.05.022. View

2.
Baran N, Lodi A, Dhungana Y, Herbrich S, Collins M, Sweeney S . Inhibition of mitochondrial complex I reverses NOTCH1-driven metabolic reprogramming in T-cell acute lymphoblastic leukemia. Nat Commun. 2022; 13(1):2801. PMC: 9120040. DOI: 10.1038/s41467-022-30396-3. View

3.
Harrington J, Ryter S, Plataki M, Price D, Choi A . Mitochondria in health, disease, and aging. Physiol Rev. 2023; 103(4):2349-2422. PMC: 10393386. DOI: 10.1152/physrev.00058.2021. View

4.
Gay N, Suwanjang W, Ruankham W, Songtawee N, Wongchitrat P, Prachayasittikul V . Butein, isoliquiritigenin, and scopoletin attenuate neurodegeneration antioxidant enzymes and SIRT1/ADAM10 signaling pathway. RSC Adv. 2022; 10(28):16593-16606. PMC: 9053097. DOI: 10.1039/c9ra06056a. View

5.
Serralha R, Rodrigues I, Bertolini A, Lima D, Nascimento M, Mouro M . Esculin reduces P2X7 and reverses mitochondrial dysfunction in the renal cortex of diabetic rats. Life Sci. 2020; 254:117787. DOI: 10.1016/j.lfs.2020.117787. View