Effect of citrus peels‐supplemented diet on longevity, memory index, redox status, cholinergic and monoaminergic enzymes in Drosophila melanogaster model

2021 ◽  
Vol 45 (2) ◽  
Author(s):  
Ganiyu Oboh ◽  
Damilola M. Olatunde ◽  
Ayokunle O. Ademosun ◽  
Opeyemi B. Ogunsuyi
2021 ◽  
Vol 2 (1) ◽  
pp. 26-37
Author(s):  
O.O. Dosumu ◽  
◽  
E.N. Akang ◽  
O.K. Idowu ◽  
G.J. Adeyemi

Background: Parkinson's disease (PD) is a multifactorial neurodegenerative disease with pathogenic mechanisms traceable to oxidative damage and mitochondrial dysfunction. Rotenone, a chemical compound commonly found in pesticides, has been found to inhibit mitochondrial complex-I and initiate PD-like symptoms in mammals and several invertebrates. Virgin Coconut Oil (VCNO) obtained from the coconut fruit has been found to possess anti-oxidative and anti-inflammatory properties. Objectives: The present study evaluated the effect of VCNO on rotenone-induced Parkinsonism in fruit flies- Drosophila melanogaster (D. melanogaster). Methods: Canton special (CS) strains of D. melanogaster, aged between 1 to 3 days were orally exposed for 7 days to 0, 250, 500 and 750 μM rotenone diet for toxicity assay, and 0, 2.5, 5 and 10 % w/w VCNO diet for longevity assay. Thereafter, 5 % VCNO diet was selected for evaluation against 500 μM rotenone. Subsequently, behavioural test (negative geotaxis), markers for redox status and enzyme activities were evaluated. Results: The results showed that rotenone induced toxicity in the flies, while VCNO increased the lifespan of D. melanogaster in a dose-dependent manner. In addition, VCNO ameliorated rotenone-induced locomotor deficits, elevated MDA, as well as the depleted GSH levels. It also mitigated the inhibited activities of SOD, CAT and ATPase in the flies. Conclusions: VCNO protected D. melanogaster against rotenone-induced toxicity by extending longevity, preventing locomotor deficits and reducing oxidative stress.


Cell Reports ◽  
2015 ◽  
Vol 11 (12) ◽  
pp. 1856-1865 ◽  
Author(s):  
Katja E. Menger ◽  
Andrew M. James ◽  
Helena M. Cochemé ◽  
Michael E. Harbour ◽  
Edward T. Chouchani ◽  
...  

Cell Reports ◽  
2015 ◽  
Vol 13 (6) ◽  
pp. 1285 ◽  
Author(s):  
Katja E. Menger ◽  
Andrew M. James ◽  
Helena M. Cochemé ◽  
Michael E. Harbour ◽  
Edward T. Chouchani ◽  
...  

Author(s):  
Opeyemi B. Ogunsuyi ◽  
Olawande C. Olagoke ◽  
Blessing A. Afolabi ◽  
Julia S. Loreto ◽  
Adedayo O. Ademiluyi ◽  
...  

2020 ◽  
Author(s):  
Gesa F. Dinges ◽  
Alexander S. Chockley ◽  
Till Bockemühl ◽  
Kei Ito ◽  
Alexander Blanke ◽  
...  

2001 ◽  
Vol 7 (S2) ◽  
pp. 1012-1013
Author(s):  
Uyen Tram ◽  
William Sullivan

Embryonic development is a dynamic event and is best studied in live animals in real time. Much of our knowledge of the early events of embryogenesis, however, comes from immunofluourescent analysis of fixed embryos. While these studies provide an enormous amount of information about the organization of different structures during development, they can give only a static glimpse of a very dynamic event. More recently real-time fluorescent studies of living embryos have become much more routine and have given new insights to how different structures and organelles (chromosomes, centrosomes, cytoskeleton, etc.) are coordinately regulated. This is in large part due to the development of commercially available fluorescent probes, GFP technology, and newly developed sensitive fluorescent microscopes. For example, live confocal fluorescent analysis proved essential in determining the primary defect in mutations that disrupt early nuclear divisions in Drosophila melanogaster. For organisms in which GPF transgenics is not available, fluorescent probes that label DNA, microtubules, and actin are available for microinjection.


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