Increased Iron Levels and Oxidative Stress Mediate Age-Related Impairments in Male and Female Drosophila melanogaster

被引:5
|
作者
Gomes K.K. [1 ]
Dos Santos A.B. [1 ]
Dos Anjos J.S. [1 ]
Leandro L.P. [2 ]
Mariano M.T. [1 ]
Pinheiro F.L. [3 ]
Farina M. [4 ]
Franco J.L. [1 ,2 ]
Posser T. [1 ]
机构
[1] Oxidative Stress and Cell Signaling Research Group, Interdisciplinary Research Center on Biotechnology-CIPBIOTEC, Universidade Federal Do Pampa, Campus São Gabriel, RS
[2] Department of Chemistry, Post Graduate Program in Toxicological Biochemistry, Universidade Federal de Santa Maria, RS
[3] Paleontology Laboratory, Federal University of Pampa, Campus São Gabriel, RS
[4] Department of Biochemistry, Federal University of Santa Catarina, Santa Catarina, Florianopolis
关键词
Cell death - Iron;
D O I
10.1155/2023/7222462
中图分类号
学科分类号
摘要
Aging is characterized by a functional decline in the physiological functions and organic systems, causing frailty, illness, and death. Ferroptosis is an iron- (Fe-) dependent regulated cell death, which has been implicated in the pathogenesis of several disorders, such as cardiovascular and neurological diseases. The present study investigated behavioral and oxidative stress parameters over the aging of Drosophila melanogaster that, together with augmented Fe levels, indicate the occurrence of ferroptosis. Our work demonstrated that older flies (30-day-old) of both sexes presented impaired locomotion and balance when compared with younger flies (5-day-old). Older flies also produced higher reactive oxygen species (ROS) levels, decreased glutathione levels (GSH), and increased lipid peroxidation. In parallel, Fe levels were augmented in the fly's hemolymph. The GSH depletion with diethyl maleate potentiated the behavioral damage associated with age. Our data demonstrated biochemical effects that characterize the occurrence of ferroptosis over the age of D. melanogaster and reports the involvement of GSH in the age-associated damages, which could be in part attributed to the augmented levels of Fe. © 2023 Karen Kich Gomes et al.
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