Crack cocaine exposure leads to developmental alterations and mitochondrial dysfunction in the <i>Drosophila melanogaster</i> model

Crack cocaine is a highly addictive drug that may induce a plethora of health problems in users.The underlying pathophysiological and toxicity mechanisms promoted by crack cocaine use are still unclear.Here, we used the <i>Drosophila melanogaster</i> model to evaluate the dose-dependent effects of crack cocaine ingestion on several developmental and lifelong parameters, as well as the expression levels of key mitochondrial, endoplasmic reticulum, and antioxidant genes.Canton-S flies were fed increasing concentrations of crack cocaine and subjected to development, longevity, and negative geotaxis assays.Subsequently, we analyzed gene expression in L3 larvae and adult heads by quantitative real-time PCR. Crack cocaine increased larval lethality (>80%), and it affected the locomotor abilities of both larvae and adults (20-30%).This was associated with increased levels of mtDNA and transcripts for Marf, Pink1, Catalase, and Sod2 at low concentrations, suggesting mitochondrial biogenesis and remodelling.Mitochondrial and ER stress were evident at high crack concentrations, as indicated by a decrease in mtDNA copy number and increased transcript levels of parkin, spargel, Ire1, PEK, and CaMKII.Taken together, our data suggest that crack cocaine may lead to distinct harmful effects that are often apparent at very low doses, increasing adverse outcomes at high doses.

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Publication Details

Journal
Xenobiotica
Published
2025-08-09
DOI
https://doi.org/10.1080/00498254.2025.2547613
Primary Topic
Neurotransmitter Receptor Influence on Behavior
Type
article
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article

Crack cocaine exposure leads to developmental alterations and mitochondrial dysfunction in the Drosophila melanogaster model

Jean Phellipe Marques do Nascimento, Lucas Anhezini, Amanda Larissa Dias Pacheco, Kellysson Bruno Oliveira et al.
Xenobiotica
Neurotransmitter Receptor Influence on Behavior
article

Crack cocaine exposure leads to developmental alterations and mitochondrial dysfunction in the Drosophila melanogaster model

Jean Phellipe Marques do Nascimento, Lucas Anhezini, Amanda Larissa Dias Pacheco, Kellysson Bruno Oliveira, Marcos T. Oliveira, Francisco Rubens Alves dos Santos, Igor Santana de Melo, Keylla Lavínia da Silva Oliveira, Bianca Rodrigues Melo da Silva, Carlos Antônio Couto Lima, Jerusa Maria de Oliveira, Olagide Wagner de Castro, Eurípedes Alves da Silva Filho, Jucilene Freitas-Santos, Mykaella Andrade de Araújo, Luciana R. de S. Floresta, C. Silva, Isa Rafaella Rocha Brito
article en

Abstract

Crack cocaine is a highly addictive drug that may induce a plethora of health problems in users.The underlying pathophysiological and toxicity mechanisms promoted by crack cocaine use are still unclear.Here, we used the <i>Drosophila melanogaster</i> model to evaluate the dose-dependent effects of crack cocaine ingestion on several developmental and lifelong parameters, as well as the expression levels of key mitochondrial, endoplasmic reticulum, and antioxidant genes.Canton-S flies were fed increasing concentrations of crack cocaine and subjected to development, longevity, and negative geotaxis assays.Subsequently, we analyzed gene expression in L3 larvae and adult heads by quantitative real-time PCR. Crack cocaine increased larval lethality (>80%), and it affected the locomotor abilities of both larvae and adults (20-30%).This was associated with increased levels of mtDNA and transcripts for Marf, Pink1, Catalase, and Sod2 at low concentrations, suggesting mitochondrial biogenesis and remodelling.Mitochondrial and ER stress were evident at high crack concentrations, as indicated by a decrease in mtDNA copy number and increased transcript levels of parkin, spargel, Ire1, PEK, and CaMKII.Taken together, our data suggest that crack cocaine may lead to distinct harmful effects that are often apparent at very low doses, increasing adverse outcomes at high doses.

XenobioticaVol. 55(7)
Núcleo de Pesquisas Aplicadas (Brazil) (BR), Centro Universitário de Araraquara (BR), Universidade Federal de Alagoas (BR), Universidade Estadual Paulista (Unesp) (BR)
Zero hunger
Openalex Percentile: Top 77%
Neurotransmitter Receptor Influence on Behavior
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