The Influence of Caffeine on <i>Siesta</i> and Nighttime Sleep in <i>Drosophila melanogaster</i>

Caffeine, a plant-derived psychostimulant, has been demonstrated to reduce sleep and increase dopaminergic neuron activity in mammals through competitive antagonism at adenosine receptors (AdoRs). However, the extent to which it influences daytime sleep (siesta) as much as nighttime sleep and the involvement of the adenosine signaling pathway in this process remain unsolved. It is similarly unclear whether the influence of caffeine varies with age and depends on sex and what type of cells it affects most; the clock cells that are involved in sleep timing and regulation or dopaminergic neurons, which are crucial for voluntary movement. To address this question, the role of caffeine has been investigated in Drosophila melanogaster (wild-type Canton-S flies), which has also been observed to reduce sleep in response to caffeine. The siesta and nighttime sleep of 3-, 30-, and 50-day-old males and females of Canton-S Drosophila were examined. Furthermore, transgenic flies with overexpressed or silenced dAdoR in all neurons (elav-expressing cells), the circadian clock cells (tim-expressing cells), and dopaminergic neurons (th-expressing cells) were studied. We found that females exhibited greater sensitivity to caffeine than males, and that older flies slept longer during the day than young flies. However, caffeine treatment resulted in reducing siesta in flies with overexpression of dAdoR in all neurons, tim-, and th-expressing cells. Conversely, silencing of dAdoR increased siesta. Therefore, the observed differences in the daytime sleep of Drosophila appeared to depend on signaling through AdoRs.

Authors

Institutions

Publication Details

Journal
Developmental Neurobiology
Published
2025-06-17
DOI
https://doi.org/10.1002/dneu.22987
Primary Topic
Neurobiology and Insect Physiology Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

The Influence of Caffeine on Siesta and Nighttime Sleep in Drosophila melanogaster

Jolanta Górska‐Andrzejak, Elżbieta Pyza, Debarati Bhattacharya, Terence L. Al Abaquita
Developmental Neurobiology
Neurobiology and Insect Physiology Research
article

The Influence of Caffeine on Siesta and Nighttime Sleep in Drosophila melanogaster

Jolanta Górska‐Andrzejak, Elżbieta Pyza, Debarati Bhattacharya, Terence L. Al Abaquita
article en

Abstract

Caffeine, a plant-derived psychostimulant, has been demonstrated to reduce sleep and increase dopaminergic neuron activity in mammals through competitive antagonism at adenosine receptors (AdoRs). However, the extent to which it influences daytime sleep (siesta) as much as nighttime sleep and the involvement of the adenosine signaling pathway in this process remain unsolved. It is similarly unclear whether the influence of caffeine varies with age and depends on sex and what type of cells it affects most; the clock cells that are involved in sleep timing and regulation or dopaminergic neurons, which are crucial for voluntary movement. To address this question, the role of caffeine has been investigated in Drosophila melanogaster (wild-type Canton-S flies), which has also been observed to reduce sleep in response to caffeine. The siesta and nighttime sleep of 3-, 30-, and 50-day-old males and females of Canton-S Drosophila were examined. Furthermore, transgenic flies with overexpressed or silenced dAdoR in all neurons (elav-expressing cells), the circadian clock cells (tim-expressing cells), and dopaminergic neurons (th-expressing cells) were studied. We found that females exhibited greater sensitivity to caffeine than males, and that older flies slept longer during the day than young flies. However, caffeine treatment resulted in reducing siesta in flies with overexpression of dAdoR in all neurons, tim-, and th-expressing cells. Conversely, silencing of dAdoR increased siesta. Therefore, the observed differences in the daytime sleep of Drosophila appeared to depend on signaling through AdoRs.

Developmental NeurobiologyVol. 85(3)
Jagiellonian University (PL)
Good health and well-being
Openalex Percentile: Top 85%
Neurobiology and Insect Physiology Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.