The Effect of Caffeine Exposure on Sleep Patterns in Zebrafish Larvae and Its Underlying Mechanism.
Study Goal
The researchers aimed to investigate caffeine's impact on zebrafish larval sleep/wake behavior and the expression of key regulatory genes in the sleep pathway.
Results Summary
Caffeine induced sleep pattern disorders, upregulated adenosine receptor genes, decreased total sleep time and efficiency, and increased ADA activity and CREB expression, suggesting regulation of circadian clock genes via the ADA/ADORA/CREB pathway.
Population
Zebrafish larvae
Effective Dosage
31.25 μM, 62.5 μM, and 120 μM
Duration
Up to 120 h (optimal exposure time)
Interactions
None mentioned
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
caffeine | increase | sleep pattern disorders | zebrafish larvae | - | could induce | #1 |
caffeine | increase | adenosine receptor genes (adora1a, adora1b, adora2a, adora2ab, adora2b) | zebrafish larvae | p < 0.05 | significantly upregulate | #2 |
caffeine | decrease | total sleep time | zebrafish larvae | - | markedly decrease | #3 |
caffeine | decrease | sleep efficiency | zebrafish larvae | - | markedly decrease | #4 |
caffeine | increase | activity of ADA | zebrafish larvae | p < 0.001 | significantly increased | #5 |
caffeine | increase | tissue-specific expression of CREB | zebrafish larvae | - | significantly increased | #6 |
The effect of caffeine on the behavior and sleep patterns of zebrafish larvae, as well as its underlying mechanisms, has been a topic of great interest. This study aimed to investigate the impact of caffeine on zebrafish larval sleep/wake behavior and the expression of key regulatory genes such as cAMP-response element binding protein (CREB) and adenosine (ADA) in the sleep pathway. To begin, the study determined the optimal dose and duration of caffeine exposure, with the optimal doses found to be 31.25 μM, 62.5 μM, and 120 μM. Similarly, the optimal exposure time was established as no more than 120 h, ensuring a mortality rate of less than 10%. The confirmation of these conditions was achieved through the assessment of angiogenesis and the inflammatory reaction. As a result, the treatment time point of 24 h post-fertilization (hpf) was selected to examine the effects of caffeine on zebrafish larval sleep rhythm (48 h, with a light cycle of 14:10). Furthermore, the study analyzed the expression of clock genes (bmal1a, per1b, per2, per3, cry2), adenosine receptor genes (adora1a, adora1b, adora2aa, adora2ab, adora2b), and key regulatory factors (CREB and ADA). The research confirmed that caffeine could induce sleep pattern disorders, significantly upregulate adenosine receptor genes (adora1a, adora1b, adora2a, adora2ab, adora2b) (p < 0.05), and markedly decrease the total sleep time and sleep efficiency of the larvae. Additionally, the activity of ADA significantly increased during the exposure (p < 0.001), and the tissue-specific expression of CREB was also significantly increased, as assessed by immunofluorescence. Caffeine may regulate circadian clock genes through the ADA/ADORA/CREB pathway. These findings not only enhance our understanding of the effects of caffeine on zebrafish larvae but also provide valuable insights into the potential impact of caffeine on human behavior and sleep.