ArticleMolecular psychiatry2026
Transcranial photobiomodulation to enhance sleep by elevating adenosine signaling: a translational study.
Article in Molecular psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- The Roles of Transcription Factor Ets-1 in Neurological Disorders.Molecular neurobiology · 2026Review
Corrections and comments
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Authors and funding
11 authors.
Funding
Abstract
Sleep disturbances are a significant health concern in modern society, with prevalent treatments often leading to limited efficacy and unwanted side effects. Adenosine, a sleep-promoting molecule in the brain, presents a promising target for innovative therapies, yet strategies to augment intracerebral adenosine have remained largely unexamined. This study explores transcranial photobiomodulation (tPBM) as a potential intervention, employing near-infrared (NIR) light to enhance mitochondrial adenosine triphosphate (ATP) synthesis and facilitate adenosine release. Utilizing fiberoptic cannula and electroencephalographic electrodes implanted in mice, we found that tPBM significantly increased non-rapid eye movement (NREM) sleep during and after stimulation compared to sham controls. Enhanced NREM delta power and elevated adenosine concentration in the frontal cortex were confirmed. In vitro experiments further demonstrated that NIR PBM increased cellular ATP production without inducing cytotoxicity. Additionally, a double-blind randomized controlled trial with 40 subjects demonstrated significant reductions in insomnia severity, sleep disturbances, and sleep latency. These findings provide preliminary clinical and translational evidence that tPBM may represent a promising non-pharmacological approach for short-term improvement of sleep disturbances through increased homeostatic pressure.
Identifiers
42744976What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.