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Dagan, Y.

Publications and source records attributed to Dagan, Y..

2 recordsLinked to original sources

Respiration-Triggered Olfactory Stimulation ReducesObstructive Sleep Apnea Symptoms Severity: A Prospective Pilot Study

Obstructive sleep apnea (OSA) is a prevalent sleep-disordered breathing condition characterized by repetitive reduction in breathing during sleep. Current care standard for OSA is continuous positive air pressure devices, often suffering from low tolerance due to limited adherence. Capitalizing on the unique neurocircuitry of olfactory perception and its retained function during sleep, we conducted a pilot study to test transient, respiration-based olfactory stimulation as a treatment for OSA markers. Thirty-two OSA patients (Apnea-Hypopnea Index (AHI)[≥]15 events/hour) underwent two polysomnography sessions, Odor and Control, in random order. In Odor nights, patients were presented with transient respiratory-based olfactory stimulation delivered via a computer-controlled commercial olfactometer (Scentific). The olfactometer, equipped with a wireless monitoring, analyzed respiratory patterns and presented odor upon detection of respiratory events. No odors were presented in Control nights. Following exclusions, 17 patients entered analysis (4 women, 47.4 (10.5) years, BMI: 33.8 (7.8)). We observed that olfactory stimulation during sleep reduced AHI ( Odor:17.2 (20.9), Control: 28.2 (18.6), z=- 3.337, p=0.000846, BF10=57.9), reflecting an average decrease of 31.3% in event number. Relatedly, stimulation reduced the oxygen desaturation index (ODI) by 26.9% ( Odor: 12.5 (15.8), Control: 25.7 (25.9), z=-3.337, p=0.000846, BF10=9.522. This effect was not linked to baseline OSA markers severity ({rho}=-0.042, p=0.87). Olfactory stimulation did not arouse from sleep or affect sleep structure, measured as time per sleep stage (F(1,16)=0.088, p=0.77). In conclusion, olfactory stimulation during sleep was effective in reducing OSA markers severity without inducing arousals and may provide a novel treatment for OSA, prompting continued research.

physiology↗

m6A is required for resolving progenitor identity during planarian stem cell differentiation

Regeneration requires accurate production of missing cell lineages. Cell production is driven by changes to gene expression, which is shaped by multiple layers of regulation. Here, we find that the ubiquitous mRNA base-modification, m6A, is required for proper cell fate choice and cellular maturation in planarian stem cells (neoblasts). We mapped m6A-enriched regions in 7,600 planarian genes, and found that perturbation of the m6A pathway resulted in progressive deterioration of tissues and death. Using single cell RNA sequencing of >20,000 cells following perturbation of the pathway, we discovered that m6A negatively regulates transcription of histone variants, and that inhibition of the pathway resulted in accumulation of undifferentiated cells throughout the animal in an abnormal transcriptional state. Analysis of >1000 planarian gene expression datasets revealed that the inhibition of the chromatin modifying complex NuRD had almost indistinguishable consequences, unraveling an unappreciated link between m6A and chromatin modifications. Our findings reveal that m6A is critical for planarian stem cell homeostasis and gene regulation in regeneration.

developmental biology↗