Journal Article DZNE-2026-00669

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Sleep deprivation increases levels of the synaptic density marker SV2A in the human brain.

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2026
PLoS Lawrence, KS

PLoS biology 24(6), e3003816 () [10.1371/journal.pbio.3003816]

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Abstract: Sleep is essential for synaptic homeostasis, a proposed mechanism whereby wakefulness leads to synaptic potentiation and sleep facilitates synaptic down-selection. Synaptic vesicle glycoprotein 2A (SV2A), whose availability is quantifiable by [¹⁸F]SynVesT-1 positron emission tomography (PET), is commonly interpreted as a proxy for synaptic density. In this randomized study, we examined 40 healthy adults (mean age 27.5 ± 6.5 years) who underwent two [¹⁸F]SynVesT-1 PET scans on consecutive days. Half of the participants were assigned to the normal sleep (i.e., control) condition and half to the sleep deprivation condition. Scans were performed at the same circadian time point, approximately 4 h after awakening in the control group and during baseline in the sleep deprivation group or after ~28 h of continuous wakefulness in the sleep deprivation group after sleep deprivation. Sleep deprivation led to significant increases in synaptic vesicle glycoprotein 2A binding in multiple brain regions, including the thalamus (+4.6%), hippocampus (+5.6%), and parietal cortex (+3.2%), whereas no changes were observed in controls. The degree of increase in synaptic vesicle glycoprotein 2A positively correlated with elevated slow wave activity during recovery sleep, a physiological marker of sleep pressure. These findings provide in vivo support for the synaptic homeostasis hypothesis in humans and suggest that synaptic vesicle glycoprotein 2A PET imaging is sensitive to sleep-wake dependent synaptic plasticity.The study was prospectively registered on 19.01.2022 here: German Clinical Trials Registry: DRKS # DRKS00027867, https://drks.de/search/en/trial/DRKS00027867.

Keyword(s): Humans (MeSH) ; Sleep Deprivation: metabolism (MeSH) ; Sleep Deprivation: diagnostic imaging (MeSH) ; Adult (MeSH) ; Male (MeSH) ; Female (MeSH) ; Positron-Emission Tomography (MeSH) ; Membrane Glycoproteins: metabolism (MeSH) ; Brain: metabolism (MeSH) ; Brain: diagnostic imaging (MeSH) ; Nerve Tissue Proteins: metabolism (MeSH) ; Synapses: metabolism (MeSH) ; Young Adult (MeSH) ; Wakefulness: physiology (MeSH) ; Sleep: physiology (MeSH) ; Biomarkers: metabolism (MeSH) ; Membrane Glycoproteins ; Nerve Tissue Proteins ; SV2A protein, human ; Biomarkers

Classification:

Contributing Institute(s):
  1. Positron Emissions Tomography (PET) (AG Boecker)
Research Program(s):
  1. 353 - Clinical and Health Care Research (POF4-353) (POF4-353)

Database coverage:
Medline ; Creative Commons Attribution CC BY (No Version) ; DOAJ ; Article Processing Charges ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Agriculture, Biology and Environmental Sciences ; Current Contents - Life Sciences ; DOAJ Seal ; Ebsco Academic Search ; Essential Science Indicators ; Fees ; IF >= 5 ; JCR ; PubMed Central ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection ; Zoological Record
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Document types > Articles > Journal Article
Institute Collections > BN DZNE > BN DZNE-AG Boecker
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 Record created 2026-06-24, last modified 2026-06-24


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