Evidence map›Paper›PMID 26146031›Full record

ArticleBehavioural brain research2015

The homeostatic regulation of REM sleep: A role for localized expression of brain-derived neurotrophic factor in the brainstem.

Subimal Datta, Clifford M Knapp, Richa Koul-Tiwari, Abigail Barnes

Abstract read
In one paragraph

Article in Behavioural brain research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.3field-weighted citation impact, top 13% of its field
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Deficiency of orexin signaling during sleep is involved in abnormal REM sleep architecture in narcolepsy.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Chronic Paroxetine Treatment Prevents the Emergence of Abnormal Electroencephalogram Oscillations in Huntington's Disease Mice.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2017
    Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 4 institutions in 1 country.

Subimal DattaDepartment of Anesthesiology, Graduate School of Medicine, The University of Tennessee, 1924 Alcoa Highway, Knoxville, TN 37920, USA; Department of Psychology, College of Arts and Sciences, The University of Tennessee, 1404 Circle Drive, Knoxville, TN 37996, USA. Electronic address: sdatta1@utk.edu.
Clifford M KnappDepartment of Psychiatry, Boston University School of Medicine, 85 East Newton Street, Boston, MA 02118, USA.
Richa Koul-TiwariDepartment of Anesthesiology, Graduate School of Medicine, The University of Tennessee, 1924 Alcoa Highway, Knoxville, TN 37920, USA.
Abigail BarnesDepartment of Anesthesiology, Graduate School of Medicine, The University of Tennessee, 1924 Alcoa Highway, Knoxville, TN 37920, USA.
Alcoa (United States) · USBoston University · USKnoxville College · USUniversity of Tennessee at Knoxville · US

Funding

CELLULAR AND NEUROCHEMICAL MECHANISMS OF REM SLEEPR01MH059839 · NIMH · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI DATTA, SUBIMAL · 1999 to 2017
$5.7M
NIMH NIH HHS MH59839NIMH NIH HHS R01 MH059839
6 · The paper itself

Abstract

Homeostatic regulation of REM sleep plays a key role in neural plasticity and deficits in this process are implicated in the development of many neuropsychiatric disorders. Little is known, however, about the molecular mechanisms that underlie this homeostatic regulation process. This study examined the hypothesis that, during selective REM sleep deprivation (RSD), increased brain-derived neurotrophic factor (BDNF) expression in REM sleep regulating areas is critical for the development of homeostatic drive for REM sleep, as measured by an increase in the number of REM sleep transitions. Rats were assigned to RSD, non-sleep deprived (BSL), or total sleep deprivation (TSD) groups. Physiological recordings were obtained from cortical, hippocampal, and pontine EEG electrodes over a 6h period, in which sleep deprivation occurred during the first 3h. In the RSD, but not the other conditions, homeostatic drive for REM sleep increased progressively. BDNF protein expression was significantly greater in the pedunculopontine tegmentum (PPT) and subcoeruleus nucleus (SubCD) in the RSD as compared to the TSD and BSL groups, areas that regulate REM sleep, but not in the medial preoptic area, which regulates non-REM sleep. There was a significant positive correlation between RSD-induced increases in number of REM sleep episodes and increased BDNF expression in the PPT and SubCD. These increases positively correlated with levels of homeostatic drive for REM sleep. These results, for the first time, suggest that selective RSD-induced increased expression of BDNF in the PPT and SubCD are determinant factors in the development of the homeostatic drive for REM sleep.

Indexed as

HomeostasisAnimalsBrainBrain-Derived Neurotrophic FactorBrain StemBrain WavesElectroencephalographyMaleRatsRats, WistarSleep DeprivationSleep, REMWakefulnessBrain-Derived Neurotrophic FactorBDNFBrainstemDorsal subcoeruleus nucleusHomeostatic regulationPedunculopontine tegmentumSelective REM sleep deprivation

Identifiers

PMID26146031
PMCPMC4558236
OpenAlexW849299161

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.