Evidence map›Paper›PMID 24695701›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

Dorsal raphe serotonin neurons in mice: immature hyperexcitability transitions to adult state during first three postnatal weeks suggesting sensitive period for environmental perturbation.

Benjamin D Rood, Lyngine H Calizo, David Piel, Zachary P Spangler, Kaitlin Campbell, Sheryl G Beck

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
–field-weighted citation impact
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

36 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Astrocytic 5-HTExperimental & molecular medicine · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Embracing diversity in the 5-HT neuronal system.Nature reviews. Neuroscience · 2019
    Review
  14. Article
  15. Article
  16. Review
  17. Serotonin neuron development: shaping molecular and structural identities.Wiley interdisciplinary reviews. Developmental biology · 2018
    Review
  18. Article
  19. Article
  20. Review
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

6 authors.

Benjamin D RoodDepartment of Anesthesiology and Critical Care, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, and Department of Anesthesiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania 19104.
Lyngine H Calizo
David Piel
Zachary P Spangler
Kaitlin Campbell
Sheryl G Beck

Funding

Anxiety development in 5-HT1A autoreceptor knockout mice, interaction with stressRC1MH089800 · NIMH · CHILDREN'S HOSP OF PHILADELPHIA · PI BECK, SHERYL G, HEN, RENE · 2009 to 2010
$949k
Serotonin-limbic system interactions that mediate anxietyR21MH099488 · NIMH · CHILDREN'S HOSP OF PHILADELPHIA · PI BECK, SHERYL G · 2012 to 2013
$452k
NIMH NIH HHS R01 MH0754047NIMH NIH HHS R21 MH099488NIMH NIH HHS RC1 MH089800NIMH NIH HHS RC1MH089800
6 · The paper itself

Abstract

Trauma during early life is a major risk factor for the development of anxiety disorders and suggests that the developing brain may be particularly sensitive to perturbation. Increased vulnerability most likely involves altering neural circuits involved in emotional regulation. The role of serotonin in emotional regulation is well established, but little is known about the postnatal development of the raphe where serotonin is made. Using whole-cell patch-clamp recording and immunohistochemistry, we tested whether serotonin circuitry in the dorsal and median raphe was functionally mature during the first 3 postnatal weeks in mice. Serotonin neurons at postnatal day 4 (P4) were hyperexcitable. The increased excitability was due to depolarized resting membrane potential, increased resistance, increased firing rate, lack of 5-HT1A autoreceptor response, and lack of GABA synaptic activity. Over the next 2 weeks, membrane resistance decreased and resting membrane potential hyperpolarized due in part to potassium current activation. The 5-HT1A autoreceptor-mediated inhibition did not develop until P21. The frequency of spontaneous inhibitory and excitatory events increased as neurons extended and refined their dendritic arbor. Serotonin colocalized with vGlut3 at P4 as in adulthood, suggesting enhanced release of glutamate alongside enhanced serotonin release. Because serotonin affects circuit development in other brain regions, altering the developmental trajectory of serotonin neuron excitability and release could have many downstream consequences. We conclude that serotonin neuron structure and function change substantially during the first 3 weeks of life during which external stressors could potentially alter circuit formation.

Indexed as

EnvironmentAge FactorsAnimalsAnimals, NewbornBacterial ProteinsBicucullineExcitatory Amino Acid AntagonistsExcitatory Postsynaptic PotentialsGABA-A Receptor AntagonistsGuanosine 5'-O-(3-Thiotriphosphate)In Vitro TechniquesLuminescent ProteinsMaleMiceMice, TransgenicQuinoxalines5-carboxamidotryptamineBacterial ProteinsBicucullineExcitatory Amino Acid AntagonistsFev protein, mouseFG 9041GABA-A Receptor AntagonistsGuanosine 5'-O-(3-Thiotriphosphate)Luminescent ProteinsQuinoxalinesSerotoninSerotonin Receptor AgonistsTranscription Factorsyellow fluorescent protein, Bacteria

Identifiers

PMID24695701
PMCPMC3972713

What OpenQuestion holds

Textmetadata
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.