Evidence map›Paper›PMID 17920133›Full record

ArticleJournal of neuroscience methods2008

Morphological and physiological properties of serotonergic neurons in dissociated cultures from the postnatal rat dorsal raphe nucleus.

Junko Yasufuku-Takano, Shigehiro Nakajima, Yasuko Nakajima

Abstract read
In one paragraph

Article in Journal of neuroscience methods, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.2field-weighted citation impact, top 53% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Neuronal phenotype dependency of agonist-induced internalization of the 5-HT(1A) serotonin receptor.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  4. Article
  5. 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

3 authors at 1 institution in 1 country.

Junko Yasufuku-TakanoDepartment of Anatomy and Cell Biology, University of Illinois at Chicago, College of Medicine (M/C 512), 808 South Wood Street, Chicago, IL 60612, USA.
Shigehiro Nakajima
Yasuko Nakajima
University of Illinois Chicago · US

Funding

NEUROPHARMACOLOGY OF AROUSAL AND SLEEP DISORDERSR01NS043239 · NINDS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI NAKAJIMA, YASUKO · 2003 to 2006
$1.3M
MOLECULAR AND CELLULAR NEUROPHYSIOLOGY FOR MENTAL HEALTHR01MH057837 · NIMH · UNIVERSITY OF ILLINOIS AT CHICAGO · PI NAKAJIMA, SHIGEHIRO · 1998 to 2002
$528k
NIMH NIH HHS MH057837NINDS NIH HHS NS043239NINDS NIH HHS R01 NS043239
6 · The paper itself

Abstract

We have developed dissociated primary cultures of the dorsal raphe nucleus from postnatal 9-12-day-old rats. The nucleus was dissected out from brain slices, dissociated, and cultured over a glial feeder layer. Serotonin immunocytochemistry revealed that 62% of cultured neurons were serotonergic. There was no significant difference in diameters between serotonergic and non-serotonergic neurons. With the whole-cell patch-clamp method, cultured neurons were tested for responses to 8-hydroxydipropylaminotetraline (8-OH-DPAT, a selective agonist for 5-HT(1A)), and then treated with serotonin immunocytochemistry. Ninety-two percent of neurons responding to 8-OH-DPAT were serotonergic. These results were used to identify serotonergic neurons. In most cases, serotonergic neurons did not show spontaneous firings of action potentials. Constant current depolarizations elicited trains of action potentials that usually did not show marked adaptation. Application of 8-OH-DPAT inhibited action potential firing. The current-voltage relation of the 8-OH-DPAT-induced current indicated an inward rectification with its reversal potential near E(K). Serotonergic neurons were depolarized by phenylephrine, bombesin, and gastrin-releasing peptide. This culture system will serve as a useful tool for elucidating the cellular, physiological, and molecular properties of brain serotonergic neurons.

Indexed as

8-Hydroxy-2-(di-n-propylamino)tetralinAnimalsAnimals, NewbornCells, CulturedDose-Response Relationship, RadiationElectric StimulationMembrane PotentialsNeuronsNeurotransmitter AgentsPatch-Clamp TechniquesRaphe NucleiRatsSerotoninSerotonin Receptor AgonistsTime Factors8-Hydroxy-2-(di-n-propylamino)tetralinNeurotransmitter AgentsSerotoninSerotonin Receptor Agonists

Identifiers

PMID17920133
PMCPMC2234594
OpenAlexW2010051698

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.