Evidence map›Paper›PMID 21524730›Full record

ArticleBrain research2011

Glycine-activated chloride currents of neurons freshly isolated from the prefrontal cortex of young rats.

Yongli Lu, Jiang-Hong Ye

Abstract read
In one paragraph

Article in Brain research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 28% 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

19 citing papers in PubMed, 22 citations in OpenAlex.

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  9. Glycine receptor α3 and α2 subunits mediate tonic and exogenous agonist-induced currents in forebrain.Proceedings of the National Academy of Sciences of the United States of America · 2017
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  12. Extrasynaptic glycine receptors of rodent dorsal raphe serotonergic neurons: a sensitive target for ethanol.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2014
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  15. Ethanol reduces neuronal excitability of lateral orbitofrontal cortex neurons via a glycine receptor dependent mechanism.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2013
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  16. Acute effects of ethanol on GABAOpen journal of neuroscience · 2013
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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

2 authors at 2 institutions in 1 country.

Yongli LuDepartment of Anesthesiology, University of Medicine and Dentistry of New Jersey, New Jersey Medical School, Newark, NJ 07103, USA.
Jiang-Hong Ye
Rutgers New Jersey Medical SchoolRutgers, The State University of New Jersey · US

Funding

Alcohol and mesolimbic glutamatergic transmissionsR01AA016964 · NIAAA · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI YE, JIANG-HONG · 2008 to 2011
$1.4M
Glycine regulates ethanol intakeR21AA016618 · NIAAA · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI YE, JIANG-HONG · 2010 to 2011
$431k
Ethanol and mesolimbic GABAergic neuronsR21AA015925 · NIAAA · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI YE, JIANG-HONG · 2006 to 2007
$403k
NIAAA NIH HHS R01 AA016964NIAAA NIH HHS R01AA016964NIAAA NIH HHS R21 AA015925NIAAA NIH HHS R21AA015925NIAAA NIH HHS R21 AA016618NIAAA NIH HHS R21AA016618
6 · The paper itself

Abstract

Strychnine-sensitive glycine receptors (GlyR) play a major role in the excitability of CNS neurons and are also a major target of many drugs including some general anesthetics and ethanol. The prefrontal cortex (PFC) is an important substrate responsible for cognitive function and for sedation, as well as hypnosis (unconsciousness) which is induced by general anesthetics and ethanol. However, the functions and the physiological and pharmacological properties of GlyRs in mature PFC neurons have not been well studied. In this study, whole-cell currents induced by glycine (I(Gly)) were recorded from freshly isolated PFC neurons of Sprague-Dawley rats aged 5 to 39 postnatal days (neonatal, P5-12; weanling, P17-21 and peri-adolescent, P30-39). We found that most of the neurons examined were responsive to glycine and the response was concentration dependent. With the increase of age, the sensitivity to glycine was significantly decreased and the sensitivity to picrotoxin was significantly increased. Conversely, the changes in sensitivity to strychnine were not significant. Interestingly, I(Gly) of all age groups was suppressed (to different scope) by low concentrations of picrotoxin (≤ 30 μM), which selectively blocked α homomeric GlyRs. Conversely, about 20-65% of I(Gly) remained in the presence of 300 μM picrotoxin, suggesting the picrotoxin-resistant subtype the αβ heteromeric GlyR, was also present. These data provide the first evidence that there are at least two subtypes of functional GlyRs in the PFC neurons of young rats, and their physiological and pharmacological properties change substantially during maturation.

Indexed as

Age FactorsAnimalsAnimals, NewbornChloride Channel AgonistsChloride ChannelsDose-Response Relationship, DrugGABA AntagonistsGlycineGlycine AgentsIn Vitro TechniquesMembrane PotentialsNeuronsPicrotoxinPrefrontal CortexRatsRats, Sprague-DawleyChloride Channel AgonistsChloride ChannelsGABA AntagonistsGlycineGlycine AgentsPicrotoxinReceptors, GlycineStrychnine

Identifiers

PMID21524730
PMCPMC3199135
OpenAlexW2077878107

What OpenQuestion holds

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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.