Evidence map›Paper›PMID 26785258›Full record

ArticlePloS one2016

Identification of a Group of GABAergic Neurons in the Dorsomedial Area of the Locus Coeruleus.

Xin Jin, Shanshan Li, Brian Bondy, Weiwei Zhong, Max F Oginsky, Yang Wu, Christopher M Johnson, Shuang Zhang, Ningren Cui, Chun Jiang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

32 citing papers in PubMed, 60 citations in OpenAlex.

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  17. Precise and Pervasive Phasic Bursting in Locus Coeruleus during Maternal Behavior in Mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
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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

10 authors at 1 institution in 1 country.

Xin JinDepartment of Biology, Georgia State University, Atlanta, Georgia, United States of America.
Shanshan LiDepartment of Biology, Georgia State University, Atlanta, Georgia, United States of America.
Brian BondyDepartment of Biology, Georgia State University, Atlanta, Georgia, United States of America.
Weiwei ZhongDepartment of Biology, Georgia State University, Atlanta, Georgia, United States of America.
Max F OginskyDepartment of Biology, Georgia State University, Atlanta, Georgia, United States of America.
Yang WuDepartment of Biology, Georgia State University, Atlanta, Georgia, United States of America.
Christopher M JohnsonDepartment of Biology, Georgia State University, Atlanta, Georgia, United States of America.
Shuang ZhangDepartment of Biology, Georgia State University, Atlanta, Georgia, United States of America.
Ningren CuiDepartment of Biology, Georgia State University, Atlanta, Georgia, United States of America.
Chun JiangDepartment of Biology, Georgia State University, Atlanta, Georgia, United States of America.
Georgia State University · US

Funding

Breathing disorders in a mouse model of Rett syndromeR01NS073875 · NINDS · GEORGIA STATE UNIVERSITY · PI JIANG, CHUN · 2011 to 2015
$1.6M
NINDS NIH HHS NS073875NINDS NIH HHS R01 NS073875
6 · The paper itself

Abstract

The locus coeruleus (LC)-norepinephrine (NE) system in the brainstem plays a critical role in a variety of behaviors is an important target of pharmacological intervention to several neurological disorders. Although GABA is the major inhibitory neurotransmitter of LC neurons, the modulation of LC neuronal firing activity by local GABAergic interneurons remains poorly understood with respect to their precise location, intrinsic membrane properties and synaptic modulation. Here, we took an optogenetic approach to address these questions. Channelrhodopsin (ChR2) in a tandem with the yellow fluorescent protein (YFP) was expressed in GABAergic neurons under the control of glutamic acid decarboxylase 2 (GAD2) promoter. Immediately dorsomedial to the LC nucleus, a group of GABAergic neurons was observed. They had small soma and were densely packed in a small area, which we named the dorsomedial LC or dmLC nucleus. These GABAergic neurons showed fast firing activity, strong inward rectification and spike frequency adaptation. Lateral inhibition among these GABAergic neurons was observed. Optostimulation of the dmLC area drastically inhibited LC neuronal firing frequency, expanded the spike intervals, and reset their pacemaking activity. Analysis of the light evoked inhibitory postsynaptic currents (IPSCs) indicated that they were monosynaptic. Such light evoked IPSCs were not seen in slices where this group of GABAergic neurons was absent. Thus, an isolated group of GABAergic neurons is demonstrated in the LC area, whose location, somatic morphology and intrinsic membrane properties are clearly distinguishable from adjacent LC neurons. They interact with each and may inhibit LC neurons as well as a part of local neuronal circuitry in the LC.

Indexed as

AnimalsCell SeparationCell TrackingElectrophysiological PhenomenaGABAergic NeuronsInterneuronsLocus CoeruleusMaleMiceMice, Inbred C57BLMice, TransgenicOptogeneticsPatch-Clamp TechniquesSynaptic Transmission

Identifiers

PMID26785258
PMCPMC4718449
OpenAlexW2419540537

What OpenQuestion holds

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LicenceCC BY
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.