Evidence map›Paper›PMID 24751569›Full record

ArticleBrain research2014

Inhibitory and excitatory amino acid neurotransmitters are utilized by the projection from the dorsal deep mesencephalic nucleus to the sublaterodorsal nucleus REM sleep induction zone.

Chang-Lin Liang, Tin Quang Nguyen, Gerald A Marks

Abstract read
In one paragraph

Article in Brain research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

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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

3 authors.

Chang-Lin LiangVA North Texas Health Care System, Research, 4500 South Lancaster Rd., Dallas, TX 75216, USA; University of Texas Southwestern Medical Center, Department of Psychiatry, 5323 Harry Hines Blvd., Dallas, TX 75390, USA. Electronic address: Chang-Lin.Liang@va.gov.
Tin Quang NguyenVA North Texas Health Care System, Research, 4500 South Lancaster Rd., Dallas, TX 75216, USA; University of Texas Southwestern Medical Center, Department of Psychiatry, 5323 Harry Hines Blvd., Dallas, TX 75390, USA. Electronic address: Tin.Nguyen@utsouthwestern.edu.
Gerald A MarksVA North Texas Health Care System, Research, 4500 South Lancaster Rd., Dallas, TX 75216, USA; University of Texas Southwestern Medical Center, Department of Psychiatry, 5323 Harry Hines Blvd., Dallas, TX 75390, USA. Electronic address: Gerald.Marks@utsouthwestern.edu.

Funding

Basic Science Training Program in the Neurobiology of Mental IllnessT32MH076690 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI TAMMINGA, CAROL A · 2007 to 2017
$2.3M
NIMH NIH HHS T32 MH076690NIMH NIH HHS T32-MH076690
6 · The paper itself

Abstract

The sublaterodorsal nucleus (SLD) in the pons of the rat is a locus supporting short-latency induction of a REM sleep-like state following local application of a GABAA receptor antagonist or kainate, glutamate receptor agonist. One putatively relevant source of these neurotransmitters is from the region of the deep mesencephalic nucleus (DpMe) just ventrolateral to the periaquiductal gray, termed the dorsal DpMe (dDpMe). Here, the amino acid neurotransmitter innervation of SLD from dDpMe was studied utilizing anterograde tract-tracing with biotinylated dextranamine (BDA) and fluorescence immunohistochemistry visualized with laser scanning confocal microscopy. Both markers for inhibitory and excitatory amino acid neurotransmitters were found in varicose axon fibers in SLD originating from dDpMe. Vesicular glutamate transporter2 (VGLUT2) represented the largest number of anterogradely labeled varicosities followed by vesicular GABA transporter (VGAT). Numerous VGAT and VGLUT2 labeled varicosities were observed apposed to dDpMe-labeled axon fibers indicating both excitatory and inhibitory presynaptic, local modulation within the SLD. Some double-labeled BDA/VGAT varicosities were seen apposed to small somata labeled for glutamate consistent with being presynaptic to the phenotype of REM sleep-active SLD neurons. Results found support the current theoretical framework of the interaction of dDpMe and SLD in control of REM sleep, while also indicating operation of mechanisms with a greater level of complexity.

Indexed as

Amino AcidsAnimalsAxonsBiotinDextransFluorescent Antibody TechniqueGlutamate DecarboxylaseMicroscopy, ConfocalNeuroanatomical Tract-Tracing TechniquesNeuronal Tract-TracersNeuronsNeurotransmitter AgentsPonsRats, Long-EvansSleep, REMTegmentum MesencephaliAmino AcidsBiotinbiotinylated dextran amineDextransGlutamate Decarboxylaseglutamate decarboxylase 1Neuronal Tract-TracersNeurotransmitter AgentsSlc17a6 protein, ratSlc32a1 protein, ratVesicular Glutamate Transport Protein 2Vesicular Inhibitory Amino Acid Transport ProteinsBiotinylated dextran amineGABAGlutamateGlycineREM sleepVesicular transporter

Identifiers

PMID24751569
PMCPMC4077466

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Registered trials

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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.