Evidence map›Paper›PMID 33907215›Full record

ArticleScientific reports2021

Whole-brain mapping of monosynaptic inputs to midbrain cholinergic neurons.

Icnelia Huerta-Ocampo, Daniel Dautan, Nadine K Gut, Bakhtawer Khan, Juan Mena-Segovia

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 34 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Icnelia Huerta-OcampoCenter for Molecular and Behavioral Neuroscience, Rutgers University, Newark, NJ, USA.
Daniel DautanCenter for Molecular and Behavioral Neuroscience, Rutgers University, Newark, NJ, USA.
Nadine K GutCenter for Molecular and Behavioral Neuroscience, Rutgers University, Newark, NJ, USA.
Bakhtawer KhanCenter for Molecular and Behavioral Neuroscience, Rutgers University, Newark, NJ, USA.
Juan Mena-SegoviaCenter for Molecular and Behavioral Neuroscience, Rutgers University, Newark, NJ, USA. juan.mena@rutgers.edu.
Rutgers, The State University of New Jersey · US

Funding

Cholinergic brainstem signaling in striatal circuitsR01NS100824 · NINDS · RUTGERS THE STATE UNIV OF NJ NEWARK · PI MENA-SEGOVIA, JUAN · 2017 to 2021
$1.7M
NINDS NIH HHS NS100824NINDS NIH HHS R01 NS100824
6 · The paper itself

Abstract

The cholinergic midbrain is involved in a wide range of motor and cognitive processes. Cholinergic neurons of the pedunculopontine (PPN) and laterodorsal tegmental nucleus (LDT) send long-ranging axonal projections that target sensorimotor and limbic areas in the thalamus, the dopaminergic midbrain and the striatal complex following a topographical gradient, where they influence a range of functions including attention, reinforcement learning and action-selection. Nevertheless, a comprehensive examination of the afferents to PPN and LDT cholinergic neurons is still lacking, partly due to the neurochemical heterogeneity of this region. Here we characterize the whole-brain input connectome to cholinergic neurons across distinct functional domains (i.e. PPN vs LDT) using conditional transsynaptic retrograde labeling in ChAT::Cre male and female rats. We reveal that input neurons are widely distributed throughout the brain but segregated into specific functional domains. Motor related areas innervate preferentially the PPN, whereas limbic related areas preferentially innervate the LDT. The quantification of input neurons revealed that both PPN and LDT receive similar substantial inputs from the superior colliculus and the output of the basal ganglia (i.e. substantia nigra pars reticulata). Notably, we found that PPN cholinergic neurons receive preferential inputs from basal ganglia structures, whereas LDT cholinergic neurons receive preferential inputs from limbic cortical areas. Our results provide the first characterization of inputs to PPN and LDT cholinergic neurons and highlight critical differences in the connectome among brain cholinergic systems thus supporting their differential roles in behavior.

Indexed as

AnimalsBrain MappingCholine O-AcetyltransferaseCholinergic NeuronsChromosome PairingFemaleMaleNeural PathwaysPedunculopontine Tegmental NucleusRatsTegmentum MesencephaliCholine O-Acetyltransferase

Identifiers

PMID33907215
PMCPMC8079369
OpenAlexW3159661089

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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.