Evidence map›Paper›PMID 32955432›Full record

ArticleeLife2020

Chronic postnatal chemogenetic activation of forebrain excitatory neurons evokes persistent changes in mood behavior.

Sthitapranjya Pati, Kamal Saba, Sonali S Salvi, Praachi Tiwari, Pratik R Chaudhari, Vijaya Verma, Sourish Mukhopadhyay, Darshana Kapri, Shital Suryavanshi, James P Clement and 2 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. 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
1.1field-weighted citation impact, top 25% 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, 16 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

12 authors at 3 institutions in 1 country.

Sthitapranjya PatiDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, India.ORCID 0000-0001-8598-4376
Kamal Saba *Centre for Cellular and Molecular Biology, Hyderabad, India.ORCID 0000-0003-1729-9961
Sonali S Salvi *Department of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, India.
Praachi TiwariDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, India.
Pratik R ChaudhariDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, India.
Vijaya VermaNeuroscience Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluru, India.
Sourish MukhopadhyayDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, India.
Darshana KapriDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, India.
Shital SuryavanshiDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, India.
James P ClementNeuroscience Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluru, India.
Anant B PatelCentre for Cellular and Molecular Biology, Hyderabad, India.
Vidita A VaidyaDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, India.ORCID 0000-0002-3907-8580
Tata Institute of Fundamental Research · INCentre for Cellular and Molecular Biology · INJawaharlal Nehru Centre for Advanced Scientific Research · IN

Funding

Tata Institute of Fundamental Research RTI4003
6 · The paper itself

Abstract

Early adversity is a risk factor for the development of adult psychopathology. Common across multiple rodent models of early adversity is increased signaling via forebrain Gq-coupled neurotransmitter receptors. We addressed whether enhanced Gq-mediated signaling in forebrain excitatory neurons during postnatal life can evoke persistent mood-related behavioral changes. Excitatory hM3Dq DREADD-mediated chemogenetic activation of forebrain excitatory neurons during postnatal life (P2-14), but not in juvenile or adult windows, increased anxiety-, despair-, and schizophrenia-like behavior in adulthood. This was accompanied by an enhanced metabolic rate of cortical and hippocampal glutamatergic and GABAergic neurons. Furthermore, we observed reduced activity and plasticity-associated marker expression, and perturbed excitatory/inhibitory currents in the hippocampus. These results indicate that Gq-signaling-mediated activation of forebrain excitatory neurons during the critical postnatal window is sufficient to program altered mood-related behavior, as well as functional changes in forebrain glutamate and GABA systems, recapitulating aspects of the consequences of early adversity.

Indexed as

AffectAnimalsAnimals, NewbornAnxietyBehavior, AnimalFemaleGABAergic NeuronsHippocampusMaleMiceNeuronsProsencephalonReceptors, G-Protein-CoupledReceptors, G-Protein-CoupledanxietydespairDREADDearly stressmouseneuroscienceschizophrenia

Identifiers

PMID32955432
PMCPMC7652419
OpenAlexW3087714301

What OpenQuestion holds

Textmetadata
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.