Evidence map›Paper›PMID 42350627›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2026

Norepinephrine regulates hippocampal mitochondrial biogenesis via β2-adrenergic receptor signaling and PGC-1α.

Darshana Kapri, Amogh Bhaskaran Jayaprasad, Praachi Tiwari, Mukund Sharma, Angarika Balakrishnan, Aastha Singla, Ishanee Mazumder, Ullas Kolthur-Seetharam, Sashaina E Fanibunda, Ashok D B Vaidya and 1 more

Abstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Darshana KapriDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, Maharashtra, India. darshanakapri@gmail.com.
Amogh Bhaskaran JayaprasadDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, Maharashtra, India.
Praachi TiwariDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, Maharashtra, India.ORCID http://orcid.org/0000-0003-1762-0217
Mukund SharmaDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, Maharashtra, India.
Angarika BalakrishnanDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, Maharashtra, India.
Aastha SinglaDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, Maharashtra, India.
Ishanee MazumderDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, Maharashtra, India.
Ullas Kolthur-SeetharamDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, Maharashtra, India.
Sashaina E FanibundaDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, Maharashtra, India.
Ashok D B VaidyaKasturba Integrative Health Sciences - Medical Research Foundation, Mumbai, India.
Vidita A VaidyaDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, Maharashtra, India. vvaidya@tifr.res.in.ORCID http://orcid.org/0000-0002-3907-8580

Funding

Tata Institute of Fundamental Research (TIFR) RTI4003
6 · The paper itself

Abstract

Neuronal mitochondria are central to not only maintaining cellular bioenergetics, calcium dynamics, and serving as signaling platforms, but are also critical for specialized functions including synaptic plasticity and neurotransmission. While mitochondria are postulated to have a fundamental role in the functioning of neurons, it is only recently that upstream factors that influence mitochondria in neurons have been systematically investigated. Here, we identify the critical role of the neurotransmitter, norepinephrine (NE) in modulating mitochondria in the rodent hippocampus. NE increases the expression of key regulators of mitochondrial biogenesis (SIRT1 and PGC-1α), enhances mitochondrial DNA content and ATP levels in hippocampal neurons in culture. These effects of NE are mediated via the recruitment of a β

Indexed as

HippocampusMitochondriaNorepinephrineReceptors, Adrenergic, beta-2Signal TransductionTranscription FactorsAdenosine TriphosphateAnimalsCells, CulturedDNA, MitochondrialMaleNeuronsPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaRatsRats, Sprague-DawleyAdenosine TriphosphateDNA, MitochondrialNorepinephrinePeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPpargc1a protein, ratReceptors, Adrenergic, beta-2Transcription Factors

Identifiers

PMID42350627
PMCPMC13486802

What OpenQuestion holds

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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.