Evidence map›Paper›PMID 30814846›Full record

ReviewJournal of experimental neuroscience2019

Molecular Mechanisms of Neurogenic Aging in the Adult Mouse Subventricular Zone.

Giuseppe Lupo, Roberta Gioia, Paola Serena Nisi, Stefano Biagioni, Emanuele Cacci

Open access · goldAbstract readReview
In one paragraph

Review in Journal of experimental neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. The NDR family of kinases: essential regulators of aging.Frontiers in molecular neuroscience · 2024
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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.

Giuseppe LupoDepartment of Chemistry, Sapienza University of Rome, Rome, Italy.ORCID https://orcid.org/0000-0001-7218-4003
Roberta GioiaDepartment of Biology and Biotechnology "Charles Darwin", Sapienza University of Rome, Rome, Italy.ORCID https://orcid.org/0000-0002-6365-1332
Paola Serena NisiDepartment of Biology and Biotechnology "Charles Darwin", Sapienza University of Rome, Rome, Italy.ORCID https://orcid.org/0000-0002-3698-9151
Stefano BiagioniDepartment of Biology and Biotechnology "Charles Darwin", Sapienza University of Rome, Rome, Italy.ORCID https://orcid.org/0000-0003-1544-3907
Emanuele CacciDepartment of Biology and Biotechnology "Charles Darwin", Sapienza University of Rome, Rome, Italy.ORCID https://orcid.org/0000-0003-0082-6999
Sapienza University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the adult rodent brain, the continuous production of new neurons by neural stem/progenitor cells (NSPCs) residing in specialized neurogenic niches and their subsequent integration into pre-existing cerebral circuitries supports odour discrimination, spatial learning, and contextual memory capabilities. Aging is recognized as the most potent negative regulator of adult neurogenesis. The neurogenic process markedly declines in the aged brain, due to the reduction of the NSPC pool and the functional impairment of the remaining NSPCs. This decline has been linked to the progressive cognitive deficits of elderly individuals and it may also be involved in the onset/progression of neurological disorders. Since the human lifespan has been dramatically extended, the incidence of age-associated neuropsychiatric conditions in the human population has increased. This has prompted efforts to shed light on the mechanisms underpinning the age-related decline of adult neurogenesis, whose knowledge may foster therapeutic approaches to prevent or delay cognitive alterations in elderly patients. In this review, we summarize recent progress in elucidating the molecular causes of neurogenic aging in the most abundant NSPC niche of the adult mouse brain: the subventricular zone (SVZ). We discuss the age-associated changes occurring both in the intrinsic NSPC molecular networks and in the extrinsic signalling pathways acting in the complex environment of the SVZ niche, and how all these changes may steer young NSPCs towards an aged phenotype.

Indexed as

Adult neurogenesisagingneural stem/progenitor cellsnichetumour suppressor pathways

Identifiers

PMID30814846
PMCPMC6381424
OpenAlexW2916081028

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.