Evidence map›Paper›PMID 28405590›Full record

ArticleNeurogenesis (Austin, Tex.)2017

Therapeutic potential of IGF-I on hippocampal neurogenesis and function during aging.

Gustavo R Morel, Micaela López León, Maia Uriarte, Paula C Reggiani, Rodolfo G Goya

Open access · bronzeAbstract read
In one paragraph

Article in Neurogenesis (Austin, Tex.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 3 pooled it
2.6field-weighted citation impact, top 10% 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

28 citing papers in PubMed, 3 syntheses or guidelines pooled it, 43 citations in OpenAlex.

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  18. Dysregulation of IGF-1/GLP-1 signaling in the progression of ALS: potential target activators and influences on neurological dysfunctions.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2021
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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.

Gustavo R MorelINIBIOLP- Histology B - Pathology B; School of Medicine, UNLP , La Plata, Argentina.
Micaela López LeónINIBIOLP- Histology B - Pathology B; School of Medicine, UNLP , La Plata, Argentina.
Maia UriarteINIBIOLP- Histology B - Pathology B; School of Medicine, UNLP , La Plata, Argentina.
Paula C ReggianiINIBIOLP- Histology B - Pathology B; School of Medicine, UNLP , La Plata, Argentina.
Rodolfo G GoyaINIBIOLP- Histology B - Pathology B; School of Medicine, UNLP , La Plata, Argentina.
Biochemistry Research Institute of La Plata · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In rats, learning and memory performance decline during normal aging, which is paralleled by a severe reduction of the levels of neurogenesis in the hippocampal dentate gyrus (DG). A promising therapeutic strategy to restore neurogenesis in the hippocampus of old rats and their spatial memory involves the use of insulin-like growth factor-I (IGF-I). The peptide exerts pleiotropic effects in the brain, regulating multiple cellular processes. Thus, 4-week intracerebroventricular (ICV) perfusion of IGF-I significantly restored spatial memory and hippocampal neurogenesis in old male rats. Similar results were achieved by ICV IGF-I gene therapy in aging female rats. Thus, the treatment seemed to increase the number of immature neurons in the DG of 28 mo old rats, which was paralleled by an increase in the accuracy of the animals to remember specific patterns, which is known as pattern separation memory. The DG is thought to be the main hippocampal structure involved in pattern separation memory and there is evidence that the level of neurogenesis in the DG is directly related to pattern separation performance in rodents. Summing up, IGF-I emerges as a promising restorative molecule for increasing hippocampal neurogenesis and memory accuracy in aged individuals and possibly, in neurodegenerative pathologies.

Indexed as

brain aginghippocampusIGF-Imemoryneurogenesis

Identifiers

PMID28405590
PMCPMC5386180
OpenAlexW2561378381

What OpenQuestion holds

Textmetadata
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.