Evidence map›Paper›PMID 20347952›Full record

ArticleExperimental gerontology2010

Decrease in PTEN and increase in Akt expression and neuron size in aged rat spinal cord.

Miguel Augusto Rodrigues de Amorim, Luis Miguel Garcia-Segura, Rodolfo Gustavo Goya, Enrique Leo Portiansky

Open access · greenAbstract read
In one paragraph

Article in Experimental gerontology, 2010. 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
0.8field-weighted citation impact, top 29% 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, 14 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

4 authors at 4 institutions in 2 countries.

Miguel Augusto Rodrigues de AmorimInstituto Cajal, CSIC, Madrid, Spain.
Luis Miguel Garcia-Segura
Rodolfo Gustavo Goya
Enrique Leo Portiansky
Biochemistry Research Institute of La Plata · ARConsejo Superior de Investigaciones Científicas · ESInstituto Cajal · ESUniversidad Nacional de La Plata · AR

Funding

Neuroprotective Gene Therapy in the Brain of Senile RatsR01AG029798 · NIA · NATIONAL UNIVERSITY OF LA PLATA · PI GOYA, RODOLFO G · 2008 to 2010
$471k
NIA NIH HHS R01 AG029798NIA NIH HHS R01AG029798-2
6 · The paper itself

Abstract

PTEN is a tumor suppressor gene known to play an important role in the regulation of cell size. In this study we compared PTEN expression in the spinal cord of young (5 months old) vs. aged (32 months old) female rats and correlated them with alterations in neuron size and morphology in the same animals. Total and phosphorylated PTEN (pPTEN) as well as its downstream target phosphorylated Akt (pAkt) were assessed by Western blotting. Spinal cord neurons were morphometrically characterized. Total PTEN, pPTEN and total Akt expression were significantly higher in young rats than in aged animals. Expression of pAkt was stronger in aged animals. A significant increase in neuronal size was observed in large motoneurons of aged as compared with young rats. Our data show that in the spinal cord of rats, neuronal PTEN expression diminishes with advanced age while neuronal size increases. These results suggest that in the spinal cord, an age-related reduction in PTEN and increase of pAkt expression may be involved in the progressive enlargement of neurons.

Indexed as

Cell EnlargementAgingAnimalsBlotting, WesternFemaleFluorescent Antibody TechniqueGene Expression Regulation, NeoplasticHumansImmunohistochemistryNeuronsProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseRatsSpinal CordTumor Suppressor ProteinsProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseTumor Suppressor Proteins

Identifiers

PMID20347952
PMCPMC2862775
OpenAlexW2015507153

What OpenQuestion holds

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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.