Evidence map›Paper›PMID 19896963›Full record

ArticleMechanisms of ageing and development

Activation of proteasome by insulin-like growth factor-I may enhance clearance of oxidized proteins in the brain.

Elizabeth Crowe, Christian Sell, Jeff D Thomas, Gregg J Johannes, Claudio Torres

Open access · greenAbstract read
In one paragraph

Article in Mechanisms of ageing and development. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

11 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Proteostasis and aging.Nature medicine · 2015
    Review
  7. Article
  8. Review
  9. Mice producing reduced levels of insulin-like growth factor type 1 display an increase in maximum, but not mean, life span.The journals of gerontology. Series A, Biological sciences and medical sciences · 2014
    Article
  10. The endocannabinoid system in normal and pathological brain ageing.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2012
    Review
  11. Article
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.

Elizabeth CroweDepartment of Pathology, Drexel University College of Medicine, Philadelphia, PA 19102, USA.
Christian Sell
Jeff D Thomas
Gregg J Johannes
Claudio Torres
Drexel University · US

Funding

Role of IGF-1 in Modulation of LongevityR01AG022443 · NIA · LANKENAU INSTITUTE FOR MEDICAL RESEARCH · PI SELL, CHRISTIAN · 2005 to 2009
$1.7M
NIA NIH HHS AG022443NIA NIH HHS AG022443-S1NIA NIH HHS R01 AG022443
6 · The paper itself

Abstract

The insulin-like growth factor type 1 (IGF-I) plays an important role in neuronal physiology. Reduced IGF-I levels are observed during aging and this decrease may be important to age-related changes in the brain. We studied the effects of IGF-I on total protein oxidation in brain tissues and in cell cultures. Our results indicate that in frontal cortex the level of oxidized proteins is significantly reduced in transgenic mice designed to overproduce IGF-I compared with wild-type animals. The frontal cortex of IGF-I-overproducing mice exhibited high chymotrypsin-like activity of the 20S and 26S proteasomes. The proteasome can also be activated in response to IGF-I in cell cultures. Kinetic studies revealed peak activation of the proteasome within 15 min following IGF-I stimulation. The effects of IGF-I on proteasome were not observed in R(-) cells lacking the IGF-I receptor. Experiments using specific kinase inhibitors suggested that activation of proteasome by IGF-I involves phosphatidyl inositol 3-kinase and mammalian target of rapamycin signaling. IGF-I also attenuated the increase in protein carbonyl content induced by proteasome inhibition. Thus, appropriate levels of IGF-I may be important for the elimination of oxidized proteins in the brain in a process mediated by activation of the proteasome.

Indexed as

AnimalsBrainBrain ChemistryCell LineEnzyme ActivationHumansInsulin-Like Growth Factor IMiceMice, KnockoutMice, TransgenicNerve Tissue ProteinsOxidation-ReductionProteasome Endopeptidase ComplexProtein CarbonylationReactive Oxygen SpeciesReceptor, IGF Type 1Insulin-Like Growth Factor INerve Tissue ProteinsProteasome Endopeptidase ComplexReactive Oxygen SpeciesReceptor, IGF Type 1

Identifiers

PMID19896963
PMCPMC2821674
OpenAlexW2073499357

What OpenQuestion holds

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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.