Evidence map›Paper›PMID 26534869›Full record

ArticleAging cell2016

Central insulin-like growth factor-1 (IGF-1) restores whole-body insulin action in a model of age-related insulin resistance and IGF-1 decline.

Derek M Huffman, Gabriela Farias Quipildor, Kai Mao, Xueying Zhang, Junxiang Wan, Pasha Apontes, Pinchas Cohen, Nir Barzilai

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

33 citing papers in PubMed, 47 citations in OpenAlex.

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  9. Icariin Improves Stress Resistance and Extends Lifespan inInternational journal of molecular sciences · 2023
    Article
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  19. Bring Back the Rat!The journals of gerontology. Series A, Biological sciences and medical sciences · 2020
    Review
  20. 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

8 authors at 3 institutions in 2 countries.

Derek M HuffmanDivision of Endocrinology, Department of Medicine, Albert Einstein College of Medicine, Bronx, NY, USA.
Gabriela Farias QuipildorDepartment of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, NY, USA.
Kai MaoDivision of Endocrinology, Department of Medicine, Albert Einstein College of Medicine, Bronx, NY, USA.
Xueying ZhangDivision of Endocrinology, Department of Medicine, Albert Einstein College of Medicine, Bronx, NY, USA.
Junxiang WanDavis School of Gerontology, University of Southern California, Los Angeles, CA, 90089, USA.
Pasha ApontesDivision of Endocrinology, Department of Medicine, Albert Einstein College of Medicine, Bronx, NY, USA.
Pinchas CohenDavis School of Gerontology, University of Southern California, Los Angeles, CA, 90089, USA.
Nir BarzilaiDivision of Endocrinology, Department of Medicine, Albert Einstein College of Medicine, Bronx, NY, USA.
Albert Einstein College of Medicine · USUniversity of Southern California · USChinese Academy of Sciences · CN

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI STEVEN C. ALMO · 1985 to 2026
$111.2M
RESEARCH TRAININGP30DK026687 · NIDDK · ST. LUKE'S-ROOSEVELT INST FOR HLTH SCIS · PI Anthony W Ferrante, DYMPNA GALLAGHER · 1986 to 2026
$33.0M
Translational Research CoreP30DK020541 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI STREAMSON C CHUA · 2015 to 2026
$27.7M
Core-010UL1TR001073 · NCATS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI KELLER, MARLA J, SHAMOON, HARRY · 2013 to 2017
$21.3M
Einstein's Nathan Shock Center of Excellence in Basic Biology of AgingP30AG038072 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI HUFFMAN, DEREK MAJOR · 2010 to 2024
$10.8M
ROLE OF NUTRIENTS IN AGE-RELATED INSULIN RESISTANCEP01AG021654 · NIA · YESHIVA UNIVERSITY · PI ROSSETTI, LUCIANO · 2003 to 2007
$10.6M
The Role of the Glucose-regulated Protein GRP78/BiP in Stress Resistance and AginP01AG034906 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MITCHELL, JAMES R. · 2011 to 2016
$9.3M
Dysregulation of Glucose Homeostasis in AgingR37AG018381 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI BARZILAI, NIR J · 2010 to 2019
$3.5M
Novel Mitochondrially Encoded Peptides and Their Role in Health and DiseaseR01GM090311 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI COHEN, PINCHAS · 2009 to 2013
$3.2M
LGP/LongenityR01AG046949 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI BARZILAI, NIR J · 2013 to 2017
$2.4M
Plasma Mitochondrial Peptide Assays as Biomarkers of Environmental Toxin ExposureR01ES020812 · NIEHS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI COHEN, PINCHAS · 2011 to 2015
$1.8M
Peripheral and central IGF-1 action in energy balance and longevity modulation R00AG037574 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI HUFFMAN, DEREK MAJOR · 2013 to 2015
$732k
NCATS NIH HHS UL1 TR001073NCI NIH HHS P30 CA013330NIA NIH HHS K99 AG037574NIA NIH HHS P01 AG021654NIA NIH HHS P01 AG034906NIA NIH HHS P30 AG038072NIA NIH HHS R00 AG037574NIA NIH HHS R01 AG046949NIA NIH HHS R37 AG018381NIDDK NIH HHS P30 DK020541NIDDK NIH HHS P30 DK026687NIEHS NIH HHS R01 ES020812NIGMS NIH HHS R01 GM090311
6 · The paper itself

Abstract

Low insulin-like growth factor-1 (IGF-1) signaling is associated with improved longevity, but is paradoxically linked with several age-related diseases in humans. Insulin-like growth factor-1 has proven to be particularly beneficial to the brain, where it confers protection against features of neuronal and cognitive decline. While aging is characterized by central insulin resistance in the face of hyperinsulinemia, the somatotropic axis markedly declines in older humans. Thus, we hypothesized that increasing IGF-1 in the brain may prove to be a novel therapeutic alternative to overcome central insulin resistance and restore whole-body insulin action in aging. Utilizing hyperinsulinemic-euglycemic clamps, we show that old insulin-resistant rats with age-related declines in IGF-1 level demonstrate markedly improved whole-body insulin action, when treated with central IGF-1, as compared to central vehicle or insulin (P < 0.05). Furthermore, central IGF-1, but not insulin, suppressed hepatic glucose production and increased glucose disposal rates in aging rats (P < 0.05). Taken together, IGF-1 action in the brain and periphery provides a 'balance' between its beneficial and detrimental actions. Therefore, we propose that strategies aimed at 'tipping the balance' of IGF-1 action centrally are the optimal approach to achieve healthy aging and longevity in humans.

Indexed as

AgingAnimalsBlood GlucoseGlucoseGlucose Clamp TechniqueInsulinInsulin-Like Growth Factor IInsulin ResistanceLiverMaleRats, Sprague-DawleyBlood GlucoseGlucoseInsulininsulin-like growth factor-1, ratInsulin-Like Growth Factor Iaginganimal modelscentral nervous systemendocrinologyglucose metabolisminsulin-like growth factorinsulin resistance

Identifiers

PMID26534869
PMCPMC4717281
OpenAlexW2102207014

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.