Evidence map›Paper›PMID 23197187›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2013

Decreased levels of proapoptotic factors and increased key regulators of mitochondrial biogenesis constitute new potential beneficial features of long-lived growth hormone receptor gene-disrupted mice.

Adam Gesing, Michal M Masternak, Andrzej Lewinski, Malgorzata Karbownik-Lewinska, John J Kopchick, Andrzej Bartke

Abstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. A Balanced Act: The Effects of GH-GHR-IGF1 Axis on Mitochondrial Function.Frontiers in cell and developmental biology · 2021
    Review
  5. Review
  6. Mitochondrial Function Is Compromised in Cortical Bone Osteocytes of Long-Lived Growth Hormone Receptor Null Mice.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2019
    Article
  7. A Long-lived Mouse Lacking Both Growth Hormone and Growth Hormone Receptor: A New Animal Model for Aging Studies.The journals of gerontology. Series A, Biological sciences and medical sciences · 2017
    Article
  8. Article
  9. Article
  10. Article
  11. Expression of apoptosis-related genes in liver-specific growth hormone receptor gene-disrupted mice is sex dependent.The journals of gerontology. Series A, Biological sciences and medical sciences · 2015
    Article
  12. 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

6 authors.

Adam GesingDepartment of Oncological Endocrinology, Medical University of Lodz, Lodz, Poland. adges7@wp.pl
Michal M Masternak
Andrzej Lewinski
Malgorzata Karbownik-Lewinska
John J Kopchick
Andrzej Bartke

Funding

Dietary fat, visceral fat depots and agingR01AG032290 · NIA · UNIVERSITY OF CENTRAL FLORIDA · PI MASTERNAK, MICHAL MATEUSZ · 2010 to 2014
$1.5M
NIA NIH HHS R01 AG032290
6 · The paper itself

Abstract

Decreased somatotrophic signaling is among the most important mechanisms associated with extended longevity. Mice homozygous for the targeted disruption of the growth hormone (GH) receptor gene (GH receptor knockout; GHRKO) are obese and dwarf, are characterized by a reduced weight and body size, undetectable levels of GH receptor, high concentration of serum GH, and greatly reduced plasma levels of insulin and insulin-like growth factor-I, and are remarkably long lived. Recent results suggest new features of GHRKO mice that may positively affect longevity-decreased levels of proapoptotic factors and increased levels of key regulators of mitochondrial biogenesis. The alterations in levels of the proapoptotic factors and key regulators of mitochondrial biogenesis were not further improved by two other potential life-extending interventions-calorie restriction and visceral fat removal. This may attribute the primary role to GH resistance in the regulation of apoptosis and mitochondrial biogenesis in GHRKO mice in terms of increased life span.

Indexed as

AnimalsApoptosisLongevityMiceMice, KnockoutMitochondrial TurnoverModels, AnimalReceptors, SomatotropinSignal TransductionReceptors, SomatotropinAgingApoptosisCalorie restrictionDwarf miceGHRKO miceLongevityMitochondrial biogenesisVisceral fat removal.

Identifiers

PMID23197187
PMCPMC3708518

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.