Evidence map›Paper›PMID 26092086›Full record

ArticleBiochimica et biophysica acta2015

Analysis of the effect of the mitochondrial prohibitin complex, a context-dependent modulator of longevity, on the C. elegans metabolome.

Artur B Lourenço, Celia Muñoz-Jiménez, Mónica Venegas-Calerón, Marta Artal-Sanz

Open access · hybridAbstract read
In one paragraph

Article in Biochimica et biophysica acta, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Prohibitins: A Key Link between Mitochondria and Nervous System Diseases.Oxidative medicine and cellular longevity · 2022
    Review
  3. Review
  4. Article
  5. Quo VadisMetabolites · 2021
    Review
  6. Article
  7. Article
  8. Review
  9. Review
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 2 institutions in 1 country.

Artur B LourençoAndalusian Centre for Developmental Biology (CABD), CSIC, Universidad Pablo de Olavide-Junta de Andalucía, Carretera de Utrera, km 1, 41013 Sevilla, Spain.
Celia Muñoz-JiménezAndalusian Centre for Developmental Biology (CABD), CSIC, Universidad Pablo de Olavide-Junta de Andalucía, Carretera de Utrera, km 1, 41013 Sevilla, Spain.
Mónica Venegas-CalerónDepartment of Biochemistry and Molecular Biology of Plant Products, Instituto de la Grasa (IG-CSIC), Ctra. Utrera Km 1, Campus Universitario Pablo de Olavide, 41013, Sevilla, Spain.
Marta Artal-SanzAndalusian Centre for Developmental Biology (CABD), CSIC, Universidad Pablo de Olavide-Junta de Andalucía, Carretera de Utrera, km 1, 41013 Sevilla, Spain. Electronic address: martsan@upo.es.
Centro Andaluz de Biología del Desarrollo · ESInstituto de la Grasa · ES

Funding

European Research Council 281691
6 · The paper itself

Abstract

The mitochondrial prohibitin complex, composed of two proteins, PHB-1 and PHB-2, is a context-dependent modulator of longevity. Specifically, prohibitin deficiency shortens the lifespan of otherwise wild type worms, while it dramatically extends the lifespan under compromised metabolic conditions. This extremely intriguingly phenotype has been linked to alterations in mitochondrial function and in fat metabolism. However, the true function of the mitochondrial prohibitin complex remains elusive. Here, we used gas chromatography coupled to a flame ionization detector (GC/FID) and ¹H NMR spectroscopy to gain molecular insights into the effect of prohibitin depletion on the Caenorhabditis elegans metabolome. We analysed the effect of prohibitin deficiency in two different developmental stages and under two different conditions, which result in opposing longevity phenotypes, namely wild type worms and daf-2(e1370) insulin signalling deficient mutants. Prohibitin depletion was shown to alter the fatty acid (GC/FID) and ¹H NMR metabolic profiles of wild type animals both at the fourth larval stage of development (L4) and at the young adult (YA) stage, while being more pronounced at the later stage. Furthermore, wild type and the diapause mutant daf-2(e1370), either expressing or not prohibitin, were clearly distinguishable based on their metabolic profiles, revealing changes in fatty acid composition, as well as in carbohydrate and amino acid metabolism. Moreover, the metabolic data indicate that daf-2(e1370) mutants are more robust than the wild type animals to changes induced by prohibitin depletion. The impact of prohibitin depletion on the C. elegans metabolome will be discussed herein in the scope of its effect on longevity. This article is part of a Special Issue entitled: Mitochondrial Dysfunction in Aging. Guest Editor: Aleksandra Trifunovic.

Indexed as

LongevityMetabolomeAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsFatty AcidsMagnetic Resonance SpectroscopyMitochondriaProhibitinsRepressor ProteinsCaenorhabditis elegans ProteinsFatty Acidsphb-1 protein, C elegansprohibitin 2, C elegansProhibitinsRepressor ProteinsC. elegansInsulin signallingLongevityMetabolomicsMitochondriaProhibitin

Identifiers

PMID26092086
PMCPMC4580209
OpenAlexW1886134552

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.