Evidence map›Paper›PMID 34909682›Full record

ArticleCurrent research in pharmacology and drug discovery2021

The small molecule SERCA activator CDN1163 increases energy metabolism in human skeletal muscle cells.

Abel M Mengeste, Jenny Lund, Parmeshwar Katare, Roya Ghobadi, Hege G Bakke, Per Kristian Lunde, Lars Eide, Gavin O' Mahony, Sven Göpel, Xiao-Rong Peng and 3 more

Open access · goldAbstract read
In one paragraph

Article in Current research in pharmacology and drug discovery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Review
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  5. Article
  6. SERCA blockade as a treatment strategy for obesity.European journal of applied physiology · 2025
    Review
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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

13 authors at 3 institutions in 2 countries.

Abel M MengesteSection for Pharmacology and Pharmaceutical Biosciences, Department of Pharmacy, University of Oslo, Norway.
Jenny LundSection for Pharmacology and Pharmaceutical Biosciences, Department of Pharmacy, University of Oslo, Norway.
Parmeshwar KatareSection for Pharmacology and Pharmaceutical Biosciences, Department of Pharmacy, University of Oslo, Norway.
Roya GhobadiSection for Pharmacology and Pharmaceutical Biosciences, Department of Pharmacy, University of Oslo, Norway.
Hege G BakkeSection for Pharmacology and Pharmaceutical Biosciences, Department of Pharmacy, University of Oslo, Norway.
Per Kristian LundeInstitute for Experimental Medical Research, Oslo University Hospital and University of Oslo, Norway.
Lars EideDepartment of Medical Biochemistry, Institute of Clinical Medicine, University of Oslo, Norway.
Gavin O' MahonyMedicinal Chemistry, Research and Early Development Cardiovascular, Renal and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
Sven GöpelBioscience Metabolism, Research and Early Development Cardiovascular, Renal and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
Xiao-Rong PengBioscience Metabolism, Research and Early Development Cardiovascular, Renal and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
Eili Tranheim KaseSection for Pharmacology and Pharmaceutical Biosciences, Department of Pharmacy, University of Oslo, Norway.
G Hege ThoresenSection for Pharmacology and Pharmaceutical Biosciences, Department of Pharmacy, University of Oslo, Norway.
Arild C RustanSection for Pharmacology and Pharmaceutical Biosciences, Department of Pharmacy, University of Oslo, Norway.
University of Oslo · NOAstraZeneca (Sweden) · SEOslo University Hospital · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveA number of studies have highlighted muscle-specific mechanisms of thermogenesis involving futile cycling of Ca

methodsIn this study, we used primary myotube cultures derived from muscle biopsies of the

resultsBoth acute (4 ​h) and chronic (5 days) treatment of myotubes with CDN1163 showed increased uptake and oxidation of glucose, as well as complete fatty acid oxidation in the presence of carbonyl cyanide 4-(trifluromethoxy)phenylhydrazone (FCCP). These effects were supported by measurement of oxygen consumption rate, in which the oxidative spare capacity and maximal respiration were enhanced after CDN1163-treatment. In addition, chronic treatment with CDN1163 improved cellular uptake of oleic acid (OA) and fatty acid β-oxidation. The increased OA metabolism was accompanied by enhanced mRNA-expression of carnitine palmitoyl transferase (

conclusionAltogether, these results suggest that SERCA activation by CDN1163 enhances energy metabolism in human myotubes, which might be favourable in relation to disorders that are related to metabolic dysfunction such as obesity and type 2 diabetes mellitus.

Indexed as

AMPKAMPK, AMP-activated protein kinaseASM, acid-soluble metabolitesCE, cholesteryl esterDAG, diacylglycerolFA, fatty acidFCCP, 4-(trifluromethoxy)phenylhydrazoneGlucose metabolismLipid metabolismOA, oleic acidObesityOCR, oxygen consumption rateSCD1, stearoyl-CoA desaturase 1SERCASERCA, sarco(endo)plasmic reticulum Ca2+-ATPaseSkeletal muscleT2DM, type 2 diabetes mellitusType 2 diabetes

Identifiers

PMID34909682
PMCPMC8663964
OpenAlexW3203884548

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.