Evidence map›Paper›PMID 22961106›Full record

ArticleNature medicine2012

Sarcolipin is a newly identified regulator of muscle-based thermogenesis in mammals.

Naresh C Bal, Santosh K Maurya, Danesh H Sopariwala, Sanjaya K Sahoo, Subash C Gupta, Sana A Shaikh, Meghna Pant, Leslie A Rowland, Eric Bombardier, Sanjeewa A Goonasekera and 3 more

Erratum issuedAbstract read
In one paragraph

Article in Nature medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 310 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
310citing papers in PubMed, 2 pooled it
20.2field-weighted citation impact, top 1% 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

310 citing papers in PubMed, 2 syntheses or guidelines pooled it, 549 citations in OpenAlex.

  1. A systematic review of exposure to endocrine disruptors and energy expenditure in mice.Environmental health : a global access science source · 2025
    Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Effects of electromyostimulation on sarcolipin and CaBiochemistry and biophysics reports · 2026
    Article
  11. Advances in research on thermogenic substances.Journal of physiological anthropology · 2026
    Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Body Temperature Regulation in the Rat by Muscle Tone.Acta physiologica (Oxford, England) · 2026
    Article
  18. Review
  19. Review
  20. Article

250 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 2 countries.

Naresh C BalDepartment of Physiology and Cell Biology, Ohio State University, College of Medicine, Columbus, Ohio, USA.
Santosh K Maurya
Danesh H Sopariwala
Sanjaya K Sahoo
Subash C Gupta
Sana A Shaikh
Meghna Pant
Leslie A Rowland
Eric Bombardier
Sanjeewa A Goonasekera
A Russell Tupling
Jeffery D Molkentin
Muthu Periasamy
The Ohio State University · USUniversity of Waterloo · CACincinnati Children's Hospital Medical Center · USHoward Hughes Medical Institute · US

Funding

CIHR 106566-1Howard Hughes Medical InstituteNHLBI NIH HHS R01 HL080551
6 · The paper itself

Abstract

The role of skeletal muscle in nonshivering thermogenesis (NST) is not well understood. Here we show that sarcolipin (Sln), a newly identified regulator of the sarco/endoplasmic reticulum Ca(2+)-ATPase (Serca) pump, is necessary for muscle-based thermogenesis. When challenged to acute cold (4 °C), Sln(-/-) mice were not able to maintain their core body temperature (37 °C) and developed hypothermia. Surgical ablation of brown adipose tissue and functional knockdown of Ucp1 allowed us to highlight the role of muscle in NST. Overexpression of Sln in the Sln-null background fully restored muscle-based thermogenesis, suggesting that Sln is the basis for Serca-mediated heat production. We show that ryanodine receptor 1 (Ryr1)-mediated Ca(2+) leak is an important mechanism for Serca-activated heat generation. Here we present data to suggest that Sln can continue to interact with Serca in the presence of Ca(2+), which can promote uncoupling of the Serca pump and cause futile cycling. We further show that loss of Sln predisposes mice to diet-induced obesity, which suggests that Sln-mediated NST is recruited during metabolic overload. These data collectively suggest that SLN is an important mediator of muscle thermogenesis and whole-body energy metabolism.

Indexed as

Adipose Tissue, BrownAnimalsBody Temperature RegulationCalciumCell LineEnergy MetabolismHEK293 CellsHumansIon ChannelsMaleMiceMice, Inbred C57BLMice, KnockoutMitochondrial ProteinsMuscle ProteinsMuscle, SkeletalCalciumIon ChannelsMitochondrial ProteinsMuscle ProteinsProteolipidsRyanodine Receptor Calcium Release ChannelsarcolipinSarcoplasmic Reticulum Calcium-Transporting ATPasesUCP1 protein, humanUcp1 protein, mouseUncoupling Protein 1

Identifiers

PMID22961106
PMCPMC3676351
OpenAlexW2065656177

What OpenQuestion holds

Textmetadata
LicenceTDM
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.