Evidence map›Paper›PMID 37423391›Full record

ArticleMolecular metabolism2023

Nipsnap1-A regulatory factor required for long-term maintenance of non-shivering thermogenesis.

Yang Liu, Yue Qu, Chloe Cheng, Pei-Yin Tsai, Kaydine Edwards, Siwen Xue, Supriya Pandit, Sakura Eguchi, Navneet Sanghera, Joeva J Barrow

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. N6-methyladenosine readerWorld journal of gastroenterology · 2025
    Article
  4. Article
  5. 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

10 authors at 2 institutions in 1 country.

Yang LiuDivision of Nutritional Sciences, Cornell University, Ithaca, NY, 14850, USA.
Yue QuDivision of Nutritional Sciences, Cornell University, Ithaca, NY, 14850, USA.
Chloe ChengDepartment of Veterinary Medicine, Cornell University, Ithaca, NY, 14850, USA.
Pei-Yin TsaiDivision of Nutritional Sciences, Cornell University, Ithaca, NY, 14850, USA.
Kaydine EdwardsDivision of Nutritional Sciences, Cornell University, Ithaca, NY, 14850, USA.
Siwen XueDivision of Nutritional Sciences, Cornell University, Ithaca, NY, 14850, USA.
Supriya PanditDivision of Nutritional Sciences, Cornell University, Ithaca, NY, 14850, USA.
Sakura EguchiDivision of Nutritional Sciences, Cornell University, Ithaca, NY, 14850, USA.
Navneet SangheraDepartment of Biological Sciences, San Jose State University, San Jose, CA, 95192, USA.
Joeva J BarrowDivision of Nutritional Sciences, Cornell University, Ithaca, NY, 14850, USA. Electronic address: jb2254@cornell.edu.
Cornell University · USSan Jose State University · US

Funding

Novel Thermogenic Factors to Combat Obesity and Metabolic DiseaseR21DK122258 · NIDDK · CORNELL UNIVERSITY · PI BARROW, JOEVA J. · 2019 to 2021
$566k
NIDDK NIH HHS R21 DK122258
6 · The paper itself

Abstract

objectiveThe activation of non-shivering thermogenesis (NST) has strong potential to combat obesity and metabolic disease. The activation of NST however is extremely temporal and the mechanisms surrounding how the benefits of NST are sustained once fully activated, remain unexplored. The objective of this study is to investigate the role of 4-Nitrophenylphosphatase Domain and Non-Neuronal SNAP25-Like 1 (Nipsnap1) in NST maintenance, which is a critical regulator identified in this study.

methodsThe expression of Nipsnap1 was profiled by immunoblotting and RT-qPCR. We generated Nipsnap1 knockout mice (N1-KO) and investigated the function of Nipsnap1 in NST maintenance and whole-body metabolism using whole body respirometry analyses. We evaluate the metabolic regulatory role of Nipsnap1 using cellular and mitochondrial respiration assay.

resultsHere, we show Nipsnap1 as a critical regulator of long-term thermogenic maintenance in brown adipose tissue (BAT). Nipsnap1 localizes to the mitochondrial matrix and increases its transcript and protein levels in response to both chronic cold and β3 adrenergic signaling. We demonstrated that these mice are unable to sustain activated energy expenditure and have significantly lower body temperature in the face of an extended cold challenge. Furthermore, when mice are exposed to the pharmacological β3 agonist CL 316, 243, the N1-KO mice exhibit significant hyperphagia and altered energy balance. Mechanistically, we demonstrate that Nipsnap1 integrates with lipid metabolism and BAT-specific ablation of Nipsnap1 leads to severe defects in beta-oxidation capacity when exposed to a cold environmental challenge.

conclusionOur findings identify Nipsnap1 as a potent regulator of long-term NST maintenance in BAT.

Indexed as

Energy MetabolismThermogenesisAnimalsCold TemperatureMiceObesitySignal TransductionBrown adipose tissueEnergy expenditureLipid metabolismNipsnap1Thermogenesis maintenance

Identifiers

PMID37423391
PMCPMC10404556
OpenAlexW4383551824

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.