Evidence map›Paper›PMID 30928474›Full record

ArticleMolecular metabolism2019

Adipose Lipocalin 2 overexpression protects against age-related decline in thermogenic function of adipose tissue and metabolic deterioration.

Jessica A Deis, Hong Guo, Yingjie Wu, Chengyu Liu, David A Bernlohr, Xiaoli Chen

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
3.4field-weighted citation impact, top 7% 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

25 citing papers in PubMed, 2 syntheses or guidelines pooled it, 67 citations in OpenAlex.

  1. Pooled it
  2. Association Of Blood Lipocalin-2 Levels with Gestational Diabetes Mellitus: A Systematic Review and Meta-Analysis.Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme · 2022
    Pooled it
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  11. Sex Differences in Adiposity and Cardiovascular Diseases.International journal of molecular sciences · 2022
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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

6 authors at 3 institutions in 2 countries.

Jessica A DeisDepartment of Food Science and Nutrition, University of Minnesota, Twin Cities, MN, USA.
Hong GuoDepartment of Food Science and Nutrition, University of Minnesota, Twin Cities, MN, USA.
Yingjie WuInstitute for Genomic Engineered Animal Models of Human Diseases, Dalian Medical University, Dalian, China.
Chengyu LiuTransgenic Core, National Heart, Lung and Blood Institute, National Institute of Health, Bethesda, MD, USA.
David A BernlohrDepartment of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, Twin Cities, MN, USA.
Xiaoli ChenDepartment of Food Science and Nutrition, University of Minnesota, Twin Cities, MN, USA. Electronic address: xlchen@umn.edu.
University of Minnesota · USDalian Medical University · CNNational Heart Lung and Blood Institute · US

Funding

Transgenic CoreZICHL005907 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI LIU, CHENGYU · 2010 to 2025
$25.8M
Minnesota Obesity Prevention Training (MnOPT)T32DK083250 · NIDDK · UNIVERSITY OF MINNESOTA · PI KOTZ, CATHERINE M, LASKA, MELISSA N. · 2010 to 2024
$5.1M
Lipocalin 2 in inflammation and metabolic controlR56DK080743 · NIDDK · UNIVERSITY OF MINNESOTA · PI CHEN, XIAOLI · 2013 to 2013
$190k
NIDDK NIH HHS R56 DK080743NIDDK NIH HHS T32 DK083250
6 · The paper itself

Abstract

objectivesAging increases the risk for development of adipose tissue dysfunction, insulin resistance, dyslipidemia, and liver steatosis. Lipocalin 2 (Lcn2) deficient mice are more prone to diet-induced obesity and metabolic dysfunction, indicating a protective role for Lcn2 in younger mice. In this study, we determined whether overexpressing Lcn2 in adipose tissue can protect against age-related metabolic deterioration.

methodsWe developed ap2-promoter-driven Lcn2 transgenic (Tg) mice and aged Lcn2 Tg mice for the metabolic assessments.

resultsWe found decreased adipocyte size in inguinal white adipose tissue (iWAT) from 10-month-old Lcn2 Tg mice relative to WT. This was accompanied by increased markers of adipogenesis in iWAT and attenuation of the age-related decline in AMP-activated protein kinase (AMPK) phosphorylation in adipose tissue depots. In addition to improvements in adipose tissue function, whole-body metabolic homeostasis was maintained in aged Lcn2 Tg mice. This included improved glucose tolerance and reduced serum triglycerides in older Lcn2 Tg mice relative to WT mice. Further, liver morphology and liver lipid levels were improved in older Lcn2 Tg mice, alongside a decrease in markers of liver inflammation and fibrosis.

conclusionsWe demonstrate that overexpression of Lcn2 in adipose tissue not only preserves adipose tissue function during aging but also promotes maintenance of glucose tolerance, decreases dyslipidemia, and prevents liver lipid accumulation and steatosis.

Indexed as

ThermogenesisAdipose Tissue, BeigeAdipose Tissue, WhiteAgingAMP-Activated Protein Kinase KinasesAnimalsGlucoseLipid MetabolismLipocalin-2LiverMaleMiceMice, Inbred C57BLProtein KinasesAMP-Activated Protein Kinase KinasesGlucoseLcn2 protein, mouseLipocalin-2Protein KinasesAdipose beigingAdipose tissueHealthspanLipocalin 2

Identifiers

PMID30928474
PMCPMC6531839
OpenAlexW2922618449

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.