Evidence map›Paper›PMID 29750602›Full record

ArticlePhysiological genomics2018

Tpcn2 knockout mice have improved insulin sensitivity and are protected against high-fat diet-induced weight gain.

Hong He, Katie Holl, Sarah DeBehnke, Chay Teng Yeo, Polly Hansen, Abraham K Gebre, Sandra Leone-Kabler, Margarida Ruas, John S Parks, John Parrington and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Physiological genomics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 45% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Two-pore channels: going with the flows.Biochemical Society transactions · 2022
    Article
  3. 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

11 authors at 3 institutions in 2 countries.

Hong HeDepartment of Pediatrics, Medical College of Wisconsin , Milwaukee, Wisconsin.
Katie HollDepartment of Pediatrics, Medical College of Wisconsin , Milwaukee, Wisconsin.
Sarah DeBehnkeDepartment of Pediatrics, Medical College of Wisconsin , Milwaukee, Wisconsin.
Chay Teng YeoDepartment of Pediatrics, Medical College of Wisconsin , Milwaukee, Wisconsin.
Polly HansenDepartment of Pediatrics, Medical College of Wisconsin , Milwaukee, Wisconsin.
Abraham K GebreDepartment of Internal Medicine-Section on Molecular Medicine, Wake Forest School of Medicine , Winston Salem, North Carolina.
Sandra Leone-KablerDepartment of Internal Medicine-Section on Molecular Medicine, Wake Forest School of Medicine , Winston Salem, North Carolina.
Margarida RuasDepartment of Pharmacology, University of Oxford , Oxford , United Kingdom.
John S ParksDepartment of Internal Medicine-Section on Molecular Medicine, Wake Forest School of Medicine , Winston Salem, North Carolina.
John ParringtonDepartment of Pharmacology, University of Oxford , Oxford , United Kingdom.
Leah C Solberg WoodsDepartment of Internal Medicine-Section on Molecular Medicine, Wake Forest School of Medicine , Winston Salem, North Carolina.
Medical College of Wisconsin · USWake Forest University · USUniversity of Oxford · GB

Funding

The Role of Hepatocyte ABCA1 in Lipid Mobilization and TransportR01HL119962 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PARKS, JOHN S · 2013 to 2022
$3.9M
Systems Genetics of Adiposity Traits in Outbred RatsR01DK106386 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SOLBERG WOODS, LEAH CATHERINE · 2015 to 2018
$2.6M
Genome-wide fine-mapping of metabolic traits in heterogeneous stock ratsR01DK088975 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI SOLBERG WOODS, LEAH CATHERINE · 2010 to 2014
$1.9M
NHLBI NIH HHS R01 HL119962NIDDK NIH HHS R01 DK088975NIDDK NIH HHS R01 DK106386
6 · The paper itself

Abstract

Type 2 diabetes is a complex disorder affected by multiple genes and the environment. Our laboratory has shown that in response to a glucose challenge, two-pore channel 2 ( Tpcn2) knockout mice exhibit a decreased insulin response but normal glucose clearance, suggesting they have improved insulin sensitivity compared with wild-type mice. We tested the hypothesis that improved insulin sensitivity in Tpcn2 knockout mice would protect against the negative effects of a high fat diet. Male and female Tpcn2 knockout (KO), heterozygous (Het), and wild-type (WT) mice were fed a low-fat (LF) or high-fat (HF) diet for 24 wk. HF diet significantly increases body weight in WT mice relative to those on the LF diet; this HF diet-induced increase in body weight is blunted in the Het and KO mice. Despite the protection against diet-induced weight gain, however, Tpcn2 KO mice are not protected against HF-diet-induced changes in glucose or insulin area under the curve during glucose tolerance tests in female mice, while HF diet has no significant effect on glucose tolerance in the male mice, regardless of genotype. Glucose disappearance during an insulin tolerance test is augmented in male KO mice, consistent with our previous findings suggesting enhanced insulin sensitivity in these mice. Male KO mice exhibit increased fasting plasma total cholesterol and triglyceride concentrations relative to WT mice on the LF diet, but this difference disappears in HF diet-fed mice where there is increased cholesterol and triglycerides across all genotypes. These data demonstrate that knockout of Tpcn2 may increase insulin action in male, but not female, mice. In addition, both male and female KO mice are protected against diet-induced weight gain, but this protection is likely independent from glucose tolerance, insulin sensitivity, and plasma lipid levels.

Indexed as

AnimalsCalcium ChannelsCholesterolDiabetes Mellitus, Type 2Diet, High-FatFemaleGlucose Tolerance TestInsulin ResistanceMaleMice, 129 StrainMice, Inbred C57BLMice, KnockoutObesitySex FactorsTriglyceridesWeight GainCalcium ChannelsCholesterolTPCN2 protein, mouseTriglyceridescholesteroldiet-induced obesitytriglyceridestwo-pore channel 2

Identifiers

PMID29750602
PMCPMC6139634
OpenAlexW2802173366

What OpenQuestion holds

Textmetadata
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.