Evidence map›Paper›PMID 27806985›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2016

High-fat diet-induced glucose dysregulation is independent of changes in islet ACE2 in mice.

Harshita Chodavarapu, Kavaljit H Chhabra, Huijing Xia, Vinayak Shenoy, Xinping Yue, Eric Lazartigues

Abstract read
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

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  9. Biological plausibility for interactions between dietary fat, resveratrol,American journal of physiology. Endocrinology and metabolism · 2020
    Article
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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 1 institution in 1 country.

Harshita ChodavarapuDepartment of Pharmacology and Experimental Therapeutics and Cardiovascular Center of Excellence, Louisiana State University Health Sciences Center, New Orleans, Louisiana.
Kavaljit H ChhabraDepartment of Pharmacology and Experimental Therapeutics and Cardiovascular Center of Excellence, Louisiana State University Health Sciences Center, New Orleans, Louisiana.
Huijing XiaDepartment of Pharmacology and Experimental Therapeutics and Cardiovascular Center of Excellence, Louisiana State University Health Sciences Center, New Orleans, Louisiana.
Vinayak ShenoyDepartment of Pharmacology, California Health Sciences University, Clovis, California; and.
Xinping YueDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans, Louisiana.
Eric LazartiguesDepartment of Pharmacology and Experimental Therapeutics and Cardiovascular Center of Excellence, Louisiana State University Health Sciences Center, New Orleans, Louisiana; elazar@lsuhsc.edu.
Louisiana State University Health Sciences Center New Orleans · US

Funding

VASCULAR SMOOTH MUSCLE PLASTICITY IN NITRIC OXIDEP20RR018766 · NCRR · LSU HEALTH SCIENCES CENTER · PI WORTHYLAKE, REBECCA · 2003 to 2011
$18.5M
Vascular and Cardiac Function Core - "Mentoring in Cardiovascular BiologyP30GM106392 · NIGMS · LSU HEALTH SCIENCES CENTER · PI KAPUSTA, DANIEL R · 2014 to 2018
$5.5M
Mechanisms of ACE2 Regulation in Neurogenic HypertensionR01HL093178 · NHLBI · LSU HEALTH SCIENCES CENTER · PI LAZARTIGUES, ERIC D · 2008 to 2017
$3.4M
NCRR NIH HHS P20 RR018766NHLBI NIH HHS R01 HL093178NIGMS NIH HHS P30 GM106392
6 · The paper itself

Abstract

While restoration of ACE2 activity in the pancreas leads to improvement of glycemia in experimental models of Type 2 diabetes, global deficiency in ACE2 disrupts β-cell function and impairs glucose tolerance in mice, demonstrating the physiological role of ACE2 in glucose homeostasis. Although the contribution of pancreatic ACE2 to glucose regulation has been demonstrated in genetic models of diabetes and in models with overexpression of the renin-angiotensin system (RAS), it is unclear whether islet ACE2 is involved in glycemic control in common models of human Type 2 diabetes. To determine whether diet-induced diabetes deregulates glucose homeostasis via reduction of ACE2 in the pancreatic islets, wild-type (WT) and ACE2 knockout (KO) male mice were fed a high-fat diet (HFD) for 16 wk. ACE2 KO mice were more susceptible than WT mice to HFD-mediated glycemic dysregulation. Islet ACE2 activity and expression of various genes, including ANG II type 1a receptor (mAT

Indexed as

Angiotensin-Converting Enzyme 2AnimalsDietary FatsDiet, High-FatGlucoseGlucose Metabolism DisordersInsulinInsulin ResistanceInsulin SecretionIslets of LangerhansMaleMiceMice, Inbred C57BLMice, KnockoutPeptidyl-Dipeptidase AACE2 protein, humanAce2 protein, mouseAngiotensin-Converting Enzyme 2Dietary FatsGlucoseInsulinPeptidyl-Dipeptidase AACE2high-fat dietpancreatic isletsrenin-angiotensin systemType 2 diabetes

Identifiers

PMID27806985
PMCPMC5256982
OpenAlexW2548118737

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.