Evidence map›Paper›PMID 31661297›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2019

Cardiac overexpression of perilipin 2 induces atrial steatosis, connexin 43 remodeling, and atrial fibrillation in aged mice.

Satsuki Sato, Jinya Suzuki, Masamichi Hirose, Mika Yamada, Yasuo Zenimaru, Takahiro Nakaya, Mai Ichikawa, Michiko Imagawa, Sadao Takahashi, Shoichiro Ikuyama and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

23 citing papers in PubMed, 28 citations in OpenAlex.

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  17. Metabolic Inflexibility as a Pathogenic Basis for Atrial Fibrillation.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

13 authors at 5 institutions in 2 countries.

Satsuki SatoThird Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.
Jinya SuzukiThird Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.
Masamichi HiroseDepartment of Molecular and Cellular Pharmacology, Iwate Medical University School of Pharmaceutical Sciences, Iwate, Japan.
Mika YamadaThird Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.
Yasuo ZenimaruThird Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.
Takahiro NakayaThird Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.
Mai IchikawaThird Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.
Michiko ImagawaThird Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.
Sadao TakahashiDivision of Diabetes Medicine, Ageo Central General Hospital, Saitama, Japan.
Shoichiro IkuyamaDivision of Endocrinology and Metabolism, Oita San-ai Medical Center, Oita, Japan.
Tadashi KonoshitaThird Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.
Fredric B KraemerVeterans Affairs Palo Alto Health Care System, Palo Alto, California.ORCID 0000-0003-2468-7807
Tamotsu IshizukaThird Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.
University of Fukui · JPIwate Medical University · JPKagawa Nutrition University · JPOita Medical Center · JPVA Palo Alto Health Care System · US

Funding

Stanford Islet Research CoreP30DK116074 · NIDDK · STANFORD UNIVERSITY · PI HASSAN CHAIB · 2017 to 2026
$19.5M
LipolysisI01BX000398 · VA · VETERANS ADMIN PALO ALTO HEALTH CARE SYS · PI KRAEMER, FREDRIC B. · 2009 to 2020
–
BLRD VA I01 BX000398NIDDK NIH HHS P30 DK116074
6 · The paper itself

Abstract

Atrial fibrillation (AF) is prevalent in patients with obesity and diabetes, and such patients often exhibit cardiac steatosis. Since the role of cardiac steatosis per se in the induction of AF has not been elucidated, the present study was designed to explore the relation between cardiac steatosis and AF. Transgenic (Tg) mice with cardiac-specific overexpression of perilipin 2 (PLIN2) were housed in the laboratory for more than 12 mo before the study. Electron microscopy of the atria of PLIN2-Tg mice showed accumulation of small lipid droplets around mitochondrial chains, and five- to ninefold greater atrial triacylglycerol (TAG) content compared with wild-type (WT) mice. Electrocardiography showed significantly longer RR intervals in PLIN2-Tg mice than in WT mice. Transesophageal electrical burst pacing resulted in significantly higher prevalence of sustained (>5 min) AF (69%) in PLIN2-Tg mice than in WT mice (24%), although it was comparable in younger (4-mo-old) mice. Connexin 43 (Cx43), a gap junction protein, was localized at the intercalated disks in WT atria but was heterogeneously distributed on the lateral side of cardiomyocytes in PLIN2-Tg atria. Langendorff-perfused hearts using the optical mapping technique showed slower and heterogeneous impulse propagation in PLIN2-Tg atria compared with WT atria. Cardiac overexpression of hormone-sensitive lipase in PLIN2-Tg mice resulted in atrial TAG depletion and amelioration of AF susceptibility. The results suggest that PLIN2-induced steatosis is associated with Cx43 remodeling, impaired conduction propagation, and higher incidence of AF in aged mice. Therapies targeting cardiac steatosis could be potentially beneficial against AF in patients with obesity or diabetes.

Indexed as

AnimalsAtrial FibrillationConnexin 43Gene Knock-In TechniquesHeart AtriaIsolated Heart PreparationLipid DropletsMiceMice, TransgenicMicroscopy, ElectronMyocytes, CardiacPerilipin-2Sterol EsteraseTriglyceridesVoltage-Sensitive Dye ImagingConnexin 43GJA1 protein, mousePerilipin-2Plin2 protein, mouseSterol EsteraseTriglyceridesagingcardiac steatosisgap junctionlipid dropletslipotoxic arrhythmia

Identifiers

PMID31661297
PMCPMC6957375
OpenAlexW2982288965

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.