Evidence map›Paper›PMID 30084544›Full record

ArticleJournal of diabetes investigation2019

Functional adenosine triphosphate-sensitive potassium channel is required in high-carbohydrate diet-induced increase in β-cell mass.

Masatoshi Murase, Yusuke Seino, Ryuya Maekawa, Atsushi Iida, Kaori Hosokawa, Tomohide Hayami, Shin Tsunekawa, Yoji Hamada, Norihide Yokoi, Susumu Seino and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of diabetes investigation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed, 9 citations in OpenAlex.

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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

12 authors at 3 institutions in 1 country.

Masatoshi MuraseDepartments of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Yusuke SeinoDepartments of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID http://orcid.org/0000-0002-9099-3493
Ryuya MaekawaDepartments of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Atsushi IidaDepartments of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Kaori HosokawaDepartments of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Tomohide HayamiDivision of Molecular and Metabolic Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.
Shin TsunekawaDepartments of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Yoji HamadaDepartments of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Norihide YokoiDivision of Molecular and Metabolic Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.ORCID http://orcid.org/0000-0002-5596-9754
Susumu SeinoDivision of Molecular and Metabolic Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.
Yoshitaka HayashiDivision of Stress Adaptation and Protection, Department of Genetics Research, Institute of Environmental Medicine, Nagoya University, Nagoya, Japan.ORCID http://orcid.org/0000-0002-7557-4303
Hiroshi ArimaDepartments of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Nagoya University · JPKobe University · JPAichi Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

AIMS/

introductionA high-carbohydrate diet is known to increase insulin secretion and induce obesity. However, whether or not a high-carbohydrate diet affects β-cell mass (BCM) has been little investigated. MATERIALS AND

methodsBoth wild-type (WT) mice and adenosine triphosphate-sensitive potassium channel-deficient (Kir6.2KO) mice were fed normal chow or high-starch (ST) diets for 22 weeks. BCM and the numbers of islets were analyzed by immunohistochemistry, and gene expression levels in islets were investigated by quantitative real-time reverse transcription polymerase chain reaction. MIN6-K8 β-cells were stimulated in solution containing various concentrations of glucose combined with nifedipine and glimepiride, and gene expression was analyzed.

resultsBoth WT and Kir6.2KO mice fed ST showed hyperinsulinemia and body weight gain. BCM, the number of islets and the expression levels of cyclinD2 messenger ribonucleic acid were increased in WT mice fed ST compared with those in WT mice fed normal chow. In contrast, no significant difference in BCM, the number of islets or the expression levels of cyclinD2 messenger ribonucleic acid were observed between Kir6.2KO mice fed normal chow and those fed ST. Incubation of MIN6-K8 β-cells in high-glucose media or with glimepiride increased cyclinD2 expression, whereas nifedipine attenuated a high-glucose-induced increase in cyclinD2 expression.

conclusionsThese results show that a high-starch diet increases BCM in an adenosine triphosphate-sensitive potassium channel-dependent manner, which is mediated through upregulation of cyclinD2 expression.

Indexed as

Weight GainAdenosine TriphosphateAnimalsBlood GlucoseCyclin D2Dietary CarbohydratesInsulin-Secreting CellsKcnj11 ChannelMaleMice, Inbred C57BLMice, KnockoutPotassium Channels, Inwardly RectifyingAdenosine TriphosphateBlood GlucoseCcnd2 protein, mouseCyclin D2Dietary CarbohydratesKcnj11 ChannelPotassium Channels, Inwardly RectifyingAdenosine triphosphate-sensitive potassium channelCarbohydrateβ-Cell mass

Identifiers

PMID30084544
PMCPMC6400177
OpenAlexW2885222356

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.