Evidence map›Paper›PMID 35005845›Full record

ArticlePhysiological reports2022

Pharmacological inhibition of the lipid phosphatase PTEN ameliorates heart damage and adipose tissue inflammation in stressed rats with metabolic syndrome.

Sao Ashikawa, Yuki Komatsu, Yumeno Kawai, Kiyoshi Aoyama, Shiho Nakano, Xixi Cui, Misaki Hayakawa, Nanako Sakabe, Nozomi Furukawa, Katsuhide Ikeda and 2 more

Open access · goldAbstract read
In one paragraph

Article in Physiological reports, 2022. 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
0.3field-weighted citation impact, top 50% 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, 3 citations in OpenAlex.

  1. The Impact of Intermittent Hypoxia on Metabolism and Cognition.International journal of molecular sciences · 2022
    Review
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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 1 institution in 1 country.

Sao AshikawaPathophysiology Sciences, Department of Integrated Health Sciences, Nagoya, Japan.
Yuki KomatsuPathophysiology Sciences, Department of Integrated Health Sciences, Nagoya, Japan.
Yumeno KawaiPathophysiology Sciences, Department of Integrated Health Sciences, Nagoya, Japan.
Kiyoshi AoyamaPathophysiology Sciences, Department of Integrated Health Sciences, Nagoya, Japan.
Shiho NakanoPathophysiology Sciences, Department of Integrated Health Sciences, Nagoya, Japan.
Xixi CuiPathophysiology Sciences, Department of Integrated Health Sciences, Nagoya, Japan.
Misaki HayakawaPathophysiology Sciences, Department of Integrated Health Sciences, Nagoya, Japan.
Nanako SakabePathophysiology Sciences, Department of Integrated Health Sciences, Nagoya, Japan.
Nozomi FurukawaPathophysiology Sciences, Department of Integrated Health Sciences, Nagoya, Japan.
Katsuhide IkedaPathophysiology Sciences, Department of Integrated Health Sciences, Nagoya, Japan.
Toyoaki MuroharaDepartment of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Kohzo NagataPathophysiology Sciences, Department of Integrated Health Sciences, Nagoya, Japan.ORCID 0000-0003-0089-6794
Nagoya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phosphatidylinositol 3-kinase (PI3K) signaling promotes the differentiation and proliferation of regulatory B (Breg) cells, and the lipid phosphatase phosphatase and tensin homolog deleted on chromosome 10 (PTEN) antagonizes the PI3K-Akt signaling pathway. We previously demonstrated that cardiac Akt activity is increased and that restraint stress exacerbates hypertension and both heart and adipose tissue (AT) inflammation in DS/obese rats, an animal model of metabolic syndrome (MetS). We here examined the effects of restraint stress and pharmacological inhibition of PTEN on heart and AT pathology in such rats. Nine-week-old animals were treated with the PTEN inhibitor bisperoxovanadium-pic [bpV(pic)] or vehicle in the absence or presence of restraint stress for 4 weeks. BpV(pic) treatment had no effect on body weight or fat mass but attenuated hypertension in DS/obese rats subjected to restraint stress. BpV(pic) ameliorated left ventricular (LV) inflammation, fibrosis, and diastolic dysfunction as well as AT inflammation in the stressed rats. Restraint stress reduced myocardial capillary density, and this effect was prevented by bpV(pic). In addition, bpV(pic) increased the proportions of Breg and B-1 cells as well as reduced those of CD8

Indexed as

Heart InjuriesMetabolic SyndromeAdipose TissueAnimalsInflammationLipidsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseRatsLipidsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePten protein, ratadipose tissue inflammationcardiac injurymetabolic syndromePTENregulatory B cellstress

Identifiers

PMID35005845
PMCPMC8744130
OpenAlexW4206138277

What OpenQuestion holds

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LicenceCC BY
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.