Evidence map›Paper›PMID 25427682›Full record

ArticleHypertension research : official journal of the Japanese Society of Hypertension2015

Significance of serum Zn-α2-glycoprotein for the regulation of blood pressure.

Souichi Kurita, Keisuke Takeuchi, Yoshimi Hayashi, Hisao Ueyama, Dimitar P Zankov, Xiaoling Pang, Takanobu Otsuka, Iwao Ohkubo, Osamu Ogikubo, Hisakazu Ogita

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In one paragraph

Article in Hypertension research : official journal of the Japanese Society of Hypertension, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

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  5. Rutin Attenuates Hepatotoxicity in High-Cholesterol-Diet-Fed Rats.Oxidative medicine and cellular longevity · 2016
    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

10 authors at 3 institutions in 1 country.

Souichi KuritaDivision of Molecular Medical Biochemistry, Department of Biochemistry and Molecular Biology, Shiga University of Medical Science, Shiga, Japan.
Keisuke TakeuchiDivision of Molecular Medical Biochemistry, Department of Biochemistry and Molecular Biology, Shiga University of Medical Science, Shiga, Japan.
Yoshimi HayashiDepartment of Orthopedic Surgery, Nagoya City University, Nagoya, Japan.
Hisao UeyamaDivision of Molecular Medical Biochemistry, Department of Biochemistry and Molecular Biology, Shiga University of Medical Science, Shiga, Japan.
Dimitar P ZankovDivision of Molecular Medical Biochemistry, Department of Biochemistry and Molecular Biology, Shiga University of Medical Science, Shiga, Japan.
Xiaoling PangDivision of Molecular Medical Biochemistry, Department of Biochemistry and Molecular Biology, Shiga University of Medical Science, Shiga, Japan.
Takanobu OtsukaDepartment of Orthopedic Surgery, Nagoya City University, Nagoya, Japan.
Iwao Ohkubo1] Division of Molecular Medical Biochemistry, Department of Biochemistry and Molecular Biology, Shiga University of Medical Science, Shiga, Japan [2] Department of Nutrition, Tenshi College, Hokkaido, Japan.
Osamu Ogikubo1] Department of Orthopedic Surgery, Nagoya City University, Nagoya, Japan [2] Department of Orthopedics, Nagoya City Rehabilitation Hospital, Aichi, Japan.
Hisakazu OgitaDivision of Molecular Medical Biochemistry, Department of Biochemistry and Molecular Biology, Shiga University of Medical Science, Shiga, Japan.
Shiga University of Medical Science · JPNagoya City University · JPTenshi College · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Zn-α2-glycoprotein (ZAG) (molecular weight=41 kDa) is one component in the α2 fraction of human plasma, and is reported to be associated with several diseases, such as cancers and metabolic syndromes. ZAG is also considered to be an important modulator of lipid metabolism. However, little is known about the correlation of serum ZAG levels with indicators of metabolic syndrome. Serum ZAG concentrations analyzed by enzyme-linked immunoassay were positively correlated with systolic and diastolic blood pressure in 326 subjects (236 males and 90 females) aged 17-79 years who had an annual health examination. By luciferase reporter and electrophoretic mobility shift assays, the core promoter region to regulate the ZAG gene expression was found to exist between -110 and -101. The transcription factor Sp1 interacted with this region, and Sp1 knockdown experiments showed that Sp1 critically regulated ZAG expression. Furthermore, ZAG increased the active form of RhoA, which was determined by pull-down assay. Increased serum ZAG concentrations induced, at least partly, by Sp1 may cause an increase in vascular tone through the activation of RhoA and contribute to elevated blood pressure.

Indexed as

AdolescentAdultAgedAnimalsBlood PressureCell LineFemaleGene Expression RegulationGene Knockdown TechniquesHumansHypertensionMaleMetabolic SyndromeMiddle AgedMuscle TonusPromoter Regions, GeneticrhoA GTP-Binding ProteinRHOA protein, humanSeminal Plasma ProteinsSp1 Transcription FactorZn-Alpha-2-Glycoprotein

Identifiers

PMID25427682
OpenAlexW2077995553

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.