Evidence map›Paper›PMID 25892997›Full record

ArticleInternational journal of endocrinology and metabolism2015

Resveratrol-Dependent Down-regulation of Receptor for Advanced Glycation End-products and Oxidative Stress in Kidney of Rats With Diabetes.

Heresh Moridi, Jamshid Karimi, Nasrin Sheikh, Mohammad Taghi Goodarzi, Massoud Saidijam, Reza Yadegarazari, Mohammad Khazaei, Iraj Khodadadi, Heidar Tavilani, Hossein Piri and 3 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of endocrinology and metabolism, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

27 citing papers in PubMed, 73 citations in OpenAlex.

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  12. Accelerated Kidney Aging in Diabetes Mellitus.Oxidative medicine and cellular longevity · 2020
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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 3 institutions in 1 country.

Heresh MoridiDepartment of Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamadan, IR Iran.
Jamshid KarimiDepartment of Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamadan, IR Iran.
Nasrin SheikhDepartment of Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamadan, IR Iran.
Mohammad Taghi GoodarziResearch Center for Molecular Medicine, Hamadan University of Medical Sciences, Hamadan, IR Iran.
Massoud SaidijamResearch Center for Molecular Medicine, Hamadan University of Medical Sciences, Hamadan, IR Iran.
Reza YadegarazariDepartment of Molecular Medicine and Genetics, School of Medicine, Hamadan University of Medical Sciences, Hamadan, IR Iran.
Mohammad KhazaeiDepartment of Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamadan, IR Iran.
Iraj KhodadadiDepartment of Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamadan, IR Iran.
Heidar TavilaniDepartment of Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamadan, IR Iran.
Hossein PiriDepartment of Biochemistry and Genetics, School of Medicine, Qazvin University of Medical Sciences, Qazvin, IR Iran.
Soheila AsadiDepartment of Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamadan, IR Iran.
Sadegh ZareiDepartment of Biochemistry, School of Medicine, Yazd University of Medical Sciences, Yazd, IR Iran.
Azam RezaeiDepartment of Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamadan, IR Iran.
Hamedan University of Medical Sciences · IRQazvin University of Medical Sciences · IRYazd University · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMillions of people in the world have diabetes mellitus and its prevalence is growing. Oxidative stress, advanced glycation end-products (AGEs) and receptor for advanced glycation end-products (RAGE) play key role in the pathogenesis of diabetes. New and safe strategies of remedy are needed for this disease.

objectivesWe hypothesized that resveratrol may exert a renal protective effect on diabetic rats. MATERIALS AND

methodsMale rats with diabetes were treated with or without resveratrol as 1, 5, 10 mg/kg of body weight for 30 days. The total AGEs and malondialdehyde levels in kidney tissues were determined by spectrofluorimetric method and the insulin level was assayed using ELISA. The total antioxidant capacity contents in kidney and the glucose in plasma were measured by a colorimetric assay. The expression of RAGE was assayed in kidneys of all animals using quantitative PCR.

resultsIn resveratrol-treated rats with diabetes, malondialdehyde levels, plasma glucose and expression of RAGE were significantly reduced compared with the untreated group. Moreover, the total antioxidant and insulin levels significantly increased in treated rats. There was no significant difference in the AGEs contents among all the groups.

conclusionsThese results revealed that resveratrol has beneficial effects on kidney by extenuating the oxidative stress and down-regulation of RAGE expression.

Indexed as

Advanced Glycation End-productDiabetes MellitusOxidative StressResveratrol

Identifiers

PMID25892997
PMCPMC4394675
OpenAlexW2111555573

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Registered trials

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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.