Evidence map›Paper›PMID 34609306›Full record

ArticleThe Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology2021

Investigation of Dynamic Thiol/Disulfide Homeostasis and Nitrosative Stress in Patients with Wilson Disease.

Emine Melis Yücel, Bugra Tolga Konduk, Ahmet Saracaloglu, Sezgin Barutçu, Seniz Demiryürek, Fatma Kaba, Belma Dogan Güngen, Abdullah Tuncay Demiryürek

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Article in The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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0cells of the map it votes in
4citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Assessment of Serum Dynamic Thiol/Disulfide Homeostasis and Oxidative/Nitrosative Stress in Patients with Crohn's Disease.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2024
    Article
  3. Article
  4. Article
4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Emine Melis YücelDepartment of Gastroenterology, Faculty of Medicine, Gaziantep University, Gaziantep, Turkey.
Bugra Tolga KondukDepartment of Gastroenterology, Faculty of Medicine, Gaziantep University, Gaziantep, Turkey.
Ahmet SaracalogluDepartment of Medical Pharmacology, Faculty of Medicine, Gaziantep University, Gaziantep, Turkey.
Sezgin BarutçuDepartment of Gastroenterology, Faculty of Medicine, Gaziantep University, Gaziantep, Turkey.
Seniz DemiryürekDepartment of Physiology, Faculty of Medicine, Gaziantep University, Gaziantep, Turkey.
Fatma KabaMedical Student, Faculty of Medicine, Gaziantep University, Gaziantep, Turkey.
Belma Dogan GüngenDepartment of Neurology, Faculty of Medicine, Istanbul Rumeli University, Istanbul, Turkey.
Abdullah Tuncay DemiryürekDepartment of Medical Pharmacology, Faculty of Medicine, Gaziantep University, Gaziantep, Turkey; Vocational School of Health Services, Gaziantep University, Gaziantep, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWilson disease (WD) is an autosomal recessive inherited disorder of copper (Cu2+) metabolism, resulting in Cu2+ accumulation and liver and central nervous system toxicity. Oxidative stress may have a role in the pathogenesis of Wilson disease, but the roles of thiol/disulfide homeostasis and nitrosative stress have not been examined. The purpose of this study was to evaluate whether there is a modification in thiol/disulfide homeostasis and nitrosative stress in patients with Wilson disease.

methodsA total of 50 patients with Wilson disease (42 under drug treatment and 8 newly diagnosed patients with no drug treatment) and 50 healthy gender- and age-matched controls were enrolled for this study. Serum native thiol and total thiol levels were measured with a spectrophotometric method. The number of disulfide bonds and the related ratios were determined from these measurements. Serum nitric oxide (NO) and 3-nitrotyrosine (3-NT) levels were analyzed using chemiluminescence and ELISA assays, respectively.

resultsThe average native thiol levels of the patient group under drug treatment were found to be markedly higher than the levels of controls (P < .05). We detected no marked changes in total thiol and disulfide levels, and disulfide/total thiol, disulfide/native thiol, or native thiol/total thiol ratios between groups. We found significant elevations in NO levels in Wilson disease group before drug treatment, and the 3-NT levels in the Wilson disease groups prior to (P < .05) and under drug treatment (P < .01), when compared to controls.

conclusionOur data are the first to show that nitrosative stress and thiol/disulfide homeostasis can contribute to the pathogenesis of Wilson disease.

Indexed as

Hepatolenticular DegenerationHomeostasisNitrosative StressDisulfidesHumansSulfhydryl CompoundsDisulfidesSulfhydryl Compounds

Identifiers

PMID34609306
PMCPMC8975326

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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.