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Background: Among the chronic diseases, chronic kidney failure is one of diseases that have the most difficulty in coping with oxidative stress due to the deterioration of the antioxidant system balance in the body. Beyond being a vitamin, 1,25-dihydroxycholecalciferol (vitamin D3) is a molecule that positively or negatively affects many enzymes which are in protein structures. Thioredoxin (TRX), which has an important role in the antioxidant system, is one of these proteins. By conducting this study, we wanted to emphasize the role of vitamin D3 in reducing the oxidative stress load on patients undergoing peritoneal dialysis (PD) via serum TRX level measurement.
Methods: In this study, we evaluated the medical treatments of 69 PD patients who were followed up routinely. The patients were divided into 2 groups according to whether they used vitamin D3 or not. 49 of our patients were using vitamin D3. While requesting routine laboratory tests, we reserved a separate serum sample to measure serum TRX levels by double-antibody sandwich enzyme-linked immunosorbent assay for all patients.
Results: Only one parameter has a significant statistical relationship with serum TRX level and the treatment protocol. The serum TRX level was significantly higher (211,62 U/l ± 314,46) in the group receiving vitamin D3 compared to the group which is not using Vitamin D3 (101,63 U/l ± 215,03) ( < 0,006).
Conclusion: This study highlights the importance of appropriate dose of vitamin D3 replacement especially in PD patients who are under intense oxidative stress compared to healthy individuals.
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http://dx.doi.org/10.1155/2022/2590944 | DOI Listing |
J Pharm Pharmacol
August 2025
Clinical Pharmacology Department, Faculty of Medicine, Ain-Shams University, Cairo, 11591, Egypt.
Objectives: Oxidative stress (OS), inflammation, and pyroptosis are hallmarks of atherosclerosis pathogenesis. Thioredoxin-interacting protein (TXNIP) crosslinks them through activating nucleotide-binding domain, leucine-rich-containing family, pyrin domain-containing-3 (NLRP3) inflammasome pathway. The current work addresses the potentials of empagliflozin (EMPA) on OS markers, thioredoxin (TRX), and TXNIP, downstream mediators of NLRP3 inflammasome and the executioner of pyroptosis; gasdermin D (GSDMD) in a model of atherosclerosis.
View Article and Find Full Text PDFCurr Issues Mol Biol
July 2025
Biruni Research Center (BAMER), Faculty of Medicine, Biruni University, 34015 Istanbul, Turkey.
Oxidative stress, mitochondrial dysfunction, and inflammatory responses cause acute liver failure in most cases of acetaminophen (APAP) overdose. Tamarixetin (Trx), an antioxidant and anti-inflammatory flavonoid, has not yet been studied in models of APAP-induced hepatotoxicity. Trx was tested for its protective effects on APAP-induced liver injury in rats using biochemical, histopathological, and oxidative stress parameters.
View Article and Find Full Text PDFIran J Basic Med Sci
January 2025
Physiology-Pharmacology Research Center, Research Institute of Basic Medical Sciences, Rafsanjan University of Medical Sciences, Rafsanjan, Iran.
Objectives: Troxerutin (TRX) is a natural bioflavonoid with several medicinal properties. We assessed its protective effect on carbon tetrachloride-related hepatorenal damage in male mice.
Materials And Methods: Male mice were assigned to five groups: Control, TRX, CCL4, CCL + TRX 75 mg/kg, CCL + TRX 150 mg/kg.
J Clin Med
June 2025
Department of Advanced Medical and Surgical Sciences and Department of Precision Medicine, University of Campania 'L. Vanvitelli', Via De Crecchio 7, 80138 Naples, Italy.
Fosfomycin is an old antibiotic that has recently gained attention owing to its preserved activity against multidrug-resistant (MDR) bacteria. Data on its use in real life are limited. Thus, we evaluated the efficacy and safety of fosfomycin disodium in the context of our hospital clinical practice.
View Article and Find Full Text PDFMetabolites
May 2025
Laboratory of Clinical Biochemistry, University General Hospital 'Attikon', Medical School, National and Kapodistrian University of Athens, 12462 Athens, Greece.
Thioredoxin-interacting protein (TXNIP) is a major inhibitor of the thioredoxin (TRX) antioxidant system and an important player in the development and aggravation of intracellular oxidative stress. Although first recognized as a metabolic regulator, recent studies have identified the multifaceted role of this protein in other molecular pathways involving inflammation, apoptosis, and glucose metabolism. : This review aims to highlight the importance of TXNIP in diabetes-related pathophysiology and explore the existing evidence regarding TXNIP's role in GDM-associated pathogenetic mechanisms, revealing common regulatory pathways.
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