Oxidative Stress in Plasma from Patients with Marfan Syndrome Is Modulated by Deodorized Garlic Preliminary Findings
Author(s) -
Israel Pérez-Torres,
María Elena Soto,
Linaloe Manzano-Pech,
Eulises DíazDíaz,
Elizabeth SoriaCastro,
María Esther Rubio-Ruíz,
Verónica GuarnerLans
Publication year - 2022
Publication title -
oxidative medicine and cellular longevity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.494
H-Index - 93
eISSN - 1942-0900
pISSN - 1942-0994
DOI - 10.1155/2022/5492127
Subject(s) - antioxidant , oxidative stress , glutathione peroxidase , chemistry , lipid peroxidation , gpx3 , gpx1 , biochemistry , thioredoxin , glutathione reductase , superoxide dismutase , glutathione , peroxidase , medicine , enzyme
Marfan syndrome (MFS) is a genetic disorder of connective tissue that affects the fibrillin-1 protein (FBN-1). It is associated with the formation of aneurysms, damage to the endothelium and oxidative stress (OS). Allium sativum (garlic) has antioxidant properties; therefore, the goal of this study was to show the antioxidant effect of deodorized garlic (DG) on antioxidant enzymes and OS markers in the plasma of patients with MFS. The activity of antioxidant enzymes such as extracellular superoxide dismutase (EcSOD), peroxidases, glutathione peroxidase (GPx), gluthatione-S-tranferase (GST), and thioredoxin reductase (TrxR) was quantified, and nonenzymatic antioxidant system markers including lipid peroxidation (LPO), carbonylation, nitrates/nitrites, GSH, and vitamin C in plasma were determined in patients with MFS before and after treatment with DG. The results show that DG increased the activity of the EcSOD, peroxidases, GPx, GST, TrxR ( p ≤ 0.05 ) and decrease LPO, carbonylation, and nitrates/nitrites ( p ≤ 0.01 ). However, glutathione was increased ( p = 0.01 ) in plasma from patients with MFS. This suggests that treatment with garlic could lower the OS threshold by increasing the activity of antioxidant enzymes and could help in the prevention and mitigation of adverse OS in patients with MFS.
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