Antioxidant Activities and Oxidative Stress Byproducts in Human Hypertension
ABSTRACT—The objective was to study oxidative status, antioxidant activities, and reactive oxygen species byproducts in whole blood and mononuclear peripherals cells and their relationship with blood pressure. Sixty-six hypertensive patients and 16 normotensive volunteers as a control group were stu...
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Published in | Hypertension (Dallas, Tex. 1979) Vol. 41; no. 5; pp. 1096 - 1101 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Philadelphia, PA
American Heart Association, Inc
01.05.2003
Hagerstown, MD Lippincott |
Subjects | |
Online Access | Get full text |
ISSN | 0194-911X 1524-4563 1524-4563 |
DOI | 10.1161/01.HYP.0000068370.21009.38 |
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Abstract | ABSTRACT—The objective was to study oxidative status, antioxidant activities, and reactive oxygen species byproducts in whole blood and mononuclear peripherals cells and their relationship with blood pressure. Sixty-six hypertensive patients and 16 normotensive volunteers as a control group were studied. In both, whole blood and peripheral mononuclear cells oxidized/reduced glutathione ratio and malondialdehyde was significantly higher, and the activity of superoxide dismutase, catalase, and glutathione peroxidase was significantly lower in hypertensive patients when compared with normal subjects. The content of damaged base 8-oxo-2′-deoxyguanosine in nuclear and mitochondrial deoxyribonucleoproteins of hypertensive subjects was also significantly higher than that of the normotensive control subjects. No differences in these measurements were found among hypertensive subjects grouped in tertiles of 24-hour average mean blood pressure or between “white-coat” and established hypertensive subjects. Furthermore, no relationship was observed between the average of 24-hour mean blood pressure and oxidized/reduced glutathione ratio, reactive oxygen species byproducts, malondialdehide, or genomic 8-oxo-2′-deoxyguanosine. In whole blood and in mononuclear cells from hypertensive subjects, there was an increase in oxidative stress and a reduction in the activity of antioxidant mechanisms that appeared to be independent of the blood pressure values. |
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AbstractList | The objective was to study oxidative status, antioxidant activities, and reactive oxygen species byproducts in whole blood and mononuclear peripherals cells and their relationship with blood pressure. Sixty-six hypertensive patients and 16 normotensive volunteers as a control group were studied. In both, whole blood and peripheral mononuclear cells oxidized/reduced glutathione ratio and malondialdehyde was significantly higher, and the activity of superoxide dismutase, catalase, and glutathione peroxidase was significantly lower in hypertensive patients when compared with normal subjects. The content of damaged base 8-oxo-2'-deoxyguanosine in nuclear and mitochondrial deoxyribonucleoproteins of hypertensive subjects was also significantly higher than that of the normotensive control subjects. No differences in these measurements were found among hypertensive subjects grouped in tertiles of 24-hour average mean blood pressure or between "white-coat" and established hypertensive subjects. Furthermore, no relationship was observed between the average of 24-hour mean blood pressure and oxidized/reduced glutathione ratio, reactive oxygen species byproducts, malondialdehide, or genomic 8-oxo-2'-deoxyguanosine. In whole blood and in mononuclear cells from hypertensive subjects, there was an increase in oxidative stress and a reduction in the activity of antioxidant mechanisms that appeared to be independent of the blood pressure values. ABSTRACT—The objective was to study oxidative status, antioxidant activities, and reactive oxygen species byproducts in whole blood and mononuclear peripherals cells and their relationship with blood pressure. Sixty-six hypertensive patients and 16 normotensive volunteers as a control group were studied. In both, whole blood and peripheral mononuclear cells oxidized/reduced glutathione ratio and malondialdehyde was significantly higher, and the activity of superoxide dismutase, catalase, and glutathione peroxidase was significantly lower in hypertensive patients when compared with normal subjects. The content of damaged base 8-oxo-2′-deoxyguanosine in nuclear and mitochondrial deoxyribonucleoproteins of hypertensive subjects was also significantly higher than that of the normotensive control subjects. No differences in these measurements were found among hypertensive subjects grouped in tertiles of 24-hour average mean blood pressure or between “white-coat” and established hypertensive subjects. Furthermore, no relationship was observed between the average of 24-hour mean blood pressure and oxidized/reduced glutathione ratio, reactive oxygen species byproducts, malondialdehide, or genomic 8-oxo-2′-deoxyguanosine. In whole blood and in mononuclear cells from hypertensive subjects, there was an increase in oxidative stress and a reduction in the activity of antioxidant mechanisms that appeared to be independent of the blood pressure values. The objective was to study oxidative status, antioxidant activities, and reactive oxygen species byproducts in whole blood and mononuclear peripherals cells and their relationship with blood pressure. Sixty-six hypertensive patients and 16 normotensive volunteers as a control group were studied. In both, whole blood and peripheral mononuclear cells oxidized/reduced glutathione ratio and malondialdehyde was significantly higher, and the activity of superoxide dismutase, catalase, and glutathione peroxidase was significantly lower in hypertensive patients when compared with normal subjects. The content of damaged base 8-oxo-2'-deoxyguanosine in nuclear and mitochondrial deoxyribonucleoproteins of hypertensive subjects was also significantly higher than that of the normotensive control subjects. No differences in these measurements were found among hypertensive subjects grouped in tertiles of 24-hour average mean blood pressure or between "white-coat" and established hypertensive subjects. Furthermore, no relationship was observed between the average of 24-hour mean blood pressure and oxidized/reduced glutathione ratio, reactive oxygen species byproducts, malondialdehide, or genomic 8-oxo-2'-deoxyguanosine. In whole blood and in mononuclear cells from hypertensive subjects, there was an increase in oxidative stress and a reduction in the activity of antioxidant mechanisms that appeared to be independent of the blood pressure values.The objective was to study oxidative status, antioxidant activities, and reactive oxygen species byproducts in whole blood and mononuclear peripherals cells and their relationship with blood pressure. Sixty-six hypertensive patients and 16 normotensive volunteers as a control group were studied. In both, whole blood and peripheral mononuclear cells oxidized/reduced glutathione ratio and malondialdehyde was significantly higher, and the activity of superoxide dismutase, catalase, and glutathione peroxidase was significantly lower in hypertensive patients when compared with normal subjects. The content of damaged base 8-oxo-2'-deoxyguanosine in nuclear and mitochondrial deoxyribonucleoproteins of hypertensive subjects was also significantly higher than that of the normotensive control subjects. No differences in these measurements were found among hypertensive subjects grouped in tertiles of 24-hour average mean blood pressure or between "white-coat" and established hypertensive subjects. Furthermore, no relationship was observed between the average of 24-hour mean blood pressure and oxidized/reduced glutathione ratio, reactive oxygen species byproducts, malondialdehide, or genomic 8-oxo-2'-deoxyguanosine. In whole blood and in mononuclear cells from hypertensive subjects, there was an increase in oxidative stress and a reduction in the activity of antioxidant mechanisms that appeared to be independent of the blood pressure values. |
Author | Tormos, Carmen Chaves, Javier Redón, Josep Giner, Vicente Sáez, Guillermo T. Oliva, Maria R. Iradi, Antonio |
AuthorAffiliation | From the Departments of Biochemistry and Molecular Biology (M.R.O., C.T., G.T.S.) and Physiology (A.I.), the Medical School, Valencia, Spain, and the Hypertension Clinic, Hospital Clínico Universitario (J.R., V.G., J.C.), Valencia, University of Valencia |
AuthorAffiliation_xml | – name: From the Departments of Biochemistry and Molecular Biology (M.R.O., C.T., G.T.S.) and Physiology (A.I.), the Medical School, Valencia, Spain, and the Hypertension Clinic, Hospital Clínico Universitario (J.R., V.G., J.C.), Valencia, University of Valencia |
Author_xml | – sequence: 1 givenname: Josep surname: Redón fullname: Redón, Josep organization: From the Departments of Biochemistry and Molecular Biology (M.R.O., C.T., G.T.S.) and Physiology (A.I.), the Medical School, Valencia, Spain, and the Hypertension Clinic, Hospital Clínico Universitario (J.R., V.G., J.C.), Valencia, University of Valencia – sequence: 2 givenname: Maria surname: Oliva middlename: R. fullname: Oliva, Maria R. – sequence: 3 givenname: Carmen surname: Tormos fullname: Tormos, Carmen – sequence: 4 givenname: Vicente surname: Giner fullname: Giner, Vicente – sequence: 5 givenname: Javier surname: Chaves fullname: Chaves, Javier – sequence: 6 givenname: Antonio surname: Iradi fullname: Iradi, Antonio – sequence: 7 givenname: Guillermo surname: Sáez middlename: T. fullname: Sáez, Guillermo T. |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14785806$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/12707286$$D View this record in MEDLINE/PubMed |
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Keywords | Human Hypertension hypertension, obesity Oxidative stress risk factors Pathogenesis antioxidants hypertension, renovascular DNA Cardiovascular disease Antioxidant |
Language | English |
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PublicationTitle | Hypertension (Dallas, Tex. 1979) |
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References | e_1_3_2_26_2 e_1_3_2_27_2 e_1_3_2_28_2 e_1_3_2_29_2 e_1_3_2_20_2 e_1_3_2_21_2 e_1_3_2_22_2 e_1_3_2_23_2 e_1_3_2_24_2 e_1_3_2_25_2 (e_1_3_2_30_2) 1995; 268 e_1_3_2_9_2 e_1_3_2_15_2 e_1_3_2_8_2 e_1_3_2_16_2 e_1_3_2_7_2 e_1_3_2_17_2 e_1_3_2_6_2 e_1_3_2_18_2 e_1_3_2_19_2 e_1_3_2_1_2 e_1_3_2_10_2 e_1_3_2_5_2 e_1_3_2_11_2 e_1_3_2_4_2 e_1_3_2_12_2 e_1_3_2_3_2 e_1_3_2_13_2 e_1_3_2_2_2 (e_1_3_2_14_2) 1999; 349 14756130 - Hypertension. 2004 Feb;43(2):e7-8; author reply e7-8 |
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SubjectTerms | Adult Antioxidants - metabolism Arterial hypertension. Arterial hypotension Biological and medical sciences Blood and lymphatic vessels Blood Pressure - physiology Cardiology. Vascular system Catalase - blood Clinical manifestations. Epidemiology. Investigative techniques. Etiology Deoxyguanosine - analogs & derivatives Deoxyguanosine - genetics Deoxyguanosine - metabolism DNA - genetics DNA - metabolism DNA, Mitochondrial - genetics DNA, Mitochondrial - metabolism Female Glutathione - blood Glutathione Disulfide - blood Glutathione Peroxidase - blood Humans Hypertension - blood Hypertension - genetics Hypertension - physiopathology Male Malondialdehyde - blood Medical sciences Middle Aged Oxidative Stress Reactive Oxygen Species - blood Superoxide Dismutase - blood |
Title | Antioxidant Activities and Oxidative Stress Byproducts in Human Hypertension |
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