Evaluation of the effect of vitamin C on caspase 9 and oxidative stress in rheumatoid arthritis patients
Author(s) -
M. Elshamy Amira,
K. Gaafar Nagah,
E. ElAshwah Nadia,
A. Wagih Ayman,
A. Shahba Abeer
Publication year - 2018
Publication title -
african journal of biochemistry research
Language(s) - English
Resource type - Journals
ISSN - 1996-0778
DOI - 10.5897/ajbr2018.0992
Subject(s) - oxidative stress , rheumatoid arthritis , malondialdehyde , vitamin c , antioxidant , medicine , vitamin , vitamin e , endocrinology , arthritis , vitamin d and neurology , apoptosis , immunology , chemistry , biochemistry
Rheumatoid arthritis (RA) is a chronic and an autoimmune disease of the joints and is widely distributed worldwide. It is characterized by alterations of the antioxidant defense system and increased free radical formation and pro-inflammatory cytokine. The aim of the present study was to evaluate the effect of vitamin C supplementation on oxidative stress biomarkers and caspase 9 level in rheumatoid arthritis patients. This study included 30 RA patients and 30 healthy subjects. Plasma levels of malondialdehyde (MDA), total antioxidant capacity (TAC), caspase 9 and 8-hydroxy-2′-deoxyguanosine (8 OHdG) were assayed as well as blood vitamin C level. These parameters were re-evaluated in RA patients after vitamin C supplementation for one month. Increased MDA and 8 OHdG levels and reduced TAC, caspase 9 and vitamin C. Levels were demonstrated in RA patients. After vitamin C supplementation, RA patients showed significant increase in TAC and vitamin C level and significant decrease in MDA and 8 OHdG levels, plasma caspase 9 level was not significantly affected after vitamin C supplementation. Increased oxidative stress and decreased apoptosis may have an important role in the pathogenesis of RA. The administration of vitamin C supplementation may help to relieve oxidative stress and enhance the antioxidant defense in these patients. Key words: Rheumatoid arthritis, oxidative stress, apoptosis, caspase 9, vitamin C.
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