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ABSTRACT
Received
: 01-03-14
Review completed : 13-03-14
Accepted
: 28-07-14
Website:
www.ijdr.in
PMID:
***
DOI:
10.4103/0970-9290.142547
Chakraborthy, etal.
Search methodology
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Chakraborthy, etal.
Search methodology
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Flow chart 1: Search methodology of the selected articles
500
Chakraborthy, etal.
Selection criteria
Inclusion criteria
Exclusion criteria
RESULTS
Included studies
Name of journal
Year
2003
Schwartz
Journal of American
College of Nutrition
Journal of Nutrition
Herbert
Journal of Nutrition
1996
FASEB journal
1999
Retsky etal.
1993
1999
Azmi etal.
Journal of Biological
Chemistry
American Journal of
Nutrition
F1000 Research
Naidu
Nutrition Journal
2003
Nishida etal.
Journal of
Periodontology
The American Journal
of Clinical Nutrition
2000
Lee etal.
1996
2013
2003
Country
Maryland,
USA
Bathesda
MD, USA
NewYork,
USA
Oregon,
USA
Boston,
USA
USA
Detroit,
USA
Mysore,
India
NewYork,
USA
USA
Conclusion
Prooxidant
High plasma
concentration
Strongin vivo
Chemopreventioninhibits
growth of malignant cells
Moderatein vivo
Iron induced Fenton
chemistry
Strongin vitro
Iron induced Fenton
reaction. In vitro
Stronginvivo, in vivo Copper induced
oxidation
Stronginvivo, in vitro Iron induced Fenton
reaction
Strongglutathione
Copper induced
dependent
oxidative damage
Strong under
Iron overload conditions
physiologic conditions
Nonsmokers
Smokers
Antioxidant
Strongin vitro
Strongantioxidant
in vivo
Iron overload
(Fenton chemistry)
Inference
In the oral environment
Prooxidant in pathologic
condition
Antioxidant in physiologic
condition
Prooxidant in pathologic
condition
Prooxidant in pathologic
condition
Antioxidant in physiologic
condition
Antioxidant in physiologic
condition
Paradoxical prooxidant in
the pathological condition
Antioxidant in physiologic
condition
Antioxidant in physiologic
condition
Antioxidant in physiologic
condition
501
Chakraborthy, etal.
Mechanism of action
36
Free radical scavenger
40
Redox potential(reducing agent)
9
Coadministration with glutathione
9
Coadministration with tocopherols
14
Prevention of lipid peroxidation
20
Prevention of oxidative DNA damage
25
Prevention of oxidative protein damage
45
Chemo preventive action
14
Ascorbic acid+iron overload
DISCUSSION
There is a continuing debate over the best dose schedule(the
amount and frequency of intake) of Vitamin C for
maintaining optimal oral health in humans. An average
intake by healthy adults ranges from 90 to 100mg daily;
while there is increased intake in pregnant and lactating
women or individuals under stress.[6]
Indian Journal of Dental Research, 25(4), 2014
Chakraborthy, etal.
Chakraborthy, etal.
CONCLUSION
Although the role of Vitamin C as an antioxidant is well
documented, there is little evidence that emphasizes its
prooxidant role in various conditions. Previous research
and our systemic review confirm that under normal
physiological conditions, it acts mainly as an antioxidant;
however, the transition of a healthy oral status to a highly
compromised pathologic state can trigger the prooxidant
activity of Vitamin C. The observations of this systemic
review also reflected the necessity for researchers to
determine stronger theories that would elucidate the
mechanisms and conditions that bring about the prooxidant
attributes of Vitamin C to illustrate and demarcate its
antioxidant and prooxidant properties more precisely.
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