Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/9926
Title: Protective effects of aspirin and vitamin C against corn syrup consumption-induced cardiac damage through sirtuin-1 and HIF-1? pathway
Authors: Aşcı, H.
Saygın, M.
Yeşilot, S.
Topsakal, Şenay
Cankara, F.N.
Özmen, O.
Savran, M.
Keywords: Cardiac damage
Caspase-3
Corn syrup
HIF-1?
Oxidative stress
ST-1
acetylsalicylic acid
ascorbic acid
caspase 3
corn syrup
creatine kinase
fructose
hypoxia inducible factor 1alpha
interleukin 24
lactate dehydrogenase
malonaldehyde
sirtuin 1
uric acid
antipain
Hif1a protein, rat
animal experiment
animal model
animal tissue
Article
cardiotoxicity
controlled study
heart injury
heart protection
hyperemia
immunohistochemistry
immunoreactivity
inflammatory infiltrate
male
muscle atrophy
nonhuman
oxidative stress
protein expression
rat
animal
chemically induced
drug effect
heart
maize
physiology
randomization
Sprague Dawley rat
sugar intake
Animals
Antipain
Ascorbic Acid
Aspirin
Dietary Sugars
Fructose
Heart
Heart Injuries
Hypoxia-Inducible Factor 1, alpha Subunit
Male
Random Allocation
Rats
Rats, Sprague-Dawley
Sirtuin 1
Zea mays
Publisher: Turkish Society of Cardiology
Abstract: Objective: The aim of this study was to investigate the protective effects of aspirin (AS) and vitamin C (VC) against cardiac damage induced by chronic corn syrup (CS) consumption via a mechanism involving sirtuin-1 (ST-1), hypoxia-inducible factor-1? (HIF-1?), and the caspase-3 pathway in rats. Methods: Forty male Sprague-Dawley rats (14-16 weeks) that weighed 250-300 g were randomly distributed into 5 groups, each containing 8 rats: control group, CS+AS group, CS+VC group, CS+AS+VC group, and CS group. AS (10 mg/kg/day) and VC (200 mg/kg/day) were orally given to the rats. F30 (30% fructose syrup solution) was given to the rats in drinking water for 6 weeks. The rats were sacrificed by exsanguination 24 h after the last administration. Blood samples and tissue were collected for biochemical, histopathological, and immunohistochemical examinations. Non-parametric Kruskal-Wallis test and Mann-Whitney U test used for the parameters without normal distribution and ANOVA and post-hoc LSD tests were used for parameters with a normal distribution to compare groups. Results: Uric acid, creatine kinase (CKMB), and lactate dehydrogenase (LDH) levels were increased in the CS group compared with the control group (1.45±0.39 and p=0.011; 3225.64±598.25 and p=0.004; 3906.83±1064.22 and p=0.002, respectively) and decreased in all the treatment groups. In addition, increased levels of MDA and decreased activity of CAT in the CS group (0.172±0.03 and p=0.000; 0.070±0.005 and p=0.007, respectively) were reversed with AS and VC therapy. A decrease in ST-1 activity and increases in caspase-3 and HIF-1 activities corrected by VC and AS therapy were observed. Conclusion: AS and VC, which display antioxidant and antiapoptotic activities, ameliorated cardiac damage induced by chronic fructose consumption by increasing the levels of ST-1 and decreasing the levels of HIF-1? and caspase-3. © 2016 by Turkish Society of Cardiology.
URI: https://hdl.handle.net/11499/9926
https://doi.org/10.5152/AnatolJCardiol.2015.6418
ISSN: 2149-2263
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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