Kumiss Supplementation Reduces Oxidative Stress and Activates Sirtuin Deacetylases by Regulating Antioxidant System.
Abstract: It was aimed to investigate the effects of kumiss a fermented mare horse beverage on the sirtuin deacetylases in the oxidative stress which had been induced by 1,2-dimethyl hydrazine (DMH). Forty BALB/C male mice were divided into four groups as control, kumiss (2 × 10 cfu/mL), DMH (20 mg/kg), and kumiss + DMH (2 × 10 cfu/mL + 20 mg/kg). At the end of 20-week regimen, SIRT2, SIRT3 protein expressions by western blotting, immunolocalizations, and inhibitory anti-oxidant activity analysis in liver, colon, and kidney tissues were performed. SIRT2 and SIRT3 expressions in DMH group were decreased in liver, colon, and kidney tissues and the decrease further stimulated by kumiss reinforcement. SIRT3, a mitochondrial protein, immunostaining increased in cell nuclei of tissues in response to kumiss treatments. The oxidative stress induced by DMH was determined to increase plasma 8-OH-2-deoxyguanosine, tissue oxidative stress index, and total oxidant capacity levels. Kumiss supplement was identified to reduce these levels and increase tissue total antioxidant capacity and reduced glutathione levels. Clarifying the molecular relationship between intracellular changes in the locations of SIRT2 and SIRT3 and oxidative stress might be important with regards to developing new medical treatments in the future. The kumiss may show a protective effect against DMH-induced damage by regulating the expression of sirtuin proteins and by protecting antioxidant system.
Publication Date: 2019-07-08 PubMed ID: 31282756DOI: 10.1080/01635581.2019.1635628Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research investigates the potential of kumiss, a fermented horse milk beverage, in reducing oxidative stress and inducing sirtuin deacetylases via the regulation of antioxidant systems.
Objective and Methodology
- The experiment was conducted to examine the impacts of kumiss on sirtuin deacetylases amid oxidative stress triggered by 1,2-dimethyl hydrazine (DMH).
- For the research, forty male mice of BALB/C species were categorized into four groups namely: control, kumiss, DMH, and kumiss + DMH. The dosage for each group varied, with kumiss receiving 2 x 10 cfu/mL, DMH receiving 20 mg/kg, and the final group receiving a combination of the two.
- Following a 20-week regimen, the researchers examined SIRT2 and SIRT3 protein expressions in the liver, colon, and kidney tissues of the mice subjects through western blotting, immunolocalizations, and inhibitory anti-oxidant activity analysis.
Findings
- The results showed that the DMH group had a decrease in SIRT2 and SIRT3 expressions in the liver, colon, and kidney tissues, which was further stimulated by kumiss reinforcement.
- More so, SIRT3 (a mitochondrial protein) immunostaining in the cell nuclei of tissues increased in response to treatments with kumiss.
- The researchers found out that the oxidative stress that was induced by DMH led to an increase in plasma 8-OH-2-deoxyguanosine, tissue oxidative stress index, and total oxidant capacity levels.
- Fascinatingly, kumiss supplementation was discovered to reduce these elevated levels while raising tissue total antioxidant capacity and reduced glutathione levels.
Conclusion
- In their research, the scientists concluded that making clear the molecular relationship between intracellular changes in the locations of SIRT2 and SIRT3 and oxidative stress could become crucial in enabling the development of new medical treatments in the future.
- In addition, they also concluded from their findings that kumiss might have a protective effect against DMH-induced damage by regulating the expression of sirtuin proteins and by safeguarding the antioxidant system.
Cite This Article
APA
Gulmez C, Atakisi O.
(2019).
Kumiss Supplementation Reduces Oxidative Stress and Activates Sirtuin Deacetylases by Regulating Antioxidant System.
Nutr Cancer, 72(3), 495-503.
https://doi.org/10.1080/01635581.2019.1635628 Publication
Researcher Affiliations
- Department of Pharmacy Services, Tuzluca Vocational High School, Igdir University, Igdir, Turkey.
- Department of Chemistry, Faculty Science and Letter, Kafkas University, Kars, Turkey.
MeSH Terms
- 1,2-Dimethylhydrazine / adverse effects
- 1,2-Dimethylhydrazine / pharmacology
- Animals
- Antioxidants / metabolism
- Carcinogens / pharmacology
- Colon / metabolism
- Cultured Milk Products
- Glutathione / metabolism
- Horses
- Humans
- Kidney / metabolism
- Liver / metabolism
- Male
- Mice
- Mice, Inbred BALB C
- Oxidative Stress / drug effects
- Protective Agents / pharmacology
- Sirtuin 2 / metabolism
- Sirtuin 3 / metabolism
- Sirtuins / metabolism
Citations
This article has been cited 3 times.- Valaei A, Azadeh F, Mostafavi Niaki ST, Salehi A, Shakib Khoob M, Mirebrahimi SHO, Kazemi S, Hosseini SM. Antioxidant and Anticancer Potentials of the Olive and Sesame Mixture against Dimethylhydrazine-Induced Colorectal Cancer in Wistar Rats.. Biomed Res Int 2022;2022:5440773.
- Shakib Khoob M, Hosseini SM, Kazemi S. In Vitro and In Vivo Antioxidant and Anticancer Potentials of Royal Jelly for Dimethylhydrazine-Induced Colorectal Cancer in Wistar Rats.. Oxid Med Cell Longev 2022;2022:9506026.
- Salehi A, Hosseini SM, Kazemi S. Antioxidant and Anticarcinogenic Potentials of Propolis for Dimethylhydrazine-Induced Colorectal Cancer in Wistar Rats.. Biomed Res Int 2022;2022:8497562.
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