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Asgarov S. (Azerbaijan), Alakbarov M. (Azerbaijan), Aliev Z. (Azerbaijan), Babayev N. (Uzbekistan), Chiladze G. (Georgia), Datskovsky I. (Israel), Garbuz I. (Moldova), Gleizer S. (Germany), Ershina A. (Kazakhstan), Kobzev D. (Switzerland), Kohl O. (Germany), Ktshanyan M. (Armenia), Lande D. (Ukraine), Ledvanov M. (Russia), Makats V. (Ukraine), Miletic L. (Serbia), Moskovkin V. (Ukraine), Murzagaliyeva A. (Kazakhstan), Novikov A. (Ukraine), Rahimov R. (Uzbekistan), Romanchuk A. (Ukraine), Shamshiev B. (Kyrgyzstan), Usheva M. (Bulgaria), Vasileva M. (Bulgar).
Medical sciences
Introduction
Pharmaceuticals with antimutagenic activity are promising agents for combined therapy of pathologies based on increased level of spontaneous genomic instability or induced one. However, their extensive use against environmental and industrial mutagens in healthy individuals is limited. [1]. Thus, a search for new sources of antimutagens is needed. We have encountered lots of data for grapes and red wine polyphenols such as procyanidins, antocyans, quercetin, resveratrol and others having protective genomic properties. [2, 3]. At the same time, the mechanisms underlying these positive effects are described poorly.
The aim of our work was to estimate the role of red wine polyphenols in correction of induced genomic instability in mouse bone marrow cells and in Salmonella typhimurium cells.
Material and methods
Antimutagenic effects of red wine in conditions of chromosomal instability induced by dioxidine (300 mg/kg, i.p.) were investigated by the routine cytogenetic method in mouse bone marrow cells.
Outbred mice (20-22 g, 8-10 weeks, N = 70) were used.
Bacterial reverse mutation test (Ames test) with histidine-requiring strain TA100 of Salmonella typhimurium and sodium azide (5 μg/dish) was carried out to detect possible point mutations.
Results and discussion
The results obtained from the cytogenetic examination are summarized in Table 1.
Table 1
Effects of red wine on chromosomal aberration types in mouse bone marrow cells (M±m)
Version of experiment |
Number of cells |
Single-dose introduction |
|||
Aberrations per 100 cells |
|||||
Total |
Single fragments |
Paired fragments |
Exchanges |
||
Control |
700 |
3,00±0,01 |
2,66±0,70 |
0±0 |
0,33±0,30 |
Dioxidine 300 mg/kg |
700 |
19,00± 0,08 |
17,60±1,1 |
1,40±0,02 |
0±0 |
Red wine 3,6 ml/kg + dioxidine 300 mg/kg |
700 |
14,66±1,90 |
5,33±0,30 |
2,66±0,50 |
6,66±0,20 |
Red wine 36 ml/kg + dioxidine 300 mg/kg |
700 |
28,33±2,60 |
13,33±0,90 |
7,0±0,30 |
8,00±1,10 |
Version of experiment |
Number of cells |
5-day-dose introduction |
|||
Aberrations per 100 cells |
|||||
Total |
Single fragments |
Paired fragments |
Exchanges |
||
Control |
700 |
3,00±0,01 |
2,66±0,70 |
0±0 |
0,33±0,30 |
Dioxidine 300 mg/kg |
700 |
18,33±1,30 |
11,00±1,20 |
5,00±0 |
2,33±0,70 |
Red wine 3,6 ml/kg + dioxidine 300 mg/kg |
700 |
19,00±1,20 |
9,33±0,60 |
6,66±0,90 |
3,00±0,60 |
Red wine 36 ml/kg + dioxidine 300 mg/kg |
700 |
14,20±0,70 |
5,20±0,70 |
4,20±0,80 |
4,80±1,20 |
As it follows from the quantitative data, red wine had a tendency to decrease chromosome aberrations. It was most evident for the repeat-dose introduction of 36 ml/kg.
Ames test showed results presented in Table 2.
Table 2
Effects of red wine on revertant colonies of S. typhimurium strain TA100 in vitro
Version of experiment |
Geometric mean |
Standard deviation |
Increase in number of revertants over positive control |
Spontaneous revertant |
136,45 |
1,08 |
- |
Sodium azide 5 μg/dish (positive control) |
351,92 |
1,54 |
- |
Red wine 0,1 μl/dish + sodium azide 5 μg/dish |
355,49 |
1,21 |
0,99 |
Red wine 1 μl/dish + sodium azide 5 μg/dish |
384,55 |
1,28 |
0,92 |
Red wine 10 μl/dish + sodium azide 5 μg/dish |
196,11 |
1,33 |
1,79 |
Red wine 100 μl/dish + sodium azide 5 μg/dish |
156,63 |
1,03 |
2,25 |
Red wine 1000 μl/dish + sodium azide 5 μg/dish |
128,14 |
1,08 |
2,75 |
Thus, red wine provided significant effect against sodium azide-induced mutagenesis at the doses 0,1 and 1 μl/dish.
Conclusions
In our experiments, red wine showed dose-dependent protective action against genomic instability at the gene level of organization of genetic material. The properties of the used bacterial strain and the known mechanism of specific genotoxicity of sodium azide based on intracellular increase of reactive oxygen species allow to assume that antimutagenic effect of red wine is possibly due to antioxidant action of polyphenols.
2. Bukatin M.V., Ovchinnikova O.Yu. Natural biological antioxidants in clinical practice. Fundamental’nye issledovaniya. – 2006. – № 6. – P. 29-30.
3. Goncharova R.I., Kuzhir T.D. Antimutagens as anticancerogens: molecular basis of application. Ecologicheskaya genetika. – 2005. – Volume 3. – № 3. – P.19-32.
Bukatin M.V., Kolobrodova N.A., Kuznetsova O.Yu. RED WINE POLYPHENOLS ACT AS ANTIMUTAGENS IN EXPERIMENTAL GENOTOXICITY. International Journal Of Applied And Fundamental Research. – 2016. – № 2 –
URL: www.science-sd.com/464-25181 (21.11.2024).