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Updated: Apr 20, 2026

Transformation of Probiotic Yeast and Their Recovery from Gastrointestinal Immune Tissues Following Oral Gavage in Mice
Published on: February 8, 2016
[Antimutagenesis of multiphytoadaptogene in yeast saccharomyces]
Abstract:
Multiphytoadaptogene (MPA) consists of plant extracts components including adaptogenes. Genotoxicity analysis revealed the antimutagenic activity of MPA. MPA decreased the direct mutations frequency in ADE4-ADE8 loci induced by UV radiation and nitrous acid by 3.7 and 33 times, respectively. The lethal effect of UV radiation was inhibited when the preparation was used. MPA had no effect on replicative mutagenesis. At the same time it depressed mutagenesis caused by repair errors. The data obtained suggest the antimutagenic activity of multiphytoadaptogene is associated with postreplicative repair activation.
Insights
Multiphytoadaptogene (MPA), a blend of plant extracts, demonstrated significant antimutagenic properties by reducing mutation frequencies caused by UV radiation and nitrous acid. Its activity is linked to activating post-replicative DNA repair mechanisms.
Area of Science:
- Pharmacology
- Genetics
- Molecular Biology
Background:
- Multiphytoadaptogene (MPA) is a complex preparation derived from plant extracts, containing adaptogenic compounds.
- Genotoxicity studies are crucial for evaluating the safety and potential therapeutic effects of natural compounds.
Purpose of the Study:
- To investigate the antimutagenic activity of MPA against genotoxic agents.
- To elucidate the mechanisms underlying MPA's potential protective effects against DNA damage.
Main Methods:
- Genotoxicity assays were performed to assess the effect of MPA on induced mutagenesis in yeast models (ADE4-ADE8 loci).
- The study evaluated MPA's impact on mutations induced by UV radiation and nitrous acid.
- MPA's influence on different types of mutagenesis, including replicative and repair-error-associated mutagenesis, was examined.
Main Results:
- MPA significantly reduced the frequency of direct mutations induced by UV radiation (3.7-fold) and nitrous acid (33-fold).
- MPA exhibited protective effects against the lethal impact of UV radiation.
- MPA did not affect replicative mutagenesis but suppressed mutagenesis arising from DNA repair errors.
Conclusions:
- The findings suggest that MPA possesses notable antimutagenic activity.
- The observed antimutagenic effects of MPA are likely associated with the activation of post-replicative DNA repair pathways.
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