Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2013:2013:340626.
doi: 10.1155/2013/340626. Epub 2013 Aug 29.

Protective effect of fermented soybean dried extracts against TPA-induced oxidative stress in hairless mice skin

Affiliations

Protective effect of fermented soybean dried extracts against TPA-induced oxidative stress in hairless mice skin

Sandra R Georgetti et al. Biomed Res Int. 2013.

Abstract

This study evaluated the chemical properties (polyphenol and genistein contents) of soybean extracts obtained by biotransformation and dried by spray dryer at different conditions and their in vivo ability to inhibit 12-O-tetradecanoylphorbol-13-acetate- (TPA-) induced biochemical alterations in the skin of hairless mice. By comparing the obtained data with that of the well-known active soybean extract Isoflavin beta, we evaluated the influence of the fermentation and drying process in the extracts efficacy. The results demonstrated that inlet gas temperature and adjuvant concentration for the extract drying process have significantly affected the total polyphenol contents and, to a minor degree, the genistein contents. However, the effect of topical stimulus with TPA, an oxidative stress inducer, which caused significant depletion of reduced glutathione (GSH) and catalase, with increased levels of H2O2 and lipid peroxidation (MDA) in the skin of hairless mice, was significantly prevented by the soybean extracts treatment. These results indicate that the spray drying processing resulted in a product capable of limiting the oxidative stress with possible therapeutic applicability as an antioxidant in pharmaceutical forms.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Role of pretreatment with different soybeans extracts on TPA-induced H2O2: hydroalcoholic extract (HE), spray-dried soybean extract at 115°C/45% (SE1), and spray-dried soybean extract at 150°C/70% (SE2). Bars represent means ± SD of three separate experiments with 3 animals per group per experiment.*Significant (P < 0.05) when compared with TPA treated control group.
Figure 2
Figure 2
Role of pretreatment with different soybean extracts on TPA-induced GSH depletion: hydroalcoholic extract (HE), spray-dried soybean extract at 115°C/45% (SE1), and spray-dried soybean extract at 150°C/70% (SE2). Bars represent means ± SD of three separate experiments with 3 animals per group per experiment. *Significant (P < 0.05) when compared with acetone treated control group. **Significant (P < 0.05) when compared with acetone treated control group and TPA treated control group.
Figure 3
Figure 3
Role of pretreatment with different soybeans extracts on TPA-induced catalase depletion: hydroalcoholic extract (HE), spray-dried soybean extract at 115°C/45% (SE1), and spray-dried soybean extract at 150°C/70% (SE2). Bars represent means ± SD of three separate experiments with 3 animals per group per experiment. *Significant (P < 0.05) when compared with acetone treated control group. **Significant (P < 0.05) when compared with TPA treated control group.
Figure 4
Figure 4
Effects of pretreatment with different soybeans extracts on TPA-mediated enhancement in the susceptibility of cutaneous skin for iron ascorbate-induced lipid peroxidation in mice: hydroalcoholic extract (HE), spray-dried soybean extract at 115°C/45% (SE1), and spray-dried soybean extract at 150°C/70% (SE2). Bars represent means ± SD of three separate experiments with 3 animals per group per experiment. *Significant (P < 0.05) when compared with acetone treated control group. **Significant (P < 0.05) when compared with acetone treated control group and TPA treated control group. ***Significant (P < 0.05) when compared with TPA treated control group and HE, SE1, and SE2 treated groups.

Similar articles

Cited by

References

    1. Vicentini FTMC, Simi TRM, del Ciampo JO, et al. Quercetin in w/o microemulsion: in vitro and in vivo skin penetration and efficacy against UVB-induced skin damages evaluated in vivo . European Journal of Pharmaceutics and Biopharmaceutics. 2008;69(3):948–957. - PubMed
    1. Sultana S, Saleem M. Salix caprea inhibits skin carcinogenesis in murine skin: inhibition of oxidative stress, ornithine decarboxylase activity and DNA synthesis. Journal of Ethnopharmacology. 2004;91(2-3):267–276. - PubMed
    1. Guo T, Wei L, Sun J, Hou C-L, Fan L. Antioxidant activities of extract and fractions from Tuber indicum Cooke & Massee. Food Chemistry. 2011;127(4):1634–1640.
    1. Halliwell B. Antioxidants in human health and disease. Annual Review of Nutrition. 1996;16:33–50. - PubMed
    1. Duan X-J, Zhang W-W, Li X-M, Wang B-G. Evaluation of antioxidant property of extract and fractions obtained from a red alga, Polysiphonia urceolata . Food Chemistry. 2006;95(1):37–43.

Publication types

LinkOut - more resources