Dergiler / Turkish Journal of Veterinary and Animal Sciences / 2020 / Cilt: 44 - Sayı: 2

The potential of Salvia officinalis as a suppressor of cell proliferation in animal feed and human nutrition: an experimental study

Sayfa
244–248
Yayın Tarihi
2020-03-01
DOI
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We concluded that Salvia officinalis oil may help the living organism to have a healthy digestive system by stopping excessive cell proliferation via the apoptotic pathway in the gastrointestinal system and, thus, may be used in both animal feed and human nutrition.

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Amaç & Hipotez:The objective of this study was to examine the in vitro cytotoxic activities of Salvia officinalis sage oil on human immortalized keratinocyte HaCaT cell lines by using an [3- 4,5-dimethylthiazol-2-yl -2,5-diphenyltetrazoliumbromide] MTT cytotoxicity assay after the Salvia officinalis oil administration in different doses and time-points.
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Temel Bulgular & Veri:The HaCaT cells 100 µL were cultured in 96- well plates at 2 × 104 cells per well and treated with different concentrations of Salvia officinalis oil 25 µM, 50 µM, 100 µM, 150 µM, and 200 µM for durations of 24, 48, and 72 h.
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Sonuç & Katkı:We concluded that Salvia officinalis oil may help the living organism to have a healthy digestive system by stopping excessive cell proliferation via the apoptotic pathway in the gastrointestinal system and, thus, may be used in both animal feed and human nutrition.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Cytotoxins · apoptosis · lamiaceae

Abstract

The objective of this study was to examine the in vitro cytotoxic activities of Salvia officinalis sage oil on human immortalized keratinocyte HaCaT cell lines by using an [3- 4,5-dimethylthiazol-2-yl -2,5-diphenyltetrazoliumbromide] MTT cytotoxicity assay after the Salvia officinalis oil administration in different doses and time-points. In vitro cytotoxic activities of Salvia officinalis oil on HaCaT cell lines were assessed, and MTT assays were used to determine cell viability. The HaCaT cells 100 µL were cultured in 96- well plates at 2 × 104 cells per well and treated with different concentrations of Salvia officinalis oil 25 µM, 50 µM, 100 µM, 150 µM, and 200 µM for durations of 24, 48, and 72 h. Cell death was determined by collecting and staining with 0.4% Trypan blue for 5 min at room temperature before microscopic examination. At 24 h, there was a significant difference between the 25 and 200 µM doses P = 0.034 . For the 72 h Salvia officinalis oil application, there was a significant difference between the 50 and 200 µM doses only P = 0.002 . On the other hand, for 48 h Salvia officinalis application, there were significant differences between 25 and 150 µM, 25 and 200 µM, 50 and 150 µM, 50 and 200 µM, 100 and 150 µM, and 100 and 200 µM doses P = 0.003, P = 0.000, P = 0.005, P = 0.001, P = 0.028, and P = 0.003, respectively . We concluded that Salvia officinalis oil may help the living organism to have a healthy digestive system by stopping excessive cell proliferation via the apoptotic pathway in the gastrointestinal system and, thus, may be used in both animal feed and human nutrition.

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Bu Makaleye Atıf Yap

ERHAN, M. K. (2020). The potential of Salvia officinalis as a suppressor of cell proliferation in animal feed and human nutrition: an experimental study. Turkish Journal of Veterinary and Animal Sciences, Cilt: 44 - Sayı: 2, 244–248. https://ajindex.com/articles/115890

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Kaynakça (12)

  1. Garcia CSC, Menti C, Lambert AP, Barcellos T, Moura S et al. Pharmacological perspectives from Brazilian Salvia officinalis (Lamiaceae): antioxidant, and antitumor in mammalian cells. Annals of the Brazilian Academy of Sciences 2016; 88: 281-292
  2. Martins N, Barros L, Santos-Buelga C, Henriques M, Silva S et al. Evaluation of bioactive properties and phenolic compounds in different extracts prepared from Salvia officinalis L. Food Chemistry 2015; 170: 378-385
  3. D’Angelo S, La Porta R, Napolitano M, Galletti P, Quagliuolo L et al. Effect of Annurca apple polyphenols on human HaCaT keratinocytes proliferation. Journal of Medicinal Food 2012; 15: 1024-1031
  4. Monsefi M, Nadi A, Alinejad Z. The effects of Salvia officinalis L. on granulosa cells and in vitro maturation of oocytes in mice. International Journal of Reproductive Biomedicine 2017; 15: 649
  5. Lima CF, Andrade PB, Seabra RM, Fernandes-Ferreira M, Pereira-Wilson C. The drinking of a Salvia officinalis infusion improves liver antioxidant status in mice and rats. Journal of Ethnopharmacology 2005; 97: 383-389
  6. Jiang Y, Zhang L, Rupasinghe HPV. Antiproliferative effects of extracts from Salvia officinalis L. and Saliva miltiorrhiza Bunge on hepatocellular carcinoma cells. Biomedicine & Pharmacotherapy 2017; 85: 57-67
  7. Ayatollahi SA, Shojaii A, Kobarfard F, Mohammadzadeh M, Choudhary MI. Two flavones from Salvia leriaefolia. Iranian Journal of Pharmaceutical Research 2010: 179-184
  8. Hamidpour M, Hamidpour R, Hamidpour S, Shahlari M. Chemistry, pharmacology, and medicinal property of sage (Salvia) to prevent and cure illnesses such as obesity, diabetes, depression, dementia, lupus, autism, heart disease, and cancer. Journal of Traditional and Complementary Medicine 2014; 4: 82-88
  9. El Hadri A, del Rio MAG, Sanz J, Sanz J, Coloma AG et al. Cytotoxic activity of α-humulene and transcaryophyllene from Salvia officinalis in animal and human tumor cells. Anales de la Real Academia Nacional de Farmacia 2010; 76: 343-456
  10. Lu Y, Foo LY. Antioxidant activities of polyphenols from sage (Salvia officinalis). Food Chemistry 2001; 75: 197-202
  11. Miguel G, Cruz C, Faleiro ML, Simões MT, Figueiredo AC et al. Salvia officinalis L. essential oils: effect of hydrodistillation time on the chemical composition, antioxidant and antimicrobial activities. Natural Product Research 2011; 25: 526-541
  12. Rodrigues MRA, Kanazawa LKS, das Neves TLM, da Silva CF, Horst H et al. Antinociceptive and anti-infla