Dergiler / Aquatic Research / 2022 / Cilt: 5 - Sayı: 2

Dose-dependent cytotoxic and proliferative effects of Microcystis aeruginosa extract and its fractions on human endothelial cells

Sayfa
117–128
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

These results showed that the activities of the total extract and its fractions in promoting or inhibiting cell proliferation varied depending on not only the content but also the treatment dose.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Microcystis aeruginosa, which spreads in five continents in the world and reported in drinking water resources in 257 countries, is a dangerous microalgae for human and animal health due to its toxins.
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Temel Bulgular & Veri:The aim of current study was to evaluate the effects of M. aeruginosa extract and its chromatographically separated fractions on human endothelial cells.
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Sonuç & Katkı:These results showed that the activities of the total extract and its fractions in promoting or inhibiting cell proliferation varied depending on not only the content but also the treatment dose.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Microcystis aeruginosa

Özet

Microcystis aeruginosa, which spreads in five continents in the world and reported in drinking water resources in 257 countries, is a dangerous microalgae for human and animal health due to its toxins. The aim of current study was to evaluate the effects of M. aeruginosa extract and its chromatographically separated fractions on human endothelial cells. In this context, crude extract was prepared from M. aeruginosa cultured in BG-11 medium, and it was fractionated by an optimized HPLC method. Algae extract and its six fractions were then analyzed for their cytotoxic effects on ECV304 using MTT assay. The results revealed that algae extract inhibited ECV304 cells by around 72%, a higher percentage than all fractions. The most toxic fraction was the first fraction, which inhibited the cells by 55%. Other fractions, except the third one, were also toxic with 35-40% inhibition percentages. Third fraction and certain doses of some fractions showed proliferative activity on ECV304 cells. These results showed that the activities of the total extract and its fractions in promoting or inhibiting cell proliferation varied depending on not only the content but also the treatment dose.

Anahtar kelimeler
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Bu Makaleye Atıf Yap

GÜLTEKİN, S. K., MERTOĞLU, E., YILANCIOĞLU, K., ARDA, N. (2022). Dose-dependent cytotoxic and proliferative effects of Microcystis aeruginosa extract and its fractions on human endothelial cells. Aquatic Research, Cilt: 5 - Sayı: 2, 117–128. https://ajindex.com/articles/413538

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Kaynakça (10)

  1. Abdel-Rahman, G., Sultan, Y.Y., Hassoub, M.A., Marrez, D.A. (2020). Cytotoxicity and antibacterial activity of the blue green alga Microcystis aeruginosa extracts against human cancer cell lines and foodborne bacteria. Egyptian Journal of Chemistry, 63(10), 4095-4105. https://doi.org/10.21608/EJCHEM.2020.42714.2862
  2. Alverca, E., Andrade, M., Dias, E., Bento, F.S., Batoreu, M.C.C., Jordan, P., Silva, M.J., Pereiraa, P. (2009). Morphological and ultrastructural effects of microcystin-LR from Microcystis aeruginosa extract on a kidney cell line. Toxicon, 54(3), 283-294. https://doi.org/10.1016/j.toxicon.2009.04.014
  3. Atasever-Arslan, B., Yilancioglu, K., Kalkan, Z., Timucin, A.C., Gür, H., Isik, F.B., Deniz, E., Erman, B., Cetiner, S. (2016). Screening of new antileukemic agents from essential oils of algae extracts and computational modeling of their interactions with intracellular signaling nodes. European Journal of Pharmaceutical Sciences, 83, 120-131. https://doi.org/10.1016/j.ejps.2015.12.001
  4. Babica, P., Kohoutek, J., Bláha, L., Adamovský, O., Maršálek B. (2006). Evaluation of extraction approaches linked to ELISA and HPLC for analyses of microcystin-LR, -RR and -YR in freshwater sediments with different organic material contents. Analytical and Bioanalytical Chemistry, 385, 1545-1551. https://doi.org/10.1007/s00216-006-0545-8
  5. Bagu, J.R., Sykes, B.D., Craig, M.M., Holmes, C.F. (1997). A molecular basis for different interactions of marine toxins with protein phosphatase-1. Molecular models for bound motuporin, microcystins, okadaic acid, and calyculin A. Journal of Biological Chemistry, 272, 5087-5097. https://doi.org/10.1074/jbc.272.8.5087
  6. Birungi, G., Li, S.F. (2009). Determination of cyanobacterial cyclic peptide hepatotoxins in drinking water using CE. Electrophoresis, 30(15), 2737-2742. https://doi.org/10.1002/elps.200900030
  7. Bittner, M., Štern, A., Smutná, M., Hilscherová, K., Žegura, B. (2021). Cytotoxic and genotoxic effects of cyanobacterial and algal extracts-microcystin and retinoic acid content. Toxins (Basel), 13(2), 107-132. https://doi.org/10.3390/toxins13020107.
  8. Bryant, D.A. (1994). Gene nomenclature recommendations for green photosynthetic bacteria and heliobacteria‖. Photosynthesis Research, 41, 27-28. https://doi.org/10.1007/BF02184142
  9. Campos, A., Vasconcelos, V. (2010). Molecular mechanisms of microcystin toxicity in animal cells. International Journal of Molecular Sciences, 11, 268-287. https://doi.org/10.3390/ijms11010268
  10. Carmichael, W