Page 34 - Book of Abstracts
P. 34

5 International Scientific Online Conference   DOI: https://doi.org/10.15414/2021.9788055224015

            th

                  ASSESSMENT OF LIPID PEROXIDATION IN THE HUMAN BLOOD AFTER IN VITRO
                  TREATMENT BY LEAF EXTRACTS OBTAINED FROM SOME AGLAONEMA SPECIES
                                     1
                  Lyudmyla Buyun , Halyna Tkachenko , Natalia Kurhaluk , Maryna Opryshko ,
                                                           2
                                                                                2
                                                                                                      1
                                     Myroslava Maryniuk , Oleksandr Gyrenko
                                                                                   1
                                                            1
                1 M.M. Gryshko National Botanic Garden, National Academy of Science of Ukraine, Kyiv, Ukraine;
                                                E-mail.: buyun@nbg.kiev.ua
                       2 Institute of Biology and Earth Sciences, Pomeranian University in Słupsk, Poland
                  This study aimed to evaluate the antioxidant activity of water extracts obtained from
             leaves of Aglaonema commutatum Schott, A. nitidum (Jack) Kunth, A. simplex (Blume) Blume,
             and A. modestum Schott ex Engl. plants. The effect of the extract on cellular oxidative damage
             was evaluated using in vitro bioassays by 2-thiobarbituric acid reactive substances (TBARS)
             formation as a lipid peroxidation biomarker in human erythrocytes.
                  The leaves of Aglaonema plants, cultivated under glasshouse conditions, were sampled at
             M.M. Gryshko National Botanical Garden (NBG), National Academy of Science of Ukraine (Kyiv,
             Ukraine). Freshly collected leaves were washed, weighed, crushed, and homogenized in 0.1M
             phosphate buffer (pH 7.4) (in proportion 1:19, w/w) at room temperature. The extracts were
             then filtered and used for analysis. The extracts were stored at -20 °C until use. Blood (10–20
             ml) was obtained from normal volunteers via venipuncture (4 males and 5 females aged 28–
             53-years old). The Research Ethics Committee of Regional Medical Hospital in Gdańsk (Poland)
             approved the study (KB-31/18). An erythrocyte suspension at 1 % hematocrit was incubated
             with 4 mM phosphate buffer (pH 7.4) (control) and pre-incubated with the extracts (5 mg/mL)
             at 37 °C for 60 min. This reaction mixture was shaken gently while being incubated for a fixed
             interval at 37 °C. For positive control, phosphate buffer was used. Erythrocyte aliquots were
             used  in  the  study.  The  level  of  lipid  peroxidation  was  determined  by  quantifying  the
             concentration  of  2-thiobarbituric  acid  reacting  substances  (TBARS)  with  the  Kamyshnikov
             (2004) method for determining the malonic dialdehyde (MDA) concentration. The µmol of MDA
             per L was calculated using 1.56·10  mM  cm  as the extinction coefficient. The mean ± S.E.M.
                                                           -1
                                                      -1
                                                5
             values  were  calculated  for  each  group  to  determine  the  significance  of  the  intergroup
             difference. The significance of differences between the values (significance level, p<0.05) was
             examined  using  the  Kruskal–Wallis  H  test  with  Statistica  8.0  software  (StatSoft,  Krakow,
             Poland).
                  Our results revealed, that the treatment by extracts obtained from various plants of the
             Aglaonema genus in a dose of 5 mg/mL increased the TBARS level when compared to untreated
             erythrocytes. The most potent prooxidative effect was demonstrated by the  A. nitidum and
             A. commutatum  compared  to  phosphate  buffer  as  control  samples  (an  increase  of  TBARS
             content by 85.3 and 30.2 %, p<0.05, respectively). On the contrary, the minimum increase of
             TBARS content in human erythrocyte suspensions was induced by A. simplex and A. modestum
             extracts (by 42.8 and 35.2 %, p<0,05, respectively). In conclusion, the most potent prooxidative
             effect was demonstrated by the A. nitidum and A. commutatum compared to phosphate buffer
             as a control sample. The minimum increase of TBARS content in human erythrocyte suspension
             was induced by A. modestum extract. Further research is needed to determine the effects of the
             active compounds of various plants belonging to the Aglaonema genus on oxidative damage in
             human erythrocytes.

            Keywords:  Aglaonema,  leaves,  lipid  peroxidation,  2-thiobarbituric  acid  reactive  substance,
            erythrocytes.
            Acknowledgments
            This study was carried out during the Scholarship Program supported by The Visegrad Fund in the
            Institute  of  Biology  and  Earth  Sciences,  Pomeranian  University  in  Słupsk  (Poland).  We  thank  The
            Visegrad Fund for supporting our study.



             5 International Scientific Conference Agrobiodiversity for Improving the Nutrition, Health, Quality of Life and  |33
              th
                                               Spiritual Human Development
                                                                                                          November 3  2021
                                                              rd
   29   30   31   32   33   34   35   36   37   38   39