AI Article Synopsis

  • Plant-based extracts have biological potential due to their high phytochemical content, but chlorophylls present can act as pro-oxidants, affecting applications negatively.
  • Olive leaf extracts (OLE) were rich in compounds like hydroxytyrosol and oleuropein, while green tea extracts (GTE) contained catechins and caffeine; both showed strong antioxidant and anticancer activities.
  • Removing chlorophylls reduced the cytotoxic effects of OLE and GTE on leukemic cells but did not significantly change their antioxidant abilities, highlighting the importance of these pigments in the extracts' cancer-fighting properties.

Article Abstract

Plant-based extracts possess biological potential due to their high content of phytochemicals. Nevertheless, photosynthetic pigments (e.g., chlorophylls) that are also present in plant extracts could produce undesirable pro-oxidant activity that might cause a negative impact on their eventual application. Herein, the phenolic content of olive leaf (OLE) and green tea (GTE) extracts was assayed, and their antioxidant and anticancer activities were evaluated before and after the removal of chlorophylls. Regarding phenolic content, OLE was rich in hydroxytyrosol, tyrosol as well as oleuropein, whereas the main compounds present in GTE were gallocatechin, epigallocatechin (EGC), epigallocatechin gallate (EGCG), gallocatechin gallate, and caffeine. Interestingly, fresh extracts' antioxidant ability was dependent on phenolic compounds; however, the elimination of chlorophyll compounds did not modify the antioxidant activity of extracts. In addition, both OLE and GTE had high cytotoxicity against HL-60 leukemic cell line. Of note, the removal of chlorophyll pigments remarkably reduced the cytotoxic effect in both cases. Therefore, our findings emphasize the remarkable antioxidant and anticancer potential of OLE and GTE and suggest that chlorophylls are of paramount importance for the tumor-killing ability of such plant-derived extracts.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10053222PMC
http://dx.doi.org/10.3390/molecules28062779DOI Listing

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