This study deals with total phenolic content, antiproliferative and proapoptotic activity of methanolic extracts from different Teucrium species and the effect on the prooxidant/antioxidant status in HCT-116 cells. The total phenolic content of the extracts was measured spectrophotometricaly and the obtained results ranged from 56.62 mg/g to 172.50 mg GA/g. The antiproliferative activity of methanolic extracts from different Teucrium species was determined using MTT cell viability assay, where IC50 value was used as a parameter for cytotoxicity. The type of cell death was explored by fluorescence microscopy using the acridin orange/ethidium bromide method. MTT assay showed that all extracts significantly reduced cell viability in a dose-dependent manner, with very low IC50 values. The highest content of phenolic compounds and the best cytotoxic activity on HCT-116 cells after 24 h of exposure was in T. chamaedrys extract, with IC50 values of 5.48 × 10−9 μg/mL. After 72 h, methanolic extract of T. arduini appeared to have the best cytotoxic activity on HCT-116, with IC50 values of 0.37 μg/mL. Treatments caused typical apoptotic morphological changes in HCT-116 cells and showed a high percentage of apoptotic cells. The results of the presented research indicate that some Teucrium extracts are a very rich source of phenols, which may directly contribute to high antiproliferative and proapoptotic activity.
Although cisplatin (cisPt) is one of the most often used cytotoxic drugs in the treatment of cancer, its clinical application is associated with nephrotoxicity and a cumulative anemia. In this study, we evaluated posible protective effects of selenium (Se) on hematological and oxidative stress parameters in rats, acutely treated with cisPt. Four groups of Wistar albino rats included control rats, cisPt-treated (7.5 mg/kg of body weight of cisPt, i.p.), Se-treated (6 mg/kg of body weight of Na(2)SeO(4), i.p.), and Se and cisPt co-treated rats. The rats were killed 72 h after treatment; hematological and oxidative stress parameters were followed in red blood cells. The results showed depletion in platelet number induced by high acute doses of cisPt and strong utilization of reduced glutathione, resulting in elevation of GSSG/2 GSH ratio. Se treatment was followed by stimulated erythropoiesis, increased lipid peroxidation, and GSH depletion. Se and cisPt co-treatment were followed by stimulated erythropoiesis and significant recovery of reduced glutathione status when compared with cisPt-treated rats. In conclusion, acute doses of Se and cisPt primarily act as pro-oxidants. CisPt influenced antioxidative properties of exogenous Se and their synergistic effects may partially participate in protection against cisPt-induced toxicity.
Propolis has been used in folk medicine for centuries due to its healing
properties. Ethanolic extracts of propolis (EEP) are rich sources of phenolic
acid and flavonoids. Natural phenolic compounds may exert chemoprotective
activity in cancer cells due to their ability to scavenge free radicals. The
aim of this in vitro study was to investigate the genotoxic and
anti-mutagenic effects of the EEP on human peripheral blood lymphocytes
(PBLs) and their cytotoxic potential on the human breast cancer cell line
(MDA-MB-231 cells). Both cell cultures were treated with six concentrations
(1, 10, 50, 100, 250 and 500 ?g/ml) of EEP1 and EEP2, separately and in
combination with mitomycin C (MMC). Our results show that the EEP1 and EEP2
samples of propolis after separate and combined treatments with MMC did not
influence the nuclear division index (NDI). In the combined treatment, both
tested EEPs significantly reduced MMC-induced micronuclei (MN) in PBLs. At 48
h after exposure of the MDA-MB-231 cell line to a combined treatment of EEP
samples with MMC, the IC50 values were significantly reduced (23.79 and 19.13
?g/ml, for EEP1+MMC and EEP2+MMC, respectively, in comparison to the single
treatment. In conclusion, the tested ethanolic extracts of propolis exhibited
a certain level of in vitro antimutagenic activity in PBLs from healthy
subjects, and anticancer activity in breast cancer cell line. The presented
findings suggest that the ethanolic extracts of propolis show potential in
anticancer therapeutic strategy. [Projekat Ministarstva nauke Republike
Srbije, br. III41010]
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