scholarly journals Cytotoxic and antioxidant properties in vitro of functional beverages based on blackberry (Rubus glaucus Benth) and soursop (Annona muricata L) pulps

2018 ◽  
Vol 8 (11) ◽  
pp. 531 ◽  
Author(s):  
Alexandra Zambrano ◽  
Rosa Raybaudi-Massilia ◽  
Francisco Arvelo ◽  
Felipe Sojo

Background:  There are many kinds of tropical fruit available in Venezuela. Two of these fruits are the focus of our study: blackberry (“mora”) and soursop (“guanábana”). These fruits have extraordinary bioactive components. For example, blackberry has antioxidant compounds such as anthocyanins, which are characteristic of the Rosaceae family. Acetogenins present in the Annonaceae family have been shown to possess cytotoxic properties that act against different types of tumor cells. In previous research, we have discovered how lyophilized soursop pulp has an elevated cytotoxic effect with a IC50 of 7.1940±1.06 in human cervix carcinoma cells (HeLa) and 0.8460±1.29 in human prostate carcinoma cells (PC3).Objective: This study focused on the health benefits and properties of the soursop and the blackberry. Our main focus was to determine the antioxidant and cytotoxic properties in a formulated beverage based on blackberry, soursop, and yogurt containing probiotics and prebiotics.Methods: The research includes the study of soursop pulp (SP), blackberry pulp (BP), and two formulations of the functional beverage selected through a sensorial analysis, F2 (BP + SP + Yogurt + Truvía® + Sacarose) and F3 (BP + SP + Yogurt + Truvía® + Sacarose + Sodium tripolyphosphate). Cell viability of prostate carcinoma cells (PC3), breast carcinoma without over-expression of the HER2/c-erb-2 gene (MCF-7), breast carcinoma in which the HER2/c-erb-2 gene is over-expressed (SKBr3) and healthy cells of human connective tissue used as control (Fibroblasts).  The previous indicated samples were assessed using MTT (3- (4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide). The antioxidant activity of the functional beverage was also done using a freshly preparation of 1,1-diphenyl-2-picrylhydrazyl (DPPH). Results: The BP demonstrated the highest cytotoxicity for both lines of breast cancer cell lines, MCF-7 and SKBR3. The values of the minimum concentration required to inhibit 50 % of the cell population (IC50) was 0.12 ± 1.10 and 1.81 ± 1.68% v / v respectively, followed by SP in MCF-7 and PC3 with values of 1.40 ± 1.03 and 1.34 ± 1.06 respectively. At the same time, the effectiveness of the formulations used found that 3.60 ± 1.04% v / v of F2 beverage was necessary to achieve 50 % inhibition of cell viability of MCF-7 line. For the formulation F3, it was necessary to use a concentration of 5.21 ± 1.04% v / v for that tumor cell line. However, the F2 and F3 formulations demonstrated IC50 values of 3.69 ± 1.08% v / v and 2.50 ± 1.08% v / v respectively for the PC3 cell line. On the other hand, the antioxidant capacity of BP and SP reached elevated values at 30 minutes of exposure to DPPH, obtaining a rate of 85.28 ± 0.11 and 80.94 ± 0.07 % respectively by using a concentration of 12.5 %, F2 and F3 formulations also reached values of 83.97 ± 0.46 and 85.62 ± 0.11 % at 100 % concentration of both drinks respectively.Conclusion: We discovered that the cytotoxic activity of both formulations prepared as well as the pulps were fairly good, revealing highly effective consequences for the inactivation of breast tumor cells MCF-7 and prostate tumor cells PC3. Moreover, BP and SP demonstrated a high antioxidant activity, with a synergistic effect accomplished by the mixture on F2 and F3.Keywords: Functional beverage, cytotoxic, antioxidant, soursop, blackberry, yogurt.

2021 ◽  
Author(s):  
Hesham M. Abd El Fatah

Abstract Background A green, eco-friendly approach to biosynthesizing silver nanoparticles has been reported for marine macroalga Cystseira myrica extract as a reducing agent. Methods Algal extract was prepared from the marine brown seaweed Cystoseira myrica. Different pH and temperature impact the green synthesis of silver nanoparticles suggesting that the synthesis depends greatly on pH and temperature. Silver nanoparticles have been detected by modifying the color of the algal extract and verified by the use of UV-vis and other characterizations. The Structure and characters of synthesized nanoparticles were confirmed using TEM, DLS, XRD, and FTIR. Cytotoxicity of the biosynthesized nanoparticles using provided cell lines of breast carcinoma cells (MCF-7) and human hepatocellular carcinoma cells (HepG2). Results Shape of silver nanoparticles at pH 9, 75°C for 30 min and was found to be suitable for the biosynthesis process and the AgNPs exhibited a characteristic absorption peak at 434nm. High resolution Electron Microscope Transmission (HR-TEM) reported polydisperse and spherical shapes ranging from 8 to 15 nm. High attractive and repulsive forces between each nanoparticle were recorded with an average zeta potential value of approximately −29.3 mV for C. myrica extract NPs. The X-ray diffraction study revealed the crystalline structure of silver nanoparticles. FT-IR has shown the bioreduction of silver ions to silver nanoparticles through biomolecules found in C. myrica extract. Silver nanoparticles have been found to have anticancer activity. The cytotoxicity assay was studied against MCF-7 and HepG2 at various concentrations (100, 50, 25, 12.5, 6.25, 3.125, 1.56, 0.78, 0.39, 0.2 and 0.1 μg/mL). By increasing the concentration of AgNPs from 0.1 to 100 μg/mL the maximum percentage of viability against MCF-7 and HepG2 cell line decreased from 94.55 ± 7.55 to 19.879 ± 0.503 and from 78.56 ± 11.36 to 25.81 ± 2.66 after time exposure respectively. Conclusions The silver nanoparticles from Cystoseira myrica have cytotoxicity activity against MCF-7 breast carcinoma cell line and HepG2 human hepato cellular carcinoma cell line.


1973 ◽  
Vol 248 (17) ◽  
pp. 6251-6253 ◽  
Author(s):  
Samuel C. Brooks ◽  
Elizabeth R. Locke ◽  
Herbert D. Soule

ChemInform ◽  
2010 ◽  
Vol 32 (35) ◽  
pp. no-no ◽  
Author(s):  
Yves Jacquot ◽  
Laurent Bermont ◽  
Herve Giorgi ◽  
Bernard Refouvelet ◽  
Gerard L. Adessi ◽  
...  

2007 ◽  
Vol 22 (4) ◽  
pp. 543-550 ◽  
Author(s):  
Qing-Feng Xiong ◽  
Yue Chen ◽  
Ling He ◽  
Cun-Liang Deng ◽  
Zhan-Wen Huang ◽  
...  

2016 ◽  
Vol 38 (4) ◽  
pp. 1643-1651 ◽  
Author(s):  
Jing Yan ◽  
Bingbing Zhang ◽  
Zohreh Hosseinzadeh ◽  
Florian Lang

Background/Aims: Oscillations of cytosolic Ca2+ activity ([Ca2+]i) participate in the orchestration of tumor cell proliferation. [Ca2+]i could be increased by intracellular Ca2+ release followed by store-operated Ca2+-entry (SOCE). [Ca2+]i could be decreased by Ca2+ extrusion via Na+/Ca2+ exchange. Mechanisms accomplishing SOCE include the pore-forming ion channel unit Orai1 and its regulator STIM1, Na+/Ca2+ exchanger isoforms include NCX1. In MCF-7 breast carcinoma cells Orai1 and NCX1 have previously been shown to be modified by pharmacological inhibition of Janus activated kinase JAK2. The present study explored whether SOCE and Na+/Ca2+ exchange are similarly sensitive to pharmacological JAK3 inhibition. Methods: MCF-7 breast carcinoma cells were studied in the absence and presence of the JAK3 inhibitor WHI-P154 (22 µM). [Ca2+]i was estimated from Fura-2-fluorescence, SOCE from increase of [Ca2+]i following Ca2+ re-addition after Ca2+-store depletion with sarcoendoplasmatic Ca2+-ATPase (SERCA) inhibitor thapsigargin (1 µM), and Na+/Ca2+ exchanger activity from increase of [Ca2+]i following extracellular Na+ removal. Transcript levels were quantified with RT-PCR. Results: Addition of ATP (100 µM) was followed by a rapid increase of [Ca2+]i, which was significantly blunted by WHI-P154. Thapsigargin-induced intracellular Ca2+ release was not appreciably influenced by WHI-P154. Subsequent SOCE was, however, significantly blunted by WHI-P154. WHI-P154 further significantly decreased Orai1 transcript levels. The increase of [Ca2+]i following extracellular Na+-removal and the NCX1 transcript levels were similarly decreased by WHI-P154. Conclusions: The JAK3 inhibitor WHI-P154 decreases both, Orai1 and NCX1 transcript levels and thus impairs SOCE and Na+/Ca2+ exchange.


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