Chapters authored
Royal Jelly and Human Interferon-Alpha (HuIFN-αN3) Affect Proliferation, Glutathione Level, and Lipid Peroxidation in Human Colorectal Adenocarcinoma Cells In Vitro
The purpose was to investigate the influence of RJ-F(M), 10-hydroxy-2-decenoic acid and HuIFN-αN3 on the proliferation of CaCo-2 cells and ascertain their effects on intracellular glutathione level and lipid peroxidation. The antiproliferative (AP) activity of RJ-F (M) (0.1 g/10 mL PBS), HuIFN-αN3 (1000 IU mL−1), 10-HDA (100.0 μmol L−1) and their combinations, in the ratios 1:1, 1:2, and 2:1 on CaCo-2 cells were measured. Single RJ-F (M) had a low AP activity: 2.0 (0.5 mg mL−1). HuIFN-αN3 had an AP activity of 2.5 (208.33 IU mL−1), while 10-HDA had an AP activity of 1.5 (37.5 μmol mL−1). AP activity of 3.8 was obtained when RJ-F(M) and HuIFN-αN3 were in the ratio 2:1. In it, the level of GSH was 24.9 ± 2.4 nmol g−3 of proteins (vs. 70.2 ± 3.2 nmol g−3 in the control), and level of MDA was 72.3 ± 3.1 nmol g−3 (vs. 23.6 ± 9.1 nmol g−3 in the control). 10-HDA, together with HuIFN-αN3, is responsible for the inhibition of CaCo-2 cell proliferation in vitro. RJ-F (M) and HuIFN-αN3 applied at 2:1 decreased level of GSH and increased lipid peroxidation via MDA in CaCo-2 cells. Future studies are needed whether these GSH- and MDA-related activities of RJ-F (M), HuIFN-αN3, 10-HDA, and their combinations may decrease the tumorigenicity index and tumorigenic potential of tumor cells in vitro
Part of the book: Lipid Peroxidation Research
Square-Wave Electric Impulses of 10 ms and 100 V/cm of Field Force, Produced by PGen-1 Impulse Generator Device, Affect the Proliferation Patterns of Different Animal Cells
The influence of the medium-strength electric forces (MSE) on the proliferation of adherent chicken embryo fibroblasts (CEF), VERO, MDBK, MRC-5, and HeLa; lymphoblast cells, FB1 and K562; and cell multiplications were analyzed by growth index (GI). Impulse generator device PGen-1 provided 100 V/cm square-wave impulses of 10 ms. Treatment: Samples were subjected to one or three MSE. GIs were compared with controls after 72 hours and one or three treatments: Monolayers: CEF: GI in the control is 16.76, and after one and three MSE, it is 15.81 and 7.09. Vero cells: GI in the controls is 8.39, and after one and three MSE, it is 5.39 and 5.69. MDBK cells: GI in controls is 8.39, and after one and three MSE, it is 5.39 and 5.69. MRC-5 cells: GI in controls is 5.58, and after one and three MSE, it is 4.18 and 2.60. HeLa cells: GI in controls is 13.69, and after one and three MSE, it is 10.16 and 5.37. Suspension cells: Lymphoblast FB1: GI in controls is 6.55, and after one and three MSE, it is 13.48 and 12.25. Lymphoblast K562: GI in controls is 9.07, and after one or three MSE, it is 12.37 and 13.55. To conclude: MSE in monolayer cells inhibits the GI, depending on the nature of cells. MSE enhances the multiplication of lymphoblast FB1 or K562.
Part of the book: Electromagnetic Field Radiation in Matter