Potency of Moringa oleifera leaf extract and silver nanoparticles against immune, microbial and HT-29 colon cancer cells growth modulation.

Moringa oleifera plant grows in many countries worldwide and being utilized as a customary medication. The current study aimed to investigate the biological effect of Moringa oleifera leaf extract (MOE) alone or in combination with silver nanoparticles (AgNPs) on colon cancer, microbial cell growth. MOE was utilized in the green synthesis of AgNPs. The characterization of AgNPs was done by UV-Vis-spectrophotometry, X-ray diffraction (XRD) and scanning electron microscopy (SEM). MOE was tested for their sugars, active biomolecules, ROS, protein contents. Results revealed that created AgNPs are about 61 nm in diameter. There were no detectable sugar and protein in MOE, but it contains ROS and active biomolecules. MOE and MOE+AgNPs exerted mild antibacterial action and increased the number of apoptotic cells and p53 protein expression of HT-29 colon cancer cells. MOE and MOE+AgNPs could arrest HT-29 cells at G2/M phase and stimulate splenic cell growth. Both extract preparations showed antioxidant activities. Because MOE and MOE+AgNP stimulated immune cells and activated apoptosis in cancer cells, these preparations can be utilized as anticancer agents.

Study of the antioxidant, immunomodulatory and antibacterial properties of Origanum majorana leaf acetone extract.

Origanum majorana (OM) is known to have antioxidant properties. The present work was designed to evaluate, for the first time, the hepato/nephroprotective, immunomudulatory and antibacterial potentials of OM leaves acetone extract (OMLE). OML was collected from Al-Soudah, Aseer, Saudi Arabia, and OMLE was prepared. Active biomolecules were screened utilizing FT-IR spectroscopy, protein electrophoresis and HPLC. Reactive oxygen species (ROS) were measured using ELISA. Male rats were treated with OMLE and livers, kidneys and sera were collected. Liver enzymes, kidney function markers, antioxidants in liver and kidney tissues and tumor markers were quantitated. OMLE immunomodulatory potentials were tested using rat splenocytes. Antimicrobial power was tested against Gram negative/positive bacteria. The extract contained many functional biomolecules and ROS but no sugars and proteins. OMLE treatment did not affect liver and kidney functions or the tumor markers. There were some changes in measured antioxidant biomolecules. The extract is not harmful to hepatocytes as indicated by levels of AST and ALT. It is not carcinogenic as it did not make any changes in tumor marker levels. The extract could modulate the splenocytes. The use of OMLE is useful in protecting normal vital organs from oxidative stress. It can also be used as immunostimulant.