ABSTRACT
In the present study, the anti-food allergy activity of Eucheuma cottonii sulfated oligosaccharide (ESO) was investigated. ESO was obtained by enzymatic degradation and purified by column chromatography. RBL-2H3 cells and BALB/c mouse model were used to test the anti-food allergy activity of ESO. The effects of ESO on the regulatory T (Treg) cells and bone marrow-derived mast cells (BMMCs) were investigated by flow cytometry. The results of in vivo assay showed that ESO decreased the levels of mast cell protease-1 and histamine and inhibited the levels of specific IgE by 77.7%. In addition, the production of interleukin (IL)-4 and IL-13 was diminished in the ESO groups compared to the non-ESO-treated group. Furthermore, ESO could up-regulate Treg cells by 22.2-97.1%. In conclusion, ESO decreased the allergy response in mice by reducing basophil degranulation, up-regulating Treg cells via Forkhead box protein 3 (Foxp3), and releasing IL-10. ESO may have preventive and therapeutic potential in allergic disease.
Subject(s)
Anti-Allergic Agents/administration & dosage , Food Hypersensitivity/drug therapy , Oligosaccharides/administration & dosage , Plant Extracts/administration & dosage , Rhodophyta/chemistry , Seaweed/chemistry , T-Lymphocytes, Regulatory/immunology , Animals , Anti-Allergic Agents/isolation & purification , Disease Models, Animal , Female , Food Hypersensitivity/immunology , Humans , Immunoglobulin E/immunology , Interleukin-13/immunology , Interleukin-4/immunology , Mast Cells/drug effects , Mast Cells/immunology , Mice , Mice, Inbred BALB C , Oligosaccharides/isolation & purification , Plant Extracts/isolation & purification , T-Lymphocytes, Regulatory/drug effects , Up-Regulation/drug effectsABSTRACT
Polysaccharides from Gracilaria lemaneiformis in particular possess various bioactive functions, but their antiallergic activity remains incompletely defined. Sulfated polysaccharide from Gracilaria lemaneiformis (GLSP) was obtained by water extraction and ethanol precipitation followed by column chromatography. BALB/c mice, RBL-2H3, and KU812 cells were used for verifying the anti food allergic activity of GLSP. According to the results of mice experiment, GLSP was able to alleviate allergy symptoms, to reduce TM-specific IgE and IgG1, to suppress Th2 cell polarization, and to promote the function of regulatory T (Treg) cells. In addition, GLSP had the ability to inhibit the function of RBL-2H3 cells. Furthermore, GLSP inhibited the activation of KU812 via suppression of p38 mitogen-activated protein kinase (MAPK). In conclusion, immunosuppression as well as the reduction in the level of p38 MAPK may contribute to GLSP's putative activity against food allergy. GLSP may be used as a functional food component for allergic patients.
Subject(s)
Anti-Allergic Agents/administration & dosage , Food Hypersensitivity/drug therapy , Gracilaria/chemistry , Plant Extracts/administration & dosage , Polysaccharides/administration & dosage , p38 Mitogen-Activated Protein Kinases/immunology , Animals , Anti-Allergic Agents/chemistry , Female , Food Hypersensitivity/genetics , Food Hypersensitivity/immunology , Humans , Immunosuppression Therapy , Mast Cells/drug effects , Mast Cells/immunology , Mice , Mice, Inbred BALB C , Plant Extracts/chemistry , Polysaccharides/chemistry , Rats , Seaweed/chemistry , Th2 Cells/drug effects , Th2 Cells/immunology , p38 Mitogen-Activated Protein Kinases/geneticsABSTRACT
Custard apple (Annona squamosa L.) is an edible tropical fruit, and its seeds had been used in south China as a folk medicine to treat "malignant sore" (cancer) and as an insecticide. Phytochemical investigation of the ethanol fraction of custard apple seeds led to the isolation of six new annonaceous acetogenins: annosquacins A-D (1-4), annosquatin A (5) and annosquatin B (6). Their structures were elucidated by spectroscopic analysis. Compounds 1-4 are adjacent bistetrahydrofuran annonaceous acetogenins. Compounds 5 and 6 are non-adjacent bistetrahydrofuran annonaceous acetogenins and the first examples in which the tetrahydrofuran ring system is located between C-9 and C-20. The absolute configurations of 1-6 were defined by the application of the Mosher method. Compounds 1-6 exhibited potent cytotoxic activity in vitro against five human tumour cell lines. Compounds 5 and 6 showed a high selectivity toward the MCF-7 and A-549 cell line respectively.
Subject(s)
Acetogenins/toxicity , Annona/chemistry , Plant Extracts/toxicity , Acetogenins/chemistry , Cell Line, Tumor , Cell Survival/drug effects , Humans , Molecular Structure , Plant Extracts/chemistry , Seeds/chemistryABSTRACT
ETHNOPHARMACOLOGICAL RELEVANCE: Seeds of Annona squamosa L. have been used in the south of China as a folk remedy to treat "malignant sores" (cancer). AIM OF THE STUDY: To investigate the chemical constituents and the anti-tumor activity of the standardized A. squamosa seeds extract in vitro and in vivo. MATERIALS AND METHODS: Annonaceous acetogenin profiles of the standardized extract were determined by using Fourier transform infrared (FT-IR) and high performance liquid chromatography (HPLC) techniques. The anti-tumor activity of the extract was tested by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) cytotoxicity in vitro and H(22) hepatoma cells transplantation tumor model in vivo. RESULTS: The FT-IR spectroscopy showed the presence of annonaceous acetogenin compounds in the extract. Two major annonaceous acetogenins: 12, 15-cis-squamostatin-A and bullatacin were identified and quantified by HPLC. The seed extract showed significant anti-tumor activity against four human tumor cell lines, especially for MCF-7 (IC(50). 0.25 µg/ml) and Hep G2 (IC(50). 0.36 µg/ml) cells in vitro. The extract inhibited the growth of H(22) tumor cells in mice with a maximum inhibitory rate of 69.55% by oral administration. CONCLUSION: A. squamosa seed extract showed significant anti-tumor activities against human hepatoma cells in vitro and in vivo, indicating a potential for developing the extract as a novel anti-liver cancer drug.