Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 6 de 6
Filter
Add more filters











Database
Language
Publication year range
1.
Int J Biol Macromol ; 225: 1010-1020, 2023 Jan 15.
Article in English | MEDLINE | ID: mdl-36410539

ABSTRACT

This study reports on in vivo immunomodulatory activities mediated by WPEP-N-b, a heterogalactan from Pleurotus eryngii. Using cyclophosphamide (CTX)-induced immunosuppressed mice, we demonstrate here that WPEP-N-b enhances immunity as determined by the immune organ index, peripheral blood immune cell content, splenocyte proliferation, NK cell activity and T lymphocyte subpopulations. WPEP-N-b prevented apoptosis of bone marrow cells induced by CTX. The level of cytokines (i.e. TNF-α, IL-6 and IL-1ß) and macrophage activity in these immunocompromised mice were restored upon treated with WPEP-N-b. Mechanistically, it appears that WPEP-N-b enhances splenocyte proliferation and NK cell activity might through the Toll-like receptor 4 (TLR4)-PKC signaling axis, and increases macrophage activity by activating JNK, p38 and NF-κB signaling pathways and Toll-like receptor 2 (TLR2) is the possible receptor of WPEP-N-b in macrophages. Our findings indicate that WPEP-N-b may function as a natural immune stimulant.


Subject(s)
Macrophages , Pleurotus , Animals , Mice , Macrophages/metabolism , Cytokines/metabolism , Pleurotus/metabolism , NF-kappa B/metabolism
2.
Front Vet Sci ; 9: 870042, 2022.
Article in English | MEDLINE | ID: mdl-35585861

ABSTRACT

This study was designed to systematically elucidate the immunomodulatory and antioxidant effects of three polysaccharide fractions (ACP60, ACP80, and ACPt2) from Abrus cantoniensis on cyclophosphamide (CTX)-induced immunosuppressive mice. The experimental mice were divided into 12 groups, then modeled and administrated with different doses of three polysaccharides (50, 150, 300 mg/kg/day) by gavage. The results showed that ACP could markedly recover the CTX-induced decline in immune organ and hemocytes indexes and promote proliferation of splenocytes, earlap swelling rate, secretion of cytokines (TNF-α, IFN-γ, IL-1ß, IL-6), and immunoglobulin (Ig-M and Ig-G). Additionally, ACP improved the enzymatic activities of T-SOD and GSH-PX greatly, while the level of MDA was significantly decreased in the liver. In particular, ACPt2 had higher immunomodulatory and antioxidant activities than ACP60 and ACP80. Based on the present findings, ACP could be utilized as an efficacious candidate for immunomodulators and antioxidants, which provide a new application prospect in the food and pharmaceutical industries.

3.
Carbohydr Polym ; 251: 116930, 2021 Jan 01.
Article in English | MEDLINE | ID: mdl-33142551

ABSTRACT

The aim of this study was to investigate the surface morphological features and in vivo immunomodulatory activities of a hetero polysaccharide fraction (HEP-W) from Hericium erinaceus. SEM and AFM images revealed that HEP-W displayed a flexible random coil conformation, and these flexible winding chains further formed continuous fiber network structure. Meanwhile, Congo red assay and XRD further proved that HEP-W mainly exhibited amorphous structure with non-triple-helical conformation in solution. In vivo immunomodulatory experiments demonstrated that HEP-W possessed protective effects against cyclophosphamide-induced immunosuppression in mice by significantly enhancing immune organ index, splenocyte proliferation, NK cell activity, IL-2 production as well as improving the macrophage phagocytosis. These findings suggest that HEP-W could be explored as a natural and effective immunomodulatory agent.


Subject(s)
Cyclophosphamide/adverse effects , Cyclophosphamide/antagonists & inhibitors , Fungal Polysaccharides/chemistry , Fungal Polysaccharides/pharmacology , Immunologic Factors/chemistry , Immunologic Factors/pharmacology , Immunosuppressive Agents/adverse effects , Immunosuppressive Agents/antagonists & inhibitors , Animals , Bone Marrow Cells/drug effects , Bone Marrow Cells/immunology , Carbohydrate Conformation , Congo Red , Female , Fungal Polysaccharides/ultrastructure , Hericium/chemistry , Interleukin-2/blood , Killer Cells, Natural/drug effects , Killer Cells, Natural/immunology , Leukocytes/drug effects , Leukocytes/immunology , Lymphocyte Activation/drug effects , Male , Mice , Mice, Inbred BALB C , Microscopy, Atomic Force , Microscopy, Electron, Scanning , Phagocytosis/drug effects , Surface Properties , X-Ray Diffraction
4.
Ann Palliat Med ; 9(5): 3249-3260, 2020 Sep.
Article in English | MEDLINE | ID: mdl-32954763

ABSTRACT

BACKGROUND: Ma-Nuo-Xi decoction (MNXD), as well as its hundreds of derivative preparations, has been used in Tibetan medicine since the 14th century. MNXD is in accordance with the theory of treatment determination based on syndrome differentiation. This study aimed to compare the effect of the auxiliary MNXD prescription (MNXD-AD) with that of the basic MNXD prescription (MNXD-BD) on the immunostimulating activity of MNXD. METHODS: The immunopotentiation of MNXD, MNXD-BD, and MNXD-AD was evaluated using a cyclophosphamide (CTX)-immunosuppressed mouse model. Their influences on non-specific and specific immunity were evaluated using immune organ indexes, peripheral white blood cell (WBC) count, red blood cell (RBC) count, platelet count, phagocytosis, macrophage-secreted nitric oxide (NO) and cytokines, natural killer (NK) cytotoxic activity, lymphocyte proliferation, serum cytokines, splenic T-lymphocyte subpopulations, and quantitative hemolysis of sheep red blood cell (QHS SRBC) assays. RESULTS: MNXD, MNXD-BD, and MNXD-AD increased the spleen and thymus indexes, as well as the peripheral WBC, RBC, and platelet counts. They also promoted phagocytosis, NO and cytokine secretion from macrophages, NK cytotoxic activity, and lymphocyte proliferation, and also raised the CD4+ /CD8+ T-cell ratio, serum cytokine concentrations, and haemolysin formation in CTX-treated immunosuppressed mice. Compared with MNXD-BD and MNXD-AD, MNXD was superior in restoring the phagocytic index, concanavalin A (ConA)-induced T-lymphocyte proliferation, NO secretion from macrophages, and haemolysin formation, as well as the levels of interleukin 1 beta (IL-1ß), and serum interleukin-2 (IL-2) and interferon gamma (INF-γ). CONCLUSIONS: MNXD, MNXD-BD, and MNXD-AD have excellent immunostimulating and myelosuppression-restoring activities on CTX-immunosuppressed mice. Among them, MNXD-AD might be an immunomodulator, which may happen to be in line with the clinical experience of Tibetan medicine physicians of using it to promote the efficacy of MNXD-BD.


Subject(s)
Immunosuppression Therapy , Phagocytosis , Animals , Cyclophosphamide , Immunologic Factors/therapeutic use , Mice , Mice, Inbred BALB C , Sheep
5.
Int J Biol Macromol ; 146: 45-52, 2020 Mar 01.
Article in English | MEDLINE | ID: mdl-31838067

ABSTRACT

Ma-Nuo-Xi Decoction (MNXD) is well-known in Tibetan medicine to be in line with the theory of treatment determination based on syndrome differentiation. However, the components responsible for its immunomodulating effect are unknown. In this study, three polysaccharide components-MNXD-P, MNXD-BD-P, and MNXD-AD-P-were isolated from MNXD and its basic and auxiliary prescription decoctions, of which MNXD-BD-P is composed of ß-(1,4)-d-glucan and RG-I pectin, MNXD-AD-P contains mainly α-(1,4)-d-glucan and some amount of arabinogalactan and/or arabinorhamnogalactan, and MNXD-P contains components of both MNXD-BD-P and MNXD-AD-P. And treatment with these polysaccharides could significantly improve the host's specific and non-specific immunity, including cellular and humoral immunities, as well as promote recovery from myelosuppression in cyclophosphamide (CTX)-immunosuppressed mice. To our knowledge, this is the first report on chemical and immunoactivity study on polysaccharides from traditional Tibetan medicine compounds, which may provide a new idea for development of carbohydrate drugs from them.


Subject(s)
Adjuvants, Immunologic/pharmacology , Cyclophosphamide/adverse effects , Immunocompromised Host , Plant Extracts/pharmacology , Polysaccharides/pharmacology , Adjuvants, Immunologic/chemistry , Animals , Cyclophosphamide/pharmacology , Male , Mice , Mice, Inbred BALB C , Plant Extracts/chemistry , Polysaccharides/chemistry
6.
Carbohydr Polym ; 142: 259-67, 2016 May 20.
Article in English | MEDLINE | ID: mdl-26917398

ABSTRACT

An exopolysaccharide (EPS) was fractionated from fermentation media of a Cordyceps sinensis fungus (Cs-HK1) by ethanol precipitation at 2/5 volume ratio of ethanol/media. Its structural characteristics were elucidated by FT-IR, GC, GC-MS, 1D and 2D NMR combined with periodate oxidation, Smith degradation, partial acid hydrolysis, and methylation analysis. Furthermore, the immunomodulatory activity of EPS was evaluated by the model of cyclophosphamide-induced immunosuppression. The results from monosaccharide composition and partial acid hydrolysis indicated that EPS almost consisted of glucose excluding a trace amount of mannose. GC-MS and NMR analysis further confirmed EPS had a linear backbone of (1→3)-ß-D-glucopyranosyl residues with a single (1→6)-ß-D-glucopyranosyl side-branching unit for every three ß-D-glucopyranosyl residues, showing a comb-like ß-D-glucan with short and intensive branches, which was responsible for high viscosity. Moreover, EPS could significantly enhance immune organs and stimulate the release of major cytokines TNF-α and INF-γ, suggesting that EPS exhibited protective effect in immunocompromised mice.


Subject(s)
Cordyceps/chemistry , Cyclophosphamide/antagonists & inhibitors , Immunologic Factors/chemistry , Immunologic Factors/pharmacology , Immunosuppressive Agents/antagonists & inhibitors , beta-Glucans/chemistry , beta-Glucans/pharmacology , Animals , Cyclophosphamide/pharmacology , Female , Hydrolysis , Immunologic Factors/isolation & purification , Immunosuppression Therapy , Immunosuppressive Agents/pharmacology , Interferon-gamma/blood , Interleukin-10/blood , Mice , Spleen/drug effects , Spleen/immunology , Thymus Gland/drug effects , Thymus Gland/immunology , Tumor Necrosis Factor-alpha/blood , beta-Glucans/isolation & purification
SELECTION OF CITATIONS
SEARCH DETAIL