Table 2.
Biological activities | Polysaccharide name |
In vitro/
in vivo |
Model system | Doses/duration | Effects/mechanism | Reference |
---|---|---|---|---|---|---|
Antioxidant | ||||||
PSP | In vitro | Assay | 0.1, 0.2, 0.4, 0.6, 0.8, 1.0, 2.0, 3.0, 4.0, and 5.0 mg/mL, respectively | Scavenging IC50 rate of DPPH radical (3.07 mg/mL), ABTS (0.68 mg/mL), hydroxyl radical (1.04 mg/mL) | Bai et al. (41) | |
PSP1 | In vitro | Assay | 0.5, 1.0, 1.5, and 2.0 mg/mL, respectively | Scavenging rate of DPPH, hydroxyl, superoxide radicals of PSP1 (2.0 mg/mL) were 56.3, 57.0, and 41.7%, and ABTS of PSP1 (2.0 mg/mL) was 33.3% | Wang et al. (23) | |
Anti-obesity | PSP | In vivo | High-fat diet (HFD)-induced rat obesity model | HFD group: rat fed a HFD diet (63.6% normal chow, 20.0% sucrose, 15.0% lard, 1.2% cholesterol, and 0.2% sodium cholate), 4 weeks Low/medium/high dose group PSP group: 200, 400 and 800 mg/kg/d, 6 weeks |
Body weight, serum total cholesterol, triglyceride, LDL-C levels, ALT, AST activity, MDA content, and levels of TNF-α, IL-1β, and IL-6; Serum HDL-C levels, hepatic SOD, catalase, and glutathione peroxidase activity |
Zeng et al. (18) |
Anti-aging | PSP | In vivo | D-Gal-induced heart aging mice | Model group: D-Gal 500 mg/kg/d for 60 days; Low-dose PSP group: 200 (PSP) + 500 (D-Gal) mg/kg/d for 60 days; High-dose PSP group: 400 (PSP) + 500 (D-Gal) mg/kg/d for 60 days |
Cardiac troponin, creatine kinase, p21, and p53 levels; ROS & MDA levels; SOD level; DNA damages and lipid peroxidation induced by oxidative stress (as indicated by reduced levels of 8-OHdG and 4-HNE |
Ma et al. (60) |
PSP | In vivo | D-Gal-induced brain aging mice | Model group: D-Gal 50 mg/kg/d for 60 days; Low-dose PSP group: 200 (PSP) + 500 (D-Gal) mg/kg/d for 60 days; High-dose PSP group: 400 (PSP) + 500 (D-Gal) mg/kg/d for 60 days |
Cognitive function during brain aging Escape latency time (p < 0.05) Number of times mice crossed the platform (p < 0.05). A total of 37, 13, and 679, circRNAs, miRNAs, and mRNAs, respectively, were significantly altered by PSP treatment. |
Zhang et al. (61) | |
Immunomodulatory | ||||||
PSPC\PSPW | In vitro | RAW 264.7 cells | 12.5–200 μg/mL, 12 h | Cells viability, phagocytic capacity, acid phosphatase activity, NO production | Sun et al. (22) | |
In vivo | Spleen deficiency male mice model | PSP 200, 400, and 800 mg/kg, respectively |
Immune functions; Reversing the decline of secretions of IL-2, IL-6, TNF-α, and IFN-γ to a normal range |
|||
PSP | In vivo | Cyclophosphamide (CY)-induced immunosuppressed chickens | Negative control group: regular diets + sterile saline; CY-induced group: regular diets + 80 mg/kg CY; PSP control group: regular diets + 800 mg/kg PSP + sterile saline; CY-induced + PSP group: regular diets + 800 mg/kg PSP + treated 80 mg/kg CY |
Weight, morphologic integrity and function of thymus and spleen; Antioxidant by increasing SOD level and decreasing MDA level in serum; Proliferation of peripheral blood T lymphocytes; Stimulating serum immunoglobulin; Levels of immune-related cytokines (IL-2, IL-6 and IFN-γ). |
Shu et al. (62) | |
PSP | In vitro | Splenocytes | 100, 200, and 400 mg/mL, 48 h | Proliferative responses of splenocytes; | Chen et al. (26) | |
In vivo | CY-induced immunosuppressed mice | Positive control: levamisole hydrochloride 10 mg/kg; PSP-L group: 100 mg/kg; PSP-M group: 200 mg/kg; PSP-H group: 400 mg/kg; Negative control (CY); … |
Expression of cytokines (TNF-α and IL-2); CD4+/CD8+ ratio T lymphocytes; Phagocytosis of mononuclear macrophages; T/B lymphocyte proliferation in the spleen of mice |
|||
PSP1/PSP2/ PSP3/PSP4 |
In vitro | RAW 264.7 cells | 0, 5, 10, 25, 50, 100, 200, and 400 μg/mL, 24 h |
Nontoxic to macrophages (0–400 μg/mL); Phagocytosis of the RAW 264.7 cell line (effect order of PSP3>PSP2>PSP4>PSP1); |
Wang et al. (25) | |
PSP3 | In vivo | CY-induced immunosuppressed mice | Positive group: 0.2 mL levamisole (10 mg/kg); PSP3 group: 100, 200, 400 mg/kg |
Restoring organ indexes; Proliferation of splenocytes and activity of NK cell; IL-2 and TNF-α, IL-4 and IL-10 levels |
||
Gut microbiota regulation actvitiy | ||||||
PSP | In vivo | Mice | PSP group: PSP (200 mg/kg) once a day. Control group: the same volume of distilled water |
Levels of SCFAs including acetic acid, propionic acid, and butyric acid; Relative abundance of Firmicutes and in Bacteroidetes at the phylum level; The abundance of Lactobacillus, Lachnospiraceae and Bacteroides reduced (at the genus level) |
Luo et al. (27) | |
Osteogenic activity | ||||||
PSP50-2-1 | In vitro | MC3T3-E1 cells | 0.02, 0.1, and 0.5 μM, respectively, 48 h | No effect on ALP activity of the MC3T3-E1 cells | Liu et al. (15) | |
PSP50-2-2 | In vitro | MC3T3-E1 cells | 1.29, 2.59, and 5.19 μM, respectively, 48 h | Differentiation and mineralization of MC3T3-E1 cells significantly at 2.59 and 5.19 μM | Liu et al. (15) | |
PSP | In vitro | Bone marrow mesenchymal stem cells (BMSCs) | 0, 5, 10, 25, and 50 mg/L PSPs, respectively, were added to the BMSCs | Osteogenic differentiation of BMMSCs | Zhao et al. (17) | |
PSP | In vitro | BMSCs | 200, 300, 400, and 500 mg/mL |
Proliferation of BMSCs during osteogenic differentiation; Expression of ALP, PINP, BMP-2, OCN, BSP and SPAR in osteoblasts |
Zong et al. (7) | |
Antiglycation | ||||||
PSP | In vitro | Assay | 0.75, 1.50, and 3.00 mg/mL, respectively | Presenting the strongest inhibitory activity (30.2%) at 3 mg/mL with AGEs | Zhao et al. (2) |
increase, decrease, other phenomena or trends.