This study aims to screen and characterize the protective effect of polysaccharides from Portulaca oleracea L. (POP) against H2O2-stimulated osteoblast apoptosis in vivo and in vitro. The enzymes viscozyme, celluclast, α-amylase, and β-glucanase were used to extract POPs. Among all enzyme-assisted POPs, the first participating fraction of viscozyme extract POP (VPOP1) exhibited the highest antioxidant activity. Hoechst 33342 and acridine orange/ethidium bromide staining and flow cytometry of MC3T3 cells revealed that VPOP1 inhibited apoptosis in a dose-dependent manner. Moreover, VPOP1 increased the expression levels of heme oxygenase-1 (HO-1) and NADPH quinine oxidoreductase 1 (NQO1) and decreased the expression levels of nuclear factor (erythroid-derived 2)-like 2 (Nrf2) and Kelch-like ECH-associated protein 1 (Keap1) in H2O2-induced cells compared with their controls. The results of an in vivo experiment show that VPOP1 significantly reduced reactive oxygen species generation and lipid peroxidation in zebrafish at 72 h post-fertilization and promoted bone growth at 9 days post-fertilization. Furthermore, VPOP1 was identified via 1-phenyl-3-methyl-5-pyrazolone derivatization as an acidic heteropolysaccharide comprising mannose and possessing a molecular weight of approximately 7.6 kDa. Collectively, VPOP1 was selected as a potential anti-osteoporotic functional food because of its protective activity against H2O2-induced damage in vitro and in vivo.

Background and purpose In Asian traditional medicine, ginseng has been referred to as the “King of Herbs” because to its extensive therapeutic and pharmacologic characteristics, particularly in the treatment of type 2 diabetes mellitus and illnesses connected to diabetes. Experimental approach The 80% ethanol extracts of cultivated, red, and mountain-cultivated ginseng were liquid partitioned with hexane, chloroform, ethyl acetate, and n-butanol, respectively. The residues produced were processed with enzyme-assisted extraction by different enzymes. Cardiomyocytes, skeletal myoblasts, wild-type AB line zebrafish and Tg (kdrl:EGFP) zebrafish were used to screen and verify the protective effect of extracts. Key results APMCG-1 is precipitated by alkaline protease-assisted extract from mountain-cultivated ginseng with 30% ethanol, which has a strong scavenging effect on hydroxyl radicals. In palmitic acid-induced H9c2 cells, APMCG-1 greatly enhanced cell viability while reducing reactive oxygen species generation and lactate dehydrogenase levels. Additionally, it reduced endoplasmic reticulum and mitochondrial dysfunction by increasing the Ca2+ level and membrane potential of mitochondria in H9c2(2-1) cells. In C2C12 cells that had been exposed to palmitic acid, APMCG-1 boosted glucose uptake while lowering creatine kinase levels. More significantly, 5 days after fertilization Tg (kdrl:EGFP) zebrafish and 1-month-old wild-type zebrafish with type 2 diabetic symptoms both had lower blood sugar and lipid levels attributed to APMCG-1. Further, APMCG-1 was identified as a glycopeptide containing O-linked glycopeptide bonds. Conclusions and implications As a PI3K/AKT activator, APMCG-1 protects the dysfunction of oxidant induced cardiomyocytes and skeletal myoblasts in type 2 diabetes, and is a potential therapeutic drug for diabetes.

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