2015
DOI: 10.1080/19476337.2015.1095803
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Immune activities of the water-soluble yam (Dioscorea oppositeThunb) polysaccharides as affected by thermal, acidic and enzymatic treatments

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Cited by 15 publications
(8 citation statements)
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“…In detail, the tryptic caseinate hydrolysates with oligochitosan glycation had higher potential to increase the secretion levels of immunoglobulins, enhance spleen and thymus indices, and promote splenocyte lymphocyte proliferation and NK cell activity in the BALB/c mice [54]. When YPS was efficiently hydrolyzed by inorganic acid, the hydrolyzed products totally lost their immunomodulation; however, thermal treatment of YPS totally led to unchanged immunomodulatory activities [55]. Polyphenols are unstable upon heat treatment and thus perform various chemical reactions, including oxidation, ring cleavage, and others.…”
Section: Discussionmentioning
confidence: 98%
“…In detail, the tryptic caseinate hydrolysates with oligochitosan glycation had higher potential to increase the secretion levels of immunoglobulins, enhance spleen and thymus indices, and promote splenocyte lymphocyte proliferation and NK cell activity in the BALB/c mice [54]. When YPS was efficiently hydrolyzed by inorganic acid, the hydrolyzed products totally lost their immunomodulation; however, thermal treatment of YPS totally led to unchanged immunomodulatory activities [55]. Polyphenols are unstable upon heat treatment and thus perform various chemical reactions, including oxidation, ring cleavage, and others.…”
Section: Discussionmentioning
confidence: 98%
“…at 100°C for 30 or 60 min), but very sensitive to the severe digestion (e.g. by a HCl solution of 3 mol L −1 ) (Hao & Zhao, 2015), which verify that the WYPs will keep their structure and immune activities during thermal processing and body digestion. However, in vivo immune activities of the WYPs are not well-assessed so far.…”
Section: Introductionmentioning
confidence: 79%
“…Spleens were treated, as previously described [22], to obtain a single-cell suspension (cell viability [98%). The splenocytes at final density of 1 9 10 5 cells/mL were seeded onto a 96-well plate (50 lL/well), and then incubated with or without the extract solutions (40 lL/well) in a total volume of 100 lL of RPMI-1640 medium supplemented with 10% FBS.…”
Section: Assay Of Spleen Lymphocyte Proliferationmentioning
confidence: 99%
“…Peritoneal macrophages were prepared as previously described [22] with a cell viability of greater than 98%. Macrophages at 1 9 10 5 cells/mL in the RPMI-1640 medium containing 10% FBS were seeded onto a 96-well plate (100 lL/well), and incubated at 37°C for 4 h. The non-adherent cells were discarded, whereas the adherent cells were treated with fresh RPMI-1640 medium containing 10% FBS (100 lL/well).…”
Section: Assay Of Macrophage Phagocytosismentioning
confidence: 99%