Ginkgo biloba leaves (GBLs) are used as herbal dietary supplements and medicine worldwide. In this study, crude GBL polysaccharides (GBPSs) were extracted and further purified on a DEAE (diethylaminoethanol) Sepharose Fast Flow column to obtain GBPS-2 and GBPS-3. The molecular weights of GBPS-2 and GBPS-3 were 672 and 723 kDa, respectively. GBPS-2 and GBPS-3 were typical acidic heteropolysaccharides, composed of mannose (Man), rhamnose (Rha), glucuronic acid (GlcA), galacturonic acid (GalA), glucose (Glc), galactose (Gal), and arabinose (Ara) (molar ratio: 0.08:0.12:0.16:0.06:0.11:1.00:0.32) and Man, Rha, GlcA, GalA, Gal, and Ara (molar ratio: 0.92:1.00:0.83:0.11:0.42:0.23), respectively. GBPS-2 and GBPS-3 exhibited limited scavenging abilities for the hydroxyl and 2,2‑diphenyl‑1‑picrylhydrazyl radicals as well as noticeable scavenging effects on superoxide radicals and 2,2'‑azino‑bis(3‑ethylbenzothiazoline‑6‑sulphonic acid) radicals. Furthermore, GBPS-2 and GBPS-3 significantly increased the phagocytosis of macrophages and promoted the production of NO, tumor necrosis factor (TNF)-α, interleukin (IL)-1β, and IL-6. Thus, GBPS-2 and GBPS-3 exhibit potential application as functional food supplements.
Keywords: Antioxidant activity; Ginkgo biloba; Immunostimulating activity; Polysaccharides.
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