In present work, AlAPS-2 showed stronger scavenging abilities than AlAPS and other fractions on hydroxyl and DPPH radicals.
And the AlAPS and its fractions had hepatoprotective effects by stabilizing the plasma membrane as well as repairing the hepatic tissue damage.
Interestingly, the treatment with AlAPS and its fractions (AlAPS-1, AlAPS-2, and AlAPS3) remarkably enhanced the antioxidant enzyme activities and reduced the lipid peroxidation contents, indicating that the polysaccharides extracted and purified form A.
In conclusion, both AlAPS and its purified fractions of AlAPS-1, AlAPS-2, and AlAPS-3 from A.
Caption: Figure 1: Elution profiles on DEAE-52 chromatography of AlAPS.
Caption: Figure 2: Gas chromatographs of (a) standard monosaccharides, (b) AlAPS, (c) AlAPS-1, (d) AlAPS-2, and (e) AlAPS-3.
Caption: Figure 3: Antioxidant activities of AlAPS, AlAPS-1, AlAPS-2, and AlAPS-3 in vitro.
Caption: Figure 5: Effects of AlAPS, AlAPS-1, AlAPS-2, and AlAPS-3 on (a) ALT activities, (b) AST activities, (c) ALP activities, (d) ALB levels, (e) LDL-C levels, and (f) HDL-C levels in D-galactose induced aging mice.
