4.7 Article

A polysaccharide extracted from Astragalus membranaceus residue improves cognitive dysfunction by altering gut microbiota in diabetic mice

Journal

CARBOHYDRATE POLYMERS
Volume 205, Issue -, Pages 500-512

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.carbpol.2018.10.041

Keywords

Astragalus membranaceus-extracted waste residue polysaccharide; Diabetes; Cognitive dysfunction; Gut microbiota; Short chain fatty acids

Funding

  1. National Natural Science Foundation of China [81473216, 81673589]
  2. Postgraduate Research & Practice Innovation Program of Jiangsu Province [KYCX18_0782]
  3. Qing Lan Project of Jiangsu Province
  4. 13th of Six Talent Peak Foundation of Jiangsu Province [SWYY-068]
  5. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
  6. Innovation Team of the Double-First Class Disciplines [CPU2018GF08]
  7. 111 Project from the Ministry of Education of China
  8. State Administration of Foreign Expert Affairs of China [111-2-07]

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A novel polysaccharide named as AERP was extracted from industrial Astragalus membranaceus-extracted waste residue, which was composed of two components coded as AERP1 and AERP2. The structures of AERP1 and AERP2 were determined by HPLC-SEC-RID, HPLC-C-18-UV, FT-IR, and NMR. The results showed that AERP1 was an acidic component with a molecular weight of 2.01 x 10(6) Da and glycosidic bonds of -> 3/5-alpha-araf-(1 ->, T-alpha-araf, -> 3/3,6-beta-galp-(1 ->, -> 2/2,4-alpha-rha-(1 ->, -> 4-alpha-galpA-(1 -> and -> 4)-6-OMe-alpha-galpA-(1 ->, AERP2 was a glucan with 2.11 x 10(3) Da by -> 4/6-alpha-glcp-(1 -> linkage. In vitro, AERP retarded glucose diffusion significantly than each single component. In vivo, AERP had a hypoglycemic effect on db/db diabetic mice by alleviating the hyperglycemia, tissue impairment, and inhibiting cognitive impairment. AERP could alter the gut microbiota and modulate the composition of SCFAs. This study gives an opportunity for exploring the industrial waste of Astragalus membranaceus in diabetic complication therapy.

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