Journal
PHARMACEUTICALS
Volume 16, Issue 1, Pages -Publisher
MDPI
DOI: 10.3390/ph16010062
Keywords
Ulva pertusa; polysaccharide; structural characterization; nonalcoholic fatty liver disease
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This study elucidated the main structure of the high-sulfated derivative of Ulva pertusa polysaccharide (HU) and explored its therapeutic effect against nonalcoholic fatty liver disease (NAFLD). Results showed that HU effectively reduced blood lipid levels, improved liver function, decreased lipid droplets in the liver, and suppressed the abnormal enlargement of epididymal fat cells. HU appears to have a protective effect on the development of NAFLD.
The high-sulfated derivative of Ulva pertusa polysaccharide (HU), with unclear structure, has better anti-hyperlipidmia activity than U pertusa polysaccharide ulvan (U). In this study, we explore the main structure of HU and its therapeutic effect against nonalcoholic fatty liver disease (NAFLD). The main structure of HU was elucidated using FT-IR and NMR (13C, 1H, COSY, HSQC, HMBC). The anti-NAFLD activity of HU was explored using the high-fat diet mouse model to detect indicators of blood lipid and liver function and observe the pathologic changes in epididymal fat and the liver. Results showed that HU had these main structural fragments: -> 4)-beta-D-Glcp(1 -> 4)-alpha-L-Rhap2,3S(1 ->; -> 4)-alpha-L-Rhap3S(1 -> 4)-beta-D-Xylp2,3S(1 ->; -> 4)-alpha-L-Rhap3S(1 -> 4)-beta-D-Xylp(1 ->; -> 4)-alpha-L-IdopA3S(1 -> 4)-alpha-L-Rhap3S(1 ->; -> 4)-beta-D-GlcpA(1 -> 3)-alpha-L-Rhap(1 ->; -> 4)-alpha-L-IdopA3S(1 -> 4)-beta-D-Glcp3Me(1 ->; -> 4)-beta-D-Xylp2,3S(1 -> 4)-alpha-L-IdopA3S(1 ->; and -> 4)-beta-D-Xylp(1 -> 4)-alpha-L-IdopA3S(1 ->. Treatment results indicated that HU markedly decreased levels of TC, LDL-C, TG, and AST. Furthermore, lipid droplets in the liver were reduced, and the abnormal enlargement of epididymal fat cells was suppressed. Thus, HU appears to have a protective effect on the development of NAFLD.
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