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Sargassum fusiforme polysaccharides (SFPs), including SFP-3-40, SFP-3-60, SFP-3-80, SFP-7-40, SFP-7-60, SFP-7-80, SFP-10-40, SFP-10-60, and SFP-10-80, were extracted at different pH (3, 7, and 10), and then precipitated with graded precipitation of 40%, 60% and 80% (v /v) ethanol solution, respectively. Their physicochemical properties and α -glucosidase inhibitory activity were determined. Results showed that SFPs significantly differed in the contents of total sugar, protein, uronic acid, sulfate, the zeta potential, and molecular weight distribution. SFPs, including SFP-10-40, SFP-10-60, and SFP-10-80, had bigger absolute zeta potential value and higher respective average molecular weight in the same ethanol concentration precipitate. All samples were mainly composed of fucose, glucuronic acid, and mannose with different molar ratios. The extraction pH and precipitation ethanol solution concentration caused little changes in functional groups, but significantly altered surface morphology of SFPs. Congo red test revealed that all polysaccharides were not helical polysaccharides. Rheological measurements indicated that SFPs were pseudoplastic fluids and showed elastic behavior of the gel. Except SFP-3-40 and SFP-3-60, all other samples had a stronger α -glucosidase inhibitory activity than that of acarbose. The inhibition type of SFPs against α -glucosidase varied owing to different extraction pH and precipitation ethyl concentration. This study shows that extraction pH can significantly affect the structure and hypoglycemic activity of SFPs and provide a data support for the scientific use of Sargassum fusiforme in industrial production. [Display omitted] • Nine polysaccharide fractions were obtained from Sargassum fusiforme (Harv.) Setch at different extraction pH. • The physicochemical properties of SFPs were significant different. • SFP-7-40 showed the strongest α -glucosidase inhibitory activity with IC 50 values of 0.304 mg/mL. [ABSTRACT FROM AUTHOR]

The objective of present research was to explore whether Sargassum fusiforme polysaccharide (SFP) could partly replace acarbose against type 2 diabetes in rats. Results indicated that SFP co-administered with low-dose acarbose intervention typically mitigated diabetic symptoms and serum profiles and exhibited better anti-diabetic effects than single acarbose treatment in controlling fasting blood glucose, improving insulin resistance and mitigating kidney injuries. The RT-qPCR analysis indicated that SFP co-administered with low-dose acarbose administration distinctly activated the IRS/PI3K/AKT signaling pathway compared with single acarbose treatment. Moreover, the co-administration also restrained liver fat accumulation via affecting the expression of HMGCR and SREBP-1c genes. In addition, the 16S rRNA gene sequencing analysis indicated that SFP co-administered with low-dose acarbose significantly restored beneficial composition of gut flora in diabetic rats, such as the increase of Muribaculaceae , Lachnospiraceae , Bifidobacterium , Ruminococcaceae _UCG-014, Ruminococcus _1, Romboutsia , Eggerthellaceae , Alistipes and Faecalibaculum , and the decrease of Escherichia - Shigella. These results suggested that SFP, the novel natural adjuvant of acarbose, displayed the desirable benefits in minimizing the dose of drug, while improving the anti-diabetic efficiency. Unlabelled Image • SFP-ACAR typically mitigated diabetic symptoms and serum profiles. • SFP-ACAR showed better effects in controlling FBG, insulin, BUN and Cr levels. • SFP-ACAR distinctly restored beneficial composition of gut flora in diabetic rats. • SFP-ACAR improved IR by notably activating the IRS/PI3K/AKT signaling pathway. [ABSTRACT FROM AUTHOR]

The objective of current work was to explore the potential anti-diabetic mechanisms of Hizikia fusifarme polysaccharide (HFP) in type 2 diabetic rats. The carbohydrate loading experiment illustrated that HFP supplement could reduce blood sugar fluctuations caused by eating through inhibiting the hydrolysis of starch in mice. The analysis of typically diabetic symptoms and serum profiles showed that oral administration of HFP could mitigate hyperglycemia, insulin resistance, dyslipidemia, chronic inflammation and oxidative stress in rats. The 16s rRNA gene sequencing analysis indicated that HFP treatment could restore beneficial composition of gut flora in diabetic rats, and the correlation analysis revealed that the improvement of diabetes is closely related to the modification of gut flora by HFP intervention. Furthermore, the RT-qPCR and western blotting analysis clarified that HFP administration could increase glycogen storage in liver and skeletal muscle of diabetic rats through activating IRS/PI3K/AKT/GLUT signaling pathway and restrain gluconeogenesis via affecting the relative expression of Egr-1 and PEPCK genes. [ABSTRACT FROM AUTHOR]

Three algal polysaccharides (APs) were acquired from Scagassum (SCP), Sargassum fusiforme (Harv.) Setch. (SFP) and Macrocystis pyrifera (L.) Ag. (MAP) by hot water extraction, and their structural characterization and antidiabetic activity were investigated in high fat diet and streptozotocin-induced type 2 diabetic rats. The results revealed that there were obvious differences in extraction yield, molecular weight, compositions of monosaccharide and organic element, molecular morphology, rheological properties and the contents of total sugar, protein, uronic acid and sulfate of SCP, MAP and SFP. SFP had the highest extraction yield, the contents of total sugar and uronic acid and the smallest molecular weight. Congo red assay indicated that all polysaccharides had no triple-helix structure. Oral administration of APs prominently restrained loss of weight and increase of water intake (P <.05), and also significantly controlled the increase of levels of blood glucose, triglyceride (TG) and total cholesterol (TC) in diabetic rats (P <0.05). Diabetic rats treated with SCP had the highest high density lipoprotein cholesterol (HDL-C) level (P <.05), similar to those in normal group. MAP and SCP showed positive effect in improving the low density lipoprotein cholesterol (LDL-C) level of diabetic rats (P <.05). Meanwhile, the increased ALT and BUN contents caused by the liver and kidney damages were markedly ameliorated in the diabetic rats with APs intervention (P <.05). As a consequence, APs could be promising candidates as natural medicines and functional foods for the improvement of diabetes and its complications. • The molecular weight, compositions, rheological properties and molecular morphology of APs are different. • APs controlled prominently the levels of blood glucose, triglyceride (TG), total cholesterol (TC) Alanine transaminase (ALT) and blood urea nitrogen (BUN) in type 2 diabetic rats. • MAP and SCP showed positive effect in controlling the low density lipoprotein cholesterol (LDL-C) level of type 2 diabetic rats. • Oral administration of SCP significantly increased the high density lipoprotein cholesterol (HDL-C) level in type 2 diabetic rats. [ABSTRACT FROM AUTHOR]

Three algae polysaccharides (APs) extracted from Ascophyllum nodosum (ANP), Fucus vesiculosus (FVP) and Undaria Pinnatifida (USP) significantly differed in the zeta potential, water and oil holding capacity, monosaccharide composition, organic element composition, molecular weight distribution, microstructure and rheological properties. Antidiabetic effects of APs were compared by oral intervention at the dose of 400 mg/kg·body weight/day in high sugar and fat diets and streptozotocin injection induced type 2 diabetic rats. The analysis of body weight, water intake, fasting blood glucose, insulin, oral glucose tolerance, blood lipid indicators (including total cholesterol (TC), triglyceride (TG), low density lipoprotein cholesterol (LDL-C) and free fatty acid (FFA)), liver function indexes (involving alanine aminotransferase (ALT) and aspartate aminotransferase (AST)) and renal function profiles (comprising uric acid (UA) and urea nitrogen (BUN)) showed that APs possessed obvious antidiabetic activities, and FVP showed better effects in controlling the levels of FFA, AST, ALT, UA and BUN. Intervention of FVP reduced the total bile acid (TBA) level and elevated high density lipoprotein cholesterol (HDL-C) level of diabetic rats. Histomorphological observation further demonstrated that APs, especially FVP, could attenuate liver and kidney damage caused by diabetes. This study concluded that the antidiabetic effects of ANP, FVP and USP were distinctly different, which might be attributed to their different chemical structures. Therefore, the structure-activity relationship and antidiabetic mechanism of APs will be our future research direction. Unlabelled Image • The compositions, zeta potentials, molecular weights, rheological properties and microstructure of APs are significantly different. • USP has stronger water and oil holding capacity than ANP and FVP. • APs could ameliorate hyperglycemia, hyperlipidemia and liver and kidney damage of diabetic rats, and FVP shows better effects in controlling the levels of free fatty acid (FFA), alanine aminotransferase (ALT), aspartate aminotransferase (AST), total bile acid (TBA) and uric acid (UA). • Intervention of APs could decrease the serum insulin level of diabetic rats. • FVP could significantly increase the high density lipoprotein cholesterol (HDL-C) level of diabetic rats. • USP could more significantly reverse weight loss of diabetic rats than ANP and FVP. [ABSTRACT FROM AUTHOR]

Two polysaccharide fractions (SFPs, designated as respectively SFP-1 and SFP-2) were acquired from Sargassum fusiforme by ultrasound-assisted enzymatic extraction, and their physicochemical properties and hypoglycemic and hypolipidemic effects were investigated. Structural analysis indicated that SFPs were obvious different in the zeta potential, molecular weight distribution, characteristic organic group, microstructure and the contents of total sugar, uronic acid, sulfate and moisture. SFPs consisted of fucose, mannose, rhamnose, glucose, galactose and glucuronic acid with different molar ratios. Congo red test explained that SFPs had no triple-helix structure. SFP-1 exhibited lower viscosity due to its lower molecular weight. Regarding to hypoglycemic and hypolipidemic effects, oral administration of SFPs prominently restrained loss of body weight and increase of water intake, and also significantly controlled the increase of levels of fasting blood glucose, triglyceride (TG), total cholesterol (TC), low density lipoprotein cholesterol (LDL-C), uric acid (UA), urea nitrogen (BUN), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) of diabetic rats, and SFP-2 showed better effects in controlling fasting blood glucose, ALT, UA and BUN levels. Intervention of SFP-2 reduced the levels of insulin, FFA and TBA of diabetic rats. Histomorphological observation further demonstrated that SFPs could attenuate liver and kidney damage caused by hyperglycemia and hyperlipidemia. Data indicated that SFPs, especially SFP-2, significantly improved hyperglycemia, hyperlipidemia and liver and kidney function of diabetic rats. • The physicochemical properties of SFPs are quite different from others investigated Sargassum fusiforme polysaccharides. • The compositions, zeta potentials, molecular weights, characteristic organic groups, rheological properties and microstructure of SFPs are obviously different. • SFPs could ameliorate hyperglycemia, hyperlipidemia and liver and kidney damage of diabetic rats, and SFP-2 shows better effects in controlling the levels fasting blood glucose, free fatty acid (FFA), alanine aminotransferase (ALT), total bile acid (TBA), uric acid (UA) and urea nitrogen (BUN). • Intervention of SFP-2 could reduce the serum insulin level of diabetic rats. [ABSTRACT FROM AUTHOR]

The antidiabetic activity and underlying mechanisms of Fucus vesiculosus polysaccharide (FVP) were studied in type 2 diabetic rats. Our results exhibited that FVP intervention reversed body weight loss, alleviated hyperglycemia and insulin resistance in diabetic rats. FVP also had the potential to ameliorate dyslipidemia, liver and kidney dysfunction, decrease oxidative stress, promote glycogen synthesis, and boost short-chain fatty acid production and total bile acid excretion. 16S rRNA gene sequencing analysis suggested that FVP interfered with the gut microbiota in a beneficial manner. Moreover, RT-qPCR results demonstrated that the antidiabetic activity of FVP in connection with the acceleration of blood glucose absorption and glycogen synthesis, the inhibition of gluconeogenesis, and the regulation of lipid metabolism in the liver. These findings suggested that FVP had antidiabetic effects on high-fat diet and STZ-induced diabetic rats and could be a potential resource for treating type 2 diabetes mellitus. [Display omitted] • FVP promoted glycogen storage in diabetic rats. • FVP enhanced bile acid excretion in diabetic rats. • FVP regulated gut microbiota in diabetic rats. • FVP regulated gene expression related to glucose and lipid metabolism in diabetic rats. [ABSTRACT FROM AUTHOR]