Anti-Diabetic Activity of a Novel Exopolysaccharide Produced by the Mangrove Endophytic Fungus Penicillium janthinellum N29

• Published in: Marine drugs 2023-04, Vol.21 (5), p.270
• Main Authors: Shao, Zhuling, Tian, Yingying, Liu, Shan, Chu, Xiao, Mao, Wenjun
• Format: Article
• Language: English
• Subjects: Animals; anti-diabetic activity; Antidiabetics; Blood Glucose; Carbon; Cholesterol; Chromatography; Density; Diabetes; Diabetes mellitus; Diabetes mellitus (non-insulin dependent); Diabetes Mellitus, Type 2; Dyslipidemia; Endophytes; exopolysaccharide; Exopolysaccharides; Fermentation; Fungi; Glucose; Glucose tolerance; Glucosidase; Glycosylation; High density lipoprotein; High fat diet; Hypoglycemic Agents - pharmacology; In vivo methods and tests; Insulin; Insulin resistance; Investigations; Lipoproteins; mangrove endophytic fungus; Mangroves; Marine environment; Marine microorganisms; Mice; Microorganisms; Molecular weight; Penicillium - chemistry; Penicillium janthinellum; Serum; Spectrum analysis; Streptozocin; structure; Triglycerides; α-Glucosidase
• ISSN: 1660-3397; 1660-3397
• DOI: 10.3390/md21050270

Marine microorganisms often produce exopolysaccharides with novel structures and diverse biological activities due to their specific marine environment. The novel active exopolysaccharides from marine microorganisms have become an important research area in new drug discovery, and show enormous development prospects. In the present study, a homogeneous exopolysaccharide from the fermented broth of the mangrove endophytic fungus N29, designated as PJ1-1, was obtained. The results of chemical and spectroscopic analyses showed that PJ1-1 was a novel galactomannan with a molecular weight of about 10.24 kDa. The backbone of PJ1-1 was composed of →2)-α-d-Man -(1→, →4)-α-d-Man -(1→, →3)-β-d-Gal -(1→ and →2)-β-d-Gal -(1→ units with partial glycosylation at C-3 of →2)-β-d-Gal -(1→ unit. PJ1-1 had a strong hypoglycemic activity in vitro, evaluated using the assay of α-glucosidase inhibition. The anti-diabetic effect of PJ1-1 in vivo was further investigated using mice with type 2 diabetes mellitus induced by a high-fat diet and streptozotocin. The results indicated that PJ1-1 markedly reduced blood glucose level and improved glucose tolerance. Notably, PJ1-1 increased insulin sensitivity and ameliorated insulin resistance. Moreover, PJ1-1 significantly decreased the levels of serum total cholesterol, triglyceride and low-density lipoprotein cholesterol, enhanced the level of serum high-density lipoprotein cholesterol and alleviated dyslipidemia. These results revealed that PJ1-1 could be a potential source of anti-diabetic agent.