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Updated: Feb 27, 2026

An In Ovo Model for Testing Insulin-mimetic Compounds
Published on: April 23, 2018
Hypoglycemic effects of a Fructus Mori polysaccharide in vitro and in vivo
Chun Chen1, Qiang Huang, Chao Li
1College of Light Industry and Food Sciences, South China University of Technology, 381 Wushan Road, Guangzhou 510640, China. lfxfu@scut.edu.cn.
Abstract:
Mulberry fruit polysaccharide (MFP), one of the major active ingredients isolated from the mulberry fruit, possesses numerous bioactivities. In vitro hypoglycemic experiments showed that MFP had significant insulin-sensitizing activity through increasing insulin secretion and promoting pancreatic β cell proliferation. In vivo, the oral administration of MFP could significantly decrease blood glucose levels and increase body weight loss in streptozotocin (STZ)-induced diabetic mice. MFP also significantly decreased the level of malondialdehyde (MDA) and increased the activities of antioxidant enzymes superoxide dismutase (SOD), glutathione peroxidase (GPx) and catalase (CAT) in the liver in STZ-induced diabetic mice. And histopathological examination showed that MFP could markedly alleviate damage to pancreas, liver and kidney tissue in STZ-induced diabetic mice. This study suggested that MFP had antioxidant and hypoglycemic properties and could provide a protective effect on STZ-induced diabetic mice.
Insights
Mulberry fruit polysaccharide (MFP) demonstrates significant hypoglycemic and antioxidant effects. This natural compound helps lower blood glucose and protect against organ damage in diabetic mice.
Area of Science:
- Pharmacology
- Biochemistry
- Natural Product Chemistry
Background:
- Mulberry fruit polysaccharide (MFP) is a key bioactive component of mulberry fruit.
- MFP exhibits various beneficial bioactivities.
- Diabetes mellitus is a metabolic disorder characterized by hyperglycemia.
Purpose of the Study:
- To investigate the hypoglycemic and antioxidant properties of MFP.
- To evaluate the protective effects of MFP on streptozotocin (STZ)-induced diabetic mice.
Main Methods:
- In vitro experiments assessed insulin secretion and pancreatic β cell proliferation.
- In vivo studies involved oral administration of MFP to STZ-induced diabetic mice.
- Biochemical assays measured malondialdehyde (MDA) levels and antioxidant enzyme activities (SOD, GPx, CAT).
- Histopathological examination assessed tissue damage in pancreas, liver, and kidney.
Main Results:
- MFP significantly increased insulin secretion and promoted pancreatic β cell proliferation in vitro.
- Oral MFP administration reduced blood glucose levels and promoted weight loss in diabetic mice.
- MFP decreased MDA levels and increased SOD, GPx, and CAT activities in the liver.
- Histopathology revealed that MFP alleviated pancreatic, liver, and kidney tissue damage.
Conclusions:
- MFP possesses significant hypoglycemic and antioxidant properties.
- MFP offers protective effects against STZ-induced diabetes in mice.
- MFP shows potential as a therapeutic agent for managing diabetes.
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