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Application of fucoidan polysaccharide sulfate in preparing drug for preventing and/or treating diabetic cardiomyopathy

A technology of diabetic cardiomyopathy and fucoidan, applied in the field of application of fucoidan sulfate in the preparation of drugs for preventing and/or treating diabetic cardiomyopathy

Active Publication Date: 2013-08-07
CAPITAL UNIVERSITY OF MEDICAL SCIENCES
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

Recent studies have found that LMWF can protect the kidney from ischemic refocus injury [Chen, J., et al., Low Molecular Weight Fucoidan against Renal Ischemia-Reperfusion Injury via Inhibition of the MAPK Signaling Pathway. PLoS One, 2013.8(2): p.e56224.], and whether LMWF has a protective effect on diabetic cardiomyopathy has not been studied

Method used

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  • Application of fucoidan polysaccharide sulfate in preparing drug for preventing and/or treating diabetic cardiomyopathy
  • Application of fucoidan polysaccharide sulfate in preparing drug for preventing and/or treating diabetic cardiomyopathy
  • Application of fucoidan polysaccharide sulfate in preparing drug for preventing and/or treating diabetic cardiomyopathy

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Embodiment 1

[0029] Materials and Methods

[0030] 1. Grouping and administration of experimental animals

[0031] The experiment selected Goto-Kakizaki (GK) rats as animal models of type 2 diabetes. The pathological characteristics of GK mice are very similar to those of human type 2 diabetes, such as mildly elevated fasting blood glucose, elevated blood glucose after eating, stable glucose-stimulated insulin secretion and impaired glucose intolerance, and elevated basal blood pressure. Late diabetic complications .]. 12-week-old male GK rats and age-sex-matched Wistar rats were purchased, and after a week of adaptive feeding in the Department of Experimental Animals, they were randomly divided into groups. The experiment was divided into normal control group (Con, Wistar rats); diabetes group (DM, GK rats), drug treatment group (DM+F50, DM+F100, DM+F200, GK rats were given 50, 100, 200mg / kg / Day dose of LMWF drugs) 5 groups. Among them, the DM+F200 group had a small number of cases a...

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Abstract

The invention discloses a drug novel use of fucoidan polysaccharide sulfate. The use is the application of the fucoidan polysaccharide sulfate in preparing the following products: (1), a product for preventing and / or treating diabetic cardiomyopathy; (2), a product for inhibiting diabetic myocardial oxidative stress; and (3), a product for inhibiting expression and activation of PKC (Protein Kinase C) beta in diabetic cardiomyopathy; and (4), a product for relieving cardiac interstitial fibrosis of a diabetic. The fucoidan polysaccharide sulfate is preferably LMWF (Fucoidan Polysaccharide Sulfate) with weight-average molecular weight of 3-30KD. According to the pharmacodynamic experiment, the LMWF can be used for generating beneficial interference to the development of pathogenetic condition of the diabetic cardiomyopathy by strengthening the myocardial systolic function and relieving cardiac fibrosis. More importantly, the LMWF can be used for effectively inhibiting oxidative stress by regulating the activity of antioxidase, and can be used for inhibiting the expression of protein kinase C beta (PKCbeta) subtype. The LMWF is from the natural existing kelp, so that the availability and safety of the kelp are beneficial to using the fucoidan polysaccharide sulfate as a potential clinical treatment drug and preventing the diabetic cardiomyopathy.

Description

technical field [0001] The invention relates to the application of fucoidan sulfate in the preparation of drugs for preventing and / or treating diabetic cardiomyopathy. Background technique [0002] Cardiac dysfunction due to diabetic cardiomyopathy is not associated with the development of coronary atherosclerosis or hypertension. Premature diastolic dysfunction and late systolic dysfunction detected by echocardiography are two prominent mechanical injuries of the heart. Cardiac dysfunction is mainly manifested as a decrease in systolic and diastolic velocity and a decrease in myocardial contractility and compliance. Although there are many pathogenesis of diabetic cardiomyopathy, many studies related to the mechanism suggest that it is related to changes in cardiac energy metabolism [An, D. and B. Rodrigues, Role of changes in cardiac metabolism in development of diabetic cardiomyopathy. Am J Physiol Heart Circ Physiol, 2006.291(4): p.H1489-506.], impaired calcium balance...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61K31/737A23L1/09A61P9/00A61P3/10
Inventor 罗大力于新凤张超崔文通张全斌
Owner CAPITAL UNIVERSITY OF MEDICAL SCIENCES
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