Assessing the therapeutic potential of long-chain isomaltooligosaccharides in diabetic and hyperlipidemic rats
Issued Date
2024-12-01
Resource Type
eISSN
17585996
Scopus ID
2-s2.0-85198717581
Journal Title
Diabetology and Metabolic Syndrome
Volume
16
Issue
1
Rights Holder(s)
SCOPUS
Bibliographic Citation
Diabetology and Metabolic Syndrome Vol.16 No.1 (2024)
Suggested Citation
Reamtong O., Waeonukul R., Prangthip P. Assessing the therapeutic potential of long-chain isomaltooligosaccharides in diabetic and hyperlipidemic rats. Diabetology and Metabolic Syndrome Vol.16 No.1 (2024). doi:10.1186/s13098-024-01374-0 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/99760
Title
Assessing the therapeutic potential of long-chain isomaltooligosaccharides in diabetic and hyperlipidemic rats
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Corresponding Author(s)
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Abstract
Background: The global rise in diabetes prevalence necessitates effective treatments. Rats, mimicking physiological changes seen in Type 2 diabetes, serve as valuable models for studying metabolic disorders. Natural health supplements, especially prebiotics, are gaining interest for improving metabolic health. Isomaltooligosaccharides (IMOs), classified as functional oligosaccharides and prebiotics, have attracted attention due to their beneficial effects on gut microbiota balance and cholesterol reduction. However, commercial IMOs often contain undesirable sugars, leading to the development of long-chain IMOs with enhanced prebiotic properties. Methods: This study assessed the therapeutic potential of long-chain IMOs derived from Bacillus subtilis strain AP-1 compared to inulin, a widely recognized prebiotic, in addressing hyperglycemia and hyperlipidemia in rats. Results: IMOs treatment effectively reduced blood sugar and triglyceride levels similarly to inulin supplementation. Proteomic analysis revealed changes in hepatic protein profiles, with upregulated pathways including glutathione metabolism, oxidative phosphorylation, and pentose and glucuronate interconversion, while pathways related to fatty acid and amino acid biosynthesis exhibited downregulation. These results suggest promising therapeutic effects of IMOs treatment on diabetes and hyperlipidemia by influencing key metabolic pathways. Conclusions: Our findings highlight the potential of long-chain IMOs as targeted interventions for metabolic disorders, warranting further investigation into their clinical applicability and mechanisms of action.