Chitosan oligosaccharide improves diabetic nephropathy by attenuating renal fibrogenesis and strengthening intestinal barriers in type 2 diabetic rats
Issued Date
2025-10-22
Resource Type
ISSN
00092797
eISSN
18727786
Scopus ID
2-s2.0-105011975711
Journal Title
Chemico Biological Interactions
Volume
420
Rights Holder(s)
SCOPUS
Bibliographic Citation
Chemico Biological Interactions Vol.420 (2025)
Suggested Citation
Sutthasupha P., Promsan S., Pengrattanachot N., Phengpol N., Lalichatsakul C., Thongnak L., Jaikumkao K., Pichyangkura R., Muanprasat C., Lungkaphin A. Chitosan oligosaccharide improves diabetic nephropathy by attenuating renal fibrogenesis and strengthening intestinal barriers in type 2 diabetic rats. Chemico Biological Interactions Vol.420 (2025). doi:10.1016/j.cbi.2025.111680 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/111510
Title
Chitosan oligosaccharide improves diabetic nephropathy by attenuating renal fibrogenesis and strengthening intestinal barriers in type 2 diabetic rats
Corresponding Author(s)
Other Contributor(s)
Abstract
It has been demonstrated that systemic low-grade inflammation and renal oxidative stress induce renal complications and diabetic nephropathy (DN) in conditions associated with diabetes. Chitosan oligosaccharide (COS) has been shown to attenuate kidney injury by enhancing renal autophagy in prediabetic rats. This study explored the effects of COS on renal injury and the mechanisms involved in a type 2 diabetes mellitus (T2DM) model. Wistar rats were given a high‐fat diet (HFD) and streptozotocin injection to induce T2DM. COS 5 or 10 or metformin 30 mg/kg/day were given orally to T2DM rats for 8 weeks. COS exerted nephroprotection through activation of renal AMP-activated protein kinase (AMPK), alleviation of the renal oxidative stress-fibrosis axis and impaired organic anion transporter (Oat3) function. COS also strengthened intestinal barriers via suppression of myosin light chain kinase (MLCK) and stimulation of calcium-sensing receptor (CaSR), limiting leaky gut and providing anti-inflammatory effects. Metformin had no effect on CaSR. COS10 and metformin had comparable effects regarding the reduction of renal oxidative stress. Metformin showed a greater efficacy in attenuating oxidative stress than COS5. However, the anti-fibrotic efficacy of COS10 was greater than metformin partly through the inhibition of the transforming growth factor beta (TGF-β)/epithelial-mesenchymal transition (EMT) process. A clinical therapeutic approach using COS supplementation could potentially increase the efficacy regarding the attenuation of hyperlipidemia, leaky gut, and protection against kidney injury in diabetic conditions.