4.7 Article

Therapeutic Efficacy of Natural Product 'C-Phycocyanin' in Alleviating Streptozotocin-Induced Diabetes via the Inhibition of Glycation Reaction in Rats

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MDPI
DOI: 10.3390/ijms232214235

关键词

type 2 diabetes mellitus (T2DM); advanced glycation end products (AGEs); streptozotocin (STZ); Plectonema species; c-phycocyanin (C-PC)

资金

  1. Scientific Research Deanship at University of Ha'il-Saudi Arabia [MDR-22 009]

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The study found that C-phycocyanin (C-PC) obtained from Plectonema species has antioxidant, antiglycation, and antidiabetic properties. In a diabetic rat model, C-PC administration decreased blood glucose, lipids, and liver and kidney function indices, while increasing body weight. C-PC also suppressed biochemical glycation markers, maintained the redox state, and protected tissue structures.
Diabetes is a long-term metabolic disorder characterized by persistently elevated blood sugar levels. Chronic hyperglycemia enhances glucose-protein interactions, leading to the formation of advanced glycation end products (AGEs), which form irreversible cross-links with a wide variety of macromolecules, and accumulate rapidly in the body tissues. Thus, the objective of this study was to assess the therapeutic properties of C-phycocyanin (C-PC) obtained from Plectonema species against oxidative stress, glycation, and type 2 diabetes mellitus (T2DM) in a streptozotocin (STZ)-induced diabetic Wistar rat. Forty-five days of C-PC administration decreased levels of triglycerides (TGs), blood glucose, glycosylated hemoglobin, (HbA1c), total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), liver and kidney function indices, and raised body weight in diabetic rats. C-PC suppressed biochemical glycation markers, as well as serum carboxymethyllysine (CML) and fluorescent AGEs. Additionally, C-PC maintained the redox state by lowering lipid peroxidation and protein-bound carbonyl content (CC), enhancing the activity of high-density lipoprotein cholesterol (HDL-C) and renal antioxidant enzymes, and preserving retinal and renal histopathological characteristics. Thus, we infer that C-PC possesses antidiabetic and antiglycation effects in diabetic rats. C-PC may also act as an antidiabetic and antiglycation agent in vivo that may reduce the risk of secondary diabetic complications.

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