HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Novel antioxidant astaxanthin-s-allyl cysteine biconjugate diminished oxidative stress and mitochondrial dysfunction to triumph diabetes in rat model.

AbstractAIMS:
The present study determines the effect of administration of novel antioxidant astaxanthin-s-allyl cysteine biconjugate (AST-SAC) against streptozotocin-induced diabetes mellitus (DM) in rats.
MAIN METHODS:
AST-SAC (1 mg/kg/day) was treated against DM in rats for 45 days. The oxidative stress, antioxidants level, insulin secretion, activities of various carbohydrate metabolizing enzymes were studied. The glucose uptake in L6 myotubes was studied. In addition, in silico analysis of interaction of AST-SAC with proteins such as insulin receptor (IR) and 5'-adenosine monophosphate-activated protein kinase (AMPK) were carried out.
KEY FINDINGS:
Administration of AST-SAC in DM rats has protected the mitochondrial function (decreased oxidative stress and normalized oxidative phosphorylation activities) and antioxidant capacity of the pancreas which has resulted in beta cells rejuvenation and insulin secretion restoration. AST-SAC decreased the alpha-glucosidases activities to bring glycemic control in DM rats. Due to these effects the glycoprotein components and lipids were restored to near normalcy in DM rats. AST-SAC protected the antioxidant status of liver, kidney and plasma; and curbed the progression of secondary complications of DM. AST-SAC treatment stimulated glucose uptake in L6 myotubes in in vitro. To support this observation, AST-SAC interacted with proteins such as IR and AMPK in silico.
SIGNIFICANCE:
AST-SAC can be considered as "multi-target-directed ligand", that is, through these manifold effects, AST-SAC has been able to prevail over DM in rats.
AuthorsSakayanathan Penislusshiyan, Loganathan Chitra, Iruthayaraj Ancy, Poomani Kumaradhas, Thayumanavan Palvannan
JournalLife sciences (Life Sci) Vol. 245 Pg. 117367 (Mar 15 2020) ISSN: 1879-0631 [Electronic] Netherlands
PMID32001265 (Publication Type: Journal Article)
CopyrightCopyright © 2020 Elsevier Inc. All rights reserved.
Chemical References
  • Antioxidants
  • Hypoglycemic Agents
  • Triglycerides
  • Xanthophylls
  • astaxanthin-s-allyl cysteine biconjugate
  • Cholesterol
  • Glucose
  • Cysteine
Topics
  • Animals
  • Antioxidants (pharmacology, therapeutic use)
  • Cholesterol (metabolism)
  • Cysteine (analogs & derivatives, pharmacology, therapeutic use)
  • Diabetes Mellitus, Experimental (drug therapy, metabolism)
  • Glucose (metabolism)
  • Hypoglycemic Agents (therapeutic use)
  • Male
  • Mitochondria (drug effects, metabolism)
  • Molecular Docking Simulation
  • Oxidative Stress (drug effects)
  • Rats
  • Rats, Sprague-Dawley
  • Triglycerides (metabolism)
  • Xanthophylls (pharmacology, therapeutic use)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: