Effects of Spirulina platensis on lipid peroxidation, antioxidant defenses, and tissue damage in kidney of alloxan-induced diabetic rats

Appl Physiol Nutr Metab. 2018 Apr;43(4):345-354. doi: 10.1139/apnm-2017-0461. Epub 2017 Nov 1.

Abstract

Chronic hyperglycemia in diabetes causes free radicals overproduction, which contributes to the development of diabetic nephropathy. In modern medicine, no satisfactory therapy is available to cure diabetes mellitus. In that context, we investigated the potential therapeutic action of spirulina-enriched diet on renal impairment and oxidative stress in diabetic rats. Diabetes was induced by a single subcutaneous injection of alloxan (120 mg·kg-1) in rats. Following alloxan treatment, male Wistar rats were fed daily with 5% spirulina-enriched diet or treated with insulin (0.5 IU·rat-1) for 3 weeks. Diabetes was associated with hyperglycemia, increase in renal oxidative parameters (lipid peroxidation, thiobarbituric-acid reactive substances, protein carbonyl and advanced oxidation protein products levels, changes in antioxidant enzyme activities), and nephropathology markers. The renal injury induced by alloxan was confirmed by histological study of the diabetic rat kidney. Treatment with spirulina or insulin significantly ameliorated renal dysfunction by reducing oxidative stress, while rats recovered normal kidney histology. Overall, this study indicates that spirulina is efficient in inhibiting hyperglycemia and oxidative stress induced by diabetes, and suggests that the administration of this alga may be helpful in the prevention of diabetic complications. This amelioration was even more pronounced than that caused by insulin injection.

Keywords: algal diet; antidiabetic; antidiabétique; diabetes mellitus; diabète sucré; nephropathy; néphropathie; oxidative stress; régime algal; spirulina; spiruline; stress oxydatif.

Publication types

  • Comparative Study

MeSH terms

  • Alloxan*
  • Animal Feed
  • Animal Nutritional Physiological Phenomena
  • Animals
  • Antioxidants / metabolism*
  • Blood Glucose / metabolism
  • Diabetes Mellitus, Experimental / blood
  • Diabetes Mellitus, Experimental / chemically induced
  • Diabetes Mellitus, Experimental / diet therapy*
  • Diabetes Mellitus, Experimental / pathology
  • Diabetic Nephropathies / blood
  • Diabetic Nephropathies / chemically induced
  • Diabetic Nephropathies / pathology
  • Diabetic Nephropathies / prevention & control*
  • Dietary Supplements*
  • Hypoglycemic Agents / pharmacology
  • Insulin / pharmacology
  • Kidney / drug effects
  • Kidney / metabolism*
  • Kidney / pathology
  • Lipid Peroxidation* / drug effects
  • Lipids / blood
  • Male
  • Oxidative Stress* / drug effects
  • Protein Carbonylation
  • Rats, Wistar
  • Spirulina*
  • Thiobarbituric Acid Reactive Substances
  • Time Factors

Substances

  • Antioxidants
  • Blood Glucose
  • Hypoglycemic Agents
  • Insulin
  • Lipids
  • Thiobarbituric Acid Reactive Substances
  • Alloxan