Fucoxanthin-Rich Brown Algae Extract Improves Male Reproductive Function on Streptozotocin-Nicotinamide-Induced Diabetic Rat Model

Int J Mol Sci. 2019 Sep 11;20(18):4485. doi: 10.3390/ijms20184485.

Abstract

Hypogonadism and oxidative stress are occurring commonly in men with diabetes and associated male infertility. This study aimed to investigate the capability of anti-oxidative and anti-inflammatory properties of fucoxanthin as well as to evaluate its protective effects on male reproduction in diabetic rats. The RAW 264.7 macrophage cells were used to evaluate the anti-oxidative and anti-inflammatory activity. Thirty male Sprague-Dawley rats were induced by streptozotocin-nicotinamide for a diabetes model and fed either with three different doses of fucoxanthin (13, 26, and 65 mg/kg) or rosiglitazone (0.571 mg/kg) for four weeks. The fucoxanthin significantly inhibited nitric oxide production and reduced reactive oxygen species level in lipopolysaccharide-induced RAW 264.7 cells. In the animal study, fucoxanthin administration improved insulin resistance, restored sperm motility, decreased abnormal sperm number, and inhibited lipid peroxidation. Moreover, it restored GPR54 and SOCS-3 mRNA expression in the hypothalamus and recovered luteinizing hormone level, as well as the testosterone level. In conclusion, fucoxanthin not only possessed antioxidant and anti-inflammatory properties but also decreased the diabetes signs and symptoms as well as improved spermatogenesis and male reproductive function.

Keywords: diabetes; fucoxanthin; hypogonadism; male reproduction; spermatogenesis.

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Blood Glucose / metabolism
  • Cell Survival / drug effects
  • Diabetes Mellitus, Experimental / chemically induced
  • Diabetes Mellitus, Experimental / drug therapy*
  • Diabetes Mellitus, Experimental / physiopathology*
  • Disease Models, Animal
  • Inflammation Mediators / metabolism
  • Insulin / blood
  • Insulin Resistance
  • Kisspeptins / genetics
  • Kisspeptins / metabolism
  • Male
  • Malondialdehyde / metabolism
  • Mice
  • Niacinamide
  • Nitric Oxide / metabolism
  • Oxidative Stress / drug effects
  • Phaeophyceae / chemistry*
  • RAW 264.7 Cells
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats, Sprague-Dawley
  • Reactive Oxygen Species / metabolism
  • Receptors, Kisspeptin-1 / genetics
  • Receptors, Kisspeptin-1 / metabolism
  • Reproduction / drug effects*
  • Spermatozoa / drug effects
  • Spermatozoa / metabolism
  • Streptozocin
  • Suppressor of Cytokine Signaling 3 Protein / genetics
  • Suppressor of Cytokine Signaling 3 Protein / metabolism
  • Testis / drug effects
  • Testis / pathology
  • Xanthophylls / pharmacology
  • Xanthophylls / therapeutic use*

Substances

  • Antioxidants
  • Blood Glucose
  • Inflammation Mediators
  • Insulin
  • Kiss1r protein, rat
  • Kisspeptins
  • RNA, Messenger
  • Reactive Oxygen Species
  • Receptors, Kisspeptin-1
  • Suppressor of Cytokine Signaling 3 Protein
  • Xanthophylls
  • fucoxanthin
  • Niacinamide
  • Nitric Oxide
  • Malondialdehyde
  • Streptozocin