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

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.
AuthorsZwe-Ling Kong, Sabri Sudirman, Yu-Chun Hsu, Chieh-Yu Su, Hsiang-Ping Kuo
JournalInternational journal of molecular sciences (Int J Mol Sci) Vol. 20 Issue 18 (Sep 11 2019) ISSN: 1422-0067 [Electronic] Switzerland
PMID31514311 (Publication Type: Journal Article)
Chemical References
  • 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
Topics
  • Animals
  • Antioxidants (metabolism)
  • Blood Glucose (metabolism)
  • Cell Survival (drug effects)
  • Diabetes Mellitus, Experimental (chemically induced, drug therapy, physiopathology)
  • Disease Models, Animal
  • Inflammation Mediators (metabolism)
  • Insulin (blood)
  • Insulin Resistance
  • Kisspeptins (genetics, metabolism)
  • Male
  • Malondialdehyde (metabolism)
  • Mice
  • Niacinamide
  • Nitric Oxide (metabolism)
  • Oxidative Stress (drug effects)
  • Phaeophyta (chemistry)
  • RAW 264.7 Cells
  • RNA, Messenger (genetics, metabolism)
  • Rats, Sprague-Dawley
  • Reactive Oxygen Species (metabolism)
  • Receptors, Kisspeptin-1 (genetics, metabolism)
  • Reproduction (drug effects)
  • Spermatozoa (drug effects, metabolism)
  • Streptozocin
  • Suppressor of Cytokine Signaling 3 Protein (genetics, metabolism)
  • Testis (drug effects, pathology)
  • Xanthophylls (pharmacology, therapeutic use)

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