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.
|
Authors | Zwe-Ling Kong, Sabri Sudirman, Yu-Chun Hsu, Chieh-Yu Su, Hsiang-Ping Kuo |
Journal | International journal of molecular sciences
(Int J Mol Sci)
Vol. 20
Issue 18
(Sep 11 2019)
ISSN: 1422-0067 [Electronic] Switzerland |
PMID | 31514311
(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)
|