Co-administration of Selenium Nanoparticles and Metformin Abrogate Testicular Oxidative Injury by Suppressing Redox Imbalance, Augmenting Sperm Quality and Nrf2 Protein Expression in Streptozotocin-Induced Diabetic Rats

被引:24
作者
Ebokaiwe, Azubuike P. [1 ]
Obeten, Kebe E. [2 ]
Okori, Stephen O. [2 ]
David, Ebuka E. [1 ]
Olusanya, Olasehinde [3 ]
Chukwu, Chukwuma J. [1 ]
Okoro, Nworie [4 ]
Ehiri, Richard C. [1 ]
机构
[1] Alex Ekwueme Fed Univ, Dept Chem Biochem & Mol Biol, PMB 1010, Abakaliki, Ebonyi State, Nigeria
[2] Cross River Univ Technol, Dept Anat, Okuku, Cross River Sta, Nigeria
[3] Univ Benein, Dept Biochem, Benin, Nigeria
[4] Alex Ekwueme Fed Univ, Dept Biol Microbiol Biotechnol, Ndufu Alike, Nigeria
关键词
Diabetes; Testes; Selenium nanoparticles; Metformin; STRESS; GLUTATHIONE; ACID; OXIDE; ASSAY; MICE;
D O I
10.1007/s12011-020-02082-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Selenium nanoparticles (SeNPs) and metformin (Met) elicit individually protective effects against testicular oxidative injury in diabetic rats. However, the combined effects of both compounds have not been investigated. We investigated the effects of SeNPs and Met individual/co-treatment on testicular oxidative injury in diabetic rats. Diabetes was induced by a single intraperitoneal administration of streptozotocin (STZ-40 mg/kg bwt). The rats were equally divided into 6 groups: Group one-non-diabetic; group two-diabetic untreated; and group six-non-diabetic received citrate buffer (2 mL/kg bwt), while group three, four, and five received SeNPs (0.1 mg/kg bwt), Met (50 mg/kg bwt), and SeNPs/Met combined respectively, for 42 days. Results revealed that SeNPs, as well as Met treatment significantly (p < 0.001), lowered blood glucose levels and improved relative organ weights in treated rats than those of the untreated group. Moreover, a synergistic effect was observed in the co-administration group. Additionally, combined treatment elicited better effect, in augmenting the pituitary and testicular hormone (LH, FSH, prolactin, and testosterone) levels, marker enzymes/protein associated with steroidogenesis (3-beta HSD, 17-beta HSD, and StAR protein), and sperm functional parameters than those of individual treatment groups, when compared with control. Furthermore, the combinatorial effects of SeNPs and Met surpassed their influence in attenuating testicular oxidative stress/inflammation and upregulation of Nrf2 protein expression in diabetic rats when compared with control. Overall, normal rats, co-treated with SeNPs and Met, did not reveal any deleterious effect. Therefore, SeNPs and Met combined treatment may better improve testes function in diabetic conditions than an individual regimen.
引用
收藏
页码:544 / 556
页数:13
相关论文
共 32 条
[1]  
Adedara IA, 2019, EUR J PHARMACOL, V19, P14
[2]  
Aitken RJ, 2006, INT J ANDROL, V29, P69, DOI 10.1111/j.1365-2605.2005.00630.x
[3]   Anti-hyperglycemic activity of selenium nanoparticles in streptozotocin-induced diabetic rats [J].
Al-Quraishy, Saleh ;
Dkhil, Mohamed A. ;
Moneim, Ahmed Esmat Abdel .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2015, 10 :6741-6756
[4]  
Bergmeyer H.U., 1974, METHOD ENZYMAT AN, P447
[5]  
Clairborne A., 1995, Handbook of methods for oxygen Radical Research ed, P237
[6]   Selenium Nanoparticles Attenuate Oxidative Stress and Testicular Damage in Streptozotocin-Induced Diabetic Rats [J].
Dkhil, Mohamed A. ;
Zrieq, Rafat ;
Al-Quraishy, Saleh ;
Moneim, Ahmed E. Abdel .
MOLECULES, 2016, 21 (11)
[7]   Nanosized selenium and Loranthus micranthus leaves ameliorate streptozotocin-induced hepato-renal dysfunction in rats via enhancement of antioxidant system, regulation of caspase 3 and Nrf2 protein expression [J].
Ebokaiwe, Azubuike P. ;
Ijomone, Omamuyovwi M. ;
Griffin, Sharoon ;
Ehiri, Richard C. ;
Obeten, Kebe E. ;
Nwankwo, Joseph O. ;
Ejike, Chukwunonso E. C. C. ;
Keck, Cornelia M. .
PHARMANUTRITION, 2019, 9
[8]   Alteration in sperm characteristics, endocrine balance and redox status in rats rendered diabetic by streptozotocin treatment: attenuating role of Loranthus micranthus [J].
Ebokaiwe, Azubuike P. ;
Ijomone, Omamuyovwi M. ;
Osawe, Sharon O. ;
Chukwu, Chukwuma J. ;
Ejike, Chukwunonso E. C. C. ;
Zhang, Guolin ;
Wang, Fei .
REDOX REPORT, 2018, 23 (01) :194-205
[9]   Formation of nitric oxide derived inflammatory oxidants by myeloperoxidase in neutrophils [J].
Eiserich, JP ;
Hristova, M ;
Cross, CE ;
Jones, AD ;
Freeman, BA ;
Halliwell, B ;
van der Vliet, A .
NATURE, 1998, 391 (6665) :393-397
[10]   Lipid peroxidation measurement by thiobarbituric acid assay in rat cerebellar slices [J].
Garcia, YJ ;
Rodríguez-Malaver, AJ ;
Peñaloza, N .
JOURNAL OF NEUROSCIENCE METHODS, 2005, 144 (01) :127-135