Effects of ginger on spermatogenesis in streptozotocin-induced diabetic rat

Journal of Medicinal Plants

Volumn 8, Issue 31, 2009, Pages 118-124

  Nassiri, M ^a   Khaki, A ^b   Ahmadi Ashtiani, H R ^c,d,e   Rezazadeh, Sh ^e   Rastgar, H ^f   Gharachurlu, Sh ^b  

^a ISLAMIC AZAD UNIVERSITY   (Iran)

^b ISLAMIC AZAD UNIVERSITY   (Iran)

^c TARBIAT MODARES UNIVERSITY   (Iran)

^d ZANJAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^e AVICENNA RESEARCH INSTITUTE   (Iran)

^f MINISTRY OF HEALTH AND MEDICAL EDUCATION   (Iran)

Author keywords

Diabetic; Ginger rhizome; Rat; Sperm; Streptozotocin

Indexed keywords

GINGER EXTRACT; MALONALDEHYDE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANTIOXIDANT ACTIVITY; ARTICLE; GINGER; MALE; NONHUMAN; RAT; SPERMATOGENESIS; SPERMATOZOON COUNT; SPERMATOZOON MOTILITY; STREPTOZOCIN DIABETES; TESTIS;

ANIMALIA; RATTUS; ZINGIBER OFFICINALE; ZINGIBERACEAE;

EID: 77950465207     PISSN: 2717204X     EISSN: 27172058     Source Type: Journal    
DOI: None     Document Type: Article

References (26)

1. Jiang GY. Practical Diabetes 1st Edition. Beijing: People's Health Publishing House: 1996, 295-296
2. Holstein A, Hinze S, Thiessen E, Plaschke A, Egberts EH.Clinical implications of hepatogenous diabetes in liver irrhosis. J. Gastroenterol Hepatol 2002; 17: 677-680
3. Tappy L, Minehira K. New data and new concepts on the role of the liver in glucose homeostasis. Curr Opin Clin Nutr Metab Care 2001; 4: 273-277
4. Baynes JW, Thorpe SR. Role of oxidative stress in diabetic complications: a new perspective on an old paradigm. J. Diabetes 1999; 48: 1-9.
5. Wolff SP, Jiang ZY, Hunt JV .Protein glycation and oxidative stress in diabetes mellitus and ageing. J. Free Radic Biol. Med. 1991; 10: 339-352
6. Palmeira CM, Santos DL, Seica R, Moreno AJ, Santos MS.Enhanced mitochondrial testicular antioxidant capacity in Goto-Kakizaki diabetic rats: role of coenzyme Q. Am. J. Physiol. Cell Physiol. 2001; 281: C1023-8.
7. Sexton WJ, Jarow JP. Effect of diabetes mellitus upon male reproductive function. J. Urol. 1997; 49: 508-513
8. Peluso MR .Flavonoids attenuate cardiovascular disease, inhibit phosphodiesterase, and modulate lipid homeostasis in adipose tissue and liver. Exp. Biol. Med. (Maywood) 2006; 231 (8): 1287-99.
9. Mahesh T, Menon VP .Quercetin alleviates oxidative stress in streptozotocin-induced diabetic rats. Phytother Res. 2004; 18: 123-127
10. Shrilatha B, Muralidhara . Early oxidative stress in testis and epididymal sperm in streptozotocin-induced diabetic mice: its progression and genotoxic consequences. Reprod Toxicol. 2007; 23 (4): 578-587
11. Khaki A, Fathi Azad F, Nouri M, Khaki AA, Jabbari -Kh H,Hammadeh M. Evaluation of Androgenic Activity of Allium cepa on Spermatogenesis in Rat. J. Folia. Morphologica 2009; 68 (1): 45-51.
12. Khaki A, Fathiazad F, Nouri M, Khaki AA, Chelar c,ozanci, Ghafari-Novin M, Hamadeh M. The Effects of Ginger on Spermatogenesis and Sperm parameters of Rat. Iranian J. of Reproductive Med. 2009; 7 (1): 7-12.
13. Khaki A, Novin MG, Khaki AA, Nouri M, Sanati E, Nikmanesh M. Comparative study of the effects of gentamicin, neomycin, streptomycin and ofloxacin antibiotics on sperm parameters and testis apoptosis in rats. Pak. J. Biol. Sci. 2008; 11 (13): 1683-1689
14. Feng R, He W, Ochi H. A new murine oxidative stress model associated with senescence. J. Mech Ageing Dev. 2001; 122: 547-559
15. Quintanilha AT, Packer L, Davies JM, Racanelli TL, Davies KJ. Membrane effects of vitamin E deficiency: bioenergetics and surface charge density studies of skeletal muscle and liver mitochondria. Ann NY Acad Sci. 1982; 393: 32-47.
16. Huang HFS, Linsenmeyer TA, Li MT, Giglio W, Anesetti R, von Hagen J, Ottenweller JE, Pogach L. Acute effects of spinal cord injury on the pituitary-testicular hormone axis and Sertoli cell functions: a time course study. J. Androl. 1995; 16: 148-157
17. Ajay Machha, Francis I. Achike, Ali Mohd Mustafa,nd Mohd Rais Mustafa. Quercetin, a flavonoid antioxidant, modulates endothelium-derived nitric oxide bioavailability in diabetic rat aortas. J. Nitric Oxide 2007; (16): 442-447
18. Cunha WR, Arantes GM, Ferreira DS, Lucarini R, Silva ML, Furtado NA, da Silva Filho AA, Crotti AE, Araújo AR. Hypoglicemic effect of Leandra lacunosa in normal and alloxan-induced diabetic rats. Fitoterapia 2008; 79 (5): 356-360
19. Kanter M, Altan MF, Donmez S, Ocakci A, Kartal ME. The effects of quercetin on bone minerals, biomechanical behavior, and structure in streptozotocin-induced diabetic rats. J. Cell Biochem. and Function 2007; 25 (6) 747-752
20. Kato A, Minoshima Y, Yamamoto J, Adachi I, Watson AA, Nash RJ. Protective Effects of Dietary Chamomile Tea on Diabetic Complications. J. Agric Food Chem. 2008; 56 (17): 8206-8211
21. Custro N, Carroccio A, Ganci A, Scafidi V, Campagna P, Di Prima L, Montalto G. Glycemic homeostasis in chronic viral hepatitis and liver cirrhosis. Diabetes Metab. 2001; 27: 476-481
22. Lecube A, Hernandez C, Genesca J, Esteban JI, Jardi R, Simo R. High prevalence of glucose abnormalities in patients with hepatitis C virus infection: a multivariate analysis Considering the liver injury. Diabetes Care 2004; 27: 1171-1175
23. Skibola CF, Smith MT. Potential health impacts of excessive flavonoid intake. J. Free Radic Biol. Med. 2000; 29: 375-383
24. ManachC, Morand C, Crespy V, Demigne C, Texier O, Regerat F, Remesy C. Quercetin is recovered in human plasma as conjugated derivatives which retain antioxidant properties. J. FEBS Lett. 1998; 426: 331-336
25. Formica JV, Regelson W. Review of the biology of Quercetin and related bioflavonoids. Food Chem. Toxicol. 1995; 33: 1061-1080
26. Hertog MG, Hollman PC. Potential health effects of the dietary flavonol quercetin. Eur. J. Clin Nutr. 1996; 50: 63-71.