Decreased in vitro fertility in male rats exposed to fluoride-induced oxidative stress damage and mitochondrial transmembrane potential loss

Toxicology and Applied Pharmacology

Volumn 230, Issue 3, 2008, Pages 352-357

  Izquierdo Vega, Jeannett A ^a,b   Sánchez Gutiérrez, Manuel ^c   Del Razo, Luz María ^a  

^a DEPARTAMENTO DE FÍSICA   (Mexico)

^b UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO   (Mexico)

^c UNIVERSIDAD AUTÓNOMA DEL ESTADO DE HIDALGO   (Mexico)

Author keywords

Fluoride; In vitro fertilization (IVF); Mitochondrial transmembrane potential; Oxidative stress; Spermatozoa

Indexed keywords

FLUORIDE; SUPEROXIDE; SUPEROXIDE DISMUTASE; WATER;

ACROSOME REACTION; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; ENZYME ACTIVITY; FEMALE; FERTILIZATION IN VITRO; FLUOROSIS; LIPID PEROXIDATION; MALE; MALE INFERTILITY; MITOCHONDRIAL MEMBRANE POTENTIAL; NONHUMAN; OXIDATIVE STRESS; PARAMETER; RAT; SPERMATOZOON; STANDARD; TRANSMISSION ELECTRON MICROSCOPY; WISTAR ALBINO GLAXO RAT;

ACROSOME REACTION; ANIMALS; FERTILITY; FERTILIZATION IN VITRO; FLUORIDES; MALE; MEMBRANE POTENTIAL, MITOCHONDRIAL; OXIDATIVE STRESS; RATS; RATS, WISTAR; SPERM MOTILITY; SPERMATOZOA;

RATTUS; RATTUS NORVEGICUS;

EID: 46749109555     PISSN: 0041008X     EISSN: 10960333     Source Type: Journal    
DOI: 10.1016/j.taap.2008.03.008     Document Type: Article

References (46)

1. Aitken R.J., Buckingham D.W., and West K.M. Reactive oxygen species and human spermatozoa: analysis of the cellular mechanisms involved in luminol- and lucigenin-dependent chemiluminescence. J. Cell. Physiol. 15 (1992) 466-477
2. Aitken R.J., Harkiss D., and Buckingham D. Relationship between iron-catalysed lipid peroxidation potential and human sperm function. J. Reprod. Fertil. 98 (1993) 257-265
3. Aitken R.J., Paterson M., Fisher H., Buckingham D.W., and van Duin M. Redox regulation of tyrosine phosphorylation in human spermatozoa and its role in the control of human sperm function. J. Cell Sci. 108 (1995) 2017-2025
4. Aitken R.J., Gordon E., Harkiss D., Twigg J.P., Milne P., Jennings Z., and Irvine D.S. Relative impact of oxidative stress on the functional competence and genomic integrity of human spermatozoa. Biol. Reprod. 59 (1998) 1037-1046
5. Al-Hiyasat A.S., Elbetieha A.M., and Darmani H. Reproductive toxic effects of ingestion of sodium fluoride in the female rat. Fluoride 33 (2000) 79-84
6. Baker M.A., and Aitken R.J. Reactive oxygen species in spermatozoa: methods for monitoringand significance for the origins of genetic disease and infertility. Reprod. Biol. Endocrinol. 3 (2005) 67-75
7. Bendahmane M., Zeng H.T., and Tulsiani D.R. Assessment of acrosomal status in rat spermatozoa: studies on carbohydrate and non-carbohydrate agonists. Arch. Biochem. Biophys. 404 (2002) 38-47
8. Bhagaban S.V.B.K., and Raghu V. Utility of check dams in dilution of fluoride concentration in ground water and the resultant analysis of blood serum and urine of villagers, Anantapur District, Andhra Pradesh, India. Environ. Geochem. Health 27 (2005) 97-108
9. Buege J.A., and Aust S.D. Microsomal lipid peroxidation. Meth. Enzymol. 52 (1978) 302-310
10. Chinoy N.J., and Narayana M.V. In vitro fluoride toxicity in human spermatozoa. Reprod. Toxicol. 8 (1994) 155-159
11. Chinoy N.J., Narayana M.V., Dalal V., Rawat M., and Patel D. Amelioration of fluoride toxicity in some accessory reproductive glands and spermatozoa of rat. Fluoride 28 (1995) 75-86
12. Chlubek D. Fluoride and oxidative stress. Fluoride 36 (2003) 217-228
13. Cittanova M.L., Lelongt B., Verpont M.C., Geniteau-Legendre M., Wahbe F., Prie D., Coriat P., and Ronco P.M. Fluoride ion toxicity in human kidney collecting duct cells. Anesthesiology 84 (1996) 428-435
14. Dabrowska E., Balunowska M., Letko R., and Szynaka B. Ultrastructural study of the mitochondria in the submandibular gland, the pancreas and the liver of young rats, exposed to NaF in drinking water. Ann. Acad. Med. Bialost. 49 (2004) 180-181
15. De Iuliis G.N., Wingate J.K., Koppers A.J., McLaughlin E.A., and Aitken R.J. Definitive evidence for the nonmitochondrial production of superoxide anion by human spermatozoa. J. Clin. Endocrinol. Metab. 91 (2006) 1968-1975
16. de Lamirande E., and Gagnon C. Impact of reactive oxygen species on spermatozoa: a balancing act between beneficial and detrimental effects. Hum. Reprod. 10 (1995) 15-21
17. de Lamirande E., Jiang H., Zini A., Kodama H., and Gagnon C. Reactive oxygen species and sperm physiology. Rev. Reprod. 2 (1997) 48-54
18. Del Razo L.M., Corona J.C., García-Vargas G., Albores A., and Cebrián M.E. Fluoride levels in well-water from a chronic arsenicism area of northern Mexico. Environ. Pollut. 80 (1993) 91-94
19. Dvořáková-Hortová K, Sandera M, Jursová M, Vašinová J, Pěknicová J,, in press. The influence of fluorides on mouse sperm capacitation. Anim. Reprod. Sci. doi:10.1016/j.anireprosci.2007.07.015.
20. Ford W.C., and Harrison A. The role of oxidative phosphorylation in the generation of ATP in human spermatozoa. J. Reprod. Fertil. 63 (1981) 271-278
21. Ford W.C.L., and Rees J.M. The bioenergetics of mammalian sperm motility. In: Gagnon C. (Ed). Control of Sperm Motility: Biological and Clinical Aspect (1990), CRC Press, Boca Raton, FL 175-202
22. Freni S.C. Exposure to high fluoride concentrations in drinking water is associated with decreased birth rates. J. Toxicol. Environ. Health 42 (1994) 109-112
23. Geiszt M., and Leto T.L. The Nox family of NAD(P)H oxidase: host defense and beyond. J. Biol. Chem. 279 (2004) 51715-51718
24. Ghosh D., Das S., Maiti R., Jana D., and Das U.B. Testicular toxicity in sodium fluoride treated rats; association with oxidative stress. Reprod. Toxicol. 16 (2002) 383-390
25. Gravance C.G., Garner D.L., Miller M.G., and Berger T. Fluorescent probes and flow cytometry to assess rat sperm integrity and mitochondrial function. Reprod. Toxicol. 15 (2001) 5-10
26. Guo X.Y., Sun G.F., and Shenyang Y.S. Oxidative stress from fluoride-induced hepatotoxicity in rats. Fluoride 36 (2003) 25-29
27. Gupta S.K., Mithal A., and Das B.K. Skeletal scintigraphic findings in endemic skeletal fluorosis. Nucl. Med. Common. 14 (1993) 384-390
28. Hardisson A., Rodríguez M.I., Burgos A., Díaz Flores L., Gutiérrez R., and Várela H. Fluoride levels in publicly supplied and bottled drinking water in the island of Tenerife, Spain. Bull. Environ. Contam. Toxicol. 67 (2001) 163-170
29. Krechniak J., and Inkielewicz I. Correlations between fluoride concentration and free radical parameters in soft tissues of rats. Fluoride 38 (2005) 293-296
30. Lawson P.B., and Yu M.H. Fluoride inhibition of Superoxide Dismutase (SOD) from the earthworm Eisenia fetida. Fluoride 36 (2003) 143-151
31. Mittal M., and Flora S.J. Vitamin E supplementation protects oxidative stress during arsenic and fluoride antagonism in male mice. Drug Chem. Toxicol. 3 (2007) 263-281
32. National Research Council (NRC). Fluoride in Drinking-Water. A Scientific Review of EPA's Standard. Washington D.C. (2006)
33. Ortiz-Perez D., Rodriguez-Martinez M., Martinez F., Borja-Aburto V.H., Castelo J., Grimaldo J.I., de la Cruz E., Carrizales L., and Diaz-Barriga F. Fluoride-induced disruption of reproductive hormones in men. Environ. Res. 93 (2003) 20-30
34. Primakoff P., and Myles G.D. Penetration, adhesion and fusion in mammalian sperm-egg interaction. Science 296 (2002) 2183-2185
35. Sanocka D., and Kurpisz M. Reactive oxygen species and sperm cells. Reprod. Biol. Endocrinol. 2 (2004) 1-12
36. Sen T., Sen N., Tripathi G., Chatterjee U., and Chakrabarti S. Lipid peroxidation associated cardiolipin loss and membrane depolarization in rat brain mitochondria. Neurochem. Int. 49 (2006) 20-27
37. Shanthakumari D., Srinivasalu S., and Subramanian S. Effect of fluoride intoxication on lipidperoxidation and antioxidant status in experimental rats. Toxicology 204 (2004) 219-228
38. Shivarajashankara Y.M., Shivashankara A.R., Gopalakrishna B.P., and Rao S.H. Oxidative stress in children with endemic skeletal fluorosis. Fluoride 34 (2001) 108-113
39. Verma R.J., and Guna Sherlin D.M. Sodium fluoride-induced hypoproteinemia and hypoglycemia in parental and F(1)-generation rats and amelioration by vitamins. Food Chem. Toxicol. 40 (2002) 1781-1788
40. Wang X., Sharma R.K., Sikka S.C., Thomas Jr. A.J., Falcone T., and Agarwal A. Alterations in mitochondria membrane potential and oxidative stress in infertile men: a prospective observational study. Fertil. Steril. 80 (2003) 844-850
41. Wang S.X., Wang Z.H., Cheng X.T., Li J., Sang Z.P., Zhang X.D., Han L.L., Qiao X.Y., Wu Z.M., and Wang Z.Q. Arsenic and fluoride exposure in drinking water: children's IQ and growth in Shanyin County, Shanxi province, China. Environ. Health Perspect. 115 (2007) 643-647
42. Wilde L.G., and Yu M. Effect of fluoride on superoxide dismutase (SOD) activity in germinating mung bean seedlings. Fluoride 31 (1998) 81-88
43. Wolfl J., Dagher M.C., Fuchs A., Geiszt M., and Ligeti E. In vitro activation of the NADPH oxidase by fluoride. Possible involvement of a factor activating GTP hydrolysis on Rac (Rac-GAP). Eur. J. Biochem. 239 (1996) 369-375
44. World Health Organization (WHO). Laboratory Manual for the Examination of Human Semen and Semen Cervical Mucus Interaction. 4th Ed. (2001), University Press, Cambridge, New York
45. Yanagimachi R. Mammalian fertilization. In: Knobil E., Neill J.D., Ewing L.L., Greenwald G.S., Markert C.L., and Pfaff D.W. (Eds). The Physiology of Reproduction. Vol 1 (1994), Raven Press, New York 190-302
46. Zhan X.A., Wang M., Xu Z.R., Li W.F., and Li J.X. Effects of fluoride on hepatic antioxidant system and transcription of Cu/Zn SOD gene in young pigs. J. Trace Elem. Med. Biol. 20 (2006) 83-87