The influence of fluorides on mouse sperm capacitation

Animal Reproduction Science

Volumn 108, Issue 1-2, 2008, Pages 157-170

  Dvorakova Hortova K ^a   Sandera M ^a   Jursova M ^a   Vasinova J ^a   Peknicova J ^b  

^a CHARLES UNIVERSITY   (Czech Republic)

^b INSTITUTE OF MOLECULAR GENETICS   (Czech Republic)

Author keywords

Aluminium; Capacitation; Fluorides; Sperm; Tyrosine phosphorylation

Indexed keywords

ALUMINUM; FLUORIDE;

ANIMAL; ARTICLE; BAGG ALBINO MOUSE; DOSE RESPONSE; DRUG EFFECT; MALE; MOUSE; ORGAN SIZE; PATHOLOGY; POLLUTANT; SPERMATOZOON; SPERMATOZOON CAPACITATION; TESTIS;

ALUMINUM; ANIMALS; DOSE-RESPONSE RELATIONSHIP, DRUG; ENVIRONMENTAL POLLUTANTS; FLUORIDES; MALE; MICE; MICE, INBRED BALB C; ORGAN SIZE; SPERM CAPACITATION; SPERMATOZOA; TESTIS;

MUS;

EID: 49749088954     PISSN: 03784320     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.anireprosci.2007.07.015     Document Type: Article

References (42)

1. Asquith K.L., Baleato R.M., McLaughlin E.A., Nixon B., and Aitken J. Tyrosine phosphorylation activates surface chaperones facilitating sperm-zona recognition. J. Cell. Sci. 117 16 (2004) 3645-3657
2. Baker M.A., Hetherington L., Ecroyd H., Roman S.D., and Aitken R.J. Analysis of the mechanism by which calcium negatively regulates the tyrosine phosphorylation cascade associated with sperm capacitation. J. Cell. Sci. 117 2 (2004) 211-222
3. Barnett, and Dickson. Milk production and consumption and growth of young of wild mice after ten generations in a cold environment. J. Physiol. 346 (1984) 409-417
4. Bavister B.D. A consistently successful procedure for in vitro fertilization of golden hamster eggs. Gamete Res. 23 2 (1989) 139-158
5. Baxendale R.W., and Fraser L.R. Evidence for multiple distinctly localized adenylyl cyclase isoforms in mammalian spermatozoa. Mol. Reprod. Dev. 66 (2003) 181-189
6. Bond, A.M., Hefter, G.T., 1980. Critical survey of stability constants and related thermodynamic data of fluoride complexes in aqueous solution. In: IUPAC Chemical Data Series, No. 27. Pergamon, Oxford.
7. Breitbart H., Cohen G., and Rubinstein S. Role of actin cytoskeleton in mammalian sperm capacitation and the acrosome reaction. Reproduction 129 (2005) 263-268
8. Brener E., Rubinstein S., Cohen G., Shternall K., Rivlin J., and Breitbart H. Remodeling of the actin cytoskeleton during mammalian sperm capacitation and acrosome reaction. Biol. Reprod. 68 (2003) 837-845
9. Chabre M. Aluminofluoride and beryllofluoride complexes: a new phosphate analogs in enzymology. Trends Biochem. Sci. 15 1 (1990) 6-10
10. Chinoy N.J., and Narayana M.V. In vitro fluoride toxicity in human spermatozoa. Reprod. Toxicol. 8 2 (1994) 155-159
11. Chinoy N.J., and Patel T.N. Effects of sodium fluoride and aluminium chloride on ovary and uterus of mice and their reversal by some antidotes. Fluoride 34 1 (2001) 9-20
12. Coggeshall K.M., and Altman A. Stimulation of PIP2 hydrolysis by aluminum fluoride in resting T cell subsets of normal and autoimmune-prone lpr mice. J. Immunol. 143 3 (1989) 780-786
13. Cohen G., Rubinstein S., Gur Y., and Breitbart H. Crosstalk between protein kinase A and C regulates phospholipase D and F-actin formation during sperm capacitation. Dev. Biol. 267 (2004) 230-241
14. Darmani H., Al-Hiyasat A.S., and Elbetieha A.M. Effects of sodium fluoride in drinking water on fertility in female mice. Fluoride 34 4 (2001) 242-249
15. Dong C., Huang F., Deng H., Schaffrath Ch., Spencer J.B., O'Hagan D., and Naismith J.H. Crystal structure and mechanism of a bacterial fluorinating enzyme. Nature 427 (2004) 561-565
16. Dominguez L., Diaz A., Fornes M.W., and Mayorga L.S. Reagents that activate GTP-binding proteins trigger the acrosome reaction in human spermatozoa. Int. J. Androl. 18 4 (1995) 203-207
17. Dvorakova K., Moore H.D.M., Sebkova N., and Palecek J. Cytoskeleton localization in the sperm head prior to fertilization. Reproduction 130 (2005) 61-69
18. Ghosh D., Das S.(S.), Maiti R., Jana D., and Das U.B. Testicular toxicity in sodium fluoride treated rats: association with oxidative stress. Reprod. Toxicol. 16 (2002) 385-390
19. Graybill J.R., Najvar L.K., Fothergill A., Hardin T., Rinaldi M., Lambros C., and Regen S.L. KY-62, a polyene analog of amphotericin B, for treatment of murine candidiasis. Antimicrob. Agents Chemother. 42 1 (1998) 147-150
20. Kahama R.W., Damen J.J., and ten Cate J.M. Enzymatic release of sequestered cows' milk fluoride for analysis by the hexamethyldisiloxane microdiffusion method. Analyst 122 8 (1997) 855-858
21. Kleuss C., Raw A.S., Lee E., Sprang S.R., and Gilman A.G. Mechanism of GTP hydrolysis by G-protein α subunits. Proc. Natl. Acad. Sci. U.S.A. 91 (1994) 9828-9831
22. Kumar A., and Susheela A.K. Effects of chronic fluoride toxicity on the morphology of ductus epididymis and the maturation of spermatozoa of rabbit. Int. J. Exp. Pathol. 76 1 (1995) 1-11
23. Li l., and Fleming N. Aluminum fluoride inhibits phospholipase D activation by a GTP-binding protein-independent mechanism. FEBS Lett. 458 (1999) 419-423
24. Moos J., Peknicova J., and Tesarik J. Relationship between molecular conversion of acrosin and the progression of exocytosis in the ionophore-induced AR. Biochim. Biophys. Acta 1176 (1993) 199-207
25. Narayana M.V., and Chinoy N.J. Reversible effects of sodium fluoride ingestion on spermatozoa of the rat. Int. J. Fertil. Menopausal Stud. 39 6 (1994) 337-346
26. Naz R.K., Ahmad K., and Kumar R. Role of membrane phosphotyrosine proteins in human spermatozoal function. J. Cell. Sci. 99 Pt I (1991) 157-165
27. Naz R.K., and Rajesh P.B. Role of tyrosine phosphorylation in sperm capacitation/acrosome reaction. Reprod. Biol. Endocrinol. 2 (2004) 75
28. NHDS, New Hampshire Department of Environmental Services, 2006. Fluoride: Health Information Summary. http://www.des.state.nh.us/factsheets/ehp/inc/14.html.
29. Nixon B., Paul J.W., Spiller C.M., Attwell-Heap A.G., Ashman L.K., and Aitken R.J. Evidence for the involvement of PECAM-1 in a receptor mediated signal-transduction pathway regulating capacitation-associated tyrosine phosphorylation in human spermatozoa. J. Cell. Sci. 118 20 (2005) 4865-4877
30. Nopakun J., Messer H.H., and Voller V. Fluoride absorption from the gastrointestinal tract of rats. J. Nutr. 119 10 (1989) 1411-1417
31. Ortiz-Pérez D., Rodrígues-Martínez M., Martínez F., Borja-Aburto V.H., Castelo J., Grimaldo J.I., de la Cruz E., Carrizales L., and Díaz-Barriga F. Fluoride-induced disruption of reproductive hormones in men. Environ. Res. 93 (2003) 20-30
32. Payne A.H., and O'Shaughnessy P.L. Structure, function and regulation of steroidogenic enzymes in the Leydig cell. In: Payne A., Hardy M., and Ruccell L. (Eds). The Leydig Cell (1996), Cache River Press, Viena 259-285
33. Pushpalatha T., Srinivas M., and Sreenivasula Reddy P. Exposure to high fluoride concentration in drinking water will affect spermatogenesis and steroidogenesis in male albino rats. Biometals 18 (2005) 207-212
34. Richburg J.H., Nanez A., Williams L.R., Embree M.E., and Boekelheide K. Sensitivity of testicular germ cells to toxicant-induced apoptosis in gld mice that express a nonfunctional form of Fas ligand. Endocrinology 141 2 (2002) 787-793
35. Sohn J.H., Lee H.W., Han D.P., Yeh B.I., Choi J.W., Jung S., and Kim H.W. Investigation of fluoroaluminate complex formation using NMR spectroscopy. Bull. Korean Chem. Soc. 20 4 (1999) 481-483
36. Sternweis P.C., and Gilman A.G. Aluminum: a requirement for activation of the regulatory component of adenylate cyclase by fluoride. Proc. Natl. Acad. Sci. U.S.A. 78 16 (1982) 4888-4891
37. Stunff H.L., Dokhac L., Bourgoin S., Bader M.-F., and Harbon S. Phospholipase D in rat myometrium: occurrence of a membrane-bound ARF6 (ADP-ribosylation factor 6)-regulated activity controlled by βγ subunits of heterotrimeric G-proteins. Biochem. J. 352 (2000) 491-499
38. Troullier A., Girardet J.L., and Dupont Y. Fluoroaluminate complexes are bifunctional analogues of phosphate in sarcoplasmic reticulum Ca(2+)-ATPase. J. Biol. Chem. 267 32 (1992) 22821-22829
39. Visconti P.E., Bailey J.L., Moore G.D., Dieyun P., Olds-Clarke P., and Kopf G.S. Capacitation of mouse spermatozoa I. Correlation between the capacitation state and protein tyrosine phosphorylation. Development 121 (1995) 1129-1137
40. Visconti P.E., Moore G.D., Bailey J.L., Pan D., Leclerc P., Connors S.A., Olds-Clarke P., and Kopf G.S. Capacitation of mouse spermatozoa II. capacitacion and protein tyrosine phosphorylation are regulated by a cAMP-dependent pathway. Development 121 (1995) 1139-1150
41. WHO Prevention of Oral Diseases, 1987. WHO Offset Publication 103. WHO, Geneva.
42. Woo A.L., James P.F., and Lingrel J.B. Sperm motility is dependent on a unique isoform of the Na K-ATPase. J. Biol. Chem. 275 27 (2000) 20693-20699