2013, Number 2
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Rev Mex Med Repro 2013; 5.6 (2)
Determination of the Effect of Temperature on Spontaneous Acrosomal Reaction in Seminal Samples Before Assisted Reproduction Procedures
Neri VP, Torres FV, Vielma VAV, Gaona AR
Language: Spanish
References: 24
Page: 97-103
PDF size: 740.99 Kb.
ABSTRACT
Background: Sperm capacitation is a calcium dependentprocess
and is related to a cascade of biochemical changes.
Capacitated sperm may respond to receptors of zona pellucida
and increase even more the intracellular calcium level and with
high levels of progesterone in the female genital tract acrosomal
reaction is induced.
Objective: To determine the effect of incubation temperature
on the spontaneous acrosomal reaction in capacitated seminal
samples before assisted reproduction procedures.
Material and method: A prospective study was done with semen
samples obtained from 10 normosperm patients with three
to six days of sexual abstinence; fura ff-AM fluorescent optical
marker was used, which is able to detect the increased intracellular
calcium. Each sample was divided into two equal fractions:
capacitated samples incubated at environment temperature
(25ºC) and capacitated samples incubated at 37ºC.
Results: There was no significant difference in the spontaneous
acrosomal reaction rate between capacitated seminal samples
maintained at environment temperature and those incubated at
37ºC, even after four hours of capacitation; however, spontaneous
acrosomal reaction tended slightly to be higher in samples
incubated at 37ºC, because after progesterone addition, calcium
influx was lower.
Conclusions: Even though temperature is important for sperm
capacitation, it is not for acrosomal reaction; thus sperm maintained
at 25ºC have the same probability to do an acrosomal
reaction that those incubated at 37ºC.
REFERENCES
Darszon A, Nishigaki T, Wood C, Trevino CL, et al. Calcium channels and Ca2+ fluctuations in sperm physiology. Int Rev Cytol 2005;243:79-172.
Baldi E, Luconi M, Bonaccorsi L, Forti G. Signal transduction pathways in human spermatozoa. J Reprod Immunol 2002;53:121-131.
Cross NL, Razy-Faulkner P. Control of human sperm intracellular pH by cholesterol and its relationship to the response of the acrosome to progesterone. Biol Reprod 1997;56:1169-1174.
Suarez SS, Wolf DP, Meizel S. Induction of the acrosome reaction in human spermatozoa by a fraction of human follicular fluid. Gamete Res 1986;14:107-121.
O’Toole CM, Arnoult C, Darszon A, Steinhardt RA, et al. Ca(2+) entry through store-operated channels in mouse sperm is initiated by egg ZP3 and drives the acrosome reaction. Mol Biol Cell 200;11:1571-1584.
Mahi CA, Yanagimachi R. The effect of temperature, osmolarity and hydrogen ion concentration on the activation and the acrosome reaction of Golden hamster spermatozoa. J Reprod Fertil 1973;35:55-66.
Lenz RW, Ball GD, Leibfried ML, Ax RL, et al. In vitro maturation and fertilization of bovine oocytes are temperaturedependent processes. Biol Reprod 1983,29:173-179.
Fleming AD, Kuehl TJ. Effects of temperature upon capacitation of guinea pig spermatozoa. J Exp Zool 1985;233:405- 411.
Si Y. Temperature-dependent hyperactivated movement of hamster spermatozoa. Biol Reprod 1997;57:1407-1412.
White DR, Phillips DM, Bedford JM. Factors affecting the acrosome reaction in human spermatozoa. J Reprod Fertil 1990;90:71-80.
Yanagimachi R. In vitro acrosome reaction and capacitation of Golden hamster sperm by bovine follicular fluid and its fractions. J Exp Zool 1969;170:269-280.
Mortimer D, Curtis EF, Camenzind AR, Tanaka S. The spontaneous acrosome reaction of human spermatozoa incubated in vitro. Hum Reprod 1989;4:57-62.
Santi CM, Darszon A, Hernández-Cruz A. A dihydropyridinesensitive T-type Ca2+ current is the main Ca2+ current carrier in mouse primary spermatocytes. Am J Physiol 1996; 271:1583-1593.
Arnoult C, Cardullo RA, Lemos JR, Florman HM. Activation of mouse sperm T-type Ca2+ channels by adhesion to the egg zona pellucida. Proc Natl Acad Sci USA 1996;93:13004- 13009.
Arnoult C, Kazam IG, Visconti PE, Kopf GS, et al. Control of the low voltage-activated calcium channel of mouse sperm by egg ZP3 and by membrane hyperpolarization during capacitation. Proc Natl Acad Sci USA 1999;96:6757-6762.
Linares-Hernández L, Guzmán-Grenfell AM, Hicks-Gómez JJ, González-Martínez MT. Voltage dependent calcium influx in human sperm assessed by simultaneous detection of intracellular calcium and membrane potential. Biochim Biophys Acta 1998;1372:1-12.
Fraire-Zamora JJ, González-Martínez MT. Effect of intracellular pH on the depolarization-evoked calcium influx in human sperm. Am J Physiol 2004;287:1688-1696.
Torres-Flores V, Picazo-Juárez G, Hernández-Rueda Y, Darszon A, et al. Sodium influx induced by external calcium chelation decreases human sperm motility. Hum Reprod 2011;26:2626-2635.
González-Martínez MT, Bonilla-Hernández MA, Guzmán- Grenfell AM. Stimulation of voltage dependent calcium channels during capacitation and by progesterone in human sperm. Arch Biochem Biophys 2002;408:205-210.
Grynkievicz G, Poenie M, Tsien RY. A new generation of calcium indicators with greatly improved fluorescent properties. J. Biol. Chem. 1985. 260:3440-3450.
Marín-Briggiler CI, Tezón JG, Miranda PV, Vázquez-Levin MH. Effect of incubating human sperm at room temperature on capacitation-related events. Fertil Steril 2002;77:252- 259.
Harper C, Cummerson JA, White MRH, Publicover S, et al. Dynamic resolution of acrosomal exocytosis in human sperm. J Cell Sci 2008;121:2130-2135.
Tocanne JF, Dupou-Cézanne L, López A, Tournier JF. Lipid lateral diffusion and membrane organization. FEBS Lett 1989;257:10-16.
Green S, Fishel S, Rowe P. The incidence of spontaneous acrosome reaction in homogeneous populations of hyperactived human spermatozoa. Hum Reprod 1999;7:1819-1822.