Skip to main content
Journal of Assisted Reproduction and Genetics logoLink to Journal of Assisted Reproduction and Genetics
. 2001 Mar;18(3):144–150. doi: 10.1023/A:1009420306173

CLINICAL ASSISTED REPRODUCTION: Seminal Plasma and IVF Potential

Melissa F Lay 1, M Elaine Richardson 1, William R Boone 2, Ashby B Bodine 1, Ronald J Thurston 1
PMCID: PMC3455596  PMID: 11411429

Abstract

Purpose: Many components of seminal plasma play a role in sperm motility by serving as energy sources. Human seminal plasma contains over 30 proteins, including forward motility proteins, antifertility proteins, and coagulation/liquefaction proteins. This study was designed to determine any correlation between motility or fertilization rates and concentrations of fructose, lactic acid, citric acid, carnitine, and protein in human seminal plasma.

Methods: Fertilization rates were determined by in vitro methods. Fructose, lactic acid, citric acid, and carnitine concentrations were ascertained using high performance liquid chromatography. Protein concentration was determined by Bradford assay.

Results: Protein concentrations were significantly different as a function of sperm motility levels. Other constituents of human seminal plasma showed an overall correlation, though not significant. No constituent exhibited significant differences as a function of fertility levels.

Conclusions: Protein concentration was significantly lower for samples with high motility. No significant differences between fertility levels and constituents measured were found.

Keywords: amines, carbohydrates, in vitro fertilization, semen, seminal plasma

Full Text

The Full Text of this article is available as a PDF (66.4 KB).

REFERENCES

  • 1.Yablonsky T. Male Fertility Testing. Lab Med. 1996;27(6):378–383. [Google Scholar]
  • 2.Setchell BP, Brooks DE. Anatomy, vasculature, innervation and fluids of the male reproductive tract. In: Knobil E, Neill JD, editors. The Physiology of Reproduction. 2nd Ed. New York: Raven Press; 1994. p. 814. [Google Scholar]
  • 3.Ayyagari RR, Fazleabas AT, Dawood MY. Seminal plasma proteins of fertile and infertile men analyzed by two-dimensional electrophoresis. Am J Obst Gyn. 1987;157(6):1528–1533. doi: 10.1016/s0002-9378(87)80257-0. [DOI] [PubMed] [Google Scholar]
  • 4.Mann T, Lutwak-Mann C. Male Reproductive Function and Semen. New York: Springer-Verlag, Berlin; 1981. [Google Scholar]
  • 5.Mann T. The Biochemistry of Semen and of the Male Reproductive Tract. New York: JohnWiley and Sons; 1964. [Google Scholar]
  • 6.Zaneveld LJD, Chatterton RT. Biochemistry of Mammalian Reproduction. New York: JohnWiley and Sons; 1982. [Google Scholar]
  • 7.Quinlivan WLG. Analysis of the proteins in human seminal plasma. Arch Bioch Biophy. 1968;127:680–687. doi: 10.1016/0003-9861(68)90278-6. [DOI] [PubMed] [Google Scholar]
  • 8.Tauber PF, Zaneveld LJD, Propping D, Schumacher GFB. Components of human split ejaculates. I. Spermatozoa, fructose, immunoglobulins, albumin, lactoferrin, transferrin and other plasma proteins. J Reprod Fert. 1975;43:249–267. doi: 10.1530/jrf.0.0430249. [DOI] [PubMed] [Google Scholar]
  • 9.Davis ME, McCune WW. Fructolysis of human spermatozoa. Fert Ster. 1950;1(4):362–372. doi: 10.1016/s0015-0282(16)30246-1. [DOI] [PubMed] [Google Scholar]
  • 10.Dhanotiya RS, Srivastava RK. Relationship between sperm concentration, initial fructose concentration and different measures of fructolysis in buffalo semen. J Agr Sci in Cambridge. 1979;92:545–547. [Google Scholar]
  • 11.Calvin J, Tubbs PK. Mitochondrial transport processes and oxidation of NADH by hypotonically-treated boar spermatozoa. European J Bioch. 1978;89:315–320. doi: 10.1111/j.1432-1033.1978.tb20929.x. [DOI] [PubMed] [Google Scholar]
  • 12.Storey BT, Kayne FJ. Energy metabolism of spermatozoa. VI. Direct intramitochondrial lactate oxidation by rabbit sperm mitochondria. Bio Reprod. 1977;16:549–556. [PubMed] [Google Scholar]
  • 13.Pande SV, Parvin R. Carnitine-acylcarnitine translocasemediated transport of fatty acids into mitochondria: Its involvement in the control of fatty acid oxidation in liver. In: Frenkel RA, McGary JD, editors. Carnitine Biosynthesis, Metabolism and Functions. London: Academic Press; 1980. pp. 143–155. [Google Scholar]
  • 14.Menchini-Fabris GF, Canale D, Izzo PL, Olivieri L, Bartelloni M. Free L-carnitine in human semen: Its variability in different andrological pathologies. Fert Ster. 1984;42(2):263–267. doi: 10.1016/s0015-0282(16)48024-6. [DOI] [PubMed] [Google Scholar]
  • 15.Brooks DE. Carnitine in the male reproductive tract and its relation to the metabolism of the epididymis and spermatozoa. In: Frankel RA, McGary JD, editors. Carnitine Biosynthesis, Metabolism, and Functions. London: Academic Press; 1980. pp. 219–235. [Google Scholar]
  • 16.Hinton BT, Brooks DE, Dott HM, Setchell BP. Effects of carnitine and some related compounds on the motility of rat spermatozoa from caput epididymis. J Reprod Fert. 1981;61:59–64. doi: 10.1530/jrf.0.0610059. [DOI] [PubMed] [Google Scholar]
  • 17.Hinton BT, Setchell BP. Concentration and uptake of carnitine in the rat epididymis: A micropuncture study. In: Frenkel RA, McGary JD, editors. Carnitine, Biosynthesis, Metabolism, and Functions. London: Academic Press; 1980. pp. 237–248. [Google Scholar]
  • 18.Hamamah S, Seguin F, Barthelemy C, Akoka S, LePape A, Lansac J, Royere D. H nuclear magnetic resonance studies of seminal plasma from fertile and infertile men. J Reprod Fert. 1993;97:51–55. doi: 10.1530/jrf.0.0970051. [DOI] [PubMed] [Google Scholar]
  • 19.Kavanagh JP. Sodium, potassium, calcium, magnesium, zinc, citrate and chloride content of human prostatic and seminal fluid. J Reprod Fert. 1985;75:35–41. doi: 10.1530/jrf.0.0750035. [DOI] [PubMed] [Google Scholar]
  • 20.Huggins C. The physiology of the prostate gland. Phys Rev. 1945;25:281–293. [Google Scholar]
  • 21.Rolf C, Behre HM, Cooper TG, Koppers B, Nieschlag E. Creatine kinase activity in human spermatozoa and seminal plasma lacks predictive value for male fertility in in vitro fertilization. Fert Ster. 1998;69(2):727–734. doi: 10.1016/s0015-0282(97)00570-0. [DOI] [PubMed] [Google Scholar]
  • 22.Spiessens C, D'Hooghe T, Wouters E, Meuleman C, Vanderschueren D. α-Glycosidase activity in seminal plasma: Predictive value for outcome in intrauterine insemination and in vitro fertilization. Fert Ster. 1998;69(4):735–739. doi: 10.1016/s0015-0282(97)00569-4. [DOI] [PubMed] [Google Scholar]
  • 23.WHO Laboratory Manual for the Examination of Human Semen and Sperm-Cervical Mucus Interaction. 3rd Ed. Cambridge: Cambridge University Press; 1992. [Google Scholar]
  • 24.Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Bioch. 1976;72:248–254. doi: 10.1006/abio.1976.9999. [DOI] [PubMed] [Google Scholar]
  • 25.Biswas S, Ferguson KM, Stedronska J, Baffoe G, Mansfield MD, Kosbab MH. Fructose and hormone levels in semen: Their correlations with sperm counts and motility. Fert Ster. 1978;30(2):200–204. doi: 10.1016/s0015-0282(16)43460-6. [DOI] [PubMed] [Google Scholar]
  • 26.Sakkas D, Urner F, Menezo Y, Leppens G. Effects of glucose and fructose on fertilization, cleavage and viability of mouse embryos in vitro. Bio Reprod. 1993;49:1288–1292. doi: 10.1095/biolreprod49.6.1288. [DOI] [PubMed] [Google Scholar]
  • 27.Jeyendran RS, Van der Ven HH, Rosecrans R, Perez-Pelaez M, Al-Ha S, Zaneveld LJD. Chemical constituents of human seminal plasma: Relationship to fertility. Andrologia. 1989;21(5):423–428. [PubMed] [Google Scholar]
  • 28.Oefner P, Bonn G, Bartsch G. High-performance liquid chromatographic analysis of citric acid, inositol and fructose in boar and bull seminal plasma. Andrologia. 1985;17(3):250–253. doi: 10.1111/j.1439-0272.1985.tb00997.x. [DOI] [PubMed] [Google Scholar]
  • 29.Bremer J. Carnitine-metabolism and functions. Phys Rev. 1983;63(4):1420–1465. doi: 10.1152/physrev.1983.63.4.1420. [DOI] [PubMed] [Google Scholar]
  • 30.Suter DA, Holland MK. The concentrations of free L-carnitine and L-O-acetylcarnitine in spermatozoa and seminal plasma of normal, fresh, and frozen human semen. Fert Ster. 1979;31:541–544. doi: 10.1016/s0015-0282(16)44001-x. [DOI] [PubMed] [Google Scholar]
  • 31.Soufir JC, Ducot B, Marson J, Jouannet P, Feneux D, Soumah A, Spira A. Levels of seminal free L (-) carnitine in fertile and infertile men. Int J Androl. 1984;7:188–197. doi: 10.1111/j.1365-2605.1984.tb00776.x. [DOI] [PubMed] [Google Scholar]
  • 32.Brooks DE. Carnitinine, acetylcarnitine and the activity of carnitine acyltransferases in seminal plasma and spermatozoa of men, rams and rats. J Reprod Fert. 1979;56:667–673. doi: 10.1530/jrf.0.0560667. [DOI] [PubMed] [Google Scholar]
  • 33.Lewin LM, Beer R, Lunenfeld B. Epididymis and seminal vesicle as sources of carnitine in human seminal fluid: The clinical significance of the carnitine concentration in human seminal fluid. Fert Ster. 1976;27(1):9–13. doi: 10.1016/s0015-0282(16)41589-x. [DOI] [PubMed] [Google Scholar]
  • 34.Kohengkul S, Tanphaichitr V, Muangmun V., Tanphaichitr N. Levels of L-carnitine and L-O-acetylcarnitine in normal and infertile human semen: A lower level of L-O acetylcarnitine in infertile semen. Fert Ster. 1977;28(12):1333–1336. doi: 10.1016/s0015-0282(16)42979-1. [DOI] [PubMed] [Google Scholar]
  • 35.Casillas ER, Erickson BJ. The role of carnitine in spermatozoan metabolism: Substrate-induced elevations in the acetylation state of carnitine and Coenzyme A in bovine and monkey semen. Biol Reprod. 1975;12:275–283. doi: 10.1095/biolreprod12.2.275. [DOI] [PubMed] [Google Scholar]
  • 36.Desnoyers L, Therien I, Manjunath P. Characterization of the major proteins of bovine seminal fluid by twodimensional polyacrylamide gel electrophoresis. Mol Reprod Dev. 1994;37:425–435. doi: 10.1002/mrd.1080370409. [DOI] [PubMed] [Google Scholar]
  • 37.Manjunath P, Chandonnet L, Leblond E, Desnoyers L. Major proteins of bovine seminal vesicles bind to spermatozoa. Bio Reprod. 1993;49:27–37. doi: 10.1095/biolreprod50.1.27. [DOI] [PubMed] [Google Scholar]
  • 38.Desnoyers L, Manjunath P. Major proteins of bovine seminal plasma exhibit novel interactions with phospholipd. J Biol Chem. 1992;267(14):10149–10155. [PubMed] [Google Scholar]
  • 39.Manjunath P, Sairam MR. Purification and biochemical characterization of three major acidic proteins (BSP-A1, BSP-A2, BSP-A3) from bovine seminal plasma. Bioch J. 1987;241:685–692. doi: 10.1042/bj2410685. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Brooks DE, Higgins SJ. Characterization and androgendependence of proteins associated with luminal fluid and spermatozoa in the rat epididymis. J Reprod Fert. 1980;59:363–375. doi: 10.1530/jrf.0.0590363. [DOI] [PubMed] [Google Scholar]
  • 41.Cameo MS, Blaquier JA. Androgen-controlled specific proteins in rat epididymis. J Endo. 1976;69:47–55. doi: 10.1677/joe.0.0690047. [DOI] [PubMed] [Google Scholar]
  • 42.Lindholmer C, Carlstrom A, Eliasson R. Occurrence and origin of proteins in human seminal plasma with special reference to albumin. Andrologia. 1974;6(2):181–196. doi: 10.1111/j.1439-0272.1974.tb01619.x. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Assisted Reproduction and Genetics are provided here courtesy of Springer Science+Business Media, LLC

RESOURCES