Abstract
Necrozoospermia is still a poorly understood cause of male infertility. It is defined as a condition in which spermatozoa in the ejaculated semen are dead. According to sperm norms of the World Health Organization (WHO) (1), sperm viability is higher than or equal to 75% in human semen samples. Fertility of the semen is impaired below this percentage. Necrozoospermia is a rare condition with a reported prevalence of 0.2-0.48% in infertile subjects (2,3).
This is a preview of subscription content, log in via an institution.
Buying options
Tax calculation will be finalised at checkout
Purchases are for personal use only
Learn about institutional subscriptionsPreview
Unable to display preview. Download preview PDF.
References
World Health Organization. WHO laboratory manual for the examination of human semen and sperm cervical mucus interaction, 3rd Edition. London: Cambridge University Press, 1992.
Phadke AM, Samant NR, Dewal SD. Seminal fructose content in necrospermia. Fertil Steril 1975;26:1021–27.
Wilton LJ, Temple-Smith PD, Gordon Baker HW, de Kretser DM. Human male infertility caused by degeneration and death of sperm in the epididymis. Fertil Steril 1988;49:1052–58.
Schwartzman RA, Cidlowski JA. Apoptosis: the biochemistry and molecular biology of programmed cell death. Endocrinol Rev 1993;14:133–51.
Majno G, Joris I. Apoptosis, oncosis and necrosis. Am J Pathol 1995;146:3–15.
Duvall E, Wyllie AH. Death and the cell. Immunol Today 1986;7:115–19.
Kerr JFR, Wyllie AH, Currie AR. Apoptosis: a basic biological phenomenon with wide-ranging implications in tissue kinetics. Br J Cancer 1972;26:239–57.
Martimbeau S, Tilly JL. Physiological cell death in endocrine-dependent tissues: an ovarian perspective. Clin Endocrinol 1997;46:241–54.
Vaux DL. Toward an understanding of the molecular mechanisms of physiological cell death. ProcNatl Acad Sci 1993;90:786–89.
Reed JC. Bcl-2 and the regulation of programmed cell death. J Cell Biol 1994;124:1–6.
Miyashita T, Reed JC. Tumor suppressor p53 is a direct transcriptional activator of the human box gene. Cell 1995;80:293–99.
Russell LD, Clermont Y. Degeneration of germ cells in normal, hypophysecto-mized and hormone-treated hypophysectomized rats. Anat Rec 1977;87:347–66.
Tapanainen J, Tilly JL, Vikho KK, Hsueh AJW. Hormonal control of apoptotic cell death in the testis: gonadotropins and androgens as testicular cells survival factors. Mol Endocrinol 1993;7:643–50.
Sinha Hikim AP, Wang C, Leung A, Swerdloff R. Involvement of apoptosis in the induction of germ cell degeneration in adult rats after gonadotropin-releasing hormone agonist treatment. Endocrinology 1995;136:2770–75.
Brinkworth MH, Weinbauer GF, Bergmann M, Nieshlag E. Apoptosis as a mechanism of germ cell loss in elderly men. Int J Androl 1997;20:222–28.
Roosen-Runge EC. The generation of pre-spermatogonial germ cells in the rat after birth. Anat Rec 1964;148:328.
Miething A. Germ-cell death during prespermatogenesis in the testis of the golden hamster. Cell Tissue Res 1992;267:583–90.
Hockenberry DM, Zutter M, Hickey W, Nahm M, Korsmeyer SJ. BCL2 protein is topographically restricted in tissues characterized by apopototic cell death. Proc Natl Acad Sci 1991;88:6961–65.
Knudson CM, Tung KSK, Tourtellotte WG, Brown GAJ, Korsmeyer SJ. Bax-deficient mice with lymphoid hyperplasia and male germ cell death. Science 1995;270:96–99.
Krajewski S, Krajewska M, Shabaik A, Miyashita T, Wang HG, Reed JC. Immu-nohistochemical determination of in vivo distribution of Bax, a dominant inhibitor ofBcl-2. Am J Pathol 1994;145:1323–26.
Hockenberry DM, Oltvai ZN, Yin XM, Milliman CL, Korsmeyer SJ. Bcl-2 functions as an antioxidant pathway to prevent apoptosis. Cell 1993;75:241–51.
Aitken RJ. A free radical theory of male infertility. Reprod Fertil Dev 1994;6:19–24.
de Lamirande E, Gagnon C. Reactive oxygen species and human spermatozoa. I. Effects on the motility and on sperm axonems. J Androl 1992;13:368–78.
Plante M, De Lamirande E, Gagnon C. Reactive oxygen species released by activated neutrophils, but not by deficient spermatozoa, are sufficient to affect normal sperm motility. Fertil Steril 1994;62:387–92.
Aitken RJ, Buckingham DW, Brindle J, Gomez E, Gordon Baker HW, Irvine DS. Analysis of sperm movement in relation to the oxidative stress created by leukocytes in washed sperm preparations and seminal plasma. Hum Reprod 1995;10:2061–71.
Perry ACF, Jones R, Hall L. Isolation and characterization of a rat cDNA clone encoding a secreted Superoxide dismutase reveals the epididymis to be a major site of its expression. Biochem J 1993;293:21–25.
Kobayashi T, Miyazaki T, Natori M, Nozawa S. Protective role of Superoxide dismutase in human sperm motility: Superoxide dismutase activity and lipid perox-ide in human seminal plasma and spermatozoa. Hum Reprod 1991;7:987–91.
Zini A, De Lamirande E, Gagnon C. Reactive oxygen species in semen of infertile patients: levels of superoxyde dismutase-and catalase-like activities in seminal plasma and spermatozoa. Int J Androl 1993;16:183–88.
Jeulin C, Soufir JC, Webert P, Laval-Martin D, Calvayrac R. Catalase activity in human spermatozoa and seminal plasma. Gamete Res 1989;24:185–96.
Alvarez JG, Storey BT. Role of glutathione peroxidase in protecting mammalian spermatozoa from loss of motility caused by spontaneous lipid peroxidation. Gamete Res 1989;23:77–90.
Gavella M, Lipovac V, Vucic M, Rocic B. Superoxide anion scavenging capacity of human seminal plasma. Int JAndrol 1996;19:82–90.
Benhamed M. Tumor necrosis factor in the male gonad. Contracept Fertil Sex 1997;25:569–71.
Comhaire FE, Bosmans W, Ombelet U, Punjabi H, Schoonjans F. Cytokines in semen of normal men and of patients with andrological diseases. Am J Reprod Immunol 1994;31:99–103.
Naz RK, Chaturvedi MM, Aggarwal BB. Role of cytokines and protooncogenes in sperm cell function: relevance to immunologic infertility. Am J Reprod Immunol 1994;32:26–37.
Estrada LS, Champion HC, Wang R, et al. Effect of tumour necrosis factor-alpha (TNF-alpha) and interferon-gamma (INF-gamma) on human sperm motility, viability and motion parameters. Int J Androl 1997;20:237–42.
Whitman ED, Doherty GM, Peplinski GR, Norton JA. Role of cytokines in oxydative damage. In: Aggarwal B, Puri R, editors. Human cytokines: their role in disease and therapy, Chapter 22. Oxford: Blackwell Science, 1995:333.
Sikka S, Rajasekaran M, Hellstrom W. Role of oxidative stress and antioxidants in male infertility. J Androl 1995;16:464–68.
Buch JP, Kolon TF, Maulik N, Kreutzer DL, Das DK. Cytokines stimulate membrane lipid peroxidation of human sperm. Fertil Steril 1994;62:186–88.
Nagata S, Goldstein P. The Fas death factor. Science 1995;267:1449–56.
Gerhard I, Lenhard K, Eggert-Kruse W, Runnebaum B. Clinical data which influence semen parameters in infertile men. Hum Reprod 1992;7:830–37.
Clavert A, Cranz C, Tardieu J. Epididymis and genital infections. In: Hamamah S, Mieusset R, Dacheux J-L, editors. Frontiers in endocrinology. Epididymis role and importance in male infertility treatment, Vol. 11. Rome: Ares Serono Symposia, 1995:203–10.
Cooper TJ. Functions of human epididymis. In: Hamamah S, Mieusset R, Dacheux J-L, editors. Frontiers in endocrinology. Epididymis role and importance in male infertility treatment, Vol. 11. Rome: Ares Serono Symposia, 1995:1–12.
Mortimer D, Templeton AA, Lenton EA, Coleman RA. Influence of abstinence and ejaculation-to-analysis delay on semen analysis parameters of suspected infertile men. Arch Androl 1982;8:2516–20.
Sinisi AA, di Finizio B, Pasquali D, Corini A, Apuzzo D, Bellastella A. Prevalence of antisperm antibodies by sperm MAR test in subjects undergoing a routine sperm analysis for infertility. Int J Androl 1993;16:311–14.
El Gothamy Z, El Samahy H. Ultrastructure sperm defects in addicts. Fertil Steril 1992;47:699–702.
Villegas H, Pinon M, Shor V, Karchmer S. Electron microscopy of Chlamydia trachomatis infection of the male genital tract. Arch Androl 1991;27:117–26.
Hustin J, Koulischer L. Microscopie électronique des spermatozoïdes. Indications et résultats. Acta Urol Belg 1989;57:17–28.
Gopalkrishnan K, Padwal V, D′Souza S, Shah R. Severe asthenozoospermia: a structural and functional study. Int J Androl 1995;18(Suppl l):67–74.
Lerda D, Rizzi R. Study of reproductive function in persons occupationally exposed to 2,4-dichlorophenoxyacetic acid (2,4-D). Mutat Res 1991;262:47–50.
Kleinschmidt K, Weissbach L, Holstein AF. Fruherkennung des kontralateralen zweitkarzinoms bei hodentumorpatienten durch das carcinoma in situ testis. Urologe A 1989;28:281–84.
Jardin A, Izard V, Benoit G, Testart J, Belaisch-Allart J, Volante M, et al. Fécondance in vivo et in vitro de spermatozoïdes épididymaires humains immatures. Reprod Nutr Devl 1988;28:1375–85.
Cummins JM, Temple-Smith PD, Rentrée MB. Reproduction in male honeypossum (Tarsipes rostratus Marsupialia): the epididymis. Am J Anat 1986;177:385–93.
Palermo G, Joris H, Devroey P, Van Sterteighem AC. Pregnancies after intracyto-plasmic injection of single spermatozoon into an oocyte. Lancet 1992;340:17–18.
Tournaye H, Liu J, Nagy Z, Verheyen G, Van Steirteghem A, Devroey P. The use of testicular sperm for intracytoplasmic sperm injection in patients with necrozoospermia. Fertil Steril 1996;66:331–34.
Cummins JM, Jequier AM. Concerns and recommendations for intracytoplasmic sperm injection (ICSI) treatment. Hum Reprod 1995;10(Suppl l):138–43.
Nduwayo L, Barthélémy C, Lansac J, Tharanne MJ, Lecomte P. Necrospermia and human male infertility. Contracept Fertil Sex 1995;23:682–85.
Skakkebaek NE, Giwercman A, De Kretser D. Pathogenesis and management of male infertility. Lancet 1994;343:1473–74.
Zamboni L. Sperm pathology and infertility. Fertil Steril 1987;48:726–31.
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1999 Springer Science+Business Media New York
About this chapter
Cite this chapter
Lecomte, P.J., Barthelemy, C., Nduwayo, L., Hamamah, S. (1999). Necrospermia: Etiology and Management. In: Hamamah, S., Olivennes, F., Mieusset, R., Frydman, R. (eds) Male Sterility and Motility Disorders. Serono Symposia USA. Springer, New York, NY. https://doi.org/10.1007/978-1-4612-1522-6_6
Download citation
DOI: https://doi.org/10.1007/978-1-4612-1522-6_6
Publisher Name: Springer, New York, NY
Print ISBN: 978-1-4612-7177-2
Online ISBN: 978-1-4612-1522-6
eBook Packages: Springer Book Archive