The objective of this study is to gain information concerning the biochemistry of certain human sperm acrosomal enzymes, seminal antifertility agents, and the fluids of the male and female genital tract; and how these interact during sperm transit, capacitation and fertilization. Additionally, the presence and activity of these compounds will be investigated under certain clinical conditions, and non-hormonal, chemical contraceptive methodology will be developed. Sperm acrosin and hyaluronidase are known to have an important role in the fertilization process. These enzymes will be purified from human spermatozoa and characterized. Particular emphasis will be placed on their kinetic properties, their reaction with synthetic inhibitors, and the different enzyme forms. The role of the acrosomal enzymes and their natural inhibitors in the reproductive process will be determined as well as the changes that the enzyme systems undergo during certain physiological and clinical events. A high molecular weight antifertility factor present in human seminal plasma will be purified, characterized, and its mechanism of action assesed. Synthetic enzyme inhibitors will be studied for their contraceptive properties and their clinical application. The protein components of human seminal plasma from infertile men will be measured and compared to those of normal men. A profile will be obtained of the cyclic changes of certain protein components from human uterine fluid and genital tract mucosa that may have a role in the reproductive processes. The proposed studies will therefore lead to a better understanding of reproduction in man, to the development of new contraceptives, and to improved diagnostic and treatment technology for infertility.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD019555-03
Application #
3316903
Study Section
Reproductive Biology Study Section (REB)
Project Start
1984-04-01
Project End
1987-08-31
Budget Start
1985-09-01
Budget End
1987-08-31
Support Year
3
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Rush University Medical Center
Department
Type
DUNS #
City
Chicago
State
IL
Country
United States
Zip Code
60612
Drisdel, R C; Mack, S R; Anderson, R A et al. (1995) Purification and partial characterization of acrosome reaction inhibiting glycoprotein from human seminal plasma. Biol Reprod 53:201-8
Anderson Jr, R A; Feathergill, K A; Rawlins, R G et al. (1995) Atrial natriuretic peptide: a chemoattractant of human spermatozoa by a guanylate cyclase-dependent pathway. Mol Reprod Dev 40:371-8
Bielfeld, P; Faridi, A; Zaneveld, L J et al. (1994) The zona pellucida-induced acrosome reaction of human spermatozoa is mediated by protein kinases. Fertil Steril 61:536-41
Anderson, R A; Feathergill, K A; Drisdel, R C et al. (1994) Atrial natriuretic peptide (ANP) as a stimulus of the human acrosome reaction and a component of ovarian follicular fluid: correlation of follicular ANP content with in vitro fertilization outcome. J Androl 15:61-70
Bielfeld, P; Jeyendran, R S; Zaneveld, L J (1993) Osmo-sensitivity of the human sperm acrosome reaction. Hum Reprod 8:1235-9
Blackwell, J; Kaminski, J M; Bielfeld, P et al. (1992) Human sperm acrosin. Further studies with the clinical assay and activity in a group of presumably fertile men. J Androl 13:571-8
Blackwell, J M; Zaneveld, L J (1992) Effect of abstinence on sperm acrosin, hypoosmotic swelling, and other semen variables. Fertil Steril 58:798-802
Jeyendran, R S; Van der Ven, H H; Zaneveld, L J (1992) The hypoosmotic swelling test: an update. Arch Androl 29:105-16
Mack, S R; Han, H L; De Jonge, J et al. (1992) The human sperm acrosome reaction does not depend on arachidonic acid metabolism via the cyclooxygenase and lipoxygenase pathways. J Androl 13:551-9
Zaneveld, L J; De Jonge, C J; Anderson, R A et al. (1991) Human sperm capacitation and the acrosome reaction. Hum Reprod 6:1265-74

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