Effects of antifertility drugs on epididymal protein secretion, acquisition of sperm surface proteins and fertility in male rats
- 1 December 1981
- journal article
- research article
- Published by Wiley in International Journal of Andrology
- Vol. 4 (1-6) , 703-712
- https://doi.org/10.1111/j.1365-2605.1981.tb00754.x
Abstract
The possibility that .alpha.-chlorohydrin, 6-chloro-6-deoxyglucose (6CDG) and cyproterone acetate (CPA) might affect epididymal protein secretion or acquisition of sperm surface proteins as the cause of their antifertility action in male rats was investigated. Daily administration of 9 mg/kg .alpha.-chlorohydrin for 7-14 days and 24 mg/kg 6CDG for 14-21 days induced sterility in male rats and impaired the capacity of the cauda epididymal spermatozoa to initiate motility. Treatment with CPA (30 mg/kg per day) for 21-28 days had no effect on fertility and initiation of sperm motility, although the epididymis of the treated animals underwent a loss in weight. The antifertility effects of .alpha.-chlorohydrin or 6CDG did not seem to be attributed to an interference with epididymal protein secretion. The cauda epididymal fluids of the .alpha.-chlorohydrin, 6CDG and CPA treated animals have similar protein patterns compared to those of the control animals. When the surface proteins of the spermatozoa were labeled with radioactive iodine, the sperm surface proteins of the .alpha.-chlorohydrin and 6CDG treated animals differed from those of the control animals. Two peaks (MW 32,000 and 70,000) and 1 peak (70,000) were significantly reduced in the .alpha.-chlorohydrin treated and 6CDG treated animals, respectively. Additional bands appeared on the surface of the treated (infertile) animals. CPA treatment did not affect the surface protein pattern of the epididymal spermatozoa. The antifertility affects of .alpha.-chlorohydrin and 6CDG are not due to an interference with epididymal secretion of specific proteins but to an intervention of the subsequent acquisition of these proteins by epididymal spermatozoa. This results in a decrease in the capacity of the epididymal sperm to initiate motility and hence a loss of fertilizing capacity.Keywords
This publication has 19 references indexed in Scilit:
- The effects of extracellular sodium on acid release and motility initiation in rat caudal epididymal spermatozoa in vitroExperimental Cell Research, 1981
- Use of low-dosage oral cyproterone acetate as a male contraceptiveContraception, 1980
- Absorptive and secretory functions of the perfused rat cauda epididymidis.The Journal of Physiology, 1978
- EFFECTS OF TESTOSTERONE, TESTOSTERONE METABOLITES AND ANTI-ANDROGENS ON THE FUNCTION OF THE MALE ACCESSORY GLANDS IN THE RABBIT AND RATJournal of Endocrinology, 1977
- Cyproterone Acetate: I. Microquantity Releasing Device of Cyproterone Acetate and its Failure in Inducing Functional Sterility in Male Rats*Andrologia, 1977
- Continuous oral low-dosage cyproterone acetate for fertility regulation in the male? — A trend analysis in 15 volunteers —Contraception, 1976
- Release of microquantities of cyproterone acetate from subcutaneous silastic capsules: Failure to produce an antifertility effectContraception, 1976
- Failure to induce sterility in male rats with microdoses of cyproterone acetate (CPA)Contraception, 1975
- Identification of the biochemical lesion produced by α-chlorohydrin in spermatozoaNature, 1975
- Fertility control in male rats by continuous release of microquantities of cyproterone acetate from subcutaneous silastic capsulesContraception, 1970