Modulation of post-thaw sperm functions with oviductal proteins in buffaloes

• Published in: Animal reproduction science 2005-11, Vol.90 (1), p.73-84
• Main Authors: Kumaresan, A., Ansari, M.R., Garg, Abhishek
• Format: Article
• Language: English
• Subjects: acrosome; Acrosome - drug effects; ammonium sulfate; animal proteins; Animals; artificial insemination; Buffalo; Buffaloes; Cell Size; centrifugation; Cervix Mucus; chemical precipitation; cryopreservation; Cryopreservation - veterinary; estrous cycle; Fallopian Tubes - chemistry; Female; Fertility; filtration; Hot Temperature; Hypotonic Solutions; in vitro studies; Male; Oviductal proteins; oviducts; Proteins - pharmacology; semen extenders; Semen Preservation - veterinary; Sperm functions; sperm motility; Sperm Motility - drug effects; Sperm-Ovum Interactions - drug effects; Spermatozoa; Spermatozoa - drug effects; Spermatozoa - physiology
• ISSN: 0378-4320; 1873-2232
• DOI: 10.1016/j.anireprosci.2005.01.009

A study was undertaken to determine the effects of oviductal proteins obtained from various stages of the estrous cycle on spermatozoa characteristics in buffaloes. Oviducts were collected from apparently healthy buffalo genital tracts (nonluteal and luteal stage of estrous cycle) and separated into isthmus and ampulla. Each segment of oviduct (nonluteal and luteal) was flushed with PBS (pH 7.4). The flushing obtained was centrifuged (3000 rpm; 30 min), filtered (0.2 μm) and frozen at −20 °C. The proteins in pooled nonluteal isthmic and ampullary and luteal isthmic and ampullary fluids were precipitated overnight using ammonium sulphate, centrifuged (10000 rpm; 30 min) and dialyzed (>10 kDa). After protein estimation, aliquots of samples containing 10 mg proteins were lyophilized in cryovials and stored in frozen form at −20 °C. Six pooled good-quality ejaculates collected by artificial vagina method from two Murrah buffalo bulls were utilized for the study. After fresh semen analysis, each pooled ejaculate was splited into five parts and extended in Tris–egg yolk–citrate extender (20% egg yolk; 7% glycerol), so that final dilution yielded approximately 60 million sperm cells per ml, and cryopreserved in 0.5 ml French straws (30 million sperm cells/straw) in LN 2 (−196 °C). Before freezing, nonluteal isthmic and ampullary and luteal isthmic and ampullary proteins were incorporated at the rate of 1 mg/ml of extended semen. The equilibrated and frozen-thawed (37 °C for 30 s) semen was evaluated for motility, live %, acrosomal integrity percentage, bovine cervical mucus penetration test and hypo-osmotic sperm swelling test. Besides this, spermatozoa from treatment and control groups were incubated at 37 °C for 6 h in sperm TALP. Among the nonluteal and luteal oviductal proteins, the former maintained higher ( P < 0.05) post-thaw sperm motility, live %, and acrosomal integrity than the control group. Between the isthmic and ampullary proteins, the isthmic proteins incorporated group maintained higher ( P < 0.05) post-thaw sperm motility, live %, and acrosomal integrity. Similarly, higher sperm penetration distance in cervical mucus was recorded in nonluteal isthmic proteins incorporated group. But, irrespective of the stage of an estrous cycle, isthmic proteins included group maintains higher sperm membrane integrity as revealed by higher ( P < 0.05) swollen sperm percentage in response to hypo-osmotic solution than the ampullary proteins included and control