A review on goat sperm cryopreservation

http://directory.umm.ac.id/Data%20Elmu/jurnal/A/Animal%20Reproduction%20Science/Vol62.Issue1-3.Aug2000/2029.pdf?origin=publication_detail

Production and storage of goat semen for artificial insemination

Sperm cells are the endpoint of male spermatogenesis and have particular anatomic and metabolic features. Sperm cryopreservation and storage currently require liquid nitrogen or ultralow refrigeration methods for long or short term storage, which requires routine maintenance and extensive space requirements. Conserving sperms have several purposes such as artificial reproductive technologies (ART), species conservation and clinical medicine. The combinations of storage temperature, cooling rate, chemical composition of the extender, cryoprotectant concentration, reactive oxygen species (ROS), seminal plasma composition and hygienic control are the key factors that affect the life-span of spermatozoa. Sperm preservation protocols vary among animal species owing to their inherent particularities that change extenders used for refrigeration and freezing. Extenders for freezing sperm cells contain buffers, carbohydrates (glucose, lactose, raffinose, saccharose and trehalose), salts (sodium citrate, citric acid), egg yolk and antibiotics. The use of different cryoprotectants, like trehalose or glycerol, as well as different concentrations of egg yolk and other constituents in semen extenders are being studied in our laboratory. Several cooling rates have been tested to freeze sperm cells. The use of faster rates (15-60 degrees C/min) gives rise to best sperm survivals after freezing-thawing, but more studies are needed to find the adequate cooling rates for each animal species. Sheep and goat males of some native breeds are being used in studies performed in EZN. Semen from those males has been frozen and stored as part of the Portuguese Animal Germplasm Bank. In small ruminants, individual variations in the quality of frozen semen have been observed, suggesting specific differences in sperm susceptibility to freezing methods, particularly obvious in goat males. Best quality frozen semen from small ruminants is being used in cervical artificial insemination studies aiming to increase productive parameters in selected flocks.

Cryopreservation of domestic animal sperm cells

Timed artificial insemination (TAI) is a very important tool in production systems, as it has a direct impact on cost-efficiency by reducing labour resulting from oestrus detection. However, to make TAI commercially feasible, hormonal treatments need to assure acceptable pregnancy rates and be economically viable. Recent advances in the knowledge of ovarian physiology (e.g. determination of follicular waves, sensitivity of the early corpus luteum) in small ruminants allowed the development of new treatments focused on an efficient estimation and synchronisation of the time of ovulation of the females of a treated flock/herd. In this review we summarise new information and concepts in the hormonal control of the life span of the corpus luteum, as well as methods to manipulate follicular growth in small ruminants. Additionally, we elaborate on recent studies concerning the use of TAI associated with short progestogen treatment in goats and the newly developed Synchrovine protocol (two doses of prostaglandin F(2alpha) given seven days apart) in sheep.

New treatments associated with timed artificial insemination in small ruminants.

Advanced assisted reproduction technologies (ART) in goats

Artificial breeding of adult goats and kids induced with hormones to ovulate outside the breeding season

The in vitro survival of ejaculated and epididymal goat sperm was measured in a milk diluent while being incubated at + 37 degrees C and after having been exposed to seminal plasma or to its components. Non-breeding season seminal plasma had a negative effect on sperm survival whether the cells were cooled to + 20 degrees C, chilled to + 4 degrees C or deep-frozen (- 196 degrees C) before being incubated at + 37 degrees C. Bulbo-urethral gland secretions also had a deleterious effect on the survival of washed ejaculated and epididymal sperm cooled to + 20 degrees C. The deleterious effect of the bulbo-urethral secretions on sperm survival and motility was significantly inhibited by the vesicular secretions. Non-breeding season seminal plasma contained bulbo-urethral but little or no vesicular secretions. The non-inhibition of their negative effect(s) may explain that of non-breeding season seminal plasma. Breeding season and non-breeding season washed ejaculated sperm had a better survival and a better motility than those incubated with breeding season seminal plasma. The mild washing procedure used may be responsible for the incomplete removal of seminal plasma from the sperm environment, namely that of the negative factors of the bulbo-urethral secretions. Breeding season seminal plasma would thus simply inhibit the effect of these negative factors or the factors themselves. This hypothesis is supported by the fact that breeding season seminal plasma had no effect on the survival of epididymal sperm.

/pdf/role-du-plasma-seminal-dans-la-survie-in-vitro-des-1ycsz3oo4l.pdf

J. M. Corteel

Papers

Artificial breeding of adult goats and kids induced with hormones to ovulate outside the breeding season

Rôle du plasma séminal dans la survie in vitro des spermatozoïdes de bouc

Development and application of artificial insemination with deep frozen semen and out-of-season breeding of goats in France.

Seasonal variations in the fertilizing capacity of washed deep frozen goat sperm.