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Artificial Insemination
(A technique with precise handling)
By
Nida Sajjad
Mphil Zoology
Subject : Analysis of development
Introduction
• Artificial deposition of semen
into female genital tract is
Artificial insemination.
• Artificial insemination is priority
because desirable characteristics
of a bull or other male livestock
animal can be passed on more
quickly.
• Also more progeny can result as
compared if an animal mate
with females in a natural
fashion.
History
• First documented report of successful use of artificial
insemination was by Italian Physiologist L.Spallangini
in 1780 when he impregnated a bitch.
• In India Samuath Kumaran used Artificial
insemination for the first time in 1939 at Palace Dairy
Farm in Mysore.
• Degree of success
• Uptill now it is successful in Ungulates,cat,dog and
poultry farms.
Nature of semen and its production
• Semen is the complete discharge of male during ejaculation.
• It has two components
Cellular elements (Spermatozoa)
Seminal Plasma or liquid portion
• Nature
• It is creamy or milky in appearance and yellowish grey in color.
• Consistency
• It has low viscosity in dogs and rabbit.Whereas highly viscous in cats.
• Gel formation is observed in rodents and primates.
• Variation in the volume of semen is due to secretions of accessory
glands.
Steps
Collection of semen from male
Evaluation of semen quality
Semen dilution for preservation
Deposition of semen in the female reproductive tract
1.Collection of semen from male
Management of male
• Young males are preferred with good nutritional and health status.As they
produce good quality semen.
12 months in bull
7-8 months in goat,boars and ram
24 months in stallion(male horse)
Physical status
• Mechanical exercise by bull studs for fit male farm animal.
• Nutritional status has profound effect as sexual development of testis has
direct correlation with good sperm production potential.
• Housing of male
• It should be convenient and comfortable both for animal and safe for handlers.
• Preparation of bull
• It includes pre-collection stimulation of bull(sluggish male) to get increased
volume and good %age of motile sperm.
• For this purpose change of teaser and false mounting are effective.
• Time
• Early morning before feeding as bull are alert and fresh during morning hours.
• Frequeny of semen collection
• Usual practice is to collect semen once a week in bull.However two or three
successive collections can be obtained from the same bull.
• Young bulls can be used twice a week for semen collection.
• Sometimes frequent semen collection decrease number of sperms.
Methods of semen collection
Electro-ejaculation method
• In this method weak alternating current is provided to sacral and pelvic nerves
through electrodes placed in rectum.
• Accesory gland secretion takes place at lower voltage and ejaculation at higher
voltage.
• Although semen has less contamination in this method but it cause discomfort
to animal and variable reaction.It is only prefered when male cannot be trained
for artificial collection of semen.
Massage method(outdated method)
• Massaging of rectum of vesicular gland and ampullae of vas deferns can induce
semen flow.
• But it has more chances of contamination with urine and get imbalance in its
composition.
Collection on dummy cow or manikin
• A dummy cow is prepared by heavy steel frame covered with hard leather to
give appearance of normal cow.
• An artificial vagina is prepared and fixed at suitable height at rear of dummy
cow.
• Although it has advantage over teaser cow being disease resistance but male
male do not show interest in such dummy cows.
Live mount and teasing procedure
• Live mounts using a teaser is most successful procedure.
• Estrogen treated females are selected for semen collection.
• Cow should be of same breed and color.
• Cow should be of medium height as bulls feels difficulty on mounting.
• It is better to select cow which has done 2-3 calving.
• A pregnant cow or cow on heat should be avoided.
Factors affecting semen production
After sexual maturity reproductive capacity of cattles are usually 4-7 years.
Following factors can affect semen production.
1.Continental breeds reach early sexual maturity then indigenous
2.Long distance travelling bulls have some effect on semen volume
3.Seasonal affect on spermatogenesis
4.Disease
5.Nutritional quality
6.Genetic inheritance
7.Frequency of ejaculation(more ejaculation less sperm count)
2.Evaluation of semen quality
• Assessment for fertility potential of semen sample before insemination is crucial
step.
• Semen is evaluated for color,volume,density and activity.
• If opaque in appearance it has high sperm concentration.But if translucent then
few sperms in semen sample.
• Curdy appearance indicate infection of reproductive tract from which semen
collected.
• Motility of sperms can be examined under microscope.
• Proportion of live to dead sperms is estimated by nigrosin-eosin stain.(5% w/v
nigrosin+0.6% w/v eosin+3% w/v sodium citrate)
3.Preservation of semen
• Ejaculated sperms do not servive for long period and high temprature storage is also
destructive to spermatozoa.
• So in order to preserve fertilization capacity of sperms.Many diluents are added for
different purposes
• What should be the Qualities of diluents?
1.Proper balance of mineral elements essential for live sperms.
2.Diluents should have nutrients for aerobic and anaerobic metabolic processes for
survival of sperm.
3.Lipoproteins and lecithins(phospholipids) to protect against cold shocks.
4.Diluents should have buffering capacity to negate shift in pH due to metabolism and
lactic acid production.
5.Inhibit bacterial growth
6.Increase volume of semen
Some diluting agents…….
Egg yolk Against cold shocks
Sodium citrate To preserve viability and fertility
Carbohydrates(glucose+fructose) As a source of energy.It increase
motility and survival of sperm.
Pencillin,Streptomycin To inhibit bacterial growth
• Cooling of semen is done to prolong viability and fertilization capacity by reducing
metabolic activity.
• Therefore,diluted semen vials are wrapped with cotton,placed in beaker
containing water and transferred to refrigerator for further cooling to 5C.
Deep freezing or cryopreservation
(Long-term Preservation)
• 1 of 5 cows become pregnant by deep freezing semen.
• For deep freezing glycerol is used as it is protective against lethal effects of
freezing.
Slow freezing (Ampoule):
• Slow freezing is carried out in alcohol-co2 ice bath and then transferred in liquid
nitrogen container for long preservation.
Instant freezing:
• 5-5.5 % sugar solution containing glycerol kept for 5-10 hours.After that small
drops of 0.5-0.2 ml by micro syrings for 10 min on dry ice.
• Then semen is transferred to liquid nitrogen(-196) for long term storage.
Thawing
• Thawing of frozen semen is essential before use.
• Melting of semen should be as quickly as possible to prevent
recrystallization of water into bigger crystals.
• Frozen semen is thawed at 34C for 15 second in water kept in thermos
flask.
• 4.Depostion into female reproductive tract
• Female should be healthy and at heat period.
• Deposition with the help of inseminating gun is done in cervix of female.
Inseminating equipment
• 2 ml plastic syring having inside diameter of 1mm
• Pipette is sterilized,dried,wrapped with paper and again sterilized with hot
oven.
• Diluted semen 0.8-1.2ml is sucked into pipette.Vulva area of cow is
cleaned,dilated and pippete is inserted into vagina and semen is lead to mid
cervix.
Method of insemination
• Rectovaginal (cervical fixation) method is used for large animals as it is possible
to perform intrauterine insemination by this method.
• Mid cervix is ideal place for deposition as it activate the spermatozoa and
increase capacitation.
 Detection of heat
• Crystalization pattern of cervical mucous under microscope helpful to detect
heat.
• If venation is like fern-tree leaf then female is in heat period.
Timing ideal insemination
• Cow has wide range of heat period of about 3-28 hours,18 hours being average
period.Mostly mid heat is preffered as ideal.
• Cow should not be inseminated before 50 days after calving.
• Viability of gamete in female reproductive tract is different for different
species.eg 30 hours in cows.
Adrenaline and excitement
• Cow should be handled carefully,as during insemination if cow get excited then
adrenaline is secreted which inhibit sperm travel within genital tract.
Advantages
Superior sire animals can be raised
Small quantity of semen can inseminate many females.
Proper method help in disease control
More female at heat can be inseminated simultaneously.
Golden tool for live stock economic trait.
Demerits
If veterinarians and professionals are less trained then it is just waste of
time,energy and resources.
Danger of contamination at various stages.
It is costly in case of materials required in laboratory and transportation.
THANKYOU

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Artificial insemination

  • 1. Artificial Insemination (A technique with precise handling) By Nida Sajjad Mphil Zoology Subject : Analysis of development
  • 2. Introduction • Artificial deposition of semen into female genital tract is Artificial insemination. • Artificial insemination is priority because desirable characteristics of a bull or other male livestock animal can be passed on more quickly. • Also more progeny can result as compared if an animal mate with females in a natural fashion.
  • 3. History • First documented report of successful use of artificial insemination was by Italian Physiologist L.Spallangini in 1780 when he impregnated a bitch. • In India Samuath Kumaran used Artificial insemination for the first time in 1939 at Palace Dairy Farm in Mysore. • Degree of success • Uptill now it is successful in Ungulates,cat,dog and poultry farms.
  • 4. Nature of semen and its production • Semen is the complete discharge of male during ejaculation. • It has two components Cellular elements (Spermatozoa) Seminal Plasma or liquid portion • Nature • It is creamy or milky in appearance and yellowish grey in color. • Consistency • It has low viscosity in dogs and rabbit.Whereas highly viscous in cats. • Gel formation is observed in rodents and primates. • Variation in the volume of semen is due to secretions of accessory glands.
  • 5. Steps Collection of semen from male Evaluation of semen quality Semen dilution for preservation Deposition of semen in the female reproductive tract
  • 6. 1.Collection of semen from male Management of male • Young males are preferred with good nutritional and health status.As they produce good quality semen. 12 months in bull 7-8 months in goat,boars and ram 24 months in stallion(male horse) Physical status • Mechanical exercise by bull studs for fit male farm animal. • Nutritional status has profound effect as sexual development of testis has direct correlation with good sperm production potential.
  • 7. • Housing of male • It should be convenient and comfortable both for animal and safe for handlers. • Preparation of bull • It includes pre-collection stimulation of bull(sluggish male) to get increased volume and good %age of motile sperm. • For this purpose change of teaser and false mounting are effective. • Time • Early morning before feeding as bull are alert and fresh during morning hours. • Frequeny of semen collection • Usual practice is to collect semen once a week in bull.However two or three successive collections can be obtained from the same bull. • Young bulls can be used twice a week for semen collection. • Sometimes frequent semen collection decrease number of sperms.
  • 8. Methods of semen collection Electro-ejaculation method • In this method weak alternating current is provided to sacral and pelvic nerves through electrodes placed in rectum. • Accesory gland secretion takes place at lower voltage and ejaculation at higher voltage. • Although semen has less contamination in this method but it cause discomfort to animal and variable reaction.It is only prefered when male cannot be trained for artificial collection of semen. Massage method(outdated method) • Massaging of rectum of vesicular gland and ampullae of vas deferns can induce semen flow. • But it has more chances of contamination with urine and get imbalance in its composition.
  • 9. Collection on dummy cow or manikin • A dummy cow is prepared by heavy steel frame covered with hard leather to give appearance of normal cow. • An artificial vagina is prepared and fixed at suitable height at rear of dummy cow. • Although it has advantage over teaser cow being disease resistance but male male do not show interest in such dummy cows. Live mount and teasing procedure • Live mounts using a teaser is most successful procedure. • Estrogen treated females are selected for semen collection. • Cow should be of same breed and color. • Cow should be of medium height as bulls feels difficulty on mounting. • It is better to select cow which has done 2-3 calving. • A pregnant cow or cow on heat should be avoided.
  • 10. Factors affecting semen production After sexual maturity reproductive capacity of cattles are usually 4-7 years. Following factors can affect semen production. 1.Continental breeds reach early sexual maturity then indigenous 2.Long distance travelling bulls have some effect on semen volume 3.Seasonal affect on spermatogenesis 4.Disease 5.Nutritional quality 6.Genetic inheritance 7.Frequency of ejaculation(more ejaculation less sperm count)
  • 11. 2.Evaluation of semen quality • Assessment for fertility potential of semen sample before insemination is crucial step. • Semen is evaluated for color,volume,density and activity. • If opaque in appearance it has high sperm concentration.But if translucent then few sperms in semen sample. • Curdy appearance indicate infection of reproductive tract from which semen collected. • Motility of sperms can be examined under microscope. • Proportion of live to dead sperms is estimated by nigrosin-eosin stain.(5% w/v nigrosin+0.6% w/v eosin+3% w/v sodium citrate)
  • 12. 3.Preservation of semen • Ejaculated sperms do not servive for long period and high temprature storage is also destructive to spermatozoa. • So in order to preserve fertilization capacity of sperms.Many diluents are added for different purposes • What should be the Qualities of diluents? 1.Proper balance of mineral elements essential for live sperms. 2.Diluents should have nutrients for aerobic and anaerobic metabolic processes for survival of sperm. 3.Lipoproteins and lecithins(phospholipids) to protect against cold shocks. 4.Diluents should have buffering capacity to negate shift in pH due to metabolism and lactic acid production. 5.Inhibit bacterial growth 6.Increase volume of semen
  • 13. Some diluting agents……. Egg yolk Against cold shocks Sodium citrate To preserve viability and fertility Carbohydrates(glucose+fructose) As a source of energy.It increase motility and survival of sperm. Pencillin,Streptomycin To inhibit bacterial growth • Cooling of semen is done to prolong viability and fertilization capacity by reducing metabolic activity. • Therefore,diluted semen vials are wrapped with cotton,placed in beaker containing water and transferred to refrigerator for further cooling to 5C.
  • 14. Deep freezing or cryopreservation (Long-term Preservation) • 1 of 5 cows become pregnant by deep freezing semen. • For deep freezing glycerol is used as it is protective against lethal effects of freezing. Slow freezing (Ampoule): • Slow freezing is carried out in alcohol-co2 ice bath and then transferred in liquid nitrogen container for long preservation. Instant freezing: • 5-5.5 % sugar solution containing glycerol kept for 5-10 hours.After that small drops of 0.5-0.2 ml by micro syrings for 10 min on dry ice. • Then semen is transferred to liquid nitrogen(-196) for long term storage.
  • 15. Thawing • Thawing of frozen semen is essential before use. • Melting of semen should be as quickly as possible to prevent recrystallization of water into bigger crystals. • Frozen semen is thawed at 34C for 15 second in water kept in thermos flask. • 4.Depostion into female reproductive tract • Female should be healthy and at heat period. • Deposition with the help of inseminating gun is done in cervix of female. Inseminating equipment • 2 ml plastic syring having inside diameter of 1mm • Pipette is sterilized,dried,wrapped with paper and again sterilized with hot oven.
  • 16. • Diluted semen 0.8-1.2ml is sucked into pipette.Vulva area of cow is cleaned,dilated and pippete is inserted into vagina and semen is lead to mid cervix. Method of insemination • Rectovaginal (cervical fixation) method is used for large animals as it is possible to perform intrauterine insemination by this method. • Mid cervix is ideal place for deposition as it activate the spermatozoa and increase capacitation.
  • 17.  Detection of heat • Crystalization pattern of cervical mucous under microscope helpful to detect heat. • If venation is like fern-tree leaf then female is in heat period. Timing ideal insemination • Cow has wide range of heat period of about 3-28 hours,18 hours being average period.Mostly mid heat is preffered as ideal. • Cow should not be inseminated before 50 days after calving. • Viability of gamete in female reproductive tract is different for different species.eg 30 hours in cows. Adrenaline and excitement • Cow should be handled carefully,as during insemination if cow get excited then adrenaline is secreted which inhibit sperm travel within genital tract.
  • 18. Advantages Superior sire animals can be raised Small quantity of semen can inseminate many females. Proper method help in disease control More female at heat can be inseminated simultaneously. Golden tool for live stock economic trait.
  • 19. Demerits If veterinarians and professionals are less trained then it is just waste of time,energy and resources. Danger of contamination at various stages. It is costly in case of materials required in laboratory and transportation.

Notas do Editor

  1. Nigrosin-Eosin (Hancock) Stain There are a number of variations of the Nigrosin-Eosin stain. A commonly-used formulation is Dissolve in water: 5% w/v nigrosin 0.6% w/v eosin 3% w/v sodium citrate, dihydrate (to obtain physiologic osmolarity) Adjust the pH of the stain to 7.0 by adding a few drops of 0.1 M NaH2PO4 or 0.1 M Na2HPO4 and filter through filter paper