Copulation and Fertilisation Flashcards

1
Q

External factors control reproductive cycles

A
  • Photoperiod
  • Lactation
  • Nutrition
  • Animal interaction
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2
Q

Sexual behaviour regulated by hormones

A
  • Oestrogen and gonadotrophin releasing hormone in females

* Testosterone in males

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3
Q

Sexual arousal

A

Psychogenic stimuli include; • Visual cues
Mating in others
Lordosis
• Olfactory cues
Sniffing of vulva Female urination Pheromones
Physiological factors for erection;
• Stimulation of pelvic nerve
Causes arterial dilation and increased blood flow into corpus cavernosa
• Relaxation of the retractor penis muscle Straightening of the sigmoid flexure

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4
Q

Copulation and ejaculation

A
  • Movement of sperm into epididymis and vas deferens
  • Muscles of vas deferens and accessory glands contract
  • Spermatozoa and seminal plasma expelled via penile urethra
  • Sympathetic control from autonomic nervous system
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5
Q

Hyperactivation

A
  • Increased head movement and less linearity
  • Variation in ejaculate
  • Ejaculate can be assessed, a key part of fertility assessment and following semen collection in the process of artificial insemination
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6
Q

Epididymis

A

Surface molecules added to head of sperm

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7
Q

Ejaculation

A

Surface molecules coated with seminal plasma proteins

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8
Q

Capacitatiom

A

Female tract strips some proteins leaving exposed areas for sperm egg binding

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9
Q

Fertilisation

A
  • Acrosomal enzymes digest small hole in zona pellucida
  • Sperm move into perivitelline space between zona pelucida and oocyte plasma membrane
  • Oocyte plasma membrane fuses with sperm
  • Sperm is engulfed
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10
Q

Acrosome reaction

A
  • Capacitation exposes zona pellucida binding proteins on sperm plasma membrane (ZP3)
  • Sperm binds to oocyte zona pellucida via ZP3 initiating the acrosome reaction
  • Release of enzymes to digest the zona pellucida
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11
Q

Overview of fertilisation

A
Sperm capacitation
\/
Hyperactivation
\/
Binding to zona pellucida
\/
Acrosome reaction
\/
Penetration of zona pellucida
\/
Sperm – Oocyte binding Fertilisation
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12
Q

Early embryo – zygote cleavage

A
  • Following fertilisation the zygote undergoes a series of mitotic divisions known as cleavage
  • The first cleavage division creates a two-cell embryo
  • Each of the two cells in the embryo is called a blastomere
  • Blastomeres cleave to form 4, 8, 16 cells
  • Each blastomere is genetically identical
  • After the 8-cell stage the ball of cells if called a morula
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13
Q

Formation of a blastocyst

A

• At the morula stage the cells separate into 2 distinct layers
–Inner ball of cells (inner cell mass)
–Cells at the periphery (trophoblast)
• Known as the blastocyst
• Cells in the outer cell mass pump sodium into the blastocyst creating accumulation of fluid, blastocoele
• Inner cell mass develops into the embryo
• Trophoblast cells become the placenta

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14
Q

Blastocyst hatching

A

• The blastocyst continues to move down the oviduct towards the uterus
• Implantation is prevented by the zona pellucida
• At the uterus the blastocyst hatches by digesting a hole in the zona
pelucida
• Blastocyst becomes a free-floating embryo
• Dependant on the uterus for survival

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15
Q

Implantation

A
  • Attachment of the embryo to the uterine mucosa followed by placentation
  • Requires oestrogen and progesterone to prepare the endometrium
  • May be invasive or non-invasive
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16
Q

In vitro fertilisation (IVF)

A

Harvesting of an ovum and sperm so that the fertilisation process can be achieved ‘in vitro’ prior to the embryo being placed inside the female for
implantation.

17
Q

Artificial Insemination Process

A
  • Ejaculate collected
  • Ejaculate assessed
  • Ejaculate diluted in ‘extender fluid’
  • Ejaculate stored
  • Room temperature (routinely used in pigs)
  • Frozen (routinely used in cows, sheep and humans but unsuccessful in pigs and can be transported by post)
  • Female inseminated with semen
18
Q

Why use artificial insemination?

A

–Transport of animals
stressful and expensive
–Global genetic selection
–Direction of selective breeding programmes -promote beneficial traits
–Transgenic mouse strains
Preservation of endangered species –Bio-security –HIV, Foot and Mouth