Difference between revisions of "In Vitro Fertilization - Anatomy & Physiology"

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* Donor is superovulated to provide large numbers of mature follicles.
 
* Donor is superovulated to provide large numbers of mature follicles.
 
* Pre-ovulatory follicles collected by surgical procedure involving aspiration of the follicular content.
 
* Pre-ovulatory follicles collected by surgical procedure involving aspiration of the follicular content.
* Oocytes captured in vitro.
+
* [[The_Ovary_-_Oocytes_-_Anatomy_%26_Physiology|Oocytes]] captured in vitro.
  
  
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** Follicular fluid is aspirated.
 
** Follicular fluid is aspirated.
 
** Follicular fluid forcefully returned to the [[The_Ovary_-_Follicles_-_Anatomy_%26_Physiology|follicle]].
 
** Follicular fluid forcefully returned to the [[The_Ovary_-_Follicles_-_Anatomy_%26_Physiology|follicle]].
** Repeated 2-3 times to dislodge oocytes.
+
** Repeated 2-3 times to dislodge [[The_Ovary_-_Oocytes_-_Anatomy_%26_Physiology|oocytes]].
  
  
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** Ovary transrectally positioned against the dorsal vaginal wall directly over the transducer head so that the [[The_Ovary_-_Follicles_-_Anatomy_%26_Physiology|follicle]] can be visualized.
 
** Ovary transrectally positioned against the dorsal vaginal wall directly over the transducer head so that the [[The_Ovary_-_Follicles_-_Anatomy_%26_Physiology|follicle]] can be visualized.
 
** Hypodermic needle is advanced through the [[Female_Reproductive_Tract_-The_Vagina/Vestibule_-_Anatomy_%26_Physiology|vaginal wall]] into the antral follicle.
 
** Hypodermic needle is advanced through the [[Female_Reproductive_Tract_-The_Vagina/Vestibule_-_Anatomy_%26_Physiology|vaginal wall]] into the antral follicle.
** Follicular fluid containing the oocyte is aspirated under constant vacuum.
+
** Follicular fluid containing the [[The_Ovary_-_Oocytes_-_Anatomy_%26_Physiology|oocyte]] is aspirated under constant vacuum.
  
  
* Aspirated oocytes are placed in a culture vessel with [[Copulation_-Sperm_in_the_Female_Tract_-_Anatomy_%26_Physiology#Capacitation|capacitated]] spermatozoa.
+
* Aspirated [[The_Ovary_-_Oocytes_-_Anatomy_%26_Physiology|oocytes]] are placed in a culture vessel with [[Copulation_-Sperm_in_the_Female_Tract_-_Anatomy_%26_Physiology#Capacitation|capacitated]] spermatozoa.
 
** Could also be cultured in a 'nurse animal' in vivo.
 
** Could also be cultured in a 'nurse animal' in vivo.
 
* Embryos are incubated for a further period to the appropriate stage for transfer.
 
* Embryos are incubated for a further period to the appropriate stage for transfer.

Revision as of 09:45, 17 July 2008

BACK TO REPRODUCTIVE SYSTEM
BACK TO REPRODUCTIVE TECHNOLOGIES


Oocyte Collection

  • Donor is superovulated to provide large numbers of mature follicles.
  • Pre-ovulatory follicles collected by surgical procedure involving aspiration of the follicular content.
  • Oocytes captured in vitro.


  • Direct follicle aspiration:
    • A hyperdermic needle is inserted into the follicle.
    • Follicular fluid is aspirated.
    • Follicular fluid forcefully returned to the follicle.
    • Repeated 2-3 times to dislodge oocytes.


  • Transvaginal Aspiration in the Mare:
    • Prior to the procedure, mares are injected with propatheline bromide (sedative) to relax the rectum.
    • Lubricated ultrasound transducer is inserted into the vagina and held in the fornix vagina.
    • Ovary transrectally positioned against the dorsal vaginal wall directly over the transducer head so that the follicle can be visualized.
    • Hypodermic needle is advanced through the vaginal wall into the antral follicle.
    • Follicular fluid containing the oocyte is aspirated under constant vacuum.


  • Aspirated oocytes are placed in a culture vessel with capacitated spermatozoa.
    • Could also be cultured in a 'nurse animal' in vivo.
  • Embryos are incubated for a further period to the appropriate stage for transfer.
  • Embryos transferred to recipient female.
  • Can be transferred at the correct stage of the recipient's oestrous cycle.
  • Embryos transferred around the blastocyst stage.
  • Success rates are improving.
  • Embryos can be frozen, eliminating the need for tight synchronisation. This allows them to be shipped to other locations.
  • Increases incidence of large offspring syndrome.