FROM THE TESTES TO THE OVARIES
often not meiotically competent. Regular examina- tion can allow scheduling of the follicular aspiration when the largest population of follicles in the appro- priate size range are present.
Follicular Aspiration
Fig. 1. Simple aspiration setup with the use of thermostatically controlled baby-bottle warmers as water baths.
ration needle. The controlled flushing set has an automatic three-way valve that allows an assistant to alternatively rapidly fill the syringe and then infuse flush medium into the follicle by simply mov- ing the syringe plunger. Tubing from the aspira- tion port of the needle (the center lumen) is attached to the collection bottle placed in a 37°C water bath. The vacuum pump, regulated to 150 mm Hg, sup- plies the vacuum through the collection bottle (Fig. 1). The needle is inserted into the needle guide, with care taken to avoid contamination and to pre- vent dulling the needle.
Mare Preparation
DSF Oocytes Oocytes are firmly adhered to the wall of the follicle. After the luteinizing hormone (LH) surge, as ovula- tion approaches, the attachment loosens in domi- nant follicles. Stimulation of the LH surge with an ovulatory agent such as deslorelin acetaten allows a timed collection of the oocyte 24 to 36 hours later.7,8 This timing allows collection of an oocyte that has become easier to flush and has also started matura- tion and will not need additional hormonal stimula- tion. A typical mare is administered 1.8 mg of deslorelin acetate after detection of a 35-mm ac- tively growing follicle during estrus in association with endometrial edema, but this will vary with breed, individual, and time of year.
IMM Oocytes
Immature oocytes can be collected from small folli- cles at any stage of the estrous cycle or from subor- dinate follicles during estrus. Equine oocytes are especially firmly adhered to the follicle wall in a broad-based hillock of cumulus cells. Considerable intra-follicular turbulence is necessary to dislodge the oocyte to allow it to be flushed out of the follicle. The greatest productive oocyte yield will generally be from follicles of 10 to 20 mm diameter, because it is difficult to create the necessary turbulence in larger follicles, and oocytes in smaller follicles are
520 2013 Vol. 59 AAEP PROCEEDINGS
All Mares Mares are restrained in stocks and tranquilized to effect with approximately 0 01 mg/kg detomidine HClo or 0.66 mg/kg xylazinep intravenously. N-bu- tylscopalammonium bromideq (0.9 mg/kg IV) is ad- ministered to encourage rectal relaxation and to prevent peristaltic waves from interfering with trans-rectal ovarian manipulation. The tail is tied up, the rectum is evacuated, and the vulva and perineum is cleaned. With a sleeved hand, approx- imately 2 oz of obstetrical lubricant is distributed over the face of the ultrasound probe and holder with the needle guide. A thin rectal sleeve is placed and then stretched over the probe and holder to prevent vaginal mucus and debris from being introduced into the needle guide channel. Obstet- rical lube is applied to the exterior of this sleeve and the probe is guided into the vagina and placed against the dorsal anterior vaginal wall lateral to the cervix. The sleeved hand is withdrawn from the vagina and introduced into the rectum. The ovary is grasped and guided to the dorsal vaginal wall next to the transducer. This requires manip- ulating the ovary and lifting it up over the uterus and is best accomplished by grasping the ovarian suspensory ligament between two fingers. The ovary and probe are aligned in such a manner that the follicle(s) to be aspirated are adjacent to and aligned with the needle guide. Penetration of the vaginal wall, ovary, and follicle with the needle is facilitated by firm pressure of the ultrasound probe against the vaginal wall opposed by firm pressure of the ovary against the peritoneal surface of the vag- inal wall. The needle is advanced to the center of the follicle, and the aspiration pump is started (Fig. 2).
Initially, the practitioner may find it easiest to
simply manipulate the probe and the ovary while having an assistant advance the needle into the follicle. This works well with dominant follicles, but smaller follicles are more efficiently aspirated when the operator handles the needle as well as the probe and ovary. This allows all to move or be stabilized in synchrony with the timing of needle puncture; which is especially important if the ani- mal is moving. The probe handle is held in the palm of the hand with forward pressure maintained by the heel of the hand. The fingers are then free to advance and manipulate the aspiration needle (Fig. 3).
DSF Oocytes
Once penetrated, the follicle is completely evacuated and then re-filled as rapidly as possible while the
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