Your browser doesn't support javascript.
loading
Successful vitrification of manually punctured equine embryos.
Wilsher, Sandra; Rigali, Florencia; Kovacsy, Sofia; Allen, Wr Twink.
Affiliation
  • Wilsher S; Sharjah Equine Hospital, Sharjah, UAE.
  • Rigali F; Sharjah Equine Hospital, Sharjah, UAE.
  • Kovacsy S; Sharjah Equine Hospital, Sharjah, UAE.
  • Allen WT; Sharjah Equine Hospital, Sharjah, UAE.
Equine Vet J ; 53(6): 1227-1233, 2021 Nov.
Article in En | MEDLINE | ID: mdl-33326638
ABSTRACT

BACKGROUND:

Successful vitrification of equine expanded blastocysts requires collapse of the blastocoele cavity using a micromanipulator-mounted biopsy pipette on an inverted microscope. Such equipment is expensive and requires user skill.

OBJECTIVES:

To develop a manual method of blastocoele collapse prior to vitrification using commercial products. STUDY

DESIGN:

In vivo experiment.

METHODS:

Seventy-nine Day 7 or 8 embryos were measured and graded. Twenty were vitrified following micromanipulator-assisted puncture and aspiration before being used to validate commercial human vitrification and warming kits containing, respectively, 2-step concentrations of DMSO and ethylene glycol (7.5%-15% vv) and decreasing concentrations of sucrose. After warming, embryos were transferred to recipient mares. Once validated, the commercial kits were used to vitrify and warm a further 39 embryos which were punctured manually using a microneedle, 2 (5%) were damaged during puncture and excluded; 20 more embryos were vitrified without puncture. Embryos were grouped as follows non-punctured ≤ 300µm (n = 10) and >300 to ≤560 µm (n = 10), punctured small (>300 to ≤560 µm; n = 17) and large (>560 µm; n = 10) and exposed to the equilibration solution (ES) in the kit for 6min. An additional group of punctured large embryos was exposed to ES for 8min (n = 10). For the initial warming step, embryos were exposed for 1min to the thawing solution at 42°C, before being moved to a dilution solution at room temperature.

RESULTS:

Vitrified, manually punctured embryos ≤560 µm exposed to ES for 6min resulted in a pregnancy rate of 82% (14/17). Unpunctured embryos ≤300 µm gave an 80% (8/10) pregnancy rate. Larger unpunctured embryos, punctured embryos >560 µm and embryos exposed to ES for 8min gave significantly reduced pregnancy rates. MAIN

LIMITATIONS:

Limited group sizes.

CONCLUSION:

High pregnancy rates can be achieved by manually puncturing ≤560 µm equine embryos prior to their vitrification and subsequent warming in commercial media.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Cryopreservation / Vitrification Limits: Animals / Pregnancy Language: En Journal: Equine Vet J Year: 2021 Type: Article

Full text: 1 Database: MEDLINE Main subject: Cryopreservation / Vitrification Limits: Animals / Pregnancy Language: En Journal: Equine Vet J Year: 2021 Type: Article