129 EFFECT OF DEVELOPMENTAL STAGE OF ICSI-PRODUCED EQUINE EMBRYOS ON PREGNANCY RATES

2009 ◽  
Vol 21 (1) ◽  
pp. 164 ◽  
Author(s):  
J. E. Stokes ◽  
E. L. Squires ◽  
T. K. Suh ◽  
J. L. Altermat ◽  
E. M. Carnevale

Intracytoplasmic sperm injection (ICSI) can be used to produce offspring from mares or stallions with fertility problems. Early embryos can be transferred into recipients’ oviducts or embryos can be cultured for nonsurgical transfer into recipients’ uteri. The aim of this research was to evaluate the optimal time to transfer ICSI-produced embryos into recipients’ uteri. The objective was to compare pregnancy rates after the nonsurgical transfer of early morulae, compact morulae, and blastocysts. Oocytes were collected by transvaginal, ultrasound-guided follicular aspirations between 20 and 24 h after administration of deslorelin (1.5 mg, i.v., Francks Pharmacy, Ocala, FL, USA) to donors. Oocytes were cultured for 16 to 18 h in M199 (Invitrogen, San Jose, CA, USA) with 10% FCS (HyClone, Logan, UT, USA), 0.2 mm pyruvate (Sigma, St. Louis, MO, USA) and 25 μg mL–1 gentamycin (Sigma, St. Louis, MO, USA) at 38.5°C and 6% CO2. Cumulus cells were denuded by gentle pipetting, after oocytes were placed into hyaluronidase (500 U mg–1, Sigma, St. Louis, MO, USA). Oocytes were injected with a single sperm from one of two stallions, with sperm being frozen or sex-sorted and refrozen (Squires EL et al. 2008). Forty-six of 62 (74%) injected oocytes cleaved. The presumptive zygotes were cultured in DMEM/F12 (Sigma, St. Louis, MO, USA) with 10% FCS at 38.5°C and an atmosphere of 5% CO2, 5% O2 and 90% N2. Embryos were placed in fresh medium every 3 days. Injected oocytes were observed for cleavage at 2 days, and embryos were assigned to a transfer group. Embryos were transferred as early morulae (EM, 8-cell to precompaction stage, n = 14), compact morulae (CM, postcompaction, n = 10) or blastocysts (B, observed blastocoele, n = 9) into recipients at 3 to 5 days (EM), 3 to 6 days (CM) or 5 to 6 days (B) after the recipient’s ovulation or follicle aspiration. Pregnancy scans were performed on Day 12, 14, and 16 after ICSI, and pregnant recipients were examined until 30 days to detect the embryo proper and heartbeat. Number of embryonic vesicles detected per transferred embryo was determined by Fisher’s Exact Test. Pregnancy rates differed (P = 0.0017) among groups (EM, 1/14, 7%; CM, 4/10, 40%; B, 7/9, 78%), with fewer (P = 0.001) EM than B resulting in embryonic vesicles; however, pregnancy rates were not significantly different between CM and other embryo stages. An embryo proper with heartbeat was observed for all pregnancies, with the exception of one pregnancy resulting from the transfer of a blastocyst. In this study, all blastocysts were transferred prior to the embryo attempting to hatch from the zona pellucida, but after the appearance of a distinct blastoceole. In our study, pregnancy rates were higher after the transfer of later v. earlier stages of embryo development.

2004 ◽  
Vol 16 (7) ◽  
pp. 675 ◽  
Author(s):  
Dirk K. Vanderwall ◽  
Gordon L. Woods ◽  
Kenneth I. Aston ◽  
Thomas D. Bunch ◽  
Guanpeng Li ◽  
...  

The objectives of the present study were to: (1) clone horses using adult cumulus cells; and (2) determine whether the cumulus cell donor affected the outcome. In vivo-matured cumulus–oocyte complexes were obtained using transvaginal ultrasound-guided follicle aspiration; oocytes were used as cytoplasts, whereas cumulus cells (from one of three different mares) were used as donor cells. Immediately following nuclear transfer and activation procedures, cloned embryos were transferred surgically to the oviduct of recipient mares (n = 2–5 embryos per recipient) that had ovulated within 24 h prior to the transfer. An initial pregnancy examination was performed between Days 14 and 16 (Day 0 = surgery); subsequent examinations were then performed every 7–10 days. A total of 136 follicles were aspirated in 96 mares, from which 72 oocytes were recovered (53%). Sixty-two cloned embryos were transferred to recipient mares, which resulted in seven (11.3%) ultrasonographically detectable conceptuses between Days 14 and 16. All seven conceptuses were lost spontaneously between Days 16 and 80. Cumulus cells from Mare 160 tended (P = 0.08) to result in a higher embryo survival rate than cumulus cells from Mare 221 (4/17 v. 1/25 respectively). To our knowledge, this is the first report documenting the establishment of cloned equine pregnancies derived from adult cumulus cells.


2010 ◽  
Vol 25 (S15) ◽  
pp. 75-78
Author(s):  
VERENA BRACHER ◽  
JOYCE PARLEVLIET ◽  
A. R. FAZELI ◽  
M. C. PIETERSE ◽  
P. L. A. M. VOS ◽  
...  

2011 ◽  
Vol 23 (1) ◽  
pp. 235
Author(s):  
I. C. Velez ◽  
J. D. Norris ◽  
Y. H. Choi ◽  
S. Loux ◽  
K. Hinrichs

Transvaginal ultrasound-guided follicle aspiration (TVA) is the most effective way to recover multiple immature oocytes from live mares. Because of the tight attachment of the equine immature oocyte to the follicle wall, TVA in this species is time consuming, taking up to 1 h per horse. Thus, it may be difficult to search follicular aspirates immediately after recovery. In 2009 in a series of 6 replicates, we observed a blastocyst development rate of 32% (13/41) after intracytoplasmic sperm injection of oocytes collected by TVA and held for ∼1.5 h at ambient temperature (26 to 32°C) before isolation from aspirated fluid (unpublished data). Therefore, in the present study we compared the effects of immediate oocyte isolation v. holding the follicular aspirate before oocyte isolation on oocyte maturation and blastocyst rates. Ten mares were used for this study; TVA was performed on each mare every 14 days, for 4 aspiration sessions per mare. Collected aspiration fluid was either processed immediately or held for 2 h at 32°C before processing. At each aspiration, one ovary was randomly assigned to each treatment [immediate (Imm) or 2-h holding (2-H)]. Follicle aspiration was performed as previously described (Jacobson et al. 2010 Theriogenology 73, 1116–1126) using M199 with Hank’s salts to flush the follicle lumen up to 8 times per follicle. Oocytes were recovered from the aspirates by filtration. Overall, 325 follicles were aspirated and 140 oocytes were obtained (43% recovery). The proportion of degenerating oocytes was not significantly different between treatments (1/68 and 0/72 for Imm and 2-H, respectively). Oocytes were held overnight in modified M199 as previously described (Choi et al. 2006 Theriogenology 66, 955–963) before maturation culture. After 30 h of maturation culture, there was no significant difference in maturation rates between treatments [75% (50/67) and 65% (46/71) for Imm and 2-H, respectively]. Fertilization was performed by intracytoplasmic sperm injection, and injected oocytes were cultured 7 to 10 days, as previously described (Choi et al. 2006). The rates of blastocyst development per injected oocyte were 23% (11/47) for Imm and 16% (7/44) for 2-H; these were not significantly different (P > 0.3). The reason for the discrepancy in blastocyst rates for held oocytes in this study (16%) compared with our 2009 observations (32%) is unclear; this could be a factor of the time held (∼1.5 v. 2 h), the temperature (26–32°C v. 32°C), or minor changes in protocol between the 2 years. From these results, we conclude that holding oocytes in the follicular aspirate for up to 2 h following collection may be performed when necessary without significantly affecting the rate of subsequent blastocyst development. This work was supported by the Link Equine Research Endowment Fund, Texas A&M University, and by Ms. Kit Knotts.


2008 ◽  
Vol 20 (1) ◽  
pp. 189
Author(s):  
J. H. M. Viana ◽  
L. S. A. Camargo ◽  
J. F. Fonseca ◽  
A. P. Oliveira ◽  
E. K. N. Arashiro ◽  
...  

Bovine in vitro embryo production (IVP) is extensively used in Brazil, associated with transvaginally guided follicle aspiration (TGFA). The good results obtained with the use of TGFA-IVP in this country are related to the ovarian physiology characteristics of zebu breeds, which include a lower persistence of dominant follicles and a greater number of follicles emerging in each follicular wave. There are, however, few reports of COC yield in these breeds in large-scale TGFA-IVP systems. The aim of this study was to analyze data on COC recovery from a Gyr (dairy zebu breed) herd in Brazil. Only pluriparous, nonlactating cows were used as donors. Follicle aspiration was performed with a portable ultrasound device, using disposable 19- or 20-gauge needles and a vacuum pressure of 80 mmHg. The follicle population before TGFA was recorded, and recovered oocyes were classified according cumulus cells layers and cytoplasm aspect. Data were analyzed by ANOVA, and means were compared by Tukey's test. Associations between variables were analyzed by Pearson's correlation method. A total of 761 TGFA sessions were performed in 54 donors, with the recovery of 8082 oocytes (10.62 � 0.32 per session) and 6208 viable COC (8.19 � 0.25 per session). Each donor underwent from 1 to 42 TGFA sessions. Both the number of total oocytes and viable COC were highly correlated with the number of follicles present in the ovaries (mean of 15.81 � 0.32) in the moment of TGFA (R = 0.86 and R = 0.83, respectively, P < 0.0001). There was a significant donor effect (P < 0.0001) in the mean number of follicles in the ovaries (ranging from 4.50 � 0.65 to 37.50 � 2.50), oocytes (from 0.75 � 0.48 to 30.50 � 8.50), and viable COC (from 0.75 � 0.48 to 25.67 � 6.12) recovered. The absolute maximum and minimum values for these parameters were 74, 67, and 44 v. 3, 0, and 0, respectively. The TGFA order also affected all parameters evaluated (P < 0.0001), with a linear decrease in the number of follicles punctured (y = –0.22x + 18.64, R2 = 0.65), total oocytes ( y = –0.25x + 13.81, R2 = 0.68) and viable oocytes (y = –0.22x + 11.05, R2 = 0.77) recovered. This decrease was probably associated with the cumulative damage in ovarian structure, once all parameters were affected, although from the first to the second TGFA session the mean number of oocytes (20.09 � 1.70 v. 14.08 � 1.11) and viable COC (16.37 � 1.27 v. 11.83 � 1.04), but not of aspirated follicles (22.28 � 1.60 v. 19.38 � 1.19), were reduced (P < 0.05). The decline in oocyte yield was greater ( y = –0.71x + 10.45, R2 = 0.95) when considering donors undergoing TGFA continuously (within intervals shorter than 8 days). Overall bastocyst rate was 28.48%, with a significant correlation between COC recovered and embryos produced (R = 0.64, P < 0.0001). These results shows that (1) follicular population is the main characteristic affecting the number of recovered COC, and consequently IVP; (2) the great variability in follicular population and in COC recovery among donors allows the selection of animals for IVF; and (3) repeated TGFA negatively affect ovarian follicle emergence and COC recovery.


2013 ◽  
Vol 79 (2) ◽  
pp. 267-273 ◽  
Author(s):  
J.H.M. Viana ◽  
M.D. Dorea ◽  
L.G.B. Siqueira ◽  
E.K.N. Arashiro ◽  
L.S.A. Camargo ◽  
...  

1992 ◽  
Vol 24 (1) ◽  
pp. 58-59 ◽  
Author(s):  
INGRID BRÜCK ◽  
KIRSTEN RAUN ◽  
BENTE SYNNESTVEDT ◽  
T. GREVE

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