scholarly journals Effect of Continuous Administration of Enalapril Maleate on the Oocyte Quality and In Vitro Production of Parthenote Embryos in Nulliparous and Multiparous Goats Undergoing Serial Laparoscopic Ovum Pick-Up

Animals ◽  
2019 ◽  
Vol 9 (11) ◽  
pp. 868
Author(s):  
Pamela A. Bravo ◽  
Maria E. Moreno ◽  
César C.L. Fernandes ◽  
Rafael Rossetto ◽  
Camila M. Cavalcanti ◽  
...  

The aim of this work was to determine the effect of enalapril maleate administration, during oocyte recovery by serial laparoscopic ovum pick-up (LOPU), on the ovarian response and in vitro embryo production (IVP). Twenty cross-bred goats were allocated equally into two groups: Nulliparous and Multiparous. In each group, five animals were selected to receive daily doses of enalapril maleate during the hormonal protocol. Estrus was synchronized by a PGF2α analog, followed 48 h later by insertion of an intravaginal device with progesterone. Forty-eight hours after, a single dose of FSH/eCG was administered. The FSH/eCG doses were repeated three times, on every four day. Oocytes were recovered by LOPU 24 h after each FSH/eCG dose. Viable oocytes were matured in vitro, to be parthenogenetically activated and cultured for 72 h to the cleavage stage. The drug treatment increased the proportion of total follicles observed at LOPU (p < 0.01) in multiparous goats. In both parity groups, enalapril administration had no effect on the proportion or quality of oocytes recovered. Furthermore, the number of embryos cleaved was similar between the groups. Thus, enalapril maleate affected the ovarian response in multiparous animals only and had no effect on the oocyte quality or IVP.

2013 ◽  
Vol 25 (1) ◽  
pp. 250
Author(s):  
N. Schlüter ◽  
A. Hanstedt ◽  
H. Stinshoff ◽  
K. Knauer ◽  
S. Wilkening ◽  
...  

The developmental competence of cumulus–oocyte complexes (COC) used for in vitro production is dependent on several factors including the stage of the oestrus cycle. In a recent study, we were able to show that circulating progesterone (P4) had no effect on follicle number, size, recovery rate, or in vitro production suitability of recovered COC (Schlüter et al. 2012 Reprod. Fertil. Dev. 24, 175–176). The aim of the present study was to determine the influence of circulating P4 concentrations on the molecular quality of bovine COC collected during repeated OPU sessions. The COC were aspirated twice per week for 5 to 6 weeks from 12 Holstein Friesian heifers. The first OPU session took place on Day 7 of the oestrous cycle after spontaneous ovulation (ovulation = Day 0). Blood samples were taken at the time of each OPU session, and P4 concentrations were determined using a radioimmunoassay. All animals showed clinical signs of oestrus and large follicles (≥8.5 mm) during the course of the OPU sessions. Following the aspiration of a large follicle, a CL-like structure (induced CL) could be detected. According to the P4 concentrations, the cycle was divided into 3 phases: CL phase after spontaneous ovulation (oCL; P4: ≥1 ng mL–1), follicle phase 1 (Fp; P4 <1 ng mL–1), and induced CL phase (iCL; P4: ≥1 ng mL–1). The length of the cycle after spontaneous ovulation did not differ significantly from that after induced ovulation (22.4 ± 3.1 days v. 23.8 ± 1.8 days, respectively). During the oCL-phase, blood P4 concentrations were significantly higher than during the iCL-phase (4.9 ± 2.3 ng mL–1 v. 3.0 ± 1.6 ng mL–1). For mRNA analysis, denuded COC were individually frozen at –80°C to analyse the relative transcript abundance using RT-qPCR. The transcripts studied play important roles during oocyte development [growth differentiation factor 9 (GDF9), bone morphogenetic protein 15 (BMP15), glucose transporter 1 (SCL2A1), hypoxia inducible factor 2α (HIF2α), progesterone receptor (PGR), progestin and adipoQ receptor 5 (PAQR5), progesterone receptor membrane component 1 and 2 (PGRMC1, PGRMC2)]. Data were tested using analysis of variance (ANOVA) followed by multiple pairwise comparisons using Tukey’s test. A P-value of ≤0.05 was considered significant. The relative abundance of all transcripts except SCL2A1 was significantly increased in oocytes collected from follicles of the oCL phase compared with that from oocytes that had been aspirated during the iCL phase. A significant increase in the relative amount of PGR, PGRMC1, PGRMC2, and BMP15 transcripts was detected in oocytes stemming from the follicular phase to those from the iCL phase. No differences in the relative abundance of all transcripts were seen comparing oocytes from oCL phase and oocytes from the follicular phase. In summary, circulating P4 concentrations had an effect on the molecular quality of COC recovered during repeated OPU session, which might affect further development. The financial support of the FBF (Förderverein Biotechnologieforschung) e.V. is gratefully acknowledged.


2016 ◽  
Vol 28 (2) ◽  
pp. 256
Author(s):  
L. M. Vieira ◽  
G. A. Bó ◽  
R. J. Mapletoft

In vitro embryo production (IVP) is an important tool to enhance genetic gain in cattle. However, oocyte quality is a limiting factor for the success of IVP programs in high-producing donors. A series of studies using protocols for follicular wave synchronization and superstimulation before ovum pickup were performed to improve the efficiency of ovum pickup and in vitro production in dairy cattle. The first study evaluated superstimulation with FSH (Folltropin-V®) before ovum pickup in lactating (n = 15) and non-lactating (n = 15) Holstein donors in a crossover design. Cows underwent synchronization of follicle wave emergence (FWE) and at the expected time of FWE, the FSH group received a total dosage of 200 mg of FSH in 4 decreasing doses 12 h apart; controls received no FSH, and ovum pickup was conducted 72 h after the expected FWE in all cows. The FSH-treated cows had a higher (P < 0.01) percentage of medium-sized follicles (6 to 10 mm) at the time of ovum pickup (55.1%) than control cows (20.8%) as well as lower cumulus‐oocyte complexes (COC) recovery rates (60.0 v. 69.8%, respectively; P = 0.002). However, FSH-treated cows had a higher blastocyst production rate (34.5 v. 19.8%; P < 0.01) and more transferable embryos per ovum pickup session (3.0 ± 0.5 v. 1.8 ± 0.4; P = 0.02). Subsequent trials evaluated plasma FSH profiles in 23 heifers and in vitro production following ovum pickup in 90 non-lactating Holstein donors superstimulated with a single IM injection of FSH in 0.5% hyaluronan (HA; MAP-5®, 50 mg). Controls received no treatment, while the F200 group received 200 mg of FSH in 4 decreasing doses 12 h apart. The F200HA and F300HA groups received 200 or 300 mg of FSH in 5 or 7.5 mL, respectively, of 0.5% HA by a single IM injection. Circulating FSH area under curve (AUC) in FSH-treated animals was greater than in the control group (P = 0.02). Although the AUC for F200 group did not differ from HA groups (P = 0.56), the total period of time plasma FSH levels were elevated was greater than in the HA groups (P < 0.01). In the IVP trial, FSH-treated cows had a greater proportion of medium-sized (6–10 mm) follicles than controls (P < 0.001). Also, numbers of follicles (P = 0.01) retrieved (control: 13.1 ± 1.0; F200: 16.5 ± 1.2; F200HA: 19.5 ± 2.1; F300HA: 15.4 ± 1.4; P = 0.01) and blastocysts produced per ovum pickup session (control: 2.4 ± 0.5; F200: 3.7 ± 0.7; F200HA: 4.7 ± 0.7; F300HA: 3.1 ± 0.6; P = 0.06) were greater in cows receiving FSH, regardless of treatment. Cows in the F200HA group had a greater recovery rate (P = 0.009), number of COC cultured (P = 0.04), and blastocysts per ovum pickup session (P = 0.06) than cows in the F300HA group. In conclusion, superstimulation of Holstein donors before ovum pickup increased the efficiency of in vitro production. Additionally, a single IM dose of FSH in 0.5% HA resulted in similar plasma FSH profiles to twice-daily FSH treatment. Non-lactating donors treated with FSH produced more embryos per ovum pickup session regardless of FSH treatment. Lastly, all in vitro-produced endpoints were greater following a single dose of 200 mg of FSH in 0.5% HA than 300 mg of FSH in 0.5% HA.


2017 ◽  
Vol 102 ◽  
pp. 29-34 ◽  
Author(s):  
M. Kafi ◽  
M. Azari ◽  
O. Chashnigir ◽  
S. Gharibzadeh ◽  
Z. Aghabozorgi ◽  
...  

2010 ◽  
Vol 22 (1) ◽  
pp. 258 ◽  
Author(s):  
C. E. Pope ◽  
M. C. Gómez ◽  
B. L. Dresser

The clouded leopard, a spotted, mid-sized cat native to southeast Asia, is classified as Endangered by the U.S. Fish and Wildlife Service. The Species Survival Plan (SSP) program has designated that clouded leopards in North American zoological institutions are a research population with the focus of enhancing management and developing assisted reproductive techniques. In this study, we examined (1) ovarian response to exogenous gonadotropin stimulation, (2) in vitro production of embryos by IVF and intracytoplasmic sperm injection (ICSI), and (3) in vivo developmental ability of in vitro-derived embryos. Eight females at Audubon Center for Research of Endangered Species (ACRES) in New Orleans, LA, were used as oocyte donors and embryo recipients. During non-estrual, but otherwise unknown, stages of the estrous cycle, females 4 to 10 years old at our first treatment were administered a total of 15 (n = 8) or 20 (n = 7) IU of porcine FSH (i.m; Sioux Biochemical Co., Sioux City, IA) daily for 4 days. On Day 5, 10 (n = 8) or 15 (n = 7) IU of porcine LH (i.m; Sioux Biochemical Co.) was given and laparoscopic oocyte retrieval (LOR) was done 24 h later. One, 2, or 3 LOR were performed on 3, 3, and 2 females, respectively (total n LOR = 15), 10 (67%) of which were done on females that were 8 to 12 years of age. A total of 176 pre-ovulatory oocytes (mean = 14.7; range = 3-31) were recovered from 12 LOR performed on 6 females. Two females, a 5-year-old and an 11-year-old, did not respond to gonadotropin treatment. Of 5 females with ≥2 LOR, an average of 16.2 and 14.6 oocytes were recovered at the first and second LOR, respectively. Luteal tissue was present on the ovaries at 3 of 4 LOR performed during January-April as compared with 0 of 11 LOR performed from June-December. Semen was obtained by electroejaculation of 3 males (6, 9, and 11 years of age) and used after cryopreservation [TEST-yolk (media prepared with egg yolk, TES, and Tris) + 6% glycerol] or after storage at 4°C for 24 h (cooled). In vitro production, cryopreservation, and transfer of embryos were done as described by Pope et al. (2006 Theriogenology 66, 1518-1524). Cleavage frequency was 43% overall, 55% (64/117) after IVF, and 20% after ICSI with frozen (10/43) or cooled (2/16) sperm. After IVF with frozen sperm, cleavage rate was 63% (48/76) v. 39% (16/41) with cooled sperm. On Days 5, 57, 26, and 17% of embryos were morula (> 16 cells), early morula (≈16 cells) and pre-morula (< 16 cells), respectively. Forty-four Day 5 embryos were cryopreserved at a slow, controlled rate, 24 of which were thawed and transferred by laparotomy to the uteri of 3 Day 5 gonadotropin-treated recipients (7-9 embryos/female). Similarly, 28 Day 5 fresh embryos were auto-transferred to 3 Day 5 recipients (5-15 embryos/female). Most embryos transferred were morulae (83%) produced by IVF using frozen sperm (71%). None of the recipients established pregnancies, a failure that, undoubtedly, was multifaceted. Age may have been a factor because most recipients were 8 to 11 years old. Nonetheless, we have (1) shown that clouded leopard females are responsive to exogenous gonadotropins, (2) produced embryos in vitro, both by IVF and ICSI, using both cryopreserved and cooled sperm, and (3) provided further evidence of seasonality in ovarian activity.


2016 ◽  
Vol 28 (2) ◽  
pp. 218
Author(s):  
L. G. B. Siqueira ◽  
P. Tribulo ◽  
A. C. Denicol ◽  
M. S. Ortega ◽  
V. M. Negrón-Pérez ◽  
...  

In vitro production (IVP) of embryos can disrupt fetal and placental development and increase risk of abnormal fetal growth. Maternal factors play a role in developmental programming of the early embryo. Colony-stimulating factor 2 (CSF2) is present in the oviduct and endometrium and has improved competence of the pre-implantation embryo to establish pregnancy in cattle. The objective was to determine whether CSF2 during embryo culture alters fetal development and alleviates abnormalities associated with IVP. Holstein oocytes were matured and fertilised in vitro with X-sorted semen from a Holstein bull. Putative zygotes were cultured in SOF-BE1 at 5% CO2 and 5% O2 for 5 days and then randomly assigned to receive vehicle (IVP-control) or 10 ng mL–1 CSF2 (IVP-CSF2). Grade I blastocysts were transferred on Day 7 to Holstein recipients that were previously randomised to receive an IVP-control or an IVP-CSF2 embryo. A third group of cows included in the randomization was assigned to be artificially inseminated on Day 0 using the same bull as for IVP (AI). Pregnancy was terminated on Day 85 or 86. Statistical analysis was performed by analysis of variance using the GLM procedure of SAS with contrasts for AI v. (IVP-control+IVP-CSF2) (contrast 1; C1) and IVP-control v. IVP-CSF2 (contrast 2; C2). Results are least squares means ± s.e.M. A total of 23 morphometric measurements of placenta and fetus were made on 9 AI, 12 IVP and 7 CSF2 female singletons. Conceptuses derived by IVP (IVP-control and IVP-CSF2) differed from those derived by AI for 4 characteristics including fetal bodyweight (142.9 ± 4.7, 157.2 ± 4.4, and 162.6 ± 6.1 g for AI, IVP-control and IVP-CSF2, respectively; C1, P = 0.0237), eviscerated weight (102.9 ± 3.4, 113.6 ± 3.2, and 112.2 ± 4.4 g; C1, P = 0.0602), crown-rump length (CRL) (13.7 ± 0.2, 14.0 ± 0.2, and 14.7 ± 0.3 g; C1, P = 0.0434; C2, P = 0.0631) and umbilical cord diameter (0.85 ± 0.08, 1.1 ± 0.08, and 0.91 ± 0.1 cm; P = 0.0519). Note that while IVP-CSF2 conceptuses were generally similar to those for IVP-control, CRL tended to be highest for IVP-CSF2. Also, umbilical cord diameter for IVP-CSF2 was similar to AI and lower than IVP-control. Data from 1 fetus in the IVP-CSF2 group was excluded from analysis because it had a phenotype consistent with large offspring syndrome. Bodyweight (354 g) was 2-fold larger than other fetuses (average = 155 g) and placental weight was 7-fold greater (1505 v. 211 g). In addition, organs were enlarged and severe ascites and hemorrhagic cotyledons were observed. In conclusion, IVP resulted in increased fetal size and umbilical cord diameter without other significant effects on placental morphometry. CSF2 did not alleviate adverse effects of culture on fetal growth, exacerbating effects on CRL, but did reduce effects of IVP on umbilical cord diameter. Gene expression analysis may be useful for further characterisation of effects and elucidation of mechanisms involved. This project was supported by USDA NIFA Grant 2011–67015–30688.


1986 ◽  
Vol 21 (2) ◽  
pp. 133-138 ◽  
Author(s):  
Zhong-Neng Xie ◽  
William C. Nettles ◽  
Richard K. Morrison ◽  
Ken Irie ◽  
S. Bradleigh Vinson

Three methods, which are more efficient than previously reported techniques, are described for in vitro production of Trichogramma pretiosum Riley in numbers ranging from a few to thousands. Several antibiotics with concentrations as high as 0.5% were not toxic to the parasitoids, reduced microbial growth, and permitted the successful rearing to the pupal stage of T. pretiosum on artificial diet composed of insect hemolymph, egg yolk, and milk. The likelihood that Trichogramma can be mass produced efficiently in vitro has been significantly increased, but it is essential that the cost and nutritional quality of the artificial diet be significantly improved.


2009 ◽  
Vol 21 (7) ◽  
pp. 901 ◽  
Author(s):  
Giovanni Giuseppe Leoni ◽  
Sara Succu ◽  
Valentina Satta ◽  
Mereu Paolo ◽  
Luisa Bogliolo ◽  
...  

This study compares the developmental capacity and cryotolerance of embryos produced from oocytes of stimulated prepubertal and adult Sarda goats. Twelve prepubertal and 13 adult goats were each given 110 and 175 IU FSH, respectively, and cumulus–oocyte complexes (COCs) were collected by laparoscopic oocyte-pick-up (LOPU). After in vitro maturation, fertilisation and culture (IVMFC), blastocysts were vitrified, warmed and blastocoel re-expansion and gene expression were evaluated. Prepubertal goats produced a higher COCs number than adults (mean ± s.e.m., 89.67 ± 5.74 and 26.69 ± 3.66, respectively; P < 0.01). Lower developmental competence was demonstrated in the prepubertal oocytes as shown by a higher number of COCs discarded before IVM (21.1% and 14.7% for prepubertals and adults, respectively; P < 0.01) and IVF (23.4% v. 9.1%; P < 0.01) and by the lower cleavage (55.6% and 70.3%, respectively; P < 0.01) and blastocyst rates (24.2% and 33.9%, respectively; P < 0.05). Compared with the adult, prepubertal vitrified/warmed blastocysts showed significantly (P < 0.05) lower in vitro viability, as determined by the re-expansion rate (62.5% and 40.3%). No differences were observed in the time required for blastocoel re-expansion or in cyclin B1, E-cadherin, Na/K ATPase, HSP90β and aquaporin 3 messenger RNA quantity. These results show that in vitro-produced embryos produced from prepubertal goat oocytes have a lower developmental rate and cryotolerance compared with their adult counterparts. However, we can assume that the quality of re-expanded embryos does not differ between the two groups.


2017 ◽  
Vol 53 (1) ◽  
pp. 226-236 ◽  
Author(s):  
TC Marques ◽  
EC da Silva Santos ◽  
TO Diesel ◽  
LO Leme ◽  
CF Martins ◽  
...  

2005 ◽  
Vol 48 (1) ◽  
pp. 32-39
Author(s):  
L. Kątska-Książkiewicz ◽  
M. Bochenek ◽  
B. Ryńska

Abstract. Bull effect on results of in vitro embryo production has been well documented. The aim of the present study was to find the relationship between quality of bull sperm chromatin and its effect on in vitro embryo production. Bovine in vitro matured oocytes were fertilized in vitro using capacitated spermatozoa (freshly ejaculated or frozen-thawed) of 12 bulls. Semen was simultaneously processed according to the sperm chromatin structure assay (SCSA) method and was analysed by flow cytometry. At least 3 replications of IVP with the same semen sample were done. The percentage of spermatozoa with abnormal chromatin ranged from 0.4% to 23.8%. All bulls used for the experiment were divided into three groups showing minimal (0.82% ± 6.82%), low (1.70% ± 15.82%) and high (18.16% ± 53.59%) percentages of spermatozoa with abnormal chromatin structure. Both cleavage rates and embryo development to the blastocyst stage were correlated significantly with sperm chromatin abnormalities and resulted in 23.1, 17.7 and 12.2% of blastocysts respectively for sperm with minimal, low and high percentages of chromatin abnormalities. The SCSA method may be used as a practical indicator of suitability of bull ejaculate for IVP purposes.


2020 ◽  
Vol 12 (1) ◽  
pp. 111-121
Author(s):  
Janderson Aguiar Rodrigues ◽  
Leandro Ferreira Domiciano ◽  
Roberta Martin Gomes da Silva Borges ◽  
Glaudson Marcos Rondon ◽  
Natalia Tousube da Rocha ◽  
...  

The objective of this work was to evaluate the influence of the tropical climate on donor races on the quantity and quality of oocytes aspirated in Nellore and Senepol cows by means of follicular aspiration, destined to the in vitro production of embryos. The experimental design was in randomized blocks, considering each bovine female as a plot and each farm being a block totaling 14 different properties, and the number of cows used were 238 for the Nelore breed and 267 for the Senepol breed totaling 505 bovine females. The evaluation of the total number of oocytes and the quality by the quality classification of oocytes aspirated in Grade I, II, III, atresic and degenerate. According to the results we can conclude that, among the two races evaluated, a greater amount of GII oocytes is observed for the Nelore breed, and the Senepol breed in tropical climate can produce a good quantity and quality of oocytes, with the lowest amount of nude in relation to the Nelore.


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