scholarly journals Meta-analysis of the effects of smooth endoplasmic reticulum aggregation on birth outcome

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Hongqin Zhang ◽  
Wenhui Hu ◽  
Ying Zhong ◽  
Zhenhua Guo
Keyword(s):  
Endoplasmic Reticulum ◽  
Oocyte Maturation ◽  
Birth Outcome ◽  
Smooth Endoplasmic Reticulum ◽  
Meta Analysis ◽  
Perinatal Complications ◽  
Vitro Fertilization ◽  
Healthy Infants ◽  
Maturation Rate

Abstract Background Smooth endoplasmic reticulum aggregation (SERa, SER+) has been reported to increase the risk of birth malformations and other abnormal outcomes, miscarriage, and perinatal complications. Other studies, however, suggest that SER+ embryos may develop into healthy infants. One report indicates that 25% of in vitro fertilization (IVF) centers discard SER+ oocytes. Thus, we investigated the effect of SER+ on birth outcomes in IVF and intracytoplasmic sperm injection. Methods We performed a literature search using PubMed, ScienceDirect, Cochrane, Embase, Ovid, and Scopus. We found a total of 1500 relevant studies between 1978 and 2020 and conducted a meta-analysis to study the effects of SER+ on live births, birth weight, and the number of metaphase II (MII) oocytes retrieved per cycle. Results Eleven eligible studies were included. If the SER+ zygote was evaluated again at the embryo transfer (ET) stage, SER+ did not affect birth or infant body weight. Stimulated ovaries producing too many oocytes per cycle were positively correlated with SER+ (OR = 1.28, 95% CI = 0.41–2.15; p = 0.004). SER+ was positively correlated with oocyte maturation rate, and observed heterogeneity in a previous meta-analysis was likely due to maternal age. Our data also showed that SER+ cycles produced more oocytes but achieved the same number of births from ET. Conclusions The use of SER+ MII oocytes is rare, with the collection of many oocytes in 1 cycle potentially inducing SER+. SER+ may be more common than we originally thought, as some SER+ is found in all oocytes. Although SER+ positively affected oocyte maturation rate, it did not affect births. We hypothesized that this is because the best embryos are chosen at every step of the process, and the oocytes with the poorest characteristics are removed. We therefore suggest a standard method for measuring SER+. Although embryos produced from SER+ cycles can be used, they should only be transferred when no other suitable embryos are available over several cycles.

scholarly journals Effect of follicle-stimulating hormone on Bligon goat oocyte maturation and embryonic development post in vitro fertilization

2020 ◽  
Vol 13 (11) ◽  
pp. 2443-2446
Author(s):  
Diah Tri Widayati ◽  
Mulyoto Pangestu
Keyword(s):  
In Vitro Fertilization ◽  
Embryonic Development ◽  
Oocyte Maturation ◽  
In Vitro Maturation ◽  
Follicle Stimulating Hormone ◽  
Fertilization In Vitro ◽  
Vitro Fertilization ◽  
Maturation Rate ◽  
Stimulating Hormone

Background and Aim: Bligon goat is a crossbreed between Etawah and Kacang goat. This crossbreed goat is mostly reared by small farmers. In vitro maturation allows female goat (does) contributes toward reproduction despite the fact that the animal has been slaughtered. The aim of this study was to determine the in vitro maturation rate of Bligon goat oocytes supplemented with follicle-stimulating hormone (FSH), and their ability for further embryonic development after in vitro fertilization. Materials and Methods: Experiment was conducted at the Laboratory of Animal Physiology and Reproduction, Faculty of Animal Science, Universitas Gadjah Mada, Yogyakarta, using Bligon goat ovaries obtained from local slaughterhouse around Yogyakarta. One thousand five hundred cumulus-oocyte complexes were matured for 24 h in tissue culture medium 199 supplemented with 50 IU/L FSH or without FSH (control). First, matured oocytes were evaluated its morphology based on the expansion of cumulus cells and PB1 extrusion. Next, 600 oocytes were then stained with 1% aceto-orcein to examine maturation based on changes in the configuration of chromosomes and nuclear membrane breakdown. Oocytes were considered mature when they reached metaphase II. To prove the ability of mature oocytes to develop into embryos, 900 oocytes were processed for fertilization in vitro. The data were analyzed using analysis of variance. Results: The results indicated that FSH supplementation significantly increased oocyte maturation rate (65.21±7.26 vs. 43.25±6.23%) as indicated by extrusion of PB1 and homologous chromosome pairing and lined in the equator. The rate of degeneration was lower in the FSH-supplemented medium (3.21±0.25 vs. 10.17±3.15%). The blastocyst stage of oocyte developed embryos was reached by 12.43±2.15% and 22.28±4.86% of the control and treatment groups, respectively. Conclusion: FSH supplementation significantly improves oocyte maturation and yields mature oocytes for future embryo development in vitro.

176 Effect of epigallocatechin-3-gallate on bovine oocyte in vitro maturation, fertilization, and development

2019 ◽  
Vol 31 (1) ◽  
pp. 212
Author(s):  
Y. Honkawa ◽  
Y. Gen ◽  
S.-H. Hyon ◽  
C. Kubota
Keyword(s):  
Oocyte Maturation ◽  
In Vitro Maturation ◽  
Polar Body ◽  
Sperm Concentration ◽  
P Value ◽  
Bovine Oocyte ◽  
Vitro Fertilization ◽  
Significant Difference ◽  
Maturation Rate

Epigallocatechin-3-gallate (EGCG) is a major ingredient of catechin polyphenols, and a strong antioxidant compound. Huang et al. (2018 Asian-australas. J. Anim. Sci.) reported that adding 50μM EGCG can improve the bovine oocyte maturation rate. In this research, we investigated the effect of EGCG supplementation on different periods in bovine IVF. Cumulus-oocyte complex (COC) collected from ovaries of slaughtered cows were cultured in maturation medium (20 to 30 oocytes per 100-µL droplet), which consisted of TCM-199 with Earle’s salts and 25mM HEPES supplemented with 10% (vol/vol) fetal bovine serum (FBS), 1µg mL−1 oestradiol, 0.02mg mL−1 FSH, and antibiotics at 38.5°C in a humidified atmosphere of 5% CO2 in air for 24h (in vitro maturation, IVM). After IVM, COC were fertilized in the fertilization medium (modified Brackett-Oliphant media supplemented with 10 µgmL−1 heparin, 10mM caffeine, and 3mg mL−1 BSA) for 6h using semen of one bull at final sperm concentration of 1×107 mL−1 (IVF). After IVF, COC were denuded and cultured in culture medium [CR1aa supplemented with 10% (vol/vol) FBS and antibiotics] at 38.5°C in a humidified atmosphere of 5% O2, 5% CO2, and 90%N2 for 8 days (in vitro culture, IVC). The EGCG was supplemented at 10, 25, 50, and 100M in IVM medium; 25 and 50 µM in IVF medium; and 50 and 100 µM in IVC medium. After 24h in IVM medium, COC were denuded by pipetting, fixed in 3:1 ethanol:acetic acid for 24h and then checked for nuclear and polar body by using aceto-orcein stain. After 18h in IVF, the pronucleus in zygote was fixed in 3:1 ethanol:acetic acid for 24h and checked by aceto-orcein staining. Embryo development was evaluated by counting the total number of embryos that had reached compacted morula by 6 to 8 days after IVF. Significant differences were analysed by chi-squared test and residual analysis. A P-value<0.05 was considered statistically significant. When EGCG was added to IVM, there was no significant difference of oocyte maturation rate between all concentrations (0v. 10v. 25v. 50v. 100 μM: 73.9% v. 56.7% v. 76.7% v. 72.7% v. 63.5%). When EGCG was added to IVF, there was no significant difference of fertilized rate (0v. 25v. 50 μM: 59.4% v. 73.7% v. 64.9%). When EGCG was added to IVC, there was no significant difference in development rate (0v. 50v. 100 μM: 26.2% v. 15.7% v. 22.0%). In this research, EGCG addition did not affect bovine in vitro fertilization.

scholarly journals The impact of Alpha/ESHRE consensus regarding oocytes with aggregates of smooth endoplasmic reticulum (SERa) on in vitro fertilization outcome

2015 ◽  
Vol 32 (11) ◽  
pp. 1629-1635 ◽  
Author(s):  
Liliana Restelli ◽  
Silvia Delle Noci ◽  
Alice Mangiarini ◽  
Stefania Ferrari ◽  
Edgardo Somigliana ◽  
...  
Keyword(s):  
Endoplasmic Reticulum ◽  
In Vitro Fertilization ◽  
Smooth Endoplasmic Reticulum ◽  
Vitro Fertilization ◽  
The Impact

scholarly journals Live birth rates in In vitro fertilization cycles with oocytes containing smooth endoplasmic reticulum aggregates and normal oocytes

2019 ◽  
Vol 12 (2) ◽  
pp. 156
Author(s):  
Sumana Gurunath ◽  
Reeta Biliangady ◽  
UmaMaheshwari Sundhararaj ◽  
Ambika Gangadharswamy ◽  
Swathi Gundlapalli ◽  
...  
Keyword(s):  
Endoplasmic Reticulum ◽  
In Vitro Fertilization ◽  
Live Birth ◽  
Smooth Endoplasmic Reticulum ◽  
Birth Rates ◽  
Vitro Fertilization ◽  
Live Birth Rates

Effect of vitrification on human oocyte maturation rate during in vitro maturation procedure: A systematic review and meta-analysis

Cryobiology ◽  
2018 ◽  
Vol 83 ◽  
pp. 84-89 ◽  
Author(s):  
Mehdi Mohsenzadeh ◽  
Amin Salehi-Abargouei ◽  
Nasim Tabibnejad ◽  
Mojgan Karimi-Zarchi ◽  
Mohammad Ali Khalili
Keyword(s):  
Systematic Review ◽  
Oocyte Maturation ◽  
In Vitro Maturation ◽  
Meta Analysis ◽  
Human Oocyte ◽  
Maturation Rate

scholarly journals Stereological Analysis of Mitochondria and Smooth Endoplasmic Reticulum Distribution in Human Oocytes at Prophase I

2008 ◽  
Vol 14 (S3) ◽  
pp. 103-104
Author(s):  
A. Luís ◽  
E. Rocha ◽  
E Oliveira ◽  
J. Silva ◽  
A. Barros ◽  
...  
Keyword(s):  
Endoplasmic Reticulum ◽  
Oocyte Maturation ◽  
Smooth Endoplasmic Reticulum ◽  
Germinal Vesicle ◽  
Human Oocytes ◽  
Stereological Analysis ◽  
Prophase I ◽  
Maturation Stages ◽  
In Vitro Oocyte Maturation

The structure of human oocytes at the different maturation stages is known based on descriptive studies of its ultrastructural composition. The tridimensional quantitative ultrastructural analysis of human oocytes would be important for understanding folliculogenesis and establishing adequate methods of in vitro oocyte maturation. In this study, stereological methods were applied to quantify the distribution of mitochondria (M) and smooth endoplasmic reticulum (SER) in oocytes at the germinal vesicle (VG) stage of prophase I.

In Vitro Induction of Crystals of MT Protein by Vinblastine-Colcemid in Mouse Spermatids

1974 ◽  
Vol 32 ◽  
pp. 132-133
Author(s):  
John J. Wolosewick ◽  
John H. D. Bryan
Keyword(s):  
Endoplasmic Reticulum ◽  
Smooth Endoplasmic Reticulum ◽  
Nuclear Ring ◽  
Rough Er ◽  
Distal Direction ◽  
In Vitro Induction

Early in spermiogenesis the manchette is rapidly assembled in a distal direction from the nuclear-ring-densities. The association of vesicles of smooth endoplasmic reticulum (SER) and the manchette microtubules (MTS) has been reported. In the mouse, osmophilic densities at the distal ends of the manchette are the organizing centers (MTOCS), and are associated with the SER. Rapid MT assembly and the lack of rough ER suggests that there is an existing pool of MT protein. Colcemid potentiates the reaction of vinblastine with tubulin and was used in this investigation to detect this protein.

Sign in / Sign up

Export Citation Format

Share Document