Male mice conceived by in vitro fertilization exhibit increased glucocorticoid receptor (GR) expression in fat tissue

2015 ◽  
Vol 104 (3) ◽  
pp. e188-e189
Author(s):  
R. Simbulan ◽  
X. Liu ◽  
A. Donjacour ◽  
S. Feuer ◽  
P. Rinaudo
2019 ◽  
Vol 120 (10) ◽  
pp. 17250-17257 ◽  
Author(s):  
Zahra Mehraban ◽  
Marefat Ghaffari Novin ◽  
Mohammad Ghasem Golmohammadi ◽  
Mohsen Sagha ◽  
Khashayar Pouriran ◽  
...  

2017 ◽  
Vol 69 ◽  
pp. 196-203 ◽  
Author(s):  
Hiwa Karimi ◽  
Pooya Mahdavi ◽  
Shohreh Fakhari ◽  
Mohammad Reza Faryabi ◽  
Parisa Esmaeili ◽  
...  

Endocrinology ◽  
2020 ◽  
Vol 161 (9) ◽  
Author(s):  
Teppei Goto ◽  
Masumi Hirabayashi ◽  
Youki Watanabe ◽  
Makoto Sanbo ◽  
Koichi Tomita ◽  
...  

Abstract Restoration of spermatogenesis and fertility is a major issue to be solved in male mammals with hypogonadotropic hypogonadism. Kiss1 knockout (KO) male mice are postulated to be a suitable animal model to investigate if hormonal replacement rescues spermatogenesis in mammals with this severe reproductive hormone deficiency, because KO mice replicate the hypothalamic disorder causing hypogonadism. The present study investigated whether testosterone supplementation was able to restore spermatogenesis and in vitro fertilization ability in Kiss1 KO mice. To this end, spermatogenesis, in vitro fertilization ability of Kiss1 KO sperm, and preimplantation development of wild-type embryos inseminated with Kiss1 KO sperm, were examined. The newly generated Kiss1 KO male mice showed infertility with cryptorchidism. Subcutaneous testosterone supplementation for 6 weeks restored plasma and intratesticular testosterone levels, elicited testicular descent, and induced complete spermatogenesis from spermatocytes to elongated spermatids in the testis, resulting in an increase in epididymal sperm number in testosterone-supplemented Kiss1 KO male mice. Epididymal sperm derived from the testosterone-supplemented Kiss1 KO mice showed normal in vitro fertilization ability, and the fertilized eggs showed normal preimplantation development, while the males failed to impregnate females. These results suggest that the failure of spermatogenesis in Kiss1 KO mice is mainly due to a lack of testosterone production, and that Kiss1 KO sperm are capable of fertilizing eggs if the animals receive the appropriate testosterone supplementation without local kisspeptin signaling in the testis and epididymis. Thus, testosterone supplementation would restore spermatogenesis of male mammals showing hypogonadotropic hypogonadism with genetic inactivation of the KISS1/Kiss1 gene.


2018 ◽  
Vol 157 ◽  
pp. 294-303 ◽  
Author(s):  
A.P. López-Cardona ◽  
I. Ibarra-Lecue ◽  
R. Laguna-Barraza ◽  
S. Pérez-Cerezales ◽  
L. Urigüen ◽  
...  

2021 ◽  
Vol 22 (19) ◽  
pp. 10650
Author(s):  
Galina Vladimirovna Kontsevaya ◽  
Ludmila Alekseevna Gerlinskaya ◽  
Yury Mikhailovich Moshkin ◽  
Margarita Vladimirovna Anisimova ◽  
Aliya Konstantinovna Stanova ◽  
...  

The latest vaccination campaign has actualized the potential impact of antigenic stimuli on reproductive functions. To address this, we mimicked vaccination’s effects by administering keyhole limpet hemocyanin (KLH ) to CD1 male mice and used their sperm for in vitro fertilization (IVF). Two-cell embryos after IVF with spermatozoa from control (C) or KLH-treated (Im) male mice were transferred to surrogate mothers mated with vasectomized control (C) or KLH-treated (Im) male mice, resulting in four experimental groups: C–C, Im–C, C–Im, and Im–Im. The pre-implantation losses were significantly lower in the Im–C group than in the C–Im group. At the same time, the resorption rates reduced markedly in the C–Im compared to the Im–C group. Embryo and placenta weights were significantly higher in the Im–Im group. Although the GM-CSF levels were lower in the amniotic fluid of the gestating surrogate mothers in the Im–Im group, they were strongly correlated with embryo mass. The number–size trade-off was only significant in the Im–Im group. This suggests a positive, cooperative effect of spermatozoa and seminal fluid from immune-primed males on embryo growth and the optimal distribution of surrogate mother maternal resources despite the negative impact of males’ antigenic challenge on the IVF success rate.


MedPharmRes ◽  
2018 ◽  
Vol 2 (2) ◽  
pp. 5-20
Author(s):  
Vu Ho ◽  
Toan Pham ◽  
Tuong Ho ◽  
Lan Vuong

IVF carries a considerable physical, emotional and financial burden. Therefore, it would be useful to be able to predict the likelihood of success for each couple. The aim of this retrospective cohort study was to develop a prediction model to estimate the probability of a live birth at 12 months after one completed IVF cycle (all fresh and frozen embryo transfers from the same oocyte retrieval). We analyzed data collected from 2600 women undergoing in vitro fertilization (IVF)/intracytoplasmic sperm injection (ICSI) at a single center in Vietnam between April 2014 and December 2015. All patients received gonadotropin-releasing hormone (GnRH) antagonist stimulation, followed by fresh and/or frozen embryo transfer (FET) on Day 3. Using Cox regression analysis, five predictive factors were identified: female age, total dose of recombinant follicle stimulating hormone used, type of trigger, fresh or FET during the first transfer, and number of subsequent FET after the first transfer. The area under the receiver operating characteristics curve for the final model was 0.63 (95% confidence interval [CI] 0.60‒0.65) and 0.60 (95% CI 0.57‒0.63) for the validation cohort. There was no significant difference between the predicted and observed probabilities of live birth (Hosmer-Lemeshow test, p > 0.05). The model developed had similar discrimination to existing models and could be implemented in clinical practice.


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