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Intromission during mating induces oxytocin release, likely shortening behavioral estrus and enhancing luteal function in ewes. Oxytocin's short half-life and limited transfer into the brain, however, restrict its exogenous use. Carbetocin, a long-acting oxytocin analog with peripheral effects, may be a practical pharmacological alternative. The aim was to determine whether systemic administration of Carbetocin could induce changes in sexual receptivity, follicular development, timing of ovulation during the estrous period, and luteal function similar to those observed after multiple matings. Timing of behavioral estrus was synchronized among 20 multiparous Merilin ewes. Upon detection of estrus, ewes were randomly assigned to a control (CON, n = 10) or Carbetocin-treated (CAR, n = 10) group. Ewes in the CAR group were administered a single intravenous dose of Carbetocin (0.2 mg/100 kg) at estrous onset. Follicular and luteal dynamics were monitored by ultrasonography, and sexual receptivity was assessed based on the ewe' immobility when mounted of a ram. Luteal images were analyzed using ImageJ™ software to quantify both total and perfused corpus luteum areas. Carbetocin treatment increased the ovulation rate (1.9 ± 0.2 and 1.4 ± 0.2; P = 0.04) and reduced the dispersion in interval between the end of estrus and time of ovulation (SD: 3.86 and 8.01, respectively, P = 0.04). In conclusion, Carbetocin administration at the onset of estrus enhanced synchrony in time of ovulation among ewes, and increased ovulation rate but compared with ewes where there were multiple matings, did not shorten duration of estrus.
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http://dx.doi.org/10.1016/j.theriogenology.2025.117600 | DOI Listing |
Proc Natl Acad Sci U S A
September 2025
Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853.
Ovulation is an intricate process that is essential for reproductive success. In , ovulation increases after mating. This increase is initiated by the male seminal fluid protein ovulin and is executed by female pathways, including octopamine (OA) neuronal signaling.
View Article and Find Full Text PDFChem Senses
September 2025
Rutgers University Department of Nutritional Sciences. 65 Dudley Road, New Brunswick, NJ 08901, USA.
Recent research has shown that KATP channels in mouse taste bud cells enhance glucose taste signaling by depolarizing the cell when ATP is present. Relatedly, estradiol has been shown to enhance glucose sensing in human pancreatic β cells via closure of KATP channels. Since taste tissue has estradiol receptors, we linked these two observations and tested whether elevated estradiol may also enhance taste sensitivity and liking for glucose in humans.
View Article and Find Full Text PDFFront Endocrinol (Lausanne)
September 2025
Gynecology/Obstetrics Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Introduction: Several studies indicate that a specific genotype profile could influence ovarian sensitivity to exogenous gonadotropin. However, most of the previous studies were observational and retrospective and thereby more prone to bias. The aim of this study was to evaluate the impact of gonadotropin single nucleotide polymorphisms (SNPs) on the outcomes of fertilization (IVF) in infertile patients undergoing their first ovarian stimulation (OS) cycle.
View Article and Find Full Text PDFJ Assist Reprod Genet
September 2025
Morsani College of Medicine, Department of Obstetrics and Gynecology, University of South Florida, 2 Tampa General Circle, STC 6th Floor, Tampa, FL, 33606, USA.
Purpose: Prior studies in fresh embryo transfer IVF cycles have associated elevated serum progesterone level on day of ovulatory trigger, particularly if ≥ 1.5 ng/ml, with decreased pregnancy rates. A similar association has been found in intrauterine insemination (IUI) cycles using gonadotropins for ovulation induction.
View Article and Find Full Text PDFHum Reprod
September 2025
IVIRMA Global Research Alliance, Genera, Clinica Valle Giulia, Rome, Italy.
Study Question: Do IVF laboratory workflows influence the mean blastulation rate per cohort of inseminated metaphase II oocytes (m-BR)?
Summary Answer: Neither the total number of procedures nor the workload per operator affected m-BR; instead, each additional hour in the interval from ovulation trigger to oocyte denudation (range 36-44 h) was associated with a measurable decline, especially beyond the 40-h threshold.
What Is Known Already: Control of laboratory conditions and standardized protocols are essential for optimizing m-BR in IVF. While advancements in technology and culture systems have improved ART outcomes, the effect of laboratory managerial decisions and procedural timing on embryological outcomes remains unclear.