LH release and ovulatory response after intramuscular, intravenous, and intrauterine administration of β-nerve growth factor of seminal plasma origin in female llamas

2015 ◽  
Vol 84 (7) ◽  
pp. 1096-1102 ◽  
Author(s):  
M. Silva ◽  
A. Fernández ◽  
C. Ulloa-Leal ◽  
G.P. Adams ◽  
M.A. Berland ◽  
...  
2020 ◽  
Vol 148 ◽  
pp. 37-47 ◽  
Author(s):  
Jamie L. Stewart ◽  
Stephanie Stella ◽  
Laís L. Cunha ◽  
Nicholas W. Dias ◽  
Igor F. Canisso ◽  
...  

2017 ◽  
Vol 17 (2) ◽  
pp. 442-453 ◽  
Author(s):  
Rosa M. Garcia-Garcia ◽  
Maria del Mar Masdeu ◽  
Ana Sanchez Rodriguez ◽  
Pilar Millan ◽  
Maria Arias-Alvarez ◽  
...  

2021 ◽  
Vol 33 (2) ◽  
pp. 152
Author(s):  
R. A. Carrasco ◽  
S. Pezo ◽  
G. P. Adams

The central inhibitory effects of progesterone on gonadotrophin secretion have been well documented in several species, including camelids. Nerve growth factor (NGF) in seminal plasma triggers ovulation in camelids and is thought to act at the level of the hypothalamus. The objective of the study was to determine the effect of progesterone on NGF-induced LH release in llamas. In Experiment 1, llamas were assigned to a low, medium, or high progesterone group (n=4 per group). The low progesterone group consisted of non-mated (non-ovulatory) llamas, the medium progesterone group consisted of mated llamas (luteal phase; 3–4 weeks pregnant), and the high progesterone group consisted of non-mated llamas given a single intramuscular (IM) dose of progesterone (300mg IM, Progesterone BioRelease LA). A jugular catheter was placed, and the following day llamas were given an intravenous dose of 1mg of NGF isolated from seminal plasma. Blood samples were taken every 30min from 1h before to 5.5h after NGF treatment. In Experiment 2, the pituitary LH response to gonadotrophin-releasing hormone (GnRH) was compared between llamas treated with either Progesterone BioRelease LA or saline (n=4 per group). Sixteen hours later, llamas in both groups were given 50µg of gonadorelin (GnRH) IV, and blood samples were collected by jugular puncture at 0.5h before and 0, 1, 2, and 4h after GnRH. Blood samples were centrifuged, and plasma was stored frozen until radioimmunoassay for LH and progesterone. Data are presented as mean±s.e.m. Data were analysed by one-way ANOVA for single-point and repeated-measures, and independent or paired t-tests. In Experiment 1, plasma progesterone concentrations in the low, medium, and high progesterone groups were 0.6±0.3, 8.2±0.4, and 14.9±1.2ng mL−1, respectively, at the time of NGF treatment (P<0.05). Circulating concentrations of LH did not differ among progesterone groups (treatment, P=0.49; time, P<0.01; treatment×time interaction, P=0.65). In all groups, LH concentrations were elevated within 30min of NGF administration, reached a peak by 2h, and remained elevated beyond the sampling period. Comparison of samples collected during the pretreatment period (i.e. −60, −30, and 0min), however, revealed that plasma LH concentrations in the high progesterone group were half that of the low and medium progesterone groups (P<0.03). In Experiment 2, plasma progesterone concentrations in the progesterone- and saline-treated groups were 12.7±2.2 and 1.3±0.3ngmL−1, respectively (P<0.01). Despite the difference in circulating progesterone concentrations, the LH response to GnRH treatment was not different between groups (treatment group, P=0.43; time, P<0.01; treatment×time interaction, P=0.84). Results demonstrate a suppressive effect of progesterone on basal LH release in llamas, but no suppressive effect on NGF- or GnRH-induced surge release from the pituitary gland. Results are consistent with the hypothesis that the site of action of NGF is downstream of the hypothalamic site of action of progesterone. This research was supported by NSERC Canada.


2018 ◽  
Vol 197 ◽  
pp. 335-342 ◽  
Author(s):  
Jamie L. Stewart ◽  
Igor F. Canisso ◽  
Robyn E. Ellerbrock ◽  
Vitor R.G. Mercadante ◽  
Fabio S. Lima

2018 ◽  
Vol 106 ◽  
pp. 30-38 ◽  
Author(s):  
Jamie L. Stewart ◽  
Vitor R.G. Mercadante ◽  
Nicholas W. Dias ◽  
Igor F. Canisso ◽  
Peter Yau ◽  
...  

Endocrinology ◽  
2016 ◽  
Vol 157 (8) ◽  
pp. 3224-3232 ◽  
Author(s):  
Marco A. Berland ◽  
Cesar Ulloa-Leal ◽  
Miguel Barría ◽  
Hollis Wright ◽  
Gregory A. Dissen ◽  
...  

Llamas are considered to be reflex ovulators. However, semen from these animals is reported to be rich in ovulation-inducing factor(s), one of which has been identified as nerve growth factor (NGF). These findings suggest that ovulation in llamas may be elicited by chemical signals contained in semen instead of being mediated by neural signals. The present study examines this notion. Llamas displaying a preovulatory follicle were assigned to four groups: group 1 received an intrauterine infusion (IUI) of PBS; group 2 received an IUI of seminal plasma; group 3 was mated to a male whose urethra had been surgically diverted (urethrostomized male); and group 4 was mated to an intact male. Ovulation (detected by ultrasonography) occurred only in llamas mated to an intact male or given an IUI of seminal plasma and was preceded by a surge in plasma LH levels initiated within an hour after coitus or IUI. In both ovulatory groups, circulating β-NGF levels increased within 15 minutes after treatment, reaching values that were greater and more sustained in llamas mated with an intact male. These results demonstrate that llamas can be induced to ovulate by seminal plasma in the absence of copulation and that copulation alone cannot elicit ovulation in the absence of seminal plasma. In addition, our results implicate β-NGF as an important mediator of seminal plasma-induced ovulation in llamas because ovulation does not occur if β-NGF levels do not increase in the bloodstream, a change that occurs promptly after copulation with an intact male or IUI of seminal plasma.


2017 ◽  
Vol 29 (1) ◽  
pp. 114
Author(s):  
J. L. Stewart ◽  
V. R. G. Mercadante ◽  
I. F. Canisso ◽  
F. S. Lima

Nerve growth factor-β (NGF) has been identified in the seminal plasma of livestock and is required for the induction of ovulation in camelids. Until recently, it was thought to play a negligible role in species with spontaneous ovulation. On the contrary, recent studies have shown that systemic administration of NGF, purified from llama seminal plasma, was associated with larger corpus luteum (CL) diameter and higher concentrations of progesterone (P) following ovulation. The objective of the current project was to determine if systemic administration of NGF, purified from bovine seminal plasma, would improve CL formation and enhance embryonic development. Our hypothesis was that systemic administration of NGF at the time of artificial insemination in cows would lead to increased CL volume, increased P secretion, and improved expression of markers of conceptus development and maternal recognition of pregnancy. Seminal plasma was harvested from semen collected by electroejaculation in Angus cross bulls. Purification of NGF was performed using a combination of anion- and cation-exchange chromatography and gradient elution. Beef cows were randomly assigned to CONT (n = 30) or NGF (n = 30) groups and synchronized using a 7-day Co-Synch + CIDR program. At time of insemination (day 0), NGF cows received 296 µg of purified NGF, reconstituted in 12 mL of PBS, and CONT cows received 12 mL of PBS intramuscularly. Blood samples were collected from the coccygeal vein of each cow at days 0, 3, 7, 10, 14, 19, 21, 28, 31, 38, 45, and 66. Ultrasound was performed at each time point for determination of ovarian structures (day 0), corpus luteum volume (all time points), and fetus detection (day 28). Statistical analysis was performed using analysis of variance with repeated-measures in R (R version 3.2.2; https://www.r-project.org/). At day 28, 17/30 (57%) CONT cows and 21/30 (70%) NGF cows were diagnosed as pregnant (P = 0.15). At day 0, cows that later became pregnant had a larger follicular diameter (1.46 cm) than those diagnosed as open (1.16 cm; P < 0.01). Follicular diameter at day 0 did not differ significantly between CONT and NGF groups for either open (P = 0.35) or pregnant (P = 0.90) cows. CL volume in open cows was affected by day (P < 0.001) with no treatment (P = 0.84) or treatment by day (P = 0.42) interaction. CL volume in pregnant cows was affected by both day (P < 0.001) and treatment (P < 0.001), with CONT cows having a higher CL volume than NGF cows. Though NGF appeared to have an inhibitory effect on CL volume in pregnant cows, results are still pending for quantification of P, insulin-like growth factor 1, pregnancy-specific protein B, and interferon-stimulated genes, which will more accurately assess the effects that NGF may have on conceptus development. The results of this study will help us to better understand the role of the seminal plasma protein, NGF, at ovulation and determine if it can be utilised to enhance insemination programs in cattle.


2014 ◽  
Vol 81 (8) ◽  
pp. 1101-1107.e1 ◽  
Author(s):  
C. Ulloa-Leal ◽  
O.A. Bogle ◽  
G.P. Adams ◽  
M.H. Ratto

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