228 Effect of seminal plasma on the interval to application of equine chorionic gonadotrophin for the recovery of cumulus-oocyte complexes in alpacas (Vicugna pacos)

2020 ◽  
Vol 32 (2) ◽  
pp. 242
Author(s):  
W. F. Huanca ◽  
J. M. Palomino ◽  
J. C. Villanueva ◽  
J. Malaga ◽  
W. Huanca

Alpacas as other camelids are induced ovulators and require an external stimulus-mounting by the male-for ovulation. NGF-β, protein present in the seminal plasma (SP) is reported as being responsible for stimulating ovulation. However, limited information exists on the effect of ovulation inducers in the new follicular wave emergence with application on protocols of superstimulation. The aim of the study was to determine the effect of two ovulation induced techniques and two different times on the interval to application of equine chorionic gonadotrophin (eCG) for the ovarian superstimulation for the recovery of COCs by ovum pick- up (OPU). Alpacas were evaluated by transrectal ultrasonography with an Aloka SSD 500 ultrasound and transducer (7.5MHz) to determine the presence of a dominant follicle=7mm. A 2×2 experimental design was used with adult female alpacas, 6 to 8 years old, which were assigned to one of the treatments when a dominant follicle=7mm was present. Alpacas were assigned randomly 1 of 2 groups (Day 0) in which follicular ovulation was induced by seminal plasma 1mL IM (SP, n=13; group 1) with application of 650IU of eCG at 36h (n=6) or 48h (n=7) post-application of SP, or by GnRH with 0.008mg of Buserelin IM (GnRH, n=10; group 2) with application of 650IU eCG at 36h (n=5) or 48h (n=5) post-application of GnRH. On Day 7, COCs were counted and the OPU procedure was performed in every group. Data were analysed using ANOVA. Results are presented in Table 1. In conclusion, both inducers of ovulation and both times of application of eCG were effective for producing follicles of 7mm and COCs acceptable for recovery in Alpacas. Table 1.Number of follicles=7mm (top) and number of COCs recovered (mean±s.e.m.) Outcome and group 36 h 48 h Total Follicles GnRH 6.8±1.93 13.4±4.34 10.10±2.50a SP 5.5±2.23 5.29±1.15 5.38±1.25b Total 6.09±1.44 8.67±2.18 7.43±1.33 COCs GnRH 5±0.97 3±1.26 4.33±0.74a SP 1±0.41 0.33±0.22 0.67±0.25b Total 3.29±0.67x 1.4±0.6y 2.5±0.53 a,bValues within columns with different letters differ significantly (P=0.05). x,yValues within columns with different letters differ significantly (P=0.05). This research funded by CIENCIACTIVA-CONCYTEC as part of the project title “Role of seminal plasma in reproductive physiology and application of biotechnologies in camelids” (149-2017).

2018 ◽  
Vol 30 (1) ◽  
pp. 189
Author(s):  
W. F. Huanca ◽  
F. Y. Hilari ◽  
J. C. Villanueva ◽  
M. Uchuari ◽  
W. Huanca

Alpacas, as other camelids, are inducer ovulators and FIO/NGF-β, a protein present in the seminal plasma (SP) is reported as the responsible of the ovulation (Kershaw-Young et al. 2012 Reprod. Fertil. Dev. 24, 1093-1097, 10.1071/RD12039). However, limited and controversial information exists regarding characteristics of follicular wave in alpacas post-induction of ovulation with SP or other stimulus. The experiment was designed to determine the effect of 3 external stimulations on the interval to follicular wave emergence and the interval to dominant follicle. Adult female alpacas between 5 and 6 years old were assigned to 1 of 3 treatments: (1) SP (n = 6): 1 mL of SP IM; (2) hCG (n = 5): 1000 IU of hCG (Pregnyl, Organon-Holland, Amsterdam, the Netherlands), via IM; or (3) follicular ablation (FA, n = 6): animals were induced by ultrasound-guided ablation of the dominant follicle ≥7 mm. Alpacas from treatments 1 and 2 were examined by ultrasonography (Aloka SSD 500, transducer 7.5 MHz; Aloka, Tokyo, Japan) at 1- to 2-h intervals between 22 and 30 h after treatment or until ovulation occurred, whichever occurred first. All animals were evaluated by ultrasonography every day from Day 2 to Day 7 post-treatment and after that on Days 9, 12, and 15 post-treatment. Data from one alpaca (FA group) was excluded because of problems in the timing of ablation. Therefore, the total number of alpaca used was 16 (SP = 6, hCG = 5, and FA = 5). Results of the effect in external stimulation were analysed using ANOVA. In conclusion, interval to the emergence of a new follicular wave on the detection of follicles ≥3 mm and interval to dominant follicle ≥7 mm differed for FA compared with hCG but not compared with SP treatment. Table 1.Follicular wave emergence (mean ± SEM) under 3 external stimulations: seminal plasma (SP), hCG, or follicular ablation (FA)


2008 ◽  
Vol 20 (1) ◽  
pp. 162 ◽  
Author(s):  
M. D. Van Steelandt ◽  
V. M. Tanco ◽  
M. H. Ratto ◽  
G. P. Adams

Systemic administration of ovulation-inducing factor (OIF), discovered recently in seminal plasma of llamas, alpacas (induced ovulators), and cattle (spontaneous ovulators), stimulated ovulation in >90% of female llamas and alpacas. The objective of the present study was to test the hypothesis that purified OIF from llama seminal plasma would induce ovulation in cattle. Peripubertal heifers, weighing 323 � 27 kg, were used to minimize the confounding effect of spontaneous ovulation. Heifers (n = 11/group) were treated intramuscularly with 1.0 mg/100 kg of purified OIF, 100 µg of GnRH (positive control), or 2.5 mL of phosphate-buffered saline (negative control). Ovarian dynamics were monitored daily by transrectal ultrasonography for 10 days post-treatment. Blood samples were collected at 0.5- to 1-h intervals for 8 h, beginning at the time of treatment. Ovulation occurred in 9/11 (82%) of GnRH-treated heifers and in 1/11 (9%) heifers in each of the OIF- and saline-treated groups (P < 0.05). A surge in plasma LH concentration was detected within 30 min of treatment in the GnRH group (2.2 � 0.1 ng mL–1; P < 0.05), but remained at the basal level in the OIF- and saline-treated groups (0.3 � 0.1 and 0.2 � 0.1 ng mL–1, respectively). The onset of regression of the dominant follicle present at the time of treatment was earlier (P < 0.05) in OIF- v. saline-treated heifers (3.1 � 0.6 days v. 6.0 � 0.7 days). The interval from treatment to follicular wave emergence was shorter (P < 0.05) in GnRH- and OIF-treated heifers than in those treated with saline (1.1 � 0.4 days, 1.5 � 0.3 days, and 3.1 � 0.3 days, respectively). A similar pattern was observed for emergence of the second follicular wave (5.1 � 0.7 days, 4.6 � 0.5 days, and 6.6 � 0.4 days, respectively). Purified OIF did not induce ovulation in heifers but hastened both the regression of the extant dominant follicle and follicular wave emergence. Results provide a rationale for the hypothesis that OIF from seminal plasma is involved in controlling follicular wave dynamics in spontaneously ovulating species (e.g., Bos taurus) through a suppressive effect on the dominant follicle. The mechanism of action on ovarian follicular wave dynamics, as well as species specificity, remains to be elucidated.


2008 ◽  
Vol 20 (1) ◽  
pp. 227
Author(s):  
A. Garcia Guerra ◽  
G. A. Bó ◽  
J. Villarreal ◽  
G. M. Brogliatti

Ovarian asynchrony and variability in response to superstimulation remain the most limiting factors in any embryo transfer program (Armstrong D 1993 Theriogenology 39, 7–24). Ovarian response can be increased and less variable if superstimulatory treatment is started at the time of follicular wave emergence (Bö GA et al. 1995 Theriogenology 43, 31–40). A combination of progesterone (P4) and estradiol have been used to synchronize follicular wave for superstimulation. A retrospective analysis was done to compare the ovarian response, superovulatory response and embryo production of cows in Argentina that received progesterone and estradol prior to superstimulation at different stages of the estrous cycle. This research was carried out using different breed of donors (n = 584, 88% Angus) during the last 4 years in Buenos Aires province, Argentina. Heat detection was performed twice a day. At random stages of the estrous cycle, donors received an intravaginal progesterone device (DIB; Syntex, Buenos Aires, Argentina), 2 mg of estradiol benzoate and 50 mg of progesterone (Syntex, Buenos Aires, Argentina) IM on the same day. On day 4 after DIB insertion, superestimulatory treatment was initiated on a decreasing dose regimen of FSH (Pluset; Callier, Spain, or Folltropin, Bioniche Animal Health Inc., Belleville, Ontario, Canada) as IM injections every 12 h over 4 d. On day 6, DIBs were removed, and cows received two doses of 2 mL of cloprostenol 12 h apart. At heat detection, all donors received a dose of 2 mL of GnRH (Dalmarelin; Fatro Von Franken, Buenos Aires, Argentina) by IM injection and were inseminated 12 and 24 h later. Seven days later, embryo collection was performed and ovarian response was evaluated as number of CL + unovulated follicles by transrectal ultrasound using a 7.5-MHz transducer (Pie Medical, Maastricht, the Netherlands). Ova/embryos were evaluated and classified according to the IETS manual. Donors were assigned to receive DIB and estradiol during the following stages of the cycle: group 1: between days 4 and 7 post-estrus (dominant follicle period), group 2: between days 8 and 12 post-estrus (emergence of the second follicular wave), and group 3: between days 13 and 21 post-estrus (dominant follicle of the second wave). Kruskal-Wallis test was used to compare variables among groups, and results are shown in Table 1. Ovarian response as CL + unovulated follicles and number of ovulations were significantly different among groups (P < 0.05). However, there was no significant difference in the number of fertilized ova or transferable embryos. Nevertheless, numeric differences that show that group 2 (started between days 8 and 12 post-estrus) was always superior for all variables. In conclusion, data suggest that estradiol may be more effective in synchronizing follicle wave emergence for superstimulation during the mid-part of the estrous cycle. Table 1. Superovulatory response in cows in which follicle wave emergence was synchronized with estradiol at different stages of the estrous cycle (mean ± SD) Research supported by Centro Genetico Bovino Eolia S.A.


2015 ◽  
Vol 27 (1) ◽  
pp. 263 ◽  
Author(s):  
R. H. Hinshaw ◽  
M. L. Switzer ◽  
R. J. Mapletoft ◽  
G. A. Bó

Although oestradiol has been used successfully to synchronize follicle wave emergence for superovulation, it cannot be used in many countries. Attention has turned to alternatives, including the use of GnRH to induce ovulation of a dominant follicle, which will be followed by emergence of a new follicular wave in 1 to 2 days. However, GnRH synchronizes follicular wave emergence only when it induces ovulation and administration of GnRH at random stages of the oestrous cycle results in ovulation in less than 60% of animals. The objective of the study was to compare superovulatory response and ova/embryo production following synchronization of follicle wave emergence for superovulation with GnRH administered 2 days after insertion of a progestin device, with a protocol in which GnRH is administered 7 days after administration of prostaglandin F2α and a progestin device. Beef donors of various breeds were placed at random into 1 of 2 groups and superstimulated by replicate so that one cow in each group had ova/embryos collected on the same day. Sixty-six superstimulations were performed in this study; 26 were performed in 13 donors that were superstimulated twice in a crossover design, and 40 donors were superstimulated once (i.e. 20 donors in each treatment group). Cows in group 1 received CIDR devices (Zoetis Animal Health, USA) on Day –2 and 100 μg of GnRH (Cystorelin, Merial USA) on Day 0; FSH treatments were initiated on Day 2 with 288 mg of Folltropin-V (Vetoquinol, Canada) given in twice-daily decreasing doses for 4 days. Prostaglandin F2α (PGF; 35 mg dinoprost, Lutalyse, Zoetis) was given with the last 2 injections of Folltropin-V and CIDR were removed with the last Folltropin-V administration (i.e. Day 6). Donors received a second GnRH at the onset of oestrus and were AI 8 and 20 h later. Donors that were still in standing oestrus at the second AI were AI again at 30 h. Ova/embryo collections were done on Day 14 and embryos were classified according to the IETS manual. Cows in group 2 received an injection of PGF and a CIDR on Day –7 and 100 μg of GnRH on Day 0; FSH treatments were initiated on Day 2 and the remainder of the treatment protocol was as in group 1. Data (total ova/embryos collected and transferable embryos) were analysed by ANOVA for mixed models, using treatment as a fixed variable and cow (i.d.) as a random variable. The group 1 cows produced a mean (± s.e.m.) of 18.6 ± 1.9 total ova/embryos of which 12.7 ± 1.5 were of transferable quality (7.2 ± 1.3 grade 1). Cows in group 2 produced a mean (± s.e.m.) of 19.5 ± 1.7 total ova/embryos, of which 14.8 ± 1.5 were of transferable quality (8.9 ± 1.2 grade 1). Although 2 more transferable embryos were obtained in group 2, differences were not significant (P > 0.3). At the same time as this experiment was done, 214 other cows were superstimulated in this practice, yielding an average of 7.9 transferable embryos per donor. Results suggest that both approaches are efficacious for the superstimulation of beef cows.Special thanks to Vetoquinol/Bioniche Animal Health, USA for support.


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.


2016 ◽  
Vol 28 (2) ◽  
pp. 168
Author(s):  
W. Huanca ◽  
J. Turin ◽  
C. Mamani ◽  
R. Sanchez ◽  
W. F. Huanca ◽  
...  

Alpacas are classified as induced ovulators, and an external stimulus is required for the occurrence of ovulation. The seminal plasma (SP) of camelids contains a protein identified as β nerve growth factor with the capacity to induce ovulation and corpus luteum formation. Alpacas have a poor reproductive efficiency and high embryo mortality rate. A study was designed to evaluate the use of SP to improve reproductive performance post natural mating (Exp. 1) and with different mounting time (MT; Exp. 2). Experiment 1: Nonpregnant alpacas (n = 117) exhibiting a dominant follicle = 7 mm, detected by transrectal ultrasonography, were bred by natural mating and then assigned randomly to 1 of 3 treatments: T1 (n = 40), 1 mL of SP IM; T2 (n = 39), 1 mL of GnRH analogue (0.0042 mg of buserelin acetate), IM; and T3 (n = 38), control. Experiment 2: Nonpregnant alpacas (n = 180) exhibiting a follicle = 7 mm were assigned randomly to the following treatments: T1 (n = 30): MT 5 min; T2 (n = 30): MT 5 min + 1 mL of SP; T3 (n = 30): MT 10 min; T4 (n = 30): MT 10 min + 1 mL of SP; T5 (n = 30): MT > 15 min; T6 (n = 30): MT > 15 min + 1 mL of SP. The same male was used for mating females in T1 and T2, T3 and T4, and T5 and T6, respectively. Animals were evaluated by ultrasound with an Aloka SSD 500 (Aloka, Tokyo, Japan) and 5.0-MHz linear transducer on Day 25 for pregnancy diagnosis. In Exp. 1 the conception rate was 67.5, 51.3, and 55.3% for T1, T2, and T3, respectively (P > 0.05). In Exp. 2 the conception rate was 46.2, 67.9, 57.1, 73.3, 61.8, and 72.7% for T1, T2, T3, T4, T5, and T6 (P < 0.05) and was significantly different between T1 v. T2 and T3 v. T4. The results suggest that the use of SP could be one method to improve reproductive performance in alpacas. Research was supported by Project N° 405-PNICP-PIAP-UNMSM.


2020 ◽  
Vol 3 (11) ◽  
pp. 1100-1104
Author(s):  
Hussein Naeem Aldhaheri ◽  
Ihsan Edan AlSaimary ◽  
Murtadha Mohammed ALMusafer

      The Aim of this study was to determine Immunogenetic expression of  Toll-like receptor gene clusters related to prostatitis, to give acknowledge about Role of TLR in prostatitis immunity in men from Basrah and Maysan provinces. A case–control study included 135 confirmed prostatitis patients And 50 persons as a control group. Data about age, marital status, working, infertility, family history and personal information like (Infection, Allergy, Steroid therapy, Residency, Smoking, Alcohol Drinking, Blood group, Body max index (BMI) and the clinical finding for all patients of Prostatitis were collected. This study shows the effect of PSA level in patients with prostatitis and control group, with P-value <0.0001 therefore the study shows a positive significant between elevated PSA levels and Prostatitis.


2020 ◽  
Vol 26 (4) ◽  
pp. 449-453
Author(s):  
Jacob A. Kahn ◽  
Jeffrey T. Waltz ◽  
Ramin M. Eskandari ◽  
Cynthia T. Welsh ◽  
Michael U. Antonucci

The authors report an unusual presentation of juvenile xanthogranuloma (JXG), a non–Langerhans cell histiocytosis of infancy and early childhood. This entity typically presents as a cutaneous head or neck nodule but can manifest with more systemic involvement including in the central nervous system. However, currently there is limited information regarding specific imaging features differentiating JXG from other neuropathological entities, with diagnosis typically made only after tissue sampling. The authors reviewed the initial images of a young patient with shunt-treated hydrocephalus and enlarging, chronic, extraaxial processes presumed to reflect subdural collections from overshunting, and they examine the operative discovery of a mass lesion that was pathologically proven to be JXG. Their results incorporate the important associated histological and advanced imaging features, including previously unreported metabolic activity on FDG PET. Ultimately, the case underscores the need to consider JXG in differential diagnoses of pediatric intracranial masses and highlights the potential role of PET in the initial diagnosis and response to treatment.


Reproduction ◽  
1974 ◽  
Vol 36 (1) ◽  
pp. 91-99 ◽  
Author(s):  
J. C. BOURSNELL ◽  
T. K. ROBERTS
Keyword(s):  

Animals ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 203
Author(s):  
María Gemma Millán de la Blanca ◽  
Eva Martínez-Nevado ◽  
Cristina Castaño ◽  
Juncal García ◽  
Berenice Bernal ◽  
...  

The American flamingo is a useful model for the development of successful semen cryopreservation procedures to be applied to threatened related species from the family Phoenicopteridae, and to permit genetic material banking. Current study sought to develop effective sperm cryopreservation protocols through examining the influences of two permeating cryoprotectants and the seminal plasma removal. During two consecutive years (April), semen samples were collected and frozen from American flamingos. In the first year, the effect of two permeating cryoprotectants, DMA (dimethylacetamide) (6%) or Me2SO (dimethylsulphoxide) (8%), on frozen–thawed sperm variables were compared in 21 males. No differences were seen between DMA and Me2SO for sperm motility, sperm viability, and DNA fragmentation after thawing. In the second year, the role of seminal plasma on sperm cryoresistance was investigated in 31 flamingos. Sperm samples were cryopreserved with and without seminal plasma, using Me2SO (8%) as a cryoprotectant. The results showed that samples with seminal plasma had higher values than samples without seminal plasma for the following sperm variables: Straight line velocity (22.40 µm/s vs. 16.64 µm/s), wobble (75.83% vs. 69.40%), (p < 0.05), linearity (62.73% vs. 52.01%) and straightness (82.38% vs. 73.79%) (p < 0.01); but acrosome integrity was lower (55.56% vs. 66.88%) (p < 0.05). The cryoresistance ratio (CR) was greater in samples frozen with seminal plasma than without seminal plasma for CR-progressive motility (138.72 vs. 54.59), CR-curvilinear velocity (105.98 vs. 89.32), CR-straight line velocity (152.77 vs. 112.58), CR-average path velocity (122.48 vs. 98.12), CR-wobble (111.75 vs. 102.04) (p < 0.05), CR-linearity (139.41 vs. 113.18), and CR-straightness (124.02 vs. 109.97) (p < 0.01). This research demonstrated that there were not differences between Me2SO and DMA to successful freezing sperm of flamingos; seminal plasma removal did not provide a benefit for sperm cryopreservation.


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