The Effect of A PRID®Delta-Based Estrus Synchronization Protocol On Pregnancy Rates In Cows With No Estrus Symptoms

The present study aimed to determine the effects of progesterone-based gonadotropin-releasing hormone (GnRH), prostaglandin F2α (PGF2α), and equine chorionic gonadotropin (eCG) injections on progesterone profiles and pregnancy rates in cows with no estrus symptoms within 60 days after parturition. A total of 80 cows were included in the study. All animals had the progesterone-releasing device PRID®Delta placed intravaginally for nine days with an injection of GnRH. On the eighth day, PGF2α was injected, and PRID®Delta was removed from the vagina on day nine. Artificial insemination was carried out 60 hours after PRID®Delta removal. In half of the animals (n = 40), 600 IU of eCG was injected when PRID®Delta was removed on the ninth day before artificial insemination 60 hours later. Blood samples were taken from the tail vein on days 0 and 8 to determine progesterone levels. The pregnancy rate in the group that received eCG was 37.5%, while it was 27.5% in those that did not (P = 0.4). While the dominant follicle diameter was 15.5 mm in cows injected with eCG during timed artificial insemination, the follicle diameter was 12.4 mm in cows with no eCG injection (P <0.001). There were no differences in serum progesterone values in blood samples taken until the time of artificial insemination. However, progesterone values in the blood taken during artificial insemination were 0.94 ng/ml in the eCG- group and 0.72 ng/ml in the eCG+ group (P <0.05). As a result, it was determined that eCG injections, in addition to progesterone-based GnRH and PGF2α applications, increased the pregnancy rates in cows without symptoms of estrus. The dominant follicle diameter was larger in cows treated with eCG during artificial insemination; however, follicle size did not increase the pregnancy rate.

Supernumerary teeth in premolar and molar area on CBCT: a pictorial review.

Objective: to build a descriptive classification of premolar and molar supernumerary teeth (ST) when preparing the cone beam computed tomography (CBCT) report. The aim is also to share wide range of CBCT images in the open access publishing model. Material and methods: For our review we systematically searched for articles from PubMed with 1) free full texts on ST in molar and premolar area and using CBCT, and 2) articles providing with information on complications related with the presence of ST in molar and premolar area. We also added to our review studies providing with classic ST classifications in premolar and molar area. Results: We found 29 cases of ST, and we freely illustrated them with 84 figures. We separated our pictorial review in: 1) unilateral ST in the mandible, 2) unilateral ST in the maxilla, 3) unilateral undersized ST, 4) bilateral ST, 5) ST with additional features, and 6) cases with major hyperdontia. Conclusions: we build up the classification matrix for premolar and molar ST with 11 descriptors and 50 boxes. The descriptors were: 1) location if the ST crown in axial view, 2) vertical location of the cusp tip in relation with closest erupted tooth in coronal view, 3) shape, 4) distribution, 5) Position (in relation to normal tooth eruption) in sagittal view, 6) State of eruption of the ST in the sagittal view, 7) Follicle size measurement in sagittal view, 8) External root resorption of adjacent teeth by ST and its location in relation to the long axis of the involved tooth, 9) Internal resorption of ST, 10) Adjacent tooth complication, and 11) Damage to surrounding structures if ST removal. The open access figures from the literature illustrated 11 boxes. With our pictorial review we were able to illustrate 45 out of 50 boxes, and freely provide the readership with the most complete description of ST in premolar and molar area on CBCT than in previously published studies.

The effect of cellular and physiological indicators on gender determination

Gender determination, in addition to having special value to parents, has particular importance in sex-linked diseases. This study aimed to investigate the cellular indicators (i.e. BMP-6 protein and PPAR? protein expression levels in granulosa cells) and the physiological indicators on gender determination. For this purpose, on 68 infertile patients referred to the clinic, ovarian stimulation was performed by different protocols and then ruptured by different HCG. Follow-up of patients was performed after they became pregnant after five months. U/S was done for knowing the gender of the baby then after labor rechecked another time. Also, granulosa-luteal cells (GLCs) were isolated from the follicular fluid of 68 women participating in the study. BMP-6 protein and PPAR? protein were measured using Western blotting. Results showed that the total number of delivered babies was 68, 41 males (60.3%) and 27 females (39.7%). About physiological indicators results, there was no significant association between the age of the mother and sex of the baby (P=0.934). No significant association was detected between the month during which the conception occurred and the sex of the baby (P=0.734). The same result was obtained for the follicle side (P=0.236), and follicle size (P=0.659), there was no significant association between the sex of the baby with the following factors: protocol of treatment (P=0.417), IVF after HCG (P=0.237), HCG type (P=0.572), parity (P=0.282), and type of infertility (P=0.376). The cellular indicators results showed that the BMP-6 protein level in granulosa cells of mothers with daughters was almost twice as high as mothers with sons (P=0.043). But there was no significant difference between mothers with daughters and mothers with sons in PPAR? protein level (P=0.12). It can be concluded that except for BMP-6 protein level, none of the cellular and physiological indicators affects gender determination. Therefore, this cell indicator can probably be evaluated as an effective indicator in determining gender.

The Reproductive Biology of Deep-Sea Elasmobranchs and Batoids from Chatham Rise and the Sub-Antarctic Region of New Zealand

<p>The reproductive biology of thirteen poorly studied deep-sea elasmobranch species, on Chatham Rise and the Sub-Antarctic region of New Zealand, was assessed. The study species are all commonly caught as bycatch in commercial fisheries and include: three viviparous species (Centroselachus crepidater, Centrophorus squamosus, Deania calcea), five deep-sea catsharks (Apristurus spp.), and five deep-sea batoid species. However, due to a lack of knowledge on their general biology, ecology, and taxonomy – the impact of fishing on these species is unknown. A species’ resilience to fishing pressure depends on its biological productivity and susceptibility to capture. Accurate assessment of maturity is critical to understanding productivity and the effects of fishing pressure on fished stocks. Maturity is commonly assessed macroscopically, using a visual assessment that lacks precision and relies on subjective judgement. The wide array of macroscopic maturity assessment keys, used internationally, employ various sets of characteristics to define the same reproductive processes, which can lead to errors and inconsistencies in maturity assessment and parameter estimates (e.g. length-at-maturity), making direct comparisons between studies difficult. Objective reproductive measurements (oviducal gland size, follicle size, uterus width, follicle number and gonad weight) were used to assess the validity and quality of the macroscopic maturity staging key used in New Zealand, towards determining the onset of maturity and accurately distinguishing between macroscopic stages. The results showed that no single measurement gave a clear-cut indicator of maturity and some fish classified as ‘maturing’ were very likely ‘mature’. Uterus width, follicle size and gonadosomatic index values were found to be the most useful attributes in determining the onset of maturity. Uterus width and follicle size were also useful in determining differences between different macroscopic stages, whilst gonadosomatic index values were useful in distinguishing between reproductive strategies. Histological observations, with a particular focus on sperm storage, were also used to inform the quality of macroscopic maturity assignment. Sperm storage was observed for the first time in Centroselachus crepidater, Centrophorus squamosus and Brochiraja asperula. This study successfully highlighted problems in the macroscopic maturity assessment key currently used in New Zealand and proposes an improved, more objective macroscopic staging key. The improved key aims: 1) to assist in distinguishing between maturity stages, particularly between stage 2 (maturing), stage 2 (resting) and stage 6 (post-partum) females, by examining the same key reproductive structures across all macroscopic stages, and 2) to provide more representative maturity data for use in fisheries and demographic models, for more robust assessment of the impacts of fishing pressure on poorly studied deep-sea chondrichthyans.</p>

The Reproductive Biology of Deep-Sea Elasmobranchs and Batoids from Chatham Rise and the Sub-Antarctic Region of New Zealand

<p>The reproductive biology of thirteen poorly studied deep-sea elasmobranch species, on Chatham Rise and the Sub-Antarctic region of New Zealand, was assessed. The study species are all commonly caught as bycatch in commercial fisheries and include: three viviparous species (Centroselachus crepidater, Centrophorus squamosus, Deania calcea), five deep-sea catsharks (Apristurus spp.), and five deep-sea batoid species. However, due to a lack of knowledge on their general biology, ecology, and taxonomy – the impact of fishing on these species is unknown. A species’ resilience to fishing pressure depends on its biological productivity and susceptibility to capture. Accurate assessment of maturity is critical to understanding productivity and the effects of fishing pressure on fished stocks. Maturity is commonly assessed macroscopically, using a visual assessment that lacks precision and relies on subjective judgement. The wide array of macroscopic maturity assessment keys, used internationally, employ various sets of characteristics to define the same reproductive processes, which can lead to errors and inconsistencies in maturity assessment and parameter estimates (e.g. length-at-maturity), making direct comparisons between studies difficult. Objective reproductive measurements (oviducal gland size, follicle size, uterus width, follicle number and gonad weight) were used to assess the validity and quality of the macroscopic maturity staging key used in New Zealand, towards determining the onset of maturity and accurately distinguishing between macroscopic stages. The results showed that no single measurement gave a clear-cut indicator of maturity and some fish classified as ‘maturing’ were very likely ‘mature’. Uterus width, follicle size and gonadosomatic index values were found to be the most useful attributes in determining the onset of maturity. Uterus width and follicle size were also useful in determining differences between different macroscopic stages, whilst gonadosomatic index values were useful in distinguishing between reproductive strategies. Histological observations, with a particular focus on sperm storage, were also used to inform the quality of macroscopic maturity assignment. Sperm storage was observed for the first time in Centroselachus crepidater, Centrophorus squamosus and Brochiraja asperula. This study successfully highlighted problems in the macroscopic maturity assessment key currently used in New Zealand and proposes an improved, more objective macroscopic staging key. The improved key aims: 1) to assist in distinguishing between maturity stages, particularly between stage 2 (maturing), stage 2 (resting) and stage 6 (post-partum) females, by examining the same key reproductive structures across all macroscopic stages, and 2) to provide more representative maturity data for use in fisheries and demographic models, for more robust assessment of the impacts of fishing pressure on poorly studied deep-sea chondrichthyans.</p>

The effect of follicle size and cryoprotectants on nuclear maturation and early embryonic development of vitrified - thawed Awassi sheep oocytes (Ovis aries)

In this study, two experiments were conducted to study the effect of both the follicle size and the cryoprotectants dimethyl sulfoxide (DMSO) and ethylene glycol (EG) on the main phases of nuclear maturation (Experiment I), cleavage stages and embryo quality (Experiment II) of Awassi sheep oocytes. Follicles were classified into two groups: small follicles (SF) (1-2 mm) and large follicles (LF) (> 2 mm). Oocytes were vitrified in three solutions: A (30% DMSO), B (30% EG) and C (15% DMSO and 15% EG). In Experiment I, the resulting vitrified-thawed oocytes in solution C achieved the best rates after the control group (fresh), respectively as the rates of maturation, germinal vesicle (GV), metaphase II(M-II), arrest, and lyses were 85.71% (P = 0.04), 8.33% (P = 0.02), 72.92% (P = 0.04); LF group, 15.25% (P = 0.04), and 5.08% (P = 0.04); SF group, respectively. In Experiment II, the same group of oocytes achieved the best rates after the control group, as the rates of fertilization, cleavage, 2-16 cell, Type3, blastocyst, and Type1 embryos were 63.28% (P = 0.001), 57.46% (P = 0.001), 40.38% (P = 0.04), 38.46% (P = 0.04); LF group, 30.00% (P = 0.01), and SF group 36.67% (P = 0.001), respectively, while the vitrified-thawed oocytes in A solution (SF group) reached the highest rate of Type 2 embryo quality (58.06%; P = 0.01). No significant differences were noticed in the germinal vesicle breakdown (GVBD), metaphase I (M-I) and morula stage. Vitrification of oocytes obtained from follicles with a diameter of more than 2 mm in a cocktail solution of DMSO (15%) and EG (15%) led to a significant increase in the yield and quality of the resulting sheep embryos.

The effectiveness of prostaglandin nanoparticles in corpus luteum regression

Research examined the formation of prostaglandin nanoparticles and their effect on corpus luteum (CL) regression carried out at IRIAP. The nanoparticles formation was carried out using the ionic gelation method. The nanoparticles have a particle size of 316.80±0.14 nm, polydispersion index of 0,453±0,001, zeta potential of +17,40±0,85 mV with 69,69±8.81% hormone entrapment. The effectiveness of nanoparticle in CL regression was observed (prostaglandin vs prostaglandin nanoparticles) using ultrasound observation, hormone profile and estrus response. Further, the size of the ovulating follicle, the time of ovulation, the size of the CL and the onset of estrus after the administration of the prostaglandins were observed. The observation showed that the intramuscular administration of prostaglandin and prostaglandin nanoparticles did not significantly differ on the onset of estrus, time of ovulation, the ovulating follicle size, size of CL and progesterone concentration. The onset of estrus occurred on 2.50 ± 0.58 and 2.33 ± 0.52 days, the ovulation time after hormone administration was on days 3.50 ± 0.55 and 2.83 ± 0.75 with the ovulation follicle size of 16, 62 ± 0.96 and 17.03 ± 1.13 mm, while the CL measures at H-3 were 13.56 ± 2.28 and 10.45 ± 0.88, the progesterone H-2 concentrations were 0.299 and 0.395, respectively for prostaglandin and prostaglandin nanoparticles. It can be concluded that the formation of nanoparticles did not impair the effectiveness of hormones in CL regression so that it can be used to increase the effectiveness of estrus synchronization

250 Effect of Pre- and Post-ai Nutrition on Ovarian Dynamics, Steroidogenesis, and Expression of Estrus in Beef Heifers

The objective of this study was to evaluate nutrition before and after artificial insemination (AI) on follicular dynamics, expression of estrus, and steroidogenesis. Seventy-nine beef heifers were randomly assigned to one of two dietary treatments (High;155% and Low;86% of maintenance energy) 30d prior to AI. Estrus was synchronized (PG 6-d CIDR protocol) and heifers received AI (d0) 8 to 12h following onset of estrus. On d0, heifers were randomly reassigned diets generating four Pre-x-Post-AI nutritional treatments; High-High (HH, n = 20), High-Low (HL, n = 20), Low-High (LH, n = 19), and Low-Low (LL, n = 20). Heifers remained on new diet treatments until embryo collection (flush; d7-8). Blood samples were collected daily from d-3 to d0, and on d1, 3, 5, 7 and 8 for plasma concentrations of estradiol (E2) and progesterone (P4). Dominant follicle diameter was evaluated on d-3 and d0, and CL diameter was recorded at flush. Statistical analyses were completed in SAS using the MIXED (body weight, E2, P4), GLIMMIX (expression of estrus), and GLM (ovarian parameters, interval to estrus) procedures. There were Pre-AI (P &lt; 0.0001) and Post-AI by time (P &lt; 0.0001) interactions on body weight; heifers in high and low treatments gained and lost weight, respectively, during both periods. Estradiol concentrations increased (P &lt; 0.0001) from d-3 (2.18±0.15pg/mL) to d0 (6.05±0.04pg/mL). Pre-AI diet increased the proportion of heifers in estrus (80±6.3% vs. 59±7.9%; P = 0.05), and dominant follicle size (11.7±1.42mm vs. 10.68±1.33mm; P = 0.0016) in High vs. Low, respectively. Additionally, High Pre-AI heifers had greater P4 after AI compared to Low Pre-AI heifers (4.85±0.37ng/mL vs. 3.53±0.38ng/mL; P = 0.015). Post-AI treatment did not influence concentrations of P4 (P = 0.88). There was no effect of Pre, Post or Pre-x-Post-AI treatment on initial follicle size, follicle growth rate, E2 concentrations, interval to estrus, or CL size at flush (P &gt; 0.10). In conclusion, nutrient restriction before AI negatively impacted ovarian function, steroidogenesis, and expression of estru.

PSXII-20 Ovarian dynamics and fertility in beef cows administered a 5-day or 6-day CO-Synch protocol for timed artificial insemination

The 5-day CO-Synch is an extensively used TAI protocol; however, it requires multiple administrations of prostaglandin F2α (PGF). The objective of the present study was to evaluate the effect of increasing progesterone (P4) device insertion from 5 to 6 days during a TAI protocol on ovarian dynamics and fertility in beef cows. Suckled beef cows (n = 867) at six locations were randomly assigned to either a 5-day or 6-day CO-Synch. Cows received an intravaginal P4 device (CIDR, Zoetis) and 100 µg of gonadorelin acetate (GnRH, Parnell) on d-9 (6-day) or d-8 (5-day). On d-3 CIDR’s were removed, an estrus detection patch applied (Estrotect, Rockway Inc.) and either one (6-day) or two (5-day) doses of PGF (500 µg of cloprostenol sodium, Estroplan, Parnell) was administered. On d0 (72 h after CIDR removal) all cows received 100 µg of GnRH, estrus expression was evaluated, and AI was performed. Pregnancy was determined by ultrasonography 34 days after TAI. Ovarian dynamics were evaluated in a subset of animals (n = 20) between d-3 and d7 to determine preovulatory follicle size, time of ovulation and corpus luteum (CL) size. Data were analyzed using generalized linear mixed models (SAS 9.4). Cows in the 6-day group tended (P = 0.09) to have a larger maximum follicle diameter (16.2±0.4mm) than cows in the 5-day group (15.0±0.6mm). In addition, CL volume on d7 was greater (P = 0.01) in the 6-day (4302±495mm3) than 5-day (2406±455mm3) group. There were, however, no differences (P = 0.15) in the interval between CIDR removal and ovulation. Cows assigned to the 6-day group had greater (P &lt; 0.05) estrus expression [56.1% (215/385) vs 41.5% (161/388)] and pregnancy rate [54.6% (236/438) vs 47.4% (207/435)] than cows in the 5-day group. In conclusion, extension of the period of P4 device insertion in a prolonged proestrus protocol increases preovulatory follicle size, estrous expression, and fertility to TAI.

Anti-Mullerian Hormone (AMH) as a Predictor of Ovarian Response to Clomiphene Citrate in Polycystic Ovarian Syndrome

Background: Serum Anti-Mullerian hormone (AMH) levels in women with polycystic ovary syndrome (PCOS) are two- to threefold higher than in ovulatory women with normal ovaries, corresponding to the two- to threefold increase in the number of small follicles in PCOS. The increased AMH has been hypothesized to reduce follicle sensitivity to follicle stimulating hormone (FSH) and estradiol production, thus preventing follicle selection, resulting in follicular arrest at the small antral phase with failure of dominance. Objective: The study was undertaken to test the hypothesis that high AMH level is associated with poor response to ovulation induction in PCOS women. Methods: This was a cross-sectional comparative study of 50 infertile women with PCOS, grouped into those with AMH level <8 ng/mL and those with AMH level [Formula: see text] 8 ng/mL. All participants received an initial dose of 100 mg/day of clomiphene citrate from 2nd to 6th day of menstrual cycle. Ovarian response (follicle size) was assessed by transvaginal monitoring on 12th day of cycle. Results: A total of 50 women were recruited, of which 4 dropped out. Women with AMH [Formula: see text] 8 ng/mL comprised only 23.91% of the PCOS women. AMH and day 12 follicle size had a statistically significant association. Adjusting for other confounding variables in linear, logarithmic, and logistic analysis, serum AMH had significant negative relationship with follicle size (r = 0.511, p < 0.001). AMH was also positively correlated with serum LH, testosterone and negatively correlated with serum follicle stimulating hormone (FSH), serum TSH and BMI. Conclusion: We observed that higher AMH level women had poor response to ovulation induction compared to women with low AMH level.