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PubMed2003

Failed fertilization: is it predictable?

PURPOSE OF REVIEW: The purpose of this review is to critically examine the ability of screening tests to predict fertilization failure. RECENT FINDINGS: Failed fertilization occurs in 5-10% of in-vitro fertilization cycles and 2-3% of intracytoplasmic sperm injection cycles. Failed fertilization may result from impaired spermatozoa, oocyte deficiencies or defects in the in-vitro sperm/oocyte medium. In the in-vitro fertilization setting most cases are caused by male factor deficiencies, whereas failure of oocyte activation is the most common cause of failed fertilization after intracytoplasmic sperm injection. Although the standard semen analysis has limited ability to predict fertilization failure, strict sperm morphology criteria, sperm-zona binding ratios and zona pellucida induced acrosome reaction tests provide increased capacity to avoid this outcome. The quality of the semen sample on the day of oocyte retrieval and fertilization performance in previous in-vitro fertilization cycles may also guide the appropriate use of intracytoplasmic sperm injection. However, the routine use of the latter technique in cases of non-male factor infertility is contraindicated. SUMMARY: The ever improving techniques highlighted in this analysis offer improved ability to predict failed fertilization.

Female↗
PubMed2002

The relationship between conspecific fertilization success and reproductive isolation among three congeneric sea urchins.

Few data are available on the effectiveness of reproductive isolating mechanisms in externally fertilizing taxa. I investigated patterns of conspecific and heterospecific fertilization among three coexisting sea urchin species, Strongylocentrotus droebachiensis, S.franciscanus, and S. purpuratus. In the laboratory, both among and within species, eggs from individual females whose eggs are more easily fertilized by conspecific sperm are also most susceptible to heterospecific fertilization. At one extreme, S. droebachiensis requires an order of magnitude fewer conspecific sperm to fertilize eggs than do the other two species and shows very little distinction between conspecific and heterospecific sperm in no choice experiments. Strongylocentrotus franciscanus has an intermediate susceptibility to fertilization by heterospecific sperm. At the other extreme, S. purpuratus rarely cross-fertilizes. Field observations indicate that S. droebachiensis is often surrounded by heterospecific sea urchins. Genetic analysis of larvae produced during heterospecific spawning events indicate that hybrids are generally produced if male conspecifics are more than 1 m from a spawning female S. droebachiensis. Laboratory cultures indicate that these hybrids suffer high mortality relative to conspecific larvae. Comparisons of reproductive success of S. droebachiensis during single-species and multispecies spawning events indicate that the benefits of producing easily fertilized eggs under conditions of sperm limitation may outweigh the costs of losing some offspring to hybrid fertilization. Patterns of variability in heterospecific fertilization are considered in light of three hypotheses: phylogenetic relatedness, reinforcement selection, and sexual selection.

Animals↗
PubMed2006

Measurement of induced acrosome reactions in human sperm using physiologic stimuli--relevance for the prediction of fertilization outcome.

Fertilization failure following standard in vitro fertilization in couples with normozoospermic men is an as yet unexplained phenomenon. A wide range of gametic disorders as well as environmental factors might contribute to this pathologic condition. One crucial condition appears to be the inability of the spermatozoa to undergo the acrosome reaction (AR). A discriminative test to distinguish fertile from non-fertile spermatozoa would be of utmost interest. In a prospective study, semen samples from men with normal semen parameters and fertilization failure were compared with semen samples from men with normal semen parameters and normal fertilization as to their capacity to undergo the AR. AR was induced using calcium ionophore as well as the physiologic stimuli progesterone and prostaglandin E(1). Discriminance analyses were undertaken to help identify patients with probable fertilization failure. Our data show that in patients with fertilization failure, the capacity of spermatozoa to undergo induced AR is greatly reduced using both unphysiologic and physiologic stimuli. However, physiologic stimuli are more suitable to identify patients with fertilization failure. Using physiologic stimuli, a formula was established to identify patients likely to fail at fertilization.

Acrosome Reaction↗
PubMed1993

Association between human in vitro fertilization rate and pregnancy outcome: a possible involvement of spermatozoal quality in subsequent embryonic viability.

A conventional view of mammalian fertilization is that the active component of the process: the spermatozoon, by virtue of its progressive motility and acrosomal enzymes, penetrates an otherwise passive oocyte. This concept has placed bias on spermatozoal normality as largely determining the outcome of fertilization; once this has been achieved then the contribution of the spermatozoon is often forgotten, and attention switches to the maternally derived "blue-print" for early embryonic development. Paternal genomic contribution is known to start at the eight-cell stage in the human, but this is usually after the time when early cleavage stage (2 to 8-cell stage) embryos are replaced in human assisted reproductive technologies (ART) procedures such as in vitro fertilization and embryo transfer (IVF-ET). Hence, fundamental abnormal contributions to embryogenesis derived from the fertilizing spermatozoon have often been ignored. Human IVF-ET has permitted far greater powers of analysis of the fertilization event, and fertilization success appears to be determined in such a system by three main factors: spermatozoal quality, oocyte quality, and quality of in vitro culture conditions (the gamete environment). If the second two factors are more carefully controlled than the first, as is the usual emphasis in routine human IVF practice, then any large variation in fertilization rates that are also significantly related to embryonic viability and ultimately pregnancy outcome, may be thought to be more directly associated with original quality of the fertilizing spermatozoon. An analysis of results of 758 IVF cases provides preliminary evidence to show that there is a close association between human in vitro fertilization rate and subsequent embryo viability following replacement. In accepting this hypothesis as a possibility, we should drastically change our attitude from one of the spermatozoon as a robust, simple initiator of embryonic development, and embrace the idea of the vulnerability of such germ cells both during and after their production, and how detrimental influences on this might profoundly affect embryogenesis after successful fertilization.

Cell Survival↗
PubMed1985

Sexual recognition and fertilization in brown algae.

Fertilization in the brown marine algae known as fucoids, is oogamous. The naked egg cell (80 micron diam.) is fertilized by small biflagellate spermatozoids and both monoecious and dioecious species are found. Fertilization is highly species-specific and this appears to be controlled during plasmogamy. Following fusion of egg and sperm, a rapid (less than 1 min) release of polyuronide cell wall material takes place from cytoplasmic vesicles within the egg. This is easily visualized using the fluorescent brightener Calcofluor, which therefore provides the basis of a quantitative fertilization bioassay. It has not proved possible to measure direct sperm binding to eggs. In experiments to investigate the molecular basis of egg-sperm recognition, the effect of exogenous agents on the initial rate of fertilization was examined. Predigestion of eggs with low concentrations of two glycosidases, alpha-fucosidase and alpha-mannosidase, caused inhibition of fertilization. The lectins concanavalin A and RCA120 bound strongly to egg surfaces, as detected using fluorescent labels, but not to sperm. The binding to eggs inhibited fertilization. On the other hand, Fucose Binding Protein bound only weakly to eggs but strongly to sperm, again causing inhibition of fertilization. It has not proved possible to quantitate lectin binding since high levels of lectin-nonspecific binding were detected using iodinated lectins. These inhibition experiments suggest that specific sugar residues may be involved in egg-sperm recognition, but the effects of lectins must be treated with caution since a large amount of variability in the sensitivity of gametes was detected. Attempts to isolate receptor fractions from egg cells have been partially successful. Egg membrane preparations bind sperm and sodium dodecyl sulphate-solubilized fractions, purified by concanavalin A affinity chromatography, have yielded low levels of a soluble receptor-like fraction that has not yet been fully characterized. Antisera raised against surface antigens of Fucus serratus sperm flagella, cause inhibition of fertilization in a species-specific manner, possibly by binding directly to the sperm fertilization receptor. A number of flagellar antigens were detected and future attempts to pinpoint the sperm receptor will make use of monoclonal antibodies.

Concanavalin A↗
PubMed1996

Plasmon analysis of Triticum (wheat) and Aegilops. 1. Production of alloplasmic common wheats and their fertilities.

Plasmons (= cytoplasms) of eight Triticum species (ten accessions) and 24 Aegilops species (36 accessions) have been introduced by repeated backcrosses to 12 genotypes of hexaploid, common wheat. At transfer problems such as crossing barrier, preferential transmission of a gametocidal or parthenogenesis-inducing chromosome, and mistagging of the material occurred, all of which hindered the plasmon transfer program. Of the 552 genotype-plasmon combinations produced, 532 (96.4%) had reached the B10 or a later backcross generation, 15 (2.7%) the B7 approximately B9 generation, and the remaining 5 (0.9%) the B4 approximately B6 generation by summer, 1996. Pollen and selfed seed fertilities were observed in plants of all the field-grown lines in the 1992-1993 winter crop season, and backcrossed and selfed seed fertilities of plants grown in a greenhouse under a long day condition (17-h light) were assessed in the five latest backcross generations. Selfed seed fertility was found to be a better parameter of male fertility than was pollen fertility. Female fertility, as estimated from the backcrossed seed fertility, was about three times more tolerant to genetic stress caused by the alien plasmon transfer than was male fertility evaluated from both the pollen and selfed seed fertilities. The plasmons studied could be classified into 14 fertility spectrum groups. Most, excluding 15 plasmons belonging to the B, D, D2, S, and Sb plasmon types, were considered the male sterile plasmon to common wheat.

Crosses, Genetic↗
PubMed1998

Enhancement of bovine oocyte fertilization in vitro with a bovine oviductal specific glycoprotein.

The purpose of this study was to determine the effect of a partially purified bovine oviductal glycoprotein (bOGP) on fertilization rates of bovine oocytes. The effect of albumin (control protein) or bOGP at 100 micrograms ml-1 during the 16-18 h fertilization period was evaluated in a standard IVF system using a sperm concentration between 0.5 and 0.125 x 10(6) spermatozoa ml-1. bOGP maintained a higher (P < 0.05) fertilization rate (62.0% versus 31.2%) at 0.125 x 10(6) spermatozoa ml-1 compared with the albumin control. The enhancement of fertilization by bOGP was blocked by the inclusion of a specific antibody to bOGP, whereas the antibody with albumin had no effect. A 2 h gamete preincubation step was subsequently included in the IVF procedure (0.125 x 10(6) spermatozoa ml-1) to determine whether the effect of bOGP was mediated through an interaction with the oocyte, the spermatozoon or both. When oocytes were preincubated with bOGP the fertilization rates were higher (P < 0.05) than with the albumin control (oocytes and spermatozoa exposed to albumin), whereas preincubation of spermatozoa with bOGP did not affect fertilization rates. There was no synergistic effect of preincubating oocytes and spermatozoa with bOGP. The increase in fertilization rate achieved by preincubating oocytes with bOGP was blocked with a specific antibody to bOGP. These results suggest that the increase in fertilization rates observed when bOGP is included during the 16-18 h fertilization period are primarily mediated through the interaction of bOGP with the oocyte since the same facilitatory effect was observed with a 2 h preincubation of oocytes before IVF. The ability to block these effects with a polyclonal antibody specifically generated against bOGP shows that this biological activity is due to bOGP. In summary, bOGP enhances fertilization in bovine oocytes whether it is included during preincubation or insemination and this appears to be due to a direct effect on the oocyte.

Animals↗
PubMed2002

Variations in modifications of sugar residues in hamster zona pellucida after in vivo fertilization and in vitro egg activation.

Lectins were used as probes in conjunction with quantitative analysis to investigate the distribution of different carbohydrate residues in hamster zona pellucida and their possible modification patterns after in vivo fertilization and in vitro egg activation. Several lectins including HPA, WGA, RCA-I, PNA, DSA, BSAIB(4), DBA, AAA and MAA were used to label the zona pellucida of both unfertilized and fertilized eggs. With the exception of PNA and BSAIB(4), the same lectins were also used to label the zona pellucida of oocytes activated in vitro. A multicomparison quantitative analysis of the density of labelling in the inner and outer regions of the zona pellucida before and after fertilization in vivo, as well as after in vitro egg activation, was performed. Of all the lectins studied, preferential localization of labelling by RCA-I and DSA to the inner zona pellucida of unfertilized eggs was observed. After in vivo fertilization, there was an increase in labelling in the inner region of the zona pellucida when thin sections of fertilized oocytes were incubated with HPA, BSAIB(4) and AAA. Although increased labelling by RCA-I was observed, a significant decrease in labelling intensity was obtained with WGA and the sequence Neu-WGA in both the inner and outer zona pellucida of fertilized oocytes. A significant increase in the density of labelling with WGA was also observed after digestion with neuraminidase. In parallel, when hamster oocytes activated in vitro were compared with those fertilized in vivo, a difference in lectin-gold labelling was observed in both the inner and outer region of the zona pellucida. Labelling with HPA, WGA, DSA and MAA increased significantly in both the inner and outer regions of the zona pellucida, whereas labelling by DBA significantly decreased in the inner portion of the zona pellucida. After neuraminidase treatment, a significant increase in labelling density was observed when thin sections of in vitro-activated oocytes were incubated with WGA. These results demonstrate: (i) the post-fertilization modifications of major saccharidic determinants that may play a role in the sperm-egg interaction process of fertilization in vivo; and (ii) that the modified properties of zonae pellucidae of fertilized and in vitro-activated eggs resulting from the action of hydrolytic enzymes, as well as glycoproteins released through exocytosis of cortical granules, are not identical.

Animals↗
PubMed2004

Impaired fertility in T-stock female mice after superovulation.

Superovulation of female mice with exogenous gonadotrophins is routinely used for increasing the number of eggs ovulated by each female in reproductive and developmental studies. We report an unusual effect of superovulation on fertilization in mice. In vivo matings of superovulated T-stock females with B6C3F1 males resulted in a two-fold reduction (P <0.001) in the frequencies of fertilized eggs compared with control B6C3F1 matings. In addition, approximately 22 h after mating, only 15% of fertilized eggs recovered in T-stock females had reached the metaphase stage of the first cleavage division versus 87% in B6C3F1 females (P <0.0001). Matings with T-stock males did not improve the reproductive performance of T-stock females. To investigate the possible cause(s) for the impaired fertilization and zygotic development, the experiments were repeated using in vitro fertilization. Under these conditions, the frequencies of fertilized eggs were not different in superovulated T-stock and B6C3F1 females (51.7 +/- 6.0 and 64.5 +/- 3.8%, P=0.10). There was a seven-fold increase in the frequencies of fertilized eggs that completed the first cell cycle of development after in vitro versus in vivo fertilization in T-stock females. These results rule out an intrinsic deficiency of the T-stock oocyte as the main reason for the impaired fertility after in vivo matings, and suggest that superovulation of T-stock females may induce a hostile oviductal and uterine environment with dramatic effects on fertilization and zygotic development.

Animals↗
PubMed2006

Cerebral palsy among children born after in vitro fertilization: the role of preterm delivery--a population-based, cohort study.

OBJECTIVE: Our aim was to assess the incidence of cerebral palsy among children conceived with in vitro fertilization and children conceived without in vitro fertilization. METHODS: A population-based, cohort study, including all live-born singletons and twins born in Denmark between January 1, 1995, and December 31, 2000, was performed. Children conceived with in vitro fertilization (9255 children) were identified through the In Vitro Fertilization Register; children conceived without in vitro fertilization (394,713) were identified through the Danish Medical Birth Register. Cerebral palsy diagnoses were obtained from the National Register of Hospital Discharges. The main outcome measure was the incidence of cerebral palsy in the in vitro fertilization and non-in vitro fertilization groups. RESULTS: Children born after in vitro fertilization had an increased risk of cerebral palsy; these results were largely unchanged after adjustment for maternal age, gender, parity, small-for-gestational age status, and educational level. The independent effect of in vitro fertilization vanished after additional adjustment for multiplicity or preterm delivery. When both multiplicity and preterm delivery were included in the multivariate models, preterm delivery remained associated strongly with the risk of cerebral palsy. CONCLUSIONS: The large proportions of preterm deliveries with in vitro fertilization, primarily for twins but also for singletons, pose an increased risk of cerebral palsy.

Adult↗
PubMed2006

Health of children born as a result of in vitro fertilization.

OBJECTIVE: The purpose of this study was to use nationwide registries to examine the health of children up to 4 years of age who were born as a result of in vitro fertilization. METHODS: Children born after in vitro fertilization (N = 4559) from 1996 to 1999 were monitored until 2003. Two control groups were selected from the Finnish Medical Birth Register as follows: all other children (excluding children born after ovulation induction) from the same period (N = 190,398, for study of perinatal health and hospitalizations) and a random sample of those children (n = 26,877, for study of health-related benefits). Mortality rates and odds ratios for perinatal outcomes, hospitalizations, health-related benefits, and long-term medication use were calculated. RESULTS: Although the health of most in vitro fertilization children was good, such children had more health problems than other children. A total of 35.7% of in vitro fertilization children and 2.2% of control children were multiple births, and the health of multiple births was worse than that of singletons. Perinatal outcomes of in vitro fertilization children were worse and hospital episodes were more common than among control children. Risks for cerebral palsy and psychological and developmental disorders were increased. Among in vitro fertilization singletons, worse results for perinatal outcomes and hospitalizations, but no increased risk for specific diseases, were found. The health of in vitro fertilization multiple births was comparable to the health of control multiple births. CONCLUSIONS: Reducing the number of transferred embryos would improve the health of in vitro fertilization children. Additional studies are needed to explain the poorer health of in vitro fertilization singletons, as well as follow-up studies to examine the health of in vitro fertilization children from 4 years onward.

Child, Preschool↗
PubMedDate not supplied

Irrigated mountain meadow fertilizer application timing effects on overland flow water quality.

Nonpoint-source pollution from agricultural activities is currently the leading cause of degradation of waterways in the United States. Applying best management practices to flood-irrigated mountain meadows may improve agricultural runoff and return flow water quality. Prior research has focused on fertilizer use for increased hay yields, while few studies have investigated the environmental implications of this practice. We examined the effects of fertilizer application timing on overland flow water quality from an irrigated mountain meadow near Gunnison, Colorado. Application of 40 kg phosphorus (P) and 19 kg nitrogen (N) ha(-1) using monoammonium phosphate (11-52-0, N-P-K) fertilizer to plots in the fall significantly reduced concentrations of reactive P and ammonium N in irrigation overland flow compared with early or late spring fertilization. Reactive P loading was 9 to almost 16 times greater when fertilizer was applied in the early or late spring, respectively, compared with in the fall. Ammonium N followed a similar trend with early spring loading more than 18 times greater and late spring loading more than 34 times greater than loads from fall-fertilized plots. Losses of 45% of the applied P and more than 17% of the N were measured in runoff when fertilizer was applied in the late spring. These results, coupled with those from previous studies, suggest that mountain meadow hay producers should apply fertilizer in the fall, especially P-based fertilizers, to improve hay yields, avoid economic losses from loss of applied fertilizers, and reduce the potential for impacts to water quality.

Agriculture↗
PubMed2006

Environmental impact of irrigation in La Violada District (Spain): II. Nitrogen fertilization and nitrate export patterns in drainage water.

Fertilizer leaching affects farm profitability and contributes to nonpoint-source pollution of receiving waters. This work aimed to establish nitrate nitrogen export from La Violada Gully in relation to nitrogen fertilization practices in its basin (La Violada Gully watershed, VGW, 19,637 ha) and especially in La Violada Irrigation District (VID, 5282 ha). Nitrogen (N) fertilization in VID (and VGW) was determined through interviews with local farmers for the hydrologic years 1995 and 1996 and NO3-N load in the gully was monitored from 1995 to 1998. The N fertilizer applied in VGW was 2175 Mg in 1995 and 2795 Mg in 1996. About 43% was applied in VID (945 Mg in 1995 and 1161 Mg in 1996). The most fertilized crop was corn: 398 kg N ha-1 (665 Mg) in 1995 and 453 kg N ha-1 (911 Mg) in 1996. Nitrogen fertilization was higher than N uptake for irrigated crops, especially for corn and rice. Nitrate N load in La Violada Gully averaged 427.4 Mg yr-1. Seventy-five percent of the exports took place during the irrigation season (321.8 Mg). During the non-irrigation season maximum NO3-N loads (3.1 Mg NO3-N d-1) were found after heavy rains following the N side-dressing of wheat in the rain-fed area of VGW (February). During the irrigation season NO3-N load was determined by outflow from the district (caused by irrigation) and to a lesser extent by changes in NO3 concentration (caused by fertilization), showing peaks in April (pre-sowing corn N fertilization and first irrigations) and June to August (highest irrigation months and corn side-dress N applications, maximum 6.3 Mg NO3-N d-1 in July). Adjusting N fertilization to crops' needs, improving irrigation efficiencies, and better scheduling N fertilization and irrigation in corn could reduce N export from VID.

Environment↗
PubMed2001

Effects of nitrogen fertilization and harvest date on yield, digestibility, fiber, and protein fractions of tropical grasses.

To evaluate the response of three tropical forage species to varying rates of nitrogen (N) fertilization [0, 39, 78, 118, 157 kg of N/(ha x cutting)] and five summer harvests, forage DM mass and nutritive value were evaluated in a randomized complete block design with a split-split plot arrangement of treatments. Plots (n = 60) were established in 1996, and five harvests were conducted every 28 d from June through September in 1997 and 1998, with fertilizer applications occuring after each harvest. Fertilization with 78 kg of N/(ha x cutting) increased forage mass in these grasses by 129% (P < 0.01) compared with no N fertilization. Additional N did not result in further increases of forage mass. Bermudagrass (Cynodon dactylon) produced more forage DM [P < 0.01; 1,536 +/- 43 kg/(ha x cutting)] than stargrass [Cynodon nlemfuensis; 1,403 +/- 43 kg/(ha x cutting)] or bahiagrass [Paspalum notatum; 1,297 +/- 43 kg/(ha x cutting)]. Peak forage mass for all species occurred in late June and July. In vitro organic matter digestibility (IVOMD) of stargrass increased (P < 0.01) linearly with fertilization. A quadratic response to N fertilization (P < 0.01) was noted in IVOMD of bermudagrass, whereas bahiagrass was not affected. Bermudagrass was more (P < 0.01) digestible (57.5 +/- 0.4) than stargrass (54.6 +/- 0.4) and bahiagrass (51.9 +/- 0.4%). As fertilization level increased, NDF decreased linearly (P < 0.01) in all three forages. Total N concentration increased (P < 0.01) linearly as N fertilization increased in all forages. Total N concentration was highest (P < 0.01) in stargrass (2.4%, DM basis) compared with bermudagrass (2.2%) and bahiagrass (2.0%). Total N concentration was depressed in all forages for late June and July harvests (P < 0.01). Fertilization increased (P < 0.05) the concentration (% of DM) of all protein fractions. In July and August, nonprotein N was reduced 11.8% (P < 0.01), whereas ADIN increased in July (P < 0.01). Bahiagrass had less N in cell contents than did bermudagrass and stargrass but had a greater concentration of N associated with the cell wall. Managerial factors, including rates of N fertilization and harvest dates, can have profound effects on the nutritional value of forage. An increased understanding of these effects is imperative to improve supplementation programs for ruminants.

Animal Feed↗
PubMed2003

Genetic evaluation of fertility using direct and correlated traits.

Poor fertility has become a major reason for involuntary culling of dairy cows in the United Kingdom. Calving interval (CI) and body condition score (BCS) are recorded, heritable, genetically correlated with each other, and could be used to extend the scope of dairy indices to include fertility traits. The use of U.K. insemination information for the evaluation of fertility has not been examined previously. Fertility and correlated traits were examined using nationally recorded milk (MILK = daily milk yield at test nearest d 110), BSC, and fertility traits (CI and the insemination traits of nonreturn rate after 56 d, NR56; days to first service, DFS; and number of inseminations per conception, INS). Genetic parameters for the traits were estimated simultaneously with a multitrait sire maternal grandsire (MGS) model and a multitrait BLUP sire MGS model was used to predict sire predicted transmitting abilities for each trait. The relationship between the fertility traits and other predicted transmitting abilities calculated in the United Kingdom was then examined. Heritabilities for the fertility traits were CI = 0.033 +/- 0.01, DFS = 0.037 +/- 0.01, NR56 = 0.018 +/- 0.001, and INS = 0.020 +/- 0.001, with a genetic correlation of 0.671 +/- 0.063 between CI and DFS and -0.939 +/- 0.031 between NR56 and INS. There was an unfavorable genetic correlation between the fertility traits and milk yield and BCS. Predicted transmitting abilities produced are similar in size and range to those produced in other studies and genetic trends are as expected. Results to date are encouraging and suggest that the planned program of work will lead to a fertility index that, when used by breeding companies, will lead to improvements in national dairy cow fertility.

Animals↗
PubMed1982

Development of extender and techniques for frozen turkey semen. 2. Fertility trials.

The effects of cryoprotectant concentrations, redilution, centrifugation, and dialysis techniques on fertility of fresh and frozen-thawed turkey semen were tested. Fresh extended semen with final concentrations of 4.8, 5.6, 9.6, and 11.2% cryoprotectant (dimethylsulfoxide and ethylene glycol, 1:1 ratio) showed a significant (P less than .05) decrease in fertility when compared to semen without cryoprotectant. Fertility of fresh semen extended with 4.8% cryoprotectant when centrifuged or rediluted and centrifuged, was unaffected when compared to cryoprotectant treated semen. Fertility of frozen-thawed semen after redilution and centrifugation was low, but samples rediluted one part semen for two parts extender yielded significantly (P less than .05) higher fertility than semen rediluted 1:1. Fresh semen extended with 11.2% cryoprotectant showed a highly significant (P less than .01) decrease in fertility despite dialysis, while semen with 9.6% cryoprotectant showed no difference when compared to dialyzed semen without cryoprotectant. Fertility of frozen-thawed semen dialyzed against blood plasma (approximately pH 7.9) and blood plasma adjusted with TES2 to pH 7.4 or pH 7.2 was not significantly different. Fertility of frozen-thawed semen dialyzed for 30 min was significantly higher (P less than .01) than semen dialyzed for 15 min or 0 min. Frozen-thawed semen dialyzed with a semen to dialysate ratio of 1:15 and 1:24 supported significantly higher (P less than .01) fertility than at 1:50 ratio. The AGPT3 dialysate yielded significantly higher (P less than .01) fertility than blood plasma adjusted to pH 7.2 with TES.

Animals↗
PubMed1996

Duration of fertility in ad libitum and feed-restricted caged broiler breeders.

It has been shown in previous studies that fertility can be reduced in overweight broiler breeder (BB) flocks. In an effort to determine the effect of ad libitum feeding on the duration of fertility in BB hens, 60 52-wk-old Shaver Starbro hens were randomly assigned to one of two treatments, ad libitum feeding (F) or restricted feeding (R) to maintain breeder target weights. All hens were reared to 52 wk under conditions of feed restriction. All birds were weighed individually on a weekly basis. At the beginning of each of two 4-wk study periods (56 to 60 wk and 60 wk to 64 wk), all birds were inseminated on 2 consecutive d with 0.05 mL pooled BB semen. All eggs were weighed and placed in a forced air incubator the same day that they were laid. After 7 to 10 d of incubation, the eggs were broken out and scored macroscopically as fertile with live embryo, fertile with dead embryo (early embryonic death), or clear (assumed infertile). The duration of fertility was defined as the number of days from the day after the second insemination to the last fertile egg before two consecutive interfile eggs. Hen BW were significantly different between treatments within each of the two 4-wk studies. The mean BW of the F hens was 4,261 g in Study 1 and 4,448 g in Study 2. The BW of the R hens were 3,459 g in Study 1 and 3,565 g in Study 2. Egg production levels and average egg weight was not different between treatments in either study. In Study 1, the duration of fertility for the F hens (12.7 d) and the R hens (12.7 d) were not different. In Study 2, the durations of fertility were significantly higher (P < 0.05) in the R hens (12.7 d) than in the F hens (10.0 d). These results support the theory that overweight BB have a reduced duration of fertility that may contribute to a reduced fertility in artificially inseminated and naturally mated flocks.

Animals↗
PubMed1999

Effectiveness of in vitro fertilization with intracytoplasmic sperm injection for severe male infertility.

BACKGROUND: In its 1993 report the Canadian Royal Commission on New Reproductive Technologies challenged the effectiveness of in vitro fertilization for severe male infertility. To address the Commission's concern, the authors compared the relative effectiveness of in vitro fertilization combined with intracytoplasmic sperm injection for severe male infertility and conventional in vitro fertilization for complete tubal occlusion in women. METHODS: This historical cohort study was done at the PROCREA Fertility Centre, a private tertiary human reproduction centre in Montreal. Three groups of infertile couples were compared: 122 couples with severe male infertility treated by in vitro fertilization with intracytoplasmic injection of fresh sperm from ejaculate (group 1); 27 couples with obstructive azoospermia treated by in vitro fertilization with intracytoplasmic injection of epididymal sperm (collected by microepididymal or percutaneous epididymal sperm aspiration) (group 2); and 98 couples with tubal factor infertility (bilateral tubal occlusion) treated with conventional in vitro fertilization (with sperm from ejaculate) (group 3). The main outcomes measured were rates of fertilization, pregnancy, clinical pregnancy and implantation. RESULTS: Pregnancy rates per started cycle were 35%, 40% and 34% for groups 1, 2 and 3 respectively. When prognostic factors were controlled for, none of the outcome measures differed significantly between the 3 groups. INTERPRETATION: In vitro fertilization with intracytoplasmic injection of sperm from the ejaculate or the epididymis is as effective for treating severe male infertility as conventional in vitro fertilization is for treating complete occlusion of the fallopian tubes in women.

Adult↗