Your browser doesn't support javascript.
loading
: 20 | 50 | 100
1 - 5 de 5
1.
Anim Sci J ; 95(1): e13947, 2024.
Article En | MEDLINE | ID: mdl-38661251

The purpose of this study is to reassess our previously reported findings on the diminished pregnancy rate of embryo transfer (ET) in summer for repeat-breeder (RB) cows compared with other seasons, with a focus on oxidative stress and energy balance. The study involved Japanese Black cattle, including 224 heifers (aged <3 years) and 278 (aged <9 years) cows with one or more deliveries, defined as RB animals. Evaluation of the effects of season on pregnancy rates revealed significantly lower rates in RB cows during summer compared with spring and autumn. Moreover, serum malondialdehyde (MDA) concentration in RB cows during summer was significantly higher than in winter, with no difference in RB heifers. Seasonal effects on serum nonesterified fatty acid (NEFA) concentration in both RB heifers and RB cows showed no significant differences. However, median MDA and NEFA concentrations in RB cows were significantly elevated compared with RB heifers, suggesting that factors contributing to low fertility should consider parity. Furthermore, our study indicated that RB cows were under oxidative stress, as demonstrated by significantly elevated MDA concentrations compared with normally reproducing cows in summer. Further investigation is necessary to gain a better understanding of these observations in the future.


Embryo Transfer , Energy Metabolism , Fatty Acids, Nonesterified , Malondialdehyde , Oxidative Stress , Pregnancy Rate , Seasons , Animals , Cattle/metabolism , Cattle/physiology , Female , Pregnancy , Malondialdehyde/blood , Malondialdehyde/metabolism , Embryo Transfer/veterinary , Fatty Acids, Nonesterified/blood
2.
BMC Genet ; 18(1): 103, 2017 Dec 06.
Article En | MEDLINE | ID: mdl-29212449

BACKGROUND: Repeat breeding, which is defined as cattle failure to conceive after three or more inseminations in the absence of clinical abnormalities, is a substantial problem in cattle breeding. To identify maternal genetic variants of repeat breeding in Japanese Black cattle, we selected 29 repeat-breeding heifers that failed to conceive following embryo transfer (ET) and conducted a genome-wide association study (GWAS) using the traits. RESULTS: We found that a single-nucleotide polymorphism (SNP; g.92,377,635A > G) in the upstream region of the FOXP3 gene on the X chromosome was highly associated with repeat breeding and failure to conceive following ET (P = 1.51 × 10-14). FOXP3 is a master gene for differentiation of regulatory T (Treg) cells that function in pregnancy maintenance. Reporter assay results revealed that the activity of the FOXP3 promoter was lower in reporter constructs with the risk-allele than in those with the non-risk-allele by approximately 0.68 fold. These findings suggest that the variant in the upstream region of FOXP3 with the risk-allele decreased FOXP3 transcription, which in turn, could reduce the number of maternal Treg cells and lead to infertility. The frequency of the risk-allele in repeat-breeding heifers is more than that in cows, suggesting that the risk-allele could be associated with infertility in repeat-breeding heifers. CONCLUSIONS: This GWAS identified a maternal variant in the upstream region of FOXP3 that was associated with infertility in repeat-breeding Japanese Black cattle that failed to conceive using ET. The variant affected the level of FOXP3 mRNA expression. Thus, the results suggest that the risk-allele could serve as a useful marker to reduce and eliminate animals with inferior fertility in Japanese Black cattle.


Cattle Diseases/genetics , Forkhead Transcription Factors/genetics , Infertility, Female/veterinary , X Chromosome , Animals , Cattle , Embryo Transfer , Female , Gene Expression , Genome-Wide Association Study , Infertility, Female/genetics
3.
Anim Sci J ; 86(7): 661-5, 2015 Jul.
Article En | MEDLINE | ID: mdl-25488699

The optimization of single-embryo culture conditions is very important, particularly in the in vitro production of bovine embryos using the ovum pick-up (OPU) procedure. The purpose of this study was to examine the development of embryos derived from oocytes obtained by OPU that were cultured either individually or in groups in medium supplemented with or without sericin and to investigate the viability of the frozen-thawed embryos after a direct transfer. When two-cell-stage embryos were cultured either individually or in groups for 7 days in CR1aa medium supplemented with or without 0.5% sericin, the rates of development to blastocysts and freezable blastocysts were significantly lower for the embryos cultured individually without sericin than for the embryos cultured in groups with or without sericin. Moreover, the rate of development to freezable blastocysts of the embryos cultured individually with sericin was significantly higher than that of the embryos cultured without sericin. When the frozen-thawed embryos were transferred directly to recipients, the rates of pregnancy, abortion, stillbirth and normal calving in the recipients were similar among the groups, irrespective of the culture conditions and sericin supplementation. Our findings indicate that supplementation with sericin during embryo culture improves the quality of the embryos cultured individually but not the viability of the frozen-thawed embryos after transfer to recipients.


Cell Survival/drug effects , Embryo Culture Techniques/methods , Embryo Transfer , Embryonic Development/drug effects , Freezing , Oocytes , Pregnancy, Animal , Sericins/pharmacology , Animals , Blastocyst , Cattle , Culture Media/pharmacology , Female , Pregnancy
4.
Cryobiology ; 67(2): 184-7, 2013 Oct.
Article En | MEDLINE | ID: mdl-23850826

Because the use of serum in the embryo cryopreservation increases the probability of animal health problems such as bovine spongiform encephalopathy (BSE) and viral infections, this study was conducted to examine the effects of sericin supplementation for serum-free freezing medium on the survival and development of bovine embryos after freezing-thawing and direct transfer to recipients. When in vitro-produced bovine embryos were frozen conventionally in the freezing medium supplemented with various concentrations (0.1%, 0.5%, and 1.0%) of sericin, the percentages of damaged zona pellucida, survival, and development of frozen-thawed embryos were similar to those of embryos frozen in freezing medium supplemented with 0.4% bovine serum albumin (BSA) and 20% fetal bovine serum (FBS) (0.4BSA/20F; control). When in vivo-derived embryos were frozen with 0.4BSA/20F (control), 0.5% sericin +20% FBS (0.5S/20F) or 0.5% sericin (0.5S) and were subsequently transferred directly to recipients, the percentages of recipients with pregnancy and normal calving in the 0.5S/20F group were higher than those in the control group (47.3% vs. 40.1% and 94.6% vs. 87.3%, respectively). Moreover, the percentages of recipients with pregnancy and normal calving (42.2% and 92.4%, respectively) in the 0.5S group were similar with those of other groups. In conclusion, these results indicate that serum-free freezing medium supplemented with sericin is available for the cryopreservation of bovine embryos and that it is beneficial for the elimination of a potential source of biological contamination by serum or BSA.


Cattle/embryology , Cryopreservation/methods , Cryoprotective Agents/metabolism , Culture Media, Serum-Free/metabolism , Embryo, Mammalian/physiology , Sericins/metabolism , Animals , Embryo Transfer , Embryo, Mammalian/embryology , Female , Pregnancy
5.
Mol Cell Proteomics ; 5(7): 1338-47, 2006 Jul.
Article En | MEDLINE | ID: mdl-16552026

We developed an integrated platform consisting of machinery and software modules that can apply vast amounts of data generated by nanoflow LC-MS to differential protein expression analyses. Unlabeled protein samples were completely digested with modified trypsin and separated by low speed (200 nl/min) one-dimensional HPLC. Mass spectra were obtained every 1 s by using the survey mode of a hybrid Q-TOF mass spectrometer and displayed in a two-dimensional plane with m/z values along the x axis, and retention time was displayed along the y axis. The time jitter of nano-LC was adjusted using newly developed software based on a dynamic programming algorithm. The comprehensiveness (60,000-160,000 peaks above the predetermined threshold detectable in 60-microg cell protein samples), reproducibility (average coefficient of variance of 0.35-0.39 and correlation coefficient of over 0.92 between duplicates), and accurate quantification with a wide dynamic range (over 10(3)) of our platform warrant its application to various types of experimental and translational proteomics.


Chromatography, High Pressure Liquid/methods , Mass Spectrometry/methods , Microfluidic Analytical Techniques/instrumentation , Peptide Fragments/chemistry , Proteomics/methods , Actinin/analysis , Actinin/metabolism , Automation/instrumentation , Blood Cells/chemistry , Cell Movement , Colorectal Neoplasms/metabolism , Diagnostic Imaging , Doxycycline/pharmacology , Gene Expression , Genes, Reporter , Humans , Microfilament Proteins/analysis , Microfilament Proteins/metabolism , Pancreatic Neoplasms/metabolism , Proteome/analysis , Proteomics/instrumentation , Software , Transfection , Tumor Cells, Cultured
...