To synchronize estrus and ovulation for improving pregnancy rate (PR) of repeat-breeder buffaloes, Controlled Internal Drug Release (CIDR) + prostaglandin (PGF2α) was used before service of repeat breeder buffaloes. Total of 20 cyclic lactating buffalo-cows (4-7 years, 400-500 kg, non-pregnant up to 90postpartum day) and 10 cyclic buffalo-heifers (2.5-4 years, 350-400 kg, not conceived after 3 services) were used in this study. In the 1 st group, a CIDR was inserted for 9 days, regardless reproductive status, and then animals were intramuscularly injected with PGF2α 24 h prior to CIDR removal. In the 2 nd group, control animals were used at the same interval. Animals in heat were naturally served and blood samples were collected on different days post-service for serum P4 determination. Pregnancy was diagnosed on day 25 post-service. Results showed that overall mean of PR was higher (P<0.01), while serum P4 at estrus was lower (P<0.001) in CIDR than in control, but both parameters were not affected significantly by animal type or CIDR x animal type interaction. Serum P4 at estrus was lower (P<0.05) in pregnant than in non-pregnant, regardless treatment or animal type. At the following post-service days, serum P4 showed the same trend of change, being higher (P<0.001) in CIDR than in control animals and in pregnant than in non-pregnant animals, regardless animal type. It could be concluded that the random usage of CIDR device for 9 days and prostaglandin F2α injection 24 h pre-CIDR withdrawal can be applied to improve pregnancy rate of repeat breeder Egyptian buffaloes.
The current study was undertaken to elucidate the effect of ovarian status in breeding and non-breeding season on the ovarian biometry, oocyte yield and oocyte quality of Baladi goats. Ovaries were collected by slicing from slaughter houses and classified with or without CLs during breeding (September-December) and non-breeding (March-July) seasons. Ovaries were weighed and measured, while oocytes were recoverded, yielded and categorized with or without CLs in breeding or non-breeding seasons. Results showed that ovarian weight and biometry (length, width and thickness) were higher in breeding than in non-breeding season, but the differences were significantly only for width. Number of follicles and oocytes/ovary (P<0.001) as well as number/ovary and proportion of oocytes at compact (P<0.0001) and denuded (P<0.05) stage were higher in breeding season than in non-breeding one. Number of degenerated oocytes/ovary was not affected significantly by season, but its proportion was lower (P<0.001) in breeding than in non-breading season. Number/ovary and proportion of partial denuded oocytes and proportion of denuded oocyte were not affected significantly by breeding season. Weight and biometry of ovaries was higher on ovaries bearing CL (CL+) than in non-bearing ones (CL-). Only ovarian width was higher (P<0.001) by 38% in CL+ than in CL-group. Ovaries bearing CL had higher (P<0.05) total follicles and oocyte yield/ovary (P<0.01) as well as oocyte recovery rate (P<0.05) than CL-ovaries. Number of compact, denuded and partial denuded oocytes/ovary was not affected by CL bearing. Number of compact oocytes tended to be greater on ovaries without than with CL. Number of degenerated oocytes/ovary was higher (P<0.05) on CL+ ovaries. Proportion of all oocyte categories was not affected by bearing CL. Finally, the effect of interaction between breeding season and bearing CL on all parameters studied was not significant. In conclusion, the goat ovaries without CL in breeding season yielded better oocyte quality than in non-breeding season, in term of COCs proportion. During non-breeding season, goats oocytes were available to be harvested from slaughtered goat does with acceptable yield and quality.
The current study investigated the effect of breeding season and presence of corpora lutea (CLs) on the ovaries with, ovarian characteristics, and yield, quality and oocyte recovery rate in sheep. Also, the effect of addition of sheep serum (SS) and bovine serum albumin (BSA) to maturation medium of sheep oocytes during breeding and non-breeding season was studied. Ovaries were collected during breeding and non-breeding seasons from slaughterhouses. Ovaries were classified with or without CLs during both seasons. Oocytes were collected by slicing and their yield, category and recovery rate were determined. Only compact oocytes (COCs) were in vitro matured as affected by breeding vs. non-breeding season and addition of 10% SS vs. BSA. Results show that only ovarian weight was higher (P<0.05) in breeding than in non-breeding season and with CL-ovaries than without CLs. Ovaries were longer and thicker in breed in than in non-breeding season. CL-ovaries during breeding season showed the highest ovarian characteristics. Number of all visible follicles/ovary tended to be higher (P<0.05) in breeding than in non-breeding season and of ovaries with than without CLs (P≥0.05). Oocyte yield/ovary was greater (P<0.05) by 41.7% in breeding than in non-breeding season. Oocyte yield was insignificantly greater on ovaries with CLs than those without CLs. Oocyte recovery rate was insignificantly higher in breeding and on ovaries with CLs than in non-breeding season and on those without CLs. Number/ovary and percentage of COCs were higher, while number/ovary were lower in breeding than in non-breeding season (P<0.05). Number and percentage of all categories were higher for oocytes recovered from ovaries with than without CLs. Percentage of oocytes at M-I stage was slightly higher in non-breeding than in breeding season. Percentage of oocytes at M-II showed an opposite trend, reflecting insignificantly higher maturation rate in breeding than in nonbreeding season. Percentage of oocytes at M-I and M-II stages was insignificantly higher in BSA than in SS-medium. Oocyte maturation rate with SS than with BSA in breeding and non-breeding season. In conclusion, sheep oocytes were available to be harvested during non-breeding season from slaughtered ewes with acceptable yield, quality and the maturation rate in vitro by addition sheep serum (10%) to maturation medium.
Various natural antioxidants, such as spirulina platensis (SP) as dietary additives, are beneficial to attenuate the detrimental effects of oxidative stress on fertility of females. The present study targeted to investigate:1) dietary SP effect (200 and 400 mg/kg LBW) on the reproductive performance, ovulatory responses and embryos development, and 2) effect of liquid SP addition to culture media (0.05 and 0.1 ml/ml) on in vitro embryos development of NZW rabbit does under heat stress. Results revealed that both dietary SP additions led to an increase (P<0.05) in ovarian weight, relative ovarian weight, total, antral follicles and CLs numbers, ovulation rate, and number and percentage of expanded blastocyst and hatched blastocysts, while decreased (P<0.05) number of bleeding follicles, number and percentage of degenerated embryos compared with control group. In vitro embryo developmental competence, in terms of number and percentage of hatched blastocysts increased (P≥0.05) by SP compared to control. Number and percentage of expanded blastocysts and degenerated embryos decreased (P≥0.05) in treatment groups as compared to control group. In conclusion addition of SP at a level of 400 mg/kg LBW in the diet of rabbit does improved reproductive traits in terms of increasing site and rate of ovulation, yield of acceptable embryos, and hatched blastocyst production. However, in vitro addition of SP in culture medium had no pronounced effect on the developmental competence of rabbit embryos.
Aim of this paper is to find the possibility of in vitro maturation of buffalo oocytes recovered from vitrified whole ovaries. Ovaries from slaughtered buffaloes (n=400) were collected; out of these ovaries, 150 were fresh and 250 buffalo ovaries were vitrified and thawed. Number of all visible follicles was recorded on fresh ovaries and on each ovarian surface pre-and post vitrification, then oocytes recovery rate was calculated in fresh or vitrified ovaries. Oocytes were recovered by aspiration. From the recovered oocytes from fresh ovaries, COCs were vitrified by straw cryodevice. Post-thawing, morphologically normal oocytes from vitrified or fresh ovaries were vitrified. Results showed that numbers of total and normal follicles, and total and normal oocytes per ovary were significantly higher in fresh than in vitrified ovaries. Total number of abnormal follicles showed significantly (P<0.01) an opposite trend, while, the difference in number of abnormal oocytes/ovary was not significant. Oocytes recovered from fresh ovaries showed significantly higher recovery and normality rates than those recovered from vitrified ovaries. Percentage of compact and expanded oocytes was significantly higher, while percentage of denuded and partial denuded oocytes was significantly lower when oocytes were recovered from fresh than from vitrified ovaries. Maturation rate (MIIoocytes percent) was higher (P<0.05) when oocytes were recovered from fresh than from vitrified ovaries and those vitrified after recovery (62.50% vs. 35.90 and 27.50%, respectively). In conclusion, vitrification of the whole buffalo ovaries is a positive tool for genetic sources cryopreservation in term of beneficial effects on in vitro maturation of oocytes when compare with those directly vitrified after recovery from fresh ovaries.
The aims of this study was to evaluate the effect of tonophosphan (TPH), as a phosphorous compound, on resumption of estrus and ovulatory activity of anestrous Egyptian buffalo heifers and anestrous post-partum buffalo cows, in relation with blood phosphorus level. Total of 24 anestrus animals with smooth ovaries and serum progesterone of <1 ng/ml up to 90 days postpartum (12 buffalo cows, weighing 470-530 kg, aging 5-7 years and between 3-4 parities. as well as 12 buffalo heifers, weighing 390-420 kg and 2.5-3 years old) were used in this study. In each of heifer and cow groups (n=12), animals were randomly divided into two subgroups (treated and control, 6 in each). Animals in treatment group (6 heifers and 6 cows) were injected twice at 7 day-interval with 4 ml/100 kg of TPH, while those in control group (6 heifers and 6 cows) were administrated with 4 ml distilled water/100 kg at the same time of TPH treatment. Estrous activity was detected twice daily to detect estrous signs. Blood samples were collected from all animals of each group on days 0, 3, 6, 10, 14, 18, 22, 26, 30, 34 and 38 of treatment. Results revealed that the estrus rate in treated animals was higher (P<0.05) in cows (83.33%) than in heifers (66.67%), while the control animals showed no estrous signs. Intensity, duration and interval from treatment to estrus were nearly similar in both heifers and cows. Concentration of serum P4 was higher (P<0.05) in cows than in heifers only on days 3 and 6 of treatment, while it was higher (P≥0.05) in cows than in heifers on other sampling days. Concentration of P4 was higher (P<0.05) in treated groups than in control on all sampling days, except during the 1 st and six days of treatment. Concentration of P4 was less than 1 ng/ml in control groups on all sampling treatment days, while P4 concentration level was ≥1 ng/ml after 10 days of treatment in treated groups. Concentration of Ca on most sampling days of treatment and P concentration on all sampling days were significantly (P<0.05-P<0.001) higher in heifers than in cows, while Ca:P ratio showed an opposite trend on all sampling days. In conclusion, Based on the foregoing results, twice tonophodphan injection of true anestrous buffalo heifers and cows at a week interval at a level of 4 ml/100 kg LBW has impact on resumption of estrous activity and achieving conception, being more effective for buffalo cows than for buffalo heifers.
To reduce early embryonic loss and improving pregnancy rate (PR) of Egyptian repeat breeder buffaloes, 45 repeat breeder animals were used in this study. Buffalo cows (n= 30) and buffalo heifers (n= 15) were allocated to three groups (10 cows and 5 heifers in each). Animals exhibiting normal heat were naturally mated. On Day 5 post-mating, a Controlled Internal Drug Release (CIDR-B) device was inserted on Day 5-9 (Protocol 1, P1), and Day 5-18 (Protocol 2, P2) post-mating. Animals in the 3 rd group (Control) were left without treatment. Blood samples were taken on different days post-mating. Results show overall pregnancy rate (PR) of 46.7, 66.7 and 13.3% in P1, P2 and control (P< 0.05), being higher in buffalo-cows than in buffalo-heifers (46.7 vs. 33.3%, P< 0.05). In controls, PR was 0 in buffalo-heifers and 20% in buffalo-cows. Level of progesterone (P 4 ) was higher (P< 0.05) in P1 and P2 than in control on most post-mating days following CIDR insertion, being higher in P2 than in P1, and higher (P≥ 0.05) in cows than in heifers. Level of P 4 at estrus decreased (P < 0.01), while post-mating P 4 levels increased for all pregnant in comparing with non-pregnant animals. In conclusion, increasing the progesterone concentrations by CIDR treatment from 5-18 days post-mating could be a useful strategy to prevent or reduce embryo mortality and is recommended for improving pregnancy in repeat breeder buffalo cows and heifers.
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