Efeito do período de suplementação com altrenogest no desempenho reprodutivo de fêmeas suínas em transição para o manejo em bandas

The synthetic progestin altrenogest (ALT) has been widely used in sow farms to concentrate artificial inseminations (AIs) during the transition of weekly productive flow for the batch farrowing system of 14 or 21 days. The objective of the present study was to investigate the effect of the duration of ALT treatment on the reproductive performance of weaned sows during transition to batch farrowing. Retrospective data was evaluated regarding the reproductive performance of primiparous and multiparous sows that were either not treated (control, n = 165) or treated with 20 mg ALT during 7 days (ALT7, n = 161) or 14 days (ALT14, n = 199) post-weaning. The interval between weaning or the end of ALT supplementation and first AI did not differ among the groups, as well as the percentage of sows inseminated up to 7 or 10 days after the end of treatment or weaning (P ≥ 0.16). There was a tendency for a lower farrowing rate (P = 0.06) in ALT7 (77.2%) when compared to ALT14 (84.5%) and control (86.3%) groups. The total number of piglets born did not differ among groups (P = 0.35). In conclusion, despite the slight delay in the estrus onset, the proportion of estrous sows was not affected, whereas the adjusted farrowing rate was reduced when ALT was administered for 7 days after weaning in multiparous sows during transition to 21 days batch farrowing system.O progestágeno sintético altrenogest (ALT) tem sido amplamente utilizado na suinocultura para agrupamento da inseminação, na transição de fluxo produtivo semanal para manejo em bandas de 14 ou 21 dias. O presente estudo investigou o efeito da duração do tratamento com ALT sobre o desempenho reprodutivo de fêmeas desmamadas na transição para o manejo em bandas. Foram coletados dados retrospectivos do desempenho reprodutivo de fêmeas primíparas e pluríparas desmamadas (n = 525) que não foram tratadas (controle, n = 165) ou tratadas diariamente com 20 mg de ALT durante 7 dias (ALT7, n = 161) ou 14 dias (ALT14, n = 199) pós-desmame. O intervalo entre o desmame ou final da suplementação de ALT e a primeira IA não diferiu entre os grupos, bem como o percentual de fêmeas inseminadas até 7 e 10 dias pós a remoção da suplementação hormonal (P ≥ 0,16). Houve uma tendência para menor taxa de parto ajustada (P = 0,06) no grupo ALT7 (77,2%), quando comparada aos grupos ALT14 (84,5%) e controle (86,3%). O número total de leitões nascidos não diferiu entre os grupos (P = 0,35). Conclui-se que, apesar do pequeno atraso no início do estro, não houve impactos na taxa de manifestação estral. Entretanto, a taxa de parto ajustada foi reduzida quando o ALT foi administrado por sete dias após o desmame na transição para o manejo em bandas de 21 dias

Endocrine Profile and Reproductive Performance in Heifers Induced to Lactation

Background: Low reproductive efficiency has been one of the main factors that lead to dairy herd culling in the reproductive age. In multiparous animals, such inefficiency and culling can occur because of various factors and may be associated with occasional endocrine failures. To avoid revenue losses that incur due to lack of lactation, lactation is artificially induced in the animals that are not pregnant, using a defined protocol. The aim of this study was, therefore, to evaluate and compare the reproductive performance of heifers submitted to the induction protocol with that of pregnant heifers during the transition period.Materials, Methods & Results: Sixty Holstein heifers, 32 ± 0.6 months of age, were divided into two groups: Control Group (Control, n = 30) comprising pregnant heifers that were accompanied since 21 days before the expected calving date until 224 days in milk (DIM) and an Induction Group (Induction, n = 30) comprising non-pregnant heifers submitted to a lactation induction protocol, accompanied from the beginning of the protocol until 224 DIM. For evaluation of the endocrine profile (progesterone and estradiol concentrations) of these animals, blood samples were collected at two periods: the pre-lactation (weeks -3, -2 and -1) and post-lactation (weeks 1 and 4). Heifers from both groups were submitted to weekly reproductive evaluations, from the beginning of lactation until 35 DIM. Uterine examinations were performed using ultrasonography and vaginoscopy to evaluate uterine content, cervical opening, and mucosal aspect. Females in good reproductive health were subjected to a hormonal protocol for timed artificial insemination (TAI). The pregnancy rate of heifers that could reproduce (Control, n = 13, and Induction, n = 20) were evaluated and inseminated until 49 DIM. Progesterone levels were similar (P > 0.05) in the two groups at both pre- and post-start of lactation. Estradiol concentrations were different (P < 0.01) among groups only in the pre-lactation period. Higher levels of progesterone (P = 0.06) were observed in the induced heifers (Induction Group = 1.07 ± 0.23 ng/mL and Control Group = 0.38 ± 0.28 ng/mL). Therefore, in the fourth week, induced heifers exhibited higher luteinic activity, the progesterone concentration was above 1 ng/mL in 42% of the animals, while just 12.5% of the Control heifers had it. The overall pregnancy rate was 47.75%. The pregnancy rate recorded for induced heifers and Control heifers was 40% and 55.55%, respectively.Discussion: Progesterone and estradiol evaluations were performed in the first week after the beginning of the lactation to evaluate the metabolism and physiological concentration of the hormones used during the protocol. The measurements were again performed in the fourth week to evaluate the return to cyclicity of the heifers in both groups. The high serum concentrations of estradiol attained during the induction, in the pre-lactation period, may have possible interfered with the uterine environment and follicular population of these animals. Furthermore, it is possible that the hormonal combination used has a central effect on the synthesis and release of gonadotrophins and/or an effect on the ovarian follicular population. Based on the hormonal profile evaluated, particularly the endocrine profile, and the reproductive performance of heifers, the results suggest that the protocol for induced lactation has a positive effect on fertility

Local regulation of antral follicle development and ovulation in monovulatory species

The identification of mutations in the genes encoding bone morphogenetic protein 15 (BMP15) and growth and differentiation factor 9 (GDF9) associated with phenotypes of sterility or increased ovulation rate in sheep aroused interest in the study of the role of local factors in preantral and antral folliculogenesis in different species. An additive mutation in the BMP15 receptor, BMPR1b, which determines an increase in the ovulatory rate, has been introduced in several sheep breeds to increase the number of lambs born. Although these mutations indicate extremely relevant functions of these factors, the literature data on the regulation of the expression and function of these proteins and their receptors are very controversial, possibly due to differences in experimental models. The present review discusses the published data and preliminary results obtained by our group on the participation of local factors in the selection of the dominant follicle, ovulation, and follicular atresia in cattle, focusing on transforming growth factors beta and their receptors. The study of the expression pattern and the functionality of proteins produced by follicular cells and their receptors will allow increasing the knowledge about this local system, known to be involved in ovarian physiopathology and with the potential to promote contraception or increase the ovulation rate in mammals

Paraoxonase 1 activity in the sperm-rich portion of boar ejaculates is positively associated with sperm quality

Associations of the activity of the paraoxonase 1 (PON1) enzyme with boar sperm quality still needs to be characterized, since boar ejaculates present distinct portions with differences in sperm concentration and quality. This study evaluated PON1 activity in the serum, in the distinct portions of boar ejaculates and estimated correlations with sperm quality parameters. Ejaculates and blood samples were collected from six boars for three weeks (two per week per boar; n = 36). Serum and post-spermatic portion PON1 activities were positively correlated (P = 0.01) but were both uncorrelated with the PON1 activity in the sperm-rich portion and in the whole ejaculate (P > 0.05). Differences in PON1 activity among boars were only observed in the sperm-rich portion of the ejaculate (P < 0.05). The PON1 activity in the serum and in the post-spermatic portion was generally negatively correlated with parameters of spermatozoa kinetics (P < 0.05). In the sperm-rich portion, PON1 activity was positively correlated with sperm concentration (P < 0.0001), curvilinear distance and velocity (both P < 0.05) and DNA integrity (P < 0.05), but negatively correlated with straightness and linearity (P < 0.05). Thus, boar ejaculates with increased PON1 activity in the sperm-rich portion may present increased concentration and spermatozoa with acceptable curvilinear velocity and distance and DNA integrity, which suggests that PON1 activity may be a biomarker for potential fertility

Bovine sperm cell motility after incubation in follicular fluid

O objetivo deste trabalho foi avaliar a motilidade de espermatozoides após inseminação artificial intrafolicular (IAIF) in vivo ou após incubação em fluído folicular in vitro. No experimento in vivo, a IAIF foi realizada com posterior recuperação do conteúdo folicular 1 a 4 horas depois, para avaliação da motilidade espermática. No experimento in vitro, os espermatozoides de um pool de doses comerciais de sêmen congelado/descongelado foram avaliados quanto à sua cinética após incubação por 1 ou 3 horas, puros (pool, controle) ou em fluído folicular (FF). Observou-se baixa motilidade dos espermatozoides nas amostras de FF, tanto in vitro como in vivo. In vitro, os principais parâmetros negativamente afetados nas células espermáticas incubadas em FF, em comparação ao controle, foram: motilidade total (MT), motilidade progressiva (MP), distância curvilínea e retilinearidade, após 1 hora de incubação; e MT, MP, velocidade média da trajetória e velocidade curvilínea, após 3 horas de incubação. O folículo ovariano e o fluído folicular não proporcionam ambiente adequado para manutenção da motilidade dos espermatozoides bovinos.The objective of this work was to evaluate sperm cell motility after intrafollicular artificial insemination (IFAI) in vivo or after incubation in follicular fluid in vitro. In the in vivo experiment, IFAI was performed, followed by the recovery of follicular content 1 to 4 hours later, in order to assess sperm motility. In the in vitro experiment, spermatozoa from a pool of commercial frozen-thawed semen were evaluated for their kinetics after incubation for 1 or 3 hours, either pure (pool, control group) or in follicular fluid (FF). A low motility of sperm cells was observed in the FF samples, both in vitro and in vivo. In vitro, the main parameters negatively affected in the sperm cells incubated in FF, compared with the control, were: total motility (TM), progressive motility (PM), curvilinear distance, and straightness, after 1 hour of incubation; and TM, PM, average path velocity, and curvilinear velocity after 3 hours of incubation. The ovarian follicle and follicular fluid do not provide a suitable environment to maintain bovine sperm cell motility

Effect of recombinant bovine somatotropin (rbST) treatment on follicular population and development in non-lactating dairy cows

The aim of this study was to evaluate the long term effects of recombinant bovine somatotropin (rbST) on follicle population and ovulatory follicle development in non-lactating dairy cows. Twenty-one Jersey cows were allocated in rbST (n=11) or control (n=10) groups. On day -60, cows in rbST group received 500 mg of somatotropin (s.c. Lactotropin, Elanco). On day 0, control and rbST cows received an intravaginal progesterone-releasing device (1.9 g, CIDR, Zoetis) and GnRH (100 mg, IM, Factrel, Zoetis). On day 8, cows received PGF2α (25 mg, IM, Lutalyse, Zoetis) and the CIDR was removed. Twelve hours after device removal (D8), serum, follicular fluid and granulosa cells samples were collected. Serum and follicular concentration of estradiol (E2) and progesterone (P4) were analyzed. Total RNA was extracted from granulosa cells to measure gene expression of LHCGR, STAR, HSD-3B1, CYP11A1, CYP19A1, CYP17A1, IGFR and PAPPA by real time PCR. Ultrasonography was performed on days -60, -53, -46, -14, -7, 0 and 8 for antral follicle count. Results were analyzed by repeated measures ANOVA and t-test. There was no effect of rbST treatment on the number of follicles during the 60 days period, as well as no effect on serum and follicular fluid E2 and follicular fluid P4 at the moment of follicle aspiration. There was a reduction in PAPPA (P = 0.006), CYP11A1 (P = 0.04) and CYP19A1 (P = 0.002) mRNA levels in granulosa cells of the pre ovulatory follicle of rbST treated cows. In conclusion, a single dose of rbST did not have long term effects on antral follicle population, serum and follicular E2/P4 concentrations in non-lactating dairy cows. Despite that, rbST injection decreased granulosa cell expression of genes related to steroidogenesis in the pre-ovulatory follicle

Analysis of nuclear maturation, DNA damage and repair gene expression of bovine oocyte and cumulus cells submitted to ionizing radiation

Radiotherapy causes destruction of tumor cells, but also threatens the integrity and survival of surrounding normal cells. Then, woman submitted to irradiation for cancer treatment may present permanent ovary damage, resulting in impaired fertility. The objective of this study was to investigate the effects of therapeutic doses of ionizing radiation (IR), used for ovarian cancer treatment in humans, on bovine cumulus-oocyte complexes (COCs) as experimental model. Bovine ovaries were exposed to 0.9 Gy, 1.8 Gy, 3.6 Gy or 18.6 Gy IR, and then COCs were collected and used to evaluate: (a) oocyte nuclear maturation; (b) presence of phosphorylated H2A.X (γH2AX), as an indicator of DNA double-strand breaks (DSBs); and (c) expression of genes involved in DNA repair (TP53BP1, RAD52, ATM, XRCC6 and XRCC5) and apoptosis (BAX). The radiation doses tested in this study had no detrimental effects on nuclear maturation and did not increase γH2AX in the oocytes. However, IR treatment altered the mRNA abundance of RAD52 (RAD52 homolog, DNA repair protein) and BAX (BCL2-associated X protein). We conclude that although IR doses had no apparent effect on oocyte nuclear maturation and DNA damage, molecular pathways involved in DNA repair and apoptosis were affected by IR exposure in cumulus cells

Intravaginal progestagen for estrus and parturition control in sows

O objetivo deste trabalho foi avaliar a utilização de dispositivos intravaginais (DIV) para o controle da reprodução em suínos. Porcas aos 112 dias de gestação receberam injeção de PGF2α (controle, n = 15) ou PGF2α com inserção de DIV contendo acetato de medroxiprogesterona (grupo DIV, n = 14) por 48 horas. As fêmeas iniciaram o parto 27,7±1,6 e 82,3±3,8 horas após aplicação de PGF2α nos grupos controle e tratado, respectivamente. Quanto ao controle do estro, dez porcas receberam DIV por 12 dias, iniciando imediatamente após o desmame, e o estro foi confirmado aos 17,25±0,17 dias após o desmame, em comparação a 4±0,25 dias no grupo controle. Dispositivos intravaginais com progestágeno podem ser utilizados no controle da reprodução em suínos.The objective of this work was to evaluate the use of intravaginal devices (IVD) for the control of reproductive events in swine. Sows at 112 days of pregnancy received an injection of PGF2α (control, n = 15) or PGF2α plus an IVD containing medroxyprogesterone acetate (IVD group, n = 14) for 48 hours. Sows initiated labor 27.7±1.6 and 82.3±3.8 h after PGF2α aplicaction, in control and treated groups, respectively. Regarding control of estrus cycle, ten sows received IVD for 12 days starting immediately after weaning, and estrus was confirmed 17.25±0.17 days after weaning, in comparison to 4.00±0.25 days for the control group. Intravaginal devices with progestagen can be applied for the control of reproduction in swine

Transforming growth factor-beta family members are regulated during induced luteolysis in cattle

The transforming growth factors beta (TGFβ) are local factors produced by ovarian cells which, after binding to their receptors, regulate follicular deviation and ovulation. However, their regulation and function during corpus luteum (CL) regression has been poorly investigated. The present study evaluated the mRNA regulation of some TGFβ family ligands and their receptors in the bovine CL during induced luteolysis in vivo. On day 10 of the estrous cycle, cows received an injection of prostaglandin F2α (PGF) and luteal samples were obtained from separate groups of cows (n= 4-5 cows per time-point) at 0, 2, 12, 24 or 48 h after treatment. Since TGF beta family comprises more than 30 ligands, we focused in some candidates genes such as activin receptors (ACVR-1A, -1B, -2A, -2B) AMH, AMHR2, BMPs (BMP-1, -2, -3, -4, -6 and -7), BMP receptors (BMPR 1A, -1B and -2), inhibin subunits (INH-A, -BA, -BB) and betaglycan (TGFBR3). The mRNA levels of BMP4, BMP6 and INHBA were higher at 2 h after PGF administration (P<0.05) in comparison to 0 h. The relative mRNA abundance of BMP1, BMP2, BMP3, BMP4, BMP6, ACVR1B, INHBA and INHBB was upregulated up to 12 h post PGF (P<0.05). On the other hand, TGFBR3 mRNA that codes for a reservoir of ligands that bind to TGF-beta receptors, was lower at 48 h. In conclusion, findings from this study demonstrated that genes encoding several TGFβ family members are expressed in a time-specific manner after PGF administration

A função da prostaglandina F2α na ovulação e na liberação de LH em vacas

O objetivo deste estudo foi avaliar o papel da prostaglandina F2α (PGF) na ovulação. No Experimento 1, as vacas foram alocadas aleatoriamente em dois tratamentos para receber 150 μg de d-Cloprostenol (Grupo PGF, n = 12) ou 2 mL de NaCl 0,9% (Grupo Controle, n = 11) e os CIDR, foram removidos 4 dias depois. Nenhuma vaca ovulou nos grupos Controle e PGF. No Experimento 2, as vacas foram separadas aleatoriamente em dois grupos experimentais para receber 4 injeções de 150 μg de d-Cloprostenol (n = 9) ou 2 mL de NaCL 0,9% (n = 9). Não foi observada ovulação em nenhum dos animais deste experimento. No Experimento 3, vacas ovariectomizadas receberam três injeções de 300μg de análogo de PGF (Grupo PGF, n = 5), 100μg de Lecirelina (Grupo GnRH, n = 5) ou 2 mL de PBS (Grupo Controle, n = 4). A concentração de LH foi maior (P &lt;0,0001) nas vacas do grupo GnRH do que nos grupos PGF e Controle. No Experimento 4, vacas com folículos pré-ovulatórios (&gt; 11,5 mm) foram tratadas com solução salina (Grupo Controle, n = 6), Lecirelina (Grupo GnRH, n = 7) ou Cloprostenol Sódico (Grupo PGF, n = 6). Houve um aumento significativo na área vascular dos folículos de 0 a 24h nos tratamentos com GnRH e PGF. Em conclusão, a PGF não foi capaz de induzir ovulação em vacas com alta ou baixa concentração plasmática de progesterona. Além disso, a PGF sozinha não foi capaz de induzir a liberação de LH e a luteinização do folículo, mas aumentou a vascularização folicular.This study aimed to evaluate the role of prostaglandin F2α (PGF) on ovulation. In Experiment 1, cows were randomly allocated to two treatments to receive 150 μg of d-Cloprostenol (PGF Group, n = 12) or 2 mL of NaCl 0.9% (Control Group, n = 11) and CIDRs, were removed 4 days later. No cow ovulated in Control and PGF groups. In Experiment 2, cows were randomly separated into two experimental groups to receive 4 injections of 150 μg of d-Cloprostenol (n = 9) or 2 mL of NaCL 0.9% (n = 9). In this experiment, ovulation was not observed in any cows. In Experiment 3, ovariectomized cows receive three injections of 300μg of PGF analog (PGF Group, n = 5), 100μg of Lecirelin (GnRH Group, n = 5) or 2 mL of PBS (Control Group, n = 4). The LH concentration was higher (P &lt;0.0001) in cows from the GnRH group than in the PGF and Control groups. In experiment 4, cows with preovulatory follicles (&gt;11.5 mm) were treated with Saline (Control Group, n = 6); Lecirelin (GnRH Group, n = 7) or Cloprostenol Sodium (PGF Group, n = 6). There was a significant increase in the vascular area of follicles from 0 to 24 h in GnRH and PGF treatments. In conclusion, PGF was not able to induce ovulation in cows with high or low plasma progesterone concentration. Additionally, PGF alone was not able to induce LH release and follicle luteinization, but increased follicular vascularization