References of "Remy, Benoît"
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See detailCryopreservation of embryos : a way to reduce the number of housed animals and the genetic drift.
Remy, Benoît ULg; Ectors, Fabien ULg; Drion, Pierre ULg

Poster (2014, January 27)

The GIGA Mouse facility platform has recently improved its mouse line cryopreservation technique. The method of embryo cryopreservation by rapid cooling also called aseptic vitrification has been selected ... [more ▼]

The GIGA Mouse facility platform has recently improved its mouse line cryopreservation technique. The method of embryo cryopreservation by rapid cooling also called aseptic vitrification has been selected. Vitrification media, key steps and timing have been optimized and validated. After a first partial exposition of the embryos to cryoprotective solutions, they are immersed in a vitrifying mixture of penetrating and non-penetrating cryoprotectants for a short time. The straw containing the embryos is immediately sealed before to be plunged in LN2, resulting in a brutal solidification in which crystallization does not have time to occur. [less ▲]

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See detailGIGA ANIMAL CARE : Mice & Zebrafish Animal Facility and Transgenesis
Remy, Benoît ULg; Ectors, Fabien ULg; Winandy, Marie ULg et al

Poster (2014, January 27)

In fundamental research, animal models allow to place molecular and cellular observations back into their physiological context. In applied research, these models still remain a mandatory step to evaluate ... [more ▼]

In fundamental research, animal models allow to place molecular and cellular observations back into their physiological context. In applied research, these models still remain a mandatory step to evaluate the efficiency and the toxicity of potential treatments, before going to clinical trials. Mouse and Zebrafish (Danio rerio) are two very interesting models because of a short live cycle and a high prolificacy. They require a limited space. Their genome is well known and shows a high homology with the human. Many tools are available to produce transgenic mice or zebrafishes. Many tests are validated using both these species. [less ▲]

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See detailLAB’INSIGHT « Toxicological Risk Assessment » - Input of ULg preclinical studies
Drion, Pierre ULg; Remy, Benoît ULg; Winandy, Marie ULg et al

Scientific conference (2013, October 24)

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See detailLower intracellular concentration of cryoprotectants after vitrification than after slow freezing despite exposure to higher concentration of cryoprotectant solutions.
Vanderzwalmen, P.; Connan, Delphine ULg; Grobet, Luc ULg et al

in Human reproduction (Oxford, England) (2013)

STUDY QUESTION: What is the intracellular concentration of cryoprotectant (ICCP) in mouse zygotes during vitrification (VIT) and slow-freezing (SLF) cryopreservation procedures? SUMMARY ANSWER: Contrary ... [more ▼]

STUDY QUESTION: What is the intracellular concentration of cryoprotectant (ICCP) in mouse zygotes during vitrification (VIT) and slow-freezing (SLF) cryopreservation procedures? SUMMARY ANSWER: Contrary to common beliefs, it was observed that the ICCP in vitrified zygotes is lower than after SLF, although the solutions used in VIT contain higher concentrations of cryoprotectants (CPs). WHAT IS KNOWN ALREADY: To reduce the likelihood of intracellular ice crystal formation, which has detrimental effects on cell organelles and membranes, VIT was introduced as an alternative to SLF to cryopreserve embryos and gametes. Combined with high cooling and warming rates, the use of high concentrations of CPs favours an intracellular environment that supports and maintains the transition from a liquid to a solid glass-like state devoid of crystals. Although the up-to-date publications are reassuring in terms of obstetric and perinatal outcomes after VIT, a fear about exposing gametes and embryos to high amounts of CPs that exceed 3-4-fold those found in SLF was central to a debate initiated by advocates of SLF procedures. STUDY DESIGN, SIZE, DURATION: Two experimental set-ups were applied. The objective of a first study was to determine the ICCP at the end of the exposure steps to the CP solutions with our VIT protocol (n = 31). The goal of the second investigation was to compare the ICCP between VIT (n = 30) and SLF (n = 30). All experiments were performed in triplicates using mouse zygotes. The study took place at the GIGA-Research Institute of the University of Liege. PARTICIPANTS/MATERIALS, SETTING, METHODS: Cell volume is modified by changes in extracellular osmolarity. Hence, we estimated the final ICCP after the incubation steps in the VIT solutions by exposing the cells to sucrose (SUC) solutions with defined molarities. The ICCP was calculated from the SUC concentration that produced no change in cell volume, i.e. when intra- and extracellular osmolarities were equivalent. Cell volume was monitored by microscopic cinematography. ICCP was compared between SLF and VIT based on the principle that a high ICCP lowers the probability of (re)crystallization during warming but increases the probability of over-swelling of the cell due to fast inflow of water. The survival rates of mouse zygotes after SLF or VIT were compared using either (i) various warming rates or (ii) various concentrations of SUC in the warming dilution medium. MAIN RESULTS AND THE ROLE OF CHANCE: The ICCP in mouse zygotes during the VIT procedure prior to plunging them in liquid nitrogen was approximately 2.14 M, i.e. one-third of the concentration in the VIT solution. After SLF, the warming rate did not affect the zygote survival rate. In contrast, only 3/30 vitrified zygotes survived when warmed slowly but as many as 30/30 zygotes survived when warming was fast (>20 000 degrees C/min). Vitrified zygotes showed significantly higher survival rates than slow-frozen zygotes when they were placed directly in the culture medium or in solutions containing low concentrations of SUC (P < 0.01). These two experiments demonstrate a lower ICCP after VIT than after SLF. LIMITATIONS, REASONS FOR CAUTION: The results should not be directly extrapolated to other stages of development or to other species due to possible differences in membrane permeability to water and CPs. WIDER IMPLICATIONS OF THE FINDINGS: The low ICCP we observed after VIT removes the concern about high ICCP after VIT, at least in murine zygotes and helps to explain the observed efficiency and lack of toxicity of VIT. STUDY FUNDING / COMPETING INTEREST(S): The study was funded by the FNRS (National Funds for Scientific Research). The authors declare that they have no competing interests. [less ▲]

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See detailBone markers in pregnant Haflinger mares _ A trimestral evaluation
Greiner, C; Remy, Benoît ULg; CAVALIER, Etienne ULg et al

in Procedings of the Hippos-Congress 2012 (2012, February 11)

Introduction Pregnancy is associated with various physiological changes that essentially affect musculoskeletal conditions in the mare. However, the influence of pregnancy on equine bone metabolism has ... [more ▼]

Introduction Pregnancy is associated with various physiological changes that essentially affect musculoskeletal conditions in the mare. However, the influence of pregnancy on equine bone metabolism has not been studied to great detail. Aim of this study was to evaluate the effect of pregnancy on bone turnover markers in clinically normal lactating mares. Materials and Methods Venous blood samples were collected three-times from 17 multiparous lactating Haflinger mares, aged four to 18 years, during the first (T1), second (T2) and third (T3) trimester of pregnancy. Blood creatinine and gamma glutamyl transferase (GGT) values were evaluated. Serum concentrations of osteocalcin and carboxy-terminal cross-linking telopeptide of type I collagen (CTX-I) were determined using an equine specific osteocalcin radioimmunoassay and an automated CTX-I electrochemiluminescent sandwich antibody assay. Results All mares had normal creatinine and GGT values. Serum CTX-I values significantly increased during the last trimester of pregnancy. Serum osteocalcin concentrations were lowest at T2 and increased thereafter at T3. Conclusions Changes in bone turnover seem to depend on the stage of pregnancy in multiparous mares. Highest values of serum CTX-I and osteocalcin were obtained in the last trimester of pregnancy. [less ▲]

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See detailSerum osteocalcin and CTX-MMP concentration in young exercising thoroughbred racehorses
Carstanjen, B.; Amory, Hélène ULg; Sulon, Joseph ULg et al

in Journal of Veterinary Medicine. A, Physiology, Pathology, Clinical Medicine (2005), 52(3), 114-120

Bone responds to exercise with changes in bone (re-)modelling, which might be monitored non-invasively with biochemical bone markers. The aim of this study was to evaluate the influence of exercise on ... [more ▼]

Bone responds to exercise with changes in bone (re-)modelling, which might be monitored non-invasively with biochemical bone markers. The aim of this study was to evaluate the influence of exercise on serum osteocalcin and serum carboxy-terminal cross-linked telopeptide of type I collagen generated by matrix metalloproteinases (CTX-MMP) concentration in young racehorses. Seventy-one 2 to 4-year-old Thoroughbreds were included in this prospective infield study. Blood sampling was performed six times (i.e. six sampling cycles) during a 9-month period. Serum samples were analysed with commercial osteocalcin and CTX-MMP radioimmunoassays. Two-year-old racehorses had higher serum osteocalcin and CTX-MMP values than 3-year-old horses. Gender and training amplitude did not significantly influence serum osteocalcin and CTX-MMP values. Two-year-old horses showed an increase in osteocalcin values between cycles 2 and 3 and an increase in serum CTX-MMP values between cycles 1 and 2. Serum osteocalcin and CTX-MMP concentrations decreased between cycles 4 and 5, and 5 and 6. Three-year-old horses showed an increase in serum osteocalcin levels between cycles 3 and 4 and an increase in serum CTX-MMP concentrations between cycles 1 and 2, and 3 and 4. Serum osteocalcin levels decreased between cycles 5 and 6, whereas serum CTX-MMP levels decreased between cycles 4 and 5, and 5 and 6. Two- and three-year-old horses showed a decreased osteocalcin/CTX-MMP ratio between cycles 1 and 2. Moreover, 2-year-old horses showed an increase in the osteocalcin/CTX-MMP ratio between cycles 2 and 3. Sore shin formation did not significantly influence serum osteocalcin and CTX-MMP values. Serum osteocalcin and CTX-MMP are promising bone markers for monitoring exercise induced changes in equine bone metabolism. [less ▲]

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See detailSerum osteocalcin in donkeys as evaluated with an equine-specific radioimmunoassay
Carstanjen, B.; Amory, Hélène ULg; Youssao, I. et al

in Journal of Animal Physiology & Animal Nutrition (2004), 88(1-2), 1-6

The purpose of this study was to validate an equine-specific osteocalcin (OC) radioimmunoassay (RIA) for use in donkeys and to establish age-related changes in serum OC concentrations in healthy donkeys ... [more ▼]

The purpose of this study was to validate an equine-specific osteocalcin (OC) radioimmunoassay (RIA) for use in donkeys and to establish age-related changes in serum OC concentrations in healthy donkeys. Serial dilutions of donkey serum showed parallelism with standard curves obtained with the equine-specific OC RIA. There was a tight linear regression between donkey serum OC values obtained with the equine specific OC RIA and a commercially available bovine-specific OC RIA. Serum OC levels of 27 healthy donkeys, analysed with the equine-specific OC RIA, showed a tight negative logarithmic regression with age. Least square means and standard error of serum OC values were 67 +/- 10 mug/l in 0.6-4-year-old donkeys (group 1), 32 +/- 9 mug/l in 5-9-year-old donkeys (group 2) and 15 +/- 11 mug/l in >9-year-old donkeys (group 3). Serum OC values were significantly (p < 0.01) higher in group 1 than in groups 2 and 3. The equine-specific OC RIA may be a useful and practical tool to assess bone metabolism and skeletal diseases in donkeys. [less ▲]

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See detailEvaluation of plasma carboxy-terminal cross-linking telopeptide of type I collagen concentration in horses.
Carstanjen, Bianca; Hoyle, Nicholas R; Gabriel, Annick ULg et al

in American Journal of Veterinary Research (2004), 65(1), 104-9

OBJECTIVE: To evaluate a human assay for quantification of carboxy-terminal cross-linking telopeptide of type I collagen (CTX-I), assess the influence of age on plasma CTX-I concentration, investigate the ... [more ▼]

OBJECTIVE: To evaluate a human assay for quantification of carboxy-terminal cross-linking telopeptide of type I collagen (CTX-I), assess the influence of age on plasma CTX-I concentration, investigate the relationship between plasma CTX-I and serum osteocalcin concentrations, and determine whether concentrations of plasma CTX-I or serum osteocalcin fluctuate in circadian manner in horses. HORSES: 75 clinically normal horses. PROCEDURE: Cross-reactivity between equine serum CTX-I and CTX-I antibodies in an automated electrochemiluminescent sandwich antibody assay (ECLIA) was evaluated via a specificity test (ie, dilution test) and recovery calculation. Serum osteocalcin concentration was measured with an equine-specific osteocalcin radioimmunoassay. To analyze diurnal variations in plasma CTX-I and serum osteocalcin concentrations, blood samples were obtained hourly during a 24-hour period. RESULTS: Results of the dilution test indicated good correlation (r > 0.99) between expected serum CTX-I concentrations and measured serum CTX-I concentrations. The calculated CTX-I recovery was 97.6% to 109.9%. Plasma CTX-I and serum osteocalcin concentrations were correlated. Plasma CTX-I concentration was inversely correlated with age of the horse. No significant circadian variations in plasma CTX-I and serum osteocalcin concentrations were detected. CONCLUSIONS AND CLINICAL RELEVANCE: Results suggest that the fully automated CTX-I ECLIA can be used for evaluation of plasma and serum samples from horses and may be a useful tool to monitor bone metabolism changes. Horses in this study did not have notable diurnal fluctuations in serum osteocalcin and plasma CTX-I concentrations. [less ▲]

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See detailIsolement et caractérisation de l'ostéocalcine équine
Carstanjen, Bianca; Wattiez, R.; Amory, Hélène ULg et al

in Annales de Médecine Vétérinaire (2002), 146

Equine bone gamma-carboxyglutamic acid containing protein - also called osteocalcin - has been isolated for the first time till homogeneity. After acid demineralisation and acid extraction, the ... [more ▼]

Equine bone gamma-carboxyglutamic acid containing protein - also called osteocalcin - has been isolated for the first time till homogeneity. After acid demineralisation and acid extraction, the purification procedure was based on reverse phase chromatography, gel filtration and ion exchange chromatography. The amino acid sequence of the primary structure has been determined to be YLDHWLGA(HYP) APYPDPL(GLA)PRR(GLA)VC (GLA)LNPDCDELADHIGF-AYRRFYGPV. The protein has a calculated molecular weight of 5,732 kDa and a calculated isoelectric point of 4,45. It contains 49 amino acids, from which 3 are gamma-carboxyglutamic acid residues at position 17, 21 and 24 and has a fully hydroxylated proline in position nine and cysteine in position 23 and 29. Equine osteocalcin shows a strong homology with bovine (98%), ovine (96%) and human (94%) osteocalcin [less ▲]

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See detailThe isolation and characterization of equine Osteocalcin
Carstanjen, B; Wattiez, R; Amory, Hélène ULg et al

in Proceedings of the 1st meeting of the International Bone and Mineral Society (IBMS) (2001)

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See detailEndocrinologie de la gestation chez les ruminants: les protéines placentaires
Zarrouk, Anissa; Remy, Benoît ULg; Sulon, Joseph ULg et al

in Annales de Médecine Vétérinaire (1998), 142

The two main groups of placental proteins of ruminants are related in this paper: Placental lactogens and Pregnancy-Specific (-Associated) Proteins. Placental lactogens belong to the prolactin and growth ... [more ▼]

The two main groups of placental proteins of ruminants are related in this paper: Placental lactogens and Pregnancy-Specific (-Associated) Proteins. Placental lactogens belong to the prolactin and growth hormone family. They stimulate mammogenesis, fetal growth hormone family. They stimulate mammogenesis, fetal growth and maternal metabolism. Pregnancy-Specific proteins and Pregnancy-Associated glycoproteins belong to the aspartic proteinase family as pepsine, cathepsine D, E. These two groups of proteins are secreted in the maternal circulation by the binucleate cells after their migration to and fusion with the uterine cells. Their profiles were determined through RIA. Further investigations are in progress to rely secretory profiles with alterations of the trophoblastic function as occuring in embryonic mortality, abortion, fetal distress... [less ▲]

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See detailSynchronization of estrus in goats: the relationship between PMSG binding in plasma, time of occurrence of estrus and fertility following artificial insemination
Baril, G.; Remy, Benoît ULg; Leboeuf, J. F. et al

in Theriogenology (1996), 45(8), 1553-1559

Radioimmunoassay (RIA) was used to measure plasma eCG binding in dairy goats (n = 524) at the beginning of a progestagen/eCG treatment and 25 d after eCG administration. The eCG binding was not dependent ... [more ▼]

Radioimmunoassay (RIA) was used to measure plasma eCG binding in dairy goats (n = 524) at the beginning of a progestagen/eCG treatment and 25 d after eCG administration. The eCG binding was not dependent on the age of the females but increased with the number of treatments they had previously received (3.4 % ± 4.8, N = 47 vs 9.6 % ± 13.2, N = 249; mean ± SD; P < 0.01 for goats treated 0 and 1 time vs those treated 2 to 5 times, respectively). The synchronization treatment led to an increase in the binding of eCG (7.1 % ± 10.9 before vs 28.3 ± 24.5 after treatment; P < 0.01). When eCG binding before treatment was higher than 5 % the onset of estrus was delayed: 37.9 % of goats came into estrus more than 30 h after sponge removal vs 7.4 % when eCG binding was lower than 5 % (P < 0.01). Fertility was significantly decreased when eCG binding was higher than 10 %. These results show that the repetition of treatment with eCG to induce estrus in goats increases eCG binding. This could explain the lowered efficiency of the hormonal treatment to synchronize estrus and the associated decrease in fertility when goats are inseminated at a predetermined time. [less ▲]

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See detailProduction of anti-PMSG antibodies and its relation to the productivity of rabbit does
Lebas, F.; Theau-Clement, M.; Remy, Benoît ULg et al

in World Rabbit Science (1996), 4(2), 57-62

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See detailCytogenetic study of bovine oocytes matured in vitro
Ectors, Fabien ULg; Koulischer, Lucien ULg; Jamar, M. et al

in Theriogenology (1995), 44(3), 445-450

Described in the present paper is a cytogenetic study of bovine oocytes matured in vitro. The cumulus-oocyte complexes (COC), punctured from ovaries recovered in a local slaughterhouse, were classified ... [more ▼]

Described in the present paper is a cytogenetic study of bovine oocytes matured in vitro. The cumulus-oocyte complexes (COC), punctured from ovaries recovered in a local slaughterhouse, were classified into 3 groups according to follicular diameter 1 to 4mm, 5 to 8mm and 9 to 13 mm. Metaphases available for observation were classified as metaphase I, haploid and diploid metaphase II. High levels of haploid metaphases II (90.6, 86.9 and 94.4 %) among the 3 groups of follicular sizes indicated successful meiotic resumption during in vitro maturation and suggested that cytoplasmic maturation may be responsible for low developmental rate after IVM, IVF and in vitro development (IVD). [less ▲]

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See detailFractionation and partial characterization of proteins extracted from the bovine fallopian tube: preparation of tools for further purifications
Remy, Benoît ULg; Rabahi, F.; Duwez, L. et al

in Theriogenology (1995), 44(1), 95-107

Described in the present paper is a combined biochemical and immunological approach to study oviductal proteins in the bovine. Antisera were raised against semi-purified proteins extracted from bovine ... [more ▼]

Described in the present paper is a combined biochemical and immunological approach to study oviductal proteins in the bovine. Antisera were raised against semi-purified proteins extracted from bovine tubal mucosal tissue and were characterized. These antisera are available to monitor puritications of specific oviductal proteins in the future. Oviducts from 170 cyclic cows were collected at a slaughterhouse, and high amounts of mucosal proteins were extracted. The proteins were fractionated after precipitation with ammonium sulfate, anti-bovine serum albumin (bSA) and anti-bovine immunoglobulins bIg) afiinity chromatography and ion exchange chromatography. Each of the 12 fractions obtained after ion exchange chromatography was used to immunize a rabbit. Conditioned media were recovered from bovine oviduct cell monolayers cultured without serum to cot&m the oviductal origin of the extracted proteins. After Western blot analysis, 15 proteins were detected in the bovine oviductal extracts, and their molecular weights and isoelectric points were determined by 2 dimensional electrophoresis. Among these 15 proteins, 11 were also detected in conditioned media of bovine oviductal cells. These results demonstrate an oviductal origin of the 11 detected proteins and strongly suggest their secretion by the oviductal cells. [less ▲]

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See detailEffects of repeated use of progestagen-PMSG treatment for estrus control in dairy goats out of breeding season
Baril, Gérard; Remy, Benoît ULg; Vallet, J. C. et al

in Reproduction in Domestic Animals (1992), 27(3), 161-168

Contents: In order to analyze the effects of repeated use of progestagen-PMSG treatment, estrus and pregnancy results have been analyzed for 1989 in a Saânen dairy goat herd in which breeding takes place ... [more ▼]

Contents: In order to analyze the effects of repeated use of progestagen-PMSG treatment, estrus and pregnancy results have been analyzed for 1989 in a Saânen dairy goat herd in which breeding takes place each year out of season after FGA/PMSG treatment. After the first 1989 treatment (169 goats), percentage of goats showing estrus and kidding have been lower for 59 multiparous than for 46 primiparous and 64 nulliparous females. Moreover, when 38 goats are treated for a second time in 1989, 44.7% exhibited estrus vs 71.0% after the first treatment (P < 0.05). The PMSG binding level before the 1st 1989 treatment is higher for multiparous (17.5 ± 23.1%) than nulli and primiparous (-0.06 ± 0.7 and 1.2 ± 1.9%) and is increased for all parities after treatment (23.2 ± 26.4 after vs 5.7 ± 15.0% before, P < 0.01). For nulliparous and primiparous females; PMSG binding levels are not different for pregnant or not pregnant nulliparous and primiparous goats. On the opposite, PMSG binding rates are higher in non pregnant (25.7 ± 23.3) than in pregnant multiparous goats (6.5 ± 15.9) (P < 0.01). However, when the binding rate is ≤ 5.12% (computerized distributions) multiparous goats exhibit estrus and pregnancy at levels not different from nulliparous or primiparous females (% estrus 95.8 vs 100 or 97.8%, % pregnancy 66.7 vs 70.3 and 63.0% respectively). Repeated use of PMSG during the female life or during one given year leads to active immunization against PMSG (as measured by percentage of binding of PMSG in plasma) decreasing the efficiency of ovarian stimulation out of breeding season. [less ▲]

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See detailObservations sur l'utilisation de traitements gonadotropes répétés chez la chèvre laitière
Baril, Gérard; Remy, Benoît ULg; Vallet, J. C. et al

in Annales de Zootechnie (1992), 41(3-4), 291-296

Observations on the repeated use of gonadotropin treatments in the dairy goat. Our studies have attempted to determine if the absence of oestrus observed in some goats after fluorogestone acetate-pregnant ... [more ▼]

Observations on the repeated use of gonadotropin treatments in the dairy goat. Our studies have attempted to determine if the absence of oestrus observed in some goats after fluorogestone acetate-pregnant mare serum gonadotropin (FGA-PMSG) treatments could be due to its repeated use. An experiment was carried out in a Saanen flock, in which she-goats were submitted to FGA-PMSG treatment each year. The first treatment of the year was performed on 169 shegoats between March and August 1989. Of the females diagnosed as non-pregnant following the first treatment, 38 were treated a second time during the same period. The proportion of females which went into oestrus after the first treatment was lower in 59 multiparous goats than in 64 nulliparous and in 46 primiparous goats (64.4 vs 100 and 97.8%; P < O.Oi). For the she-goats treated twice, the percentage of females which went into oestrus after the second treatment was lower than that observed after the first treatment (44.7 vs 71.0%; P < 0.05). The presence of anti-PMSG antibodies in plasma was investigated in blood samples taken before and after each treatment. Results are expressed as % of radioactive PMSG bound by 10 pl of blood plasma. Before the first treatment, the percentage of bound PMSG was higher in multiparous than in nulliparous and primiparous goats (17.5 t 23.1 vs -0.06 t 0.7 ; 1.2 ± 1.9 ; P < 0.01), and increased after treatment for all parities. In goats treated twice, the percentage of bound PMSG before the second treatment was higher than that observed before first treatment (22.8 t 23. vs 11.2 f 19.7; P < 0.05). For both treatments, females which did not come into oestrus showed a percentage of bound PMSG which was significantly higher than that of goats in which oestrus was observed (multiparous first treatment: 30.5 f 23.6 vs 1I 2. 9 20. 1 %; she-goats in second treatment: 33.9 ± 23.1 vs 9.2 ± 14.5T.). When the percentage of bound PMSG before treatment was low (< 5°l) in multiparous goats, the oestrus and kidding rates after the first treatment did not differ from those observed in nulliparous and primiparous goats. The decrease in the efficiency of the treatments was therefore not due to the age of animals. The repeated use of FGA-PMSG during the lifetime of goats or within the same year is followed by an increase in the levels of antibodies against PMSG. The presence of those antibodies may explain the decrease in the efficiency of these treatments in inducing and synchronizing oestrus. [less ▲]

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See detailAre porcine follicle stimulating hormone antibodies associated with decreased superovulatory response in goat ?
Beckers, Jean-François ULg; Baril, G; Vallet, JC et al

in Theriogenology (1990), 33(1), 192

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