792 research outputs found

    Genetic selection of maternal lines and digestive efficiency in rabbits: long term selection for litter size at weaning versus hyper selection for reproductive longevity

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    The objective of the present paper is to evaluate how long-term selection for litter size at weaning or short-term hyper selection for reproductive longevity, affect the digestive utilisation of growing and lactating rabbits. A digestibility trial was carried out during the 3rd week of lactation with a total of 27 multiparous does: 14 females came from a line selected for litter size at weaning over 32 generations (V), and 13 from a recently constituted, long lived-productive line (LP). Another digestibility trial was performed during the growing period with a total of 48 growing rabbits (24 from each line). After a 7 d adaptation period, faeces were collected individually for 4 d (from 13 to 16 d of lactation or from 49 to 53 d of age, respectively). Daily feed intake and weight gain recorded during the experimental growing period were similar for both lines (137 g of dry matter (DM)/d and 48 g/d, respectively). Growing rabbits from the V-line showed greater values for the digestibility of the DM and OM (+1 percentage point; P<0.10) and signifi cantly higher values for the acid detergent fi bre (+3 percentage points; P=0.03) than animals from the LP line. No signifi cant differences for the apparent digestibility coeffi cients of crude protein, neutral detergent fi bre, crude fi bre and gross energy were observed between lines, these being on average 65.7, 23.0, 10.7 and 52.6%, respectively. Females from the LP line were initially heavier (+258 g of live weight; P=0.06), and presented a signifi cantly greater daily feed intake (+22 g DM/d; P=0.04) and milk yield (+37 g/d; P=0.01) during the pre-experimental and faeces collection phases (from 6 to 16 d of lactation). V-line lactating does displayed greater values for digestibility for all those nutrients evaluated (from +0.9 and +3.7 percentage points for the crude protein and acid detergent fi bre) compared to the LP line females, although these were only signifi cant for the DM, organic matter and gross energy (+2.3, +2.5, +2.1 percentage points; P<0.05). In conclusion, rabbits selected for litter size at weaning seem to have greater effi ciency for digestive utilisation than those hyper selected for reproductive longevity.This study has been supported by the Spanish CICYT project AGL 2004-02710/GAN.Pascual Amorós, JJ.; Ródenas, L.; Martínez, E.; Cervera, C.; Blas, E.; Baselga, M. (2008). Genetic selection of maternal lines and digestive efficiency in rabbits: long term selection for litter size at weaning versus hyper selection for reproductive longevity. World Rabbit Science. 16(3). doi:10.4995/wrs.2008.62516

    Different resource allocation strategies result from selection for litter size at weaning in rabbit does

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    This study examined the effect of long-term selection of a maternal rabbit line, solely for a reproductive criterion, on the ability of female rabbits to deal with constrained environmental conditions. Female rabbits from generations 16 and 36 (n = 72 and 79, respectively) of a line founded and selected to increase litter size at weaning were compared simultaneously. Female rabbits were subjected to normal (NC), nutritional (NF) or heat (HC) challenging conditions from 1st to 3rd parturition. Animals in NC and NF were housed at normal room temperatures (18°C to 25°C) and respectively fed with control (11.6 MJ digestible energy (DE)/kg dry matter (DM), 126 g digestible protein (DP)/kg DM, and 168 g of ADF/kg DM) or low-energy fibrous diets (9.1 MJ DE/kg DM, 104 g DP/kg DM and 266 g ADF/kg DM), whereas those housed in HC were subjected to high room temperatures (25°C to 35°C) and the control diet. The litter size was lower for female rabbits housed in both NF and HC environments, but the extent and timing where this reduction took place differed between generations. In challenging conditions (NF and HC), the average reduction in the reproductive performance of female rabbits from generation 16, compared with NC, was &#8722;2.26 (P<0.05) and &#8722;0.51 kits born alive at 2nd and 3rd parturition, respectively. However, under these challenging conditions, the reproductive performance of female rabbits from generation 36 was less affected at 2nd parturition (&#8722;1.25 kits born alive), but showed a greater reduction at the 3rd parturition (&#8722;3.53 kits born alive; P<0.05) compared with NC. The results also showed differences between generations in digestible energy intake, milk yield and accretion, and use of body reserves throughout lactation in NC, HC and NF, which together indicate that there were different resource allocation strategies in the animals from the different generations. Selection to increase litter size at weaning led to increased reproductive robustness at the onset of an environmental constraint, but failure to sustain the reproductive liability when the challenge was maintained in the long term. This response could be directly related to the shortterm environmental fluctuations (less severe) that frequently occur in the environment where this line has been selected.The authors thank Professor Enrique Blas Ferrer for his valuable comments on the initial version of this document, Juan Carlos Moreno for his help in conducting the trial at the experimental farm, and the Ministry of Economy and Competitiveness (Project: AGL2011-30170-C02-01) for economic support.Savietto, D.; Cervera Fras, MC.; Ródenas Martínez, L.; Martínez Paredes, EM.; Baselga Izquierdo, M.; García Diego, FJ.; Larsen, T.... (2014). Different resource allocation strategies result from selection for litter size at weaning in rabbit does. Animal. 8(4):618-628. https://doi.org/10.1017/S1751731113002437S61862884García-Diego, F.-J., Pascual, J. J., & Marco, F. (2011). Technical Note: Design of a large variable temperature chamber for heat stress studies in rabbits. World Rabbit Science, 19(4). doi:10.4995/wrs.2011.938Ragab, M., & Baselga, M. (2011). A comparison of reproductive traits of four maternal lines of rabbits selected for litter size at weaning and founded on different criteria. Livestock Science, 136(2-3), 201-206. doi:10.1016/j.livsci.2010.09.009Friggens, N. C. (2003). Body lipid reserves and the reproductive cycle: towards a better understanding. Livestock Production Science, 83(2-3), 219-236. doi:10.1016/s0301-6226(03)00111-8Littell, R. C., Henry, P. R., & Ammerman, C. B. (1998). Statistical analysis of repeated measures data using SAS procedures. Journal of Animal Science, 76(4), 1216. doi:10.2527/1998.7641216xEstany, J., Baselga, M., Blasco, A., & Camacho, J. (1989). Mixed model methodology for the estimation of genetic response to selection in litter size of rabbits. Livestock Production Science, 21(1), 67-75. doi:10.1016/0301-6226(89)90021-3Fernández-Carmona, J., Alqedra, I., Cervera, C., Moya, J., & Pascual, J. J. (2003). Effect of lucerne-based diets on performance of reproductive rabbit does at two temperatures. Animal Science, 76(2), 283-295. doi:10.1017/s1357729800053534Fernández-Carmona, J., Cervera, C., Sabater, C., & Blas, E. (1995). Effect of diet composition on the production of rabbit breeding does housed in a traditional building and at 30°C. Animal Feed Science and Technology, 52(3-4), 289-297. doi:10.1016/0377-8401(94)00715-lHarano, Y., Ohtsuki, M., Ida, M., Kojima, H., Harada, M., Okanishi, T., … Shigeta, Y. (1985). Direct automated assay method for serum or urine levels of ketone bodies. Clinica Chimica Acta, 151(2), 177-183. doi:10.1016/0009-8981(85)90321-3Dauncey, M. J. (1990). Thyroid hormones and thermogenesis. Proceedings of the Nutrition Society, 49(2), 203-215. doi:10.1079/pns19900024Savietto, D., Blas, E., Cervera, C., Baselga, M., Friggens, N. C., Larsen, T., & Pascual, J. J. (2012). Digestive efficiency in rabbit does according to environment and genetic type. World Rabbit Science, 20(3). doi:10.4995/wrs.2012.1152Falconer, D. S. (1990). Selection in different environments: effects on environmental sensitivity (reaction norm) and on mean performance. Genetical Research, 56(1), 57-70. doi:10.1017/s0016672300028883Vicente, J., & García-Ximénez, F. (1993). Effects of strain and embryo transfer model (embryos from one versus two donor does/recipient) on results of cryopreservation in rabbit. Reproduction Nutrition Development, 33(1), 5-13. doi:10.1051/rnd:19930101Quiniou, N., Renaudeau, D., Dubois, S., & Noblet, J. (2000). Influence of high ambient temperatures on food intake and feeding behaviour of multiparous lactating sows. Animal Science, 70(3), 471-479. doi:10.1017/s1357729800051821Theilgaard, P., Sánchez, J. P., Pascual, J. J., Friggens, N. C., & Baselga, M. (2006). Effect of body fatness and selection for prolificacy on survival of rabbit does assessed using a cryopreserved control population. Livestock Science, 103(1-2), 65-73. doi:10.1016/j.livsci.2006.01.007Brecchia, G., Bonanno, A., Galeati, G., Federici, C., Maranesi, M., Gobbetti, A., … Boiti, C. (2006). Hormonal and metabolic adaptation to fasting: Effects on the hypothalamic–pituitary–ovarian axis and reproductive performance of rabbit does. Domestic Animal Endocrinology, 31(2), 105-122. doi:10.1016/j.domaniend.2005.09.006Piles, M., Garreau, H., Rafel, O., Larzul, C., Ramon, J., & Ducrocq, V. (2006). Survival analysis in two lines of rabbits selected for reproductive traits1. Journal of Animal Science, 84(7), 1658-1665. doi:10.2527/jas.2005-678Sanchez, J. P., Baselga, M., & Ducrocq, V. (2006). Genetic and environmental correlations between longevity and litter size in rabbits. Journal of Animal Breeding and Genetics, 123(3), 180-185. doi:10.1111/j.1439-0388.2006.00590.xQuevedo, F., Cervera, C., Blas, E., Baselga, M., & Pascual, J. J. (2006). Long-term effect of selection for litter size and feeding programme on the performance of reproductive rabbit does 2. Lactation and growing period. Animal Science, 82(5), 751-762. doi:10.1079/asc200688Vicente, J. S., & García-Ximénez, F. (1996). Direct transfer of vitrified rabbit embryos. Theriogenology, 45(4), 811-815. doi:10.1016/0093-691x(96)00010-6Coureaud, G., Fortun-Lamothe, L., Langlois, D., & Schaal, B. (2007). The reactivity of neonatal rabbits to the mammary pheromone as a probe for viability. animal, 1(7), 1026-1032. doi:10.1017/s1751731107000389Rommers, J. M., Boiti, C., Brecchia, G., Meijerhof, R., Noordhuizen, J. P. T. M., Decuypere, E., & Kemp, B. (2004). Metabolic adaptation and hormonal regulation in young rabbit does during long-term caloric restriction and subsequent compensatory growth. Animal Science, 79(2), 255-264. doi:10.1017/s1357729800090111Piles, M., García, M. L., Rafel, O., Ramon, J., & Baselga, M. (2006). Genetics of litter size in three maternal lines of rabbits: Repeatability versus multiple-trait models. Journal of Animal Science, 84(9), 2309-2315. doi:10.2527/jas.2005-622Garcı́a, M. L., & Baselga, M. (2002). Estimation of genetic response to selection in litter size of rabbits using a cryopreserved control population. Livestock Production Science, 74(1), 45-53. doi:10.1016/s0301-6226(01)00280-9Cervera, C., & Carmona, J. F. (s. f.). Nutrition and the climatic environment. Nutrition of the rabbit, 267-284. doi:10.1079/9781845936693.0267Nicodemus, N., Redondo, R., Pérez-Alba, L., Carabaño, R., De Blas, J. C., & García, J. (2010). Effect of level of fibre and type of grinding on the performance of rabbit does and their litters during the first three lactations. Livestock Science, 129(1-3), 186-193. doi:10.1016/j.livsci.2010.01.023Theilgaard, P., Sánchez, J., Pascual, J., Berg, P., Friggens, N. C., & Baselga, M. (2007). Late reproductive senescence in a rabbit line hyper selected for reproductive longevity, and its association with body reserves. Genetics Selection Evolution, 39(2), 207. doi:10.1186/1297-9686-39-2-207Martínez-Paredes, E., Ródenas, L., Martínez-Vallespín, B., Cervera, C., Blas, E., Brecchia, G., … Pascual, J. J. (2012). Effects of feeding programme on the performance and energy balance of nulliparous rabbit does. animal, 6(7), 1086-1095. doi:10.1017/s1751731111002643Baselga M 2004. Genetic improvement of meat rabbits. Programmes and diffusion. In Proceedings of 8th World Rabbit Science Congress, 5–7 September 2004, Puebla, Mexico, pp. 1–13

    Targeting tumorigenesis: development and use of mTOR inhibitors in cancer therapy

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    The mammalian target of rapamycin (mTOR) is an intracellular serine/threonine protein kinase positioned at a central point in a variety of cellular signaling cascades. The established involvement of mTOR activity in the cellular processes that contribute to the development and progression of cancer has identified mTOR as a major link in tumorigenesis. Consequently, inhibitors of mTOR, including temsirolimus, everolimus, and ridaforolimus (formerly deforolimus) have been developed and assessed for their safety and efficacy in patients with cancer. Temsirolimus is an intravenously administered agent approved by the US Food and Drug Administration (FDA) and the European Medicines Agency (EMEA) for the treatment of advanced renal cell carcinoma (RCC). Everolimus is an oral agent that has recently obtained US FDA and EMEA approval for the treatment of advanced RCC after failure of treatment with sunitinib or sorafenib. Ridaforolimus is not yet approved for any indication. The use of mTOR inhibitors, either alone or in combination with other anticancer agents, has the potential to provide anticancer activity in numerous tumor types. Cancer types in which these agents are under evaluation include neuroendocrine tumors, breast cancer, leukemia, lymphoma, hepatocellular carcinoma, gastric cancer, pancreatic cancer, sarcoma, endometrial cancer, and non-small-cell lung cancer. The results of ongoing clinical trials with mTOR inhibitors, as single agents and in combination regimens, will better define their activity in cancer

    Measurement of the total cross section and ρ -parameter from elastic scattering in pp collisions at √s=13 TeV with the ATLAS detector

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    Studies of new Higgs boson interactions through nonresonant HH production in the b¯bγγ fnal state in pp collisions at √s = 13 TeV with the ATLAS detector

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    A search for nonresonant Higgs boson pair production in the b ¯bγγ fnal state is performed using 140 fb−1 of proton-proton collisions at a centre-of-mass energy of 13 TeV recorded by the ATLAS detector at the CERN Large Hadron Collider. This analysis supersedes and expands upon the previous nonresonant ATLAS results in this fnal state based on the same data sample. The analysis strategy is optimised to probe anomalous values not only of the Higgs (H) boson self-coupling modifer κλ but also of the quartic HHV V (V = W, Z) coupling modifer κ2V . No signifcant excess above the expected background from Standard Model processes is observed. An observed upper limit µHH &lt; 4.0 is set at 95% confdence level on the Higgs boson pair production cross-section normalised to its Standard Model prediction. The 95% confdence intervals for the coupling modifers are −1.4 &lt; κλ &lt; 6.9 and −0.5 &lt; κ2V &lt; 2.7, assuming all other Higgs boson couplings except the one under study are fxed to the Standard Model predictions. The results are interpreted in the Standard Model efective feld theory and Higgs efective feld theory frameworks in terms of constraints on the couplings of anomalous Higgs boson (self-)interactions

    Comparison of inclusive and photon-tagged jet suppression in 5.02 TeV Pb+Pb collisions with ATLAS

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    Measurement of the H → γ γ and H → ZZ∗ → 4 cross-sections in pp collisions at √s = 13.6 TeV with the ATLAS detector

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    The inclusive Higgs boson production cross section is measured in the di-photon and the Z Z∗ → 4 decay channels using 31.4 and 29.0 fb−1 of pp collision data respectively, collected with the ATLAS detector at a centre of-mass energy of √s = 13.6 TeV. To reduce the model dependence, the measurement in each channel is restricted to a particle-level phase space that closely matches the chan nel’s detector-level kinematic selection, and it is corrected for detector effects. These measured fiducial cross-sections are σfid,γ γ = 76+14 −13 fb, and σfid,4 = 2.80 ± 0.74 fb, in agreement with the corresponding Standard Model predic tions of 67.6±3.7 fb and 3.67±0.19 fb. Assuming Standard Model acceptances and branching fractions for the two chan nels, the fiducial measurements are extrapolated to the full phase space yielding total cross-sections of σ (pp → H) = 67+12 −11 pb and 46±12 pb at 13.6 TeV from the di-photon and Z Z∗ → 4 measurements respectively. The two measure ments are combined into a total cross-section measurement of σ (pp → H) = 58.2±8.7 pb, to be compared with the Stan dard Model prediction of σ (pp → H)SM = 59.9 ± 2.6 p

    Searches for lepton-flavour-violating decays of the Higgs boson into eτ and μτ in \sqrt{s} = 13 TeV pp collisions with the ATLAS detector

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    Abstract This paper presents direct searches for lepton flavour violation in Higgs boson decays, H → eτ and H → μτ, performed using data collected with the ATLAS detector at the LHC. The searches are based on a data sample of proton-proton collisions at a centre-of-mass energy s s \sqrt{s} = 13 TeV, corresponding to an integrated luminosity of 138 fb−1. Leptonic (τ → ℓνℓντ) and hadronic (τ → hadrons ντ) decays of the τ-lepton are considered. Two background estimation techniques are employed: the MC-template method, based on data-corrected simulation samples, and the Symmetry method, based on exploiting the symmetry between electrons and muons in the Standard Model backgrounds. No significant excess of events is observed and the results are interpreted as upper limits on lepton-flavour-violating branching ratios of the Higgs boson. The observed (expected) upper limits set on the branching ratios at 95% confidence level, B B \mathcal{B} (H → eτ) < 0.20% (0.12%) and B B \mathcal{B} (H → μτ ) < 0.18% (0.09%), are obtained with the MC-template method from a simultaneous measurement of potential H → eτ and H → μτ signals. The best-fit branching ratio difference, B B \mathcal{B} (H → μτ) → B B \mathcal{B} (H → eτ), measured with the Symmetry method in the channel where the τ-lepton decays to leptons, is (0.25 ± 0.10)%, compatible with a value of zero within 2.5σ

    Search for resonant WZ production in the fully leptonic final state in proton–proton collisions at √s=13 TeV with the ATLAS detector

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