Free Access
Issue
Reprod. Nutr. Dev.
Volume 44, Number 5, September-October 2004
Page(s) 437 - 447
DOI https://doi.org/10.1051/rnd:2004050
References of Reprod. Nutr. Dev. 44 437-447
  1. Lin KC, Okamura H, Mori Y. Inhibition of hCG-induced ovulation and steroidogenesis by short-term hyperprolactinemia in female rabbits. Endocrinol Jpn 1987, 34: 675-683.
  2. Ubilla E, Rebollar PG. Influence of the postpartum day on plasma estradiol-17b levels, sexual behaviour and conception rate in artificially inseminated lactating rabbits. Anim Reprod Sci 1995, 38: 337-344 [CrossRef].
  3. Ubilla E, Rebollar PG, Pazo D, Esquifino A, Alvariño JMR. Pituitary and ovarian response to transient doe-litter separation in nursing rabbits. J Reprod Fertil 2000, 118: 361-366.
  4. Ubilla E, Rebollar PG, Pazo D, Esquifino A, Alvariño JMR. Effects of doe-litter separation on endocrinological and productivity variables in lactating rabbits. Livest Prod Sci 2000, 67: 67-74.
  5. Theau-Clèment M. Advances in biostimulation methods applied to rabbit reproduction. In: Proc 7th World Rabbit Sci, Vol A, 2000, p 61-79.
  6. Pluske JR, Hampson DJ, Williams IH. Factors influencing the structure and function of the small intestine in the weaned pig: a review. Livest Prod Sci 1997, 51: 215-236.
  7. Sangild PT, Silver M, Schmidt M, Fowden AL. The perinatal pig in pediatric gastroenterology. In: Tumbleson ME, Schnook L (Eds), Advances in Swine in Biomedical Research, Plenum Press, New York, 1996.
  8. Gutiérrez I, García P, Carabaño R, De Blas C. Effect of supplementation with animal plasma and antibiotics on jejunal morphology of early-weaned rabbits. In: Proc 7th World Rabbit Congress, Valencia, Spain, Vol C, 2000, p 263-267.
  9. Hampson DJ. Alteration in piglet small intestinal structure at weaning. Res Vet Sci 1986, 40: 32-40.
  10. Dahlquist A. Method for assay of intestinal dissaccharidases. Anal Chem 1964, 7: 18-25.
  11. Peterson GL. A simplification of the protein assay method of Lowry et al. Which is more generally applicable. Ann Biochem 1977, 83: 346-356.
  12. Spanish Royal Decree 223/88. Sobre protección de los animales utilizados para experimentación y otros fines científicos. Boletín Oficial del Estado 1988, 67: 8509-8511.
  13. SAS. SAS® Propietary Software Release 8.2. SAS Inst Inc, Cary, NC, USA, 1999-2001.
  14. Nicodemus N. Recomendaciones sobre el nivel óptimo de inclusión de fibra: FND, fibra larga y LAD, en piensos de conejos de alta productividad, Tesis doctoral, Universidad Politécnica de Madrid, España, 2000.
  15. Davis SR, Farr VC, Stelwagen K. Regulation of yield loss and milk composition during once-daily milking: a review. Livest Prod Sci 1999, 59: 77-94.
  16. Szendrö ZS, Jovanczai ZS, Theau-Clément M, Radnai I, Biro-Nemeth E, Milisits G. The effect of doe-litter separation on production performance in rabbit does and their kits. World Rabbit Sci 1999, 7: 165-169.
  17. Calvert DT, Knight CH, Peaker M. Milk accumulation and secretion in the rabbit. Q J Exp Physiol 1985, 70: 357-363.
  18. Wilde CJ, Knight CH. Metabolic adaptations in mammary gland during the declining phase of lactation. J Dairy Sci 1989, 72: 1679-1692.
  19. Knight CH. The importance of cell division in udder development and lactation. Livest Prod Sci 2000, 66: 169-176.
  20. Alvariño JMR, Bueno A, Santiago ME, Del Arco JA. Effect of a doe-litter separation on survival and growth of young rabbits. World Rabbit Sci 1999, 7: 161-163.
  21. Boiti C, Bonanno A, Brecchia G, Alabiso M, Di Grigoli A, Zampini D. Influence d'une séparation mère-jeunes pendant 48 h, sur la croissance des lapereaux et leur sensibilité à un stress. In: Proc. 9e Journ Rech Cunicole Fr, Paris, 2001, p 167-170.
  22. Bonanno A, Alabiso M, Di Grigoli A, Alicata ML. Effect of change of cage and/or 44 h mother-litter separation on productivity of non-receptive lactating rabbit does. Preliminary investigations. World Rabbit Sci 1999, 7: 107-111.
  23. Bonanno A, Alabiso M, Di Grigoli A, Alicata ML, Leto G. Effect of a 48 h delayed insemination with or without a 48 h doe-litter separation on performance of non-receptive does. World Rabbit Sci 1999, 7: 171-175.
  24. Bonanno A, Alabiso M, Di Grigoli A, Alicata ML, Montalbano L. Effect of a 48 h doe-litter separation on performance of free or controlled nursing rabbit does. In: Proc 7th World Rabbit Congress, Vol A, Valencia, Spain, 2000, p 97-103.
  25. Maertens L. Effect of flushing, mother litter separation and PMSG on the fertility of lactating does and the performance of their litter. World Rabbit Sci 1998, 6: 185-190.
  26. Virag GY, Kustos K, Szabo L. Effect of a 48 hours doe-litter separation on rabbit doe's reproductive performance and offspring's growth. World Rabbit Sci 1999, 7: 155-159.
  27. Jilge B, Hudson R. Diversity and development of circadian rhythms in the European rabbit. Chronobiol Int 2001, 18: 1-26.
  28. Bonanno A, Di Grigoli A, Alabiso M, Boiti C. Parity and number of repeated doe-litter-separation treatments affect differently the reproductive performance of lactating does. World Rabbit Sci 2002, 10: 63-70.
  29. Castellini C, Canali C, Boiti C. Effect of mother-litter separation for 24 hours by closing the nestbox or change of cage, on rabbit doe reproductive performance. World Rabbit Sci 1998, 6: 191-203.
  30. Pavois V, Le Naour J, Ducep O, Perrin G, Duperray J. Une méthode naturelle pour améliorer la réceptivité et la fertilité des lapines allaitantes en insémination artificielle. In: Proc 6e Journ Rech Cunicole, France, La Rochelle, Vol II 1994, p 528-535.
  31. Theau-Clément M, Mercier P. Effect of a 24 h doe-litter separation on rabbit doe reproductive performance and growth of the young. World Rabbit Sci 1999, 7: 177-179.
  32. Tomás N, Perucho O, Catafau J, Aloi N, Rafel O, Ramón J, Gómez EA. Estímulo de la aceptación de la monta mediante el cierre del nidal en conejas. Efecto sobre las camadas en lactación. Boletín de cunicultura 1996, 86: 14-17.
  33. Alvariño JMR, Del Arco JA, Bueno A. Effect of mother-litter separation on reproductive performance of lactating rabbit females inseminated on day 4 or 11 post-partum. World Rabbit Sci 1998, 6: 191-194.
  34. Lebas F, Laplace J-P. Mensurations viscérales chez le lapin. Ann Zootech 1972, 21: 37-47.
  35. Yu B, Chiou PWS. The morphological changes of intestinal mucose in growing rabbits. Lab Anim 1997, 31: 254-263.
  36. Campín J, Gutiérrez I, Espinosa A, Carabaño R, Rebollar PG, De Blas JC. Efecto de la fuente de proteína sobre los parámetros digestivos, parámetros histológicos y digestibilidad ileal y fecal en gazapos destetados precozmente. In: Proc. XXVII Symposium de Cunicultura, Reus, Tarragona, Spain, 2002, p 117-127.
  37. Diamond JM, Karasov WH. Trophic control of the intestinal mucose. Nature (London) 1983, 304: 18.
  38. James PS, Smith MW, Tivey DR, Wilson TJG. Epidermal growth factor selectively increases maltase and sucrase activities in neonatal piglet intestine. J Physiol 1987, 393: 583-594.
  39. Gutiérrez I, Espinosa A, García J, Carabaño R, De Blas JC. Effects of levels of starch, fiber and lactose on digestion and growth performance of early-weaned rabbits. J Anim Sci 2002, 80: 1029-1037 [PubMed].
  40. Zhang H, Malo C, Buddington RK. Suckling induces rapid intestinal growth and changes in brush border digestive functions of newborn pigs. J Nutr 1997, 127: 418-426.
  41. Sangild PT, Fowden AL, Trahair JF. How does the foetal gastrointestinal tract develop in preparation for enteral nutrition after birth. Livest Prod Sci 2000, 66: 141-150.
  42. Wang T, Xu RJ. Effects of colostrum feeding on intestinal development in newborn pigs. Biol Neonate 1996, 70: 339-348.
  43. Marounek M, Vovk SJ, Skrivanová V. Distribution of activity of hydrolitic enzymes in the digestive tract of rabbits. Br J Nutr 1995, 73: 463-469.
  44. Tsuboi KK, Kwong LK, Neu J, Sunshine P. A proposed mechanism of normal intestinal lactase decline in the post-weaned mammal. Biochem Biophys Res 1981, p 645-652.
  45. Tsuboi KK, Kwong LK, D'Harlingue AE, Stevenson DK, Kerner JA Jr, Sunshine P. The nature of maturation decline of intestinal lactase activity. Biochim Biophys Acta 1985, 840: 69-78.
  46. Allingham K, von Saldern C, Brennan PA, Distel H, Hudson R. Endogenous expression of c-Fos in hypothalamic nuclei of neonatal rabbits coincides with their circadian pattern of suckling-associated arousal. Brain Res 1998, 783: 210-218.
  47. Boiti C, Bonanno A, Brecchia G, Mazza F. Effects of neonatal deprivation on the neuroendocrine responses of rabbits. In: Boiti C, Gidenne T, Sabbioni E (Eds), COST ACTION 848 & ECVAM. JRC Ispra: Proc of Joint Scientific Meeting WG1 and WG-4, 2002, p 19.
  48. Rebollar PG, Alvariño JMR, Jiménez V, Cano P, Chacón P, Esquifino AI. Effect of doe-litter separation on FSH and LH levels of young lactating rabbits: preliminary results. In: Boiti C, Gidenne T, Sabbioni E (Eds), COST ACTION 848 & ECVAM. JRC Ispra: Proc of Joint Scientific Meeting WG1 and WG-4, 2002, p 20.
  49. Hörnicke H, Ruoff G, Vogt B, Clauss W, Ehrlein M-J. Phase relationship of the circadian rhythms of feed intake, caecal motility and production of soft and hard faeces in domestic rabbits. Lab Anim 1984, 18: 169-172 [PubMed].