Literature DB >> 16249998

Effects of feed restriction during organogenesis on embryo-fetal development in rabbit.

G D Cappon1, T L Fleeman, R E Chapin, M E Hurtt.   

Abstract

BACKGROUND: Appropriate maternal nutrition and body weight gain during pregnancy is well established as a major factor in healthy prenatal development in humans. Given the role of nutrition and body weight gain in normal development, pharmaceuticals intended to reduce appetite and promote weight loss will generate developmental toxicity data that may be challenging to interpret. To aid with this, the effects of feed restriction, and subsequent reduction in maternal body weight gain, on embryo-fetal development was investigated in the rabbit.
METHODS: Groups of 15 pregnant New Zealand White rabbits were offered 150 (control), 110, 75, 55, 35, and 15 g feed/day from gestation day (GD) 7-19. Cesarean sections were carried out on GD 29 and fetuses were examined for external, visceral, and skeletal development.
RESULTS: Maternal body weights at the end of the feed restriction period (GD 20) were 0.97, 0.98, 0.93, 0.94, and 0.86 x control for the 110, 75, 55, 35, and 15 g feed/day groups, respectively. Only at 15 g feed/day was there a net maternal body weight loss (the GD 20 body weight was 0.93 x the GD 6 body weight) at the end of the feed restriction period. Six does aborted in the 15 g feed/day group; there were no other abortions associated with feed restriction. Fetal body weight was significantly reduced at 75, 55, 35, and 15 g feed/day (0.95, 0.90, 0.86, and 0.84 x control, respectively). There were no external or visceral malformations or variations, and no skeletal malformations associated with feed restriction. The incidence of fetuses with sternebrae 5 or 6 unossified was increased at feed levels < or = 75 g/day. At a feed level of 35 g/day there was an increase in unossified metatarsals and metacarpals, and an increase in the number of fetuses with a reduced number of caudal vertebrae ossified. Although these findings were not increased at a feed level of 15 g/day, the lack of dose response was likely due to increased abortion and subsequent decrease in fetuses available for evaluation at 15 g feed/day.
CONCLUSION: These data demonstrate that feed restriction to feed levels that produce substantial reductions in maternal body weight gain can result in developmental toxicity expressed by abortion, reduced fetal weight, and alterations in ossification. Abortion only occurred when feed was restricted to an amount that produced maternal body weight loss (15 g feed/day) whereas reduced fetal weight and increased incidence of fetuses with unossified sternebrae, metatarsals, metacarpals, or caudal vertebrae were noted at feed levels of < or = 75 g/day. There were no fetal malformations associated with feed restriction. Copyright 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 16249998     DOI: 10.1002/bdrb.20058

Source DB:  PubMed          Journal:  Birth Defects Res B Dev Reprod Toxicol        ISSN: 1542-9733


  5 in total

1.  Effect of Feed Restriction during Pregnancy on Performance and Productivity of New Zealand White Rabbit Does.

Authors:  Abeer Nafeaa; Souad Abd Elfattah Ahmed; Said Fat Hallah
Journal:  Vet Med Int       Date:  2011-09-04

2.  Effects of gestational maternal undernutrition on growth, carcass composition and meat quality of rabbit offspring.

Authors:  George K Symeon; Michael Goliomytis; Iosif Bizelis; George Papadomichelakis; Olga Pagonopoulou; Zafeiris Abas; Stelios G Deligeorgis; Stella E Chadio
Journal:  PLoS One       Date:  2015-02-11       Impact factor: 3.240

3.  Competition for Materno-Fetal Resource Partitioning in a Rabbit Model of Undernourished Pregnancy.

Authors:  Jorge Lopez-Tello; Maria Arias-Alvarez; Maria Angeles Jimenez-Martinez; Rosa Maria Garcia-Garcia; Maria Rodriguez; Pedro Luis Lorenzo Gonzalez; Ruben Bermejo-Poza; Antonio Gonzalez-Bulnes; Pilar Garcia Rebollar
Journal:  PLoS One       Date:  2017-01-03       Impact factor: 3.240

4.  Delayed-Release Dimethyl Fumarate and Pregnancy: Preclinical Studies and Pregnancy Outcomes from Clinical Trials and Postmarketing Experience.

Authors:  Ralf Gold; J Theodore Phillips; Eva Havrdova; Amit Bar-Or; Ludwig Kappos; Norman Kim; Tim Thullen; Patricia Valencia; Lauren Oliva; Mark Novas; Jie Li; Marianne T Sweetser; Nuwan Kurukulasuriya; Vissia Viglietta; Robert J Fox
Journal:  Neurol Ther       Date:  2015-10-12

Review 5.  Comparison of rat and rabbit embryo-fetal developmental toxicity data for 379 pharmaceuticals: on the nature and severity of developmental effects.

Authors:  Peter T Theunissen; Sonja Beken; Bruce K Beyer; William J Breslin; Gregg D Cappon; Connie L Chen; Gary Chmielewski; Luc De Schaepdrijver; Brian Enright; Jennifer E Foreman; Wafa Harrouk; Kok-Wah Hew; Alan M Hoberman; Julia Y Hui; Thomas B Knudsen; Susan B Laffan; Susan L Makris; Matt Martin; Mary Ellen McNerney; Christine L Siezen; Dinesh J Stanislaus; Jane Stewart; Kary E Thompson; Belen Tornesi; Jan Willem Van der Laan; Gerhard F Weinbauer; Sandra Wood; Aldert H Piersma
Journal:  Crit Rev Toxicol       Date:  2016-10-19       Impact factor: 5.635

  5 in total

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