Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractMechanisms of Action of Microbial Biocontrol Agents against Botrytis cinerea    Next AbstractBiosynthesis of 2-Phenylethanol in Rose Petals Is Linked to the Expression of One Allele of RhPAAS »

Birth Defects Res B Dev Reprod Toxicol


Title:The guinea pig as an animal model for developmental and reproductive toxicology studies
Author(s):Rocca MS; Wehner NG;
Address:"TherImmune Research Corp., Gaithersburg, Maryland, USA. mrocca@amgen.com"
Journal Title:Birth Defects Res B Dev Reprod Toxicol
Year:2009
Volume:86
Issue:2
Page Number:92 - 97
DOI: 10.1002/bdrb.20188
ISSN/ISBN:1542-9741 (Electronic) 1542-9733 (Linking)
Abstract:"BACKGROUND: Regulatory guidelines for developmental and reproductive toxicology (DART) studies require selection of 'relevant' animal models as determined by kinetic, pharmacological, and toxicological data. Traditionally, rats, mice, and rabbits are the preferred animal models for these studies. However, for test articles that are pharmacologically inactive in the traditional animal models, the guinea pig may be a viable option. This choice should not be made lightly, as guinea pigs have many disadvantages compared to the traditional species, including limited historical control data, variability in pregnancy rates, small and variable litter size, long gestation, relative maturity at birth, and difficulty in dosing and breeding. METHODS: This report describes methods for using guinea pigs in DART studies and provides results of positive and negative controls. Standard study designs and animal husbandry methods were modified to allow mating on the postpartum estrus in fertility studies and were used for producing cohorts of pregnant females for developmental studies. RESULTS: A positive control study with the pregnancy-disrupting agent mifepristone resulted in the anticipated failure of embryo implantation and supported the use of the guinea pig model. Control data for reproductive endpoints collected from 5 studies are presented. CONCLUSION: In cases where the traditional animal models are not relevant, the guinea pig can be used successfully for DART studies"
Keywords:"Abortifacient Agents/toxicity Animal Husbandry/methods Animals Breeding/methods Embryo Implantation/drug effects Estrous Cycle Female Fertility Guinea Pigs/*embryology/physiology Litter Size Male Mifepristone/toxicity *Models, Animal Organ Size/drug effec;"
Notes:"MedlineRocca, Meredith S Wehner, Nancy G eng 2009/03/24 Birth Defects Res B Dev Reprod Toxicol. 2009 Apr; 86(2):92-7. doi: 10.1002/bdrb.20188"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 29-09-2024