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pubmed-article:12852482pubmed:abstractTextA review of the nonsteroidal anti-inflammatory drug (NSAID) literature suggested occurrences of low-level incidences of cardiovascular and midline defects in rabbit fetuses exposed in utero. Aspirin (acetylsalicylic acid, ASA) is a widely used NSAID that irreversibly inhibits cyclooxygenases (COXs) 1 and 2. ASA has been studied extensively in rats and has consistently increased low-incidence cardiovascular malformations and defects in midline closure. The objectives of the current study were to comprehensively define the developmental toxicology profile of ASA in rabbits by using a dosing paradigm encompassing the period of organogenesis and to test the hypothesis that maternal gastrointestinal toxicity after repeated dose administrations hampers the detection of low-incidence malformations with ASA in rabbits by limiting ASA administration to sensitive windows for cardiovascular development and midline closure.lld:pubmed
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pubmed-article:12852482pubmed:pagination38-46lld:pubmed
pubmed-article:12852482pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:12852482pubmed:articleTitleComparison of the developmental toxicity of aspirin in rabbits when administered throughout organogenesis or during sensitive windows of development.lld:pubmed
pubmed-article:12852482pubmed:affiliationPfizer Global Research & Development, Groton, Connecticut 06340, USA. gregg_d_cappon@groton.pfizer.comlld:pubmed
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pubmed-article:12852482pubmed:publicationTypeComparative Studylld:pubmed