Literature DB >> 2888203

Maternal factors in developmental toxicity.

J M DeSesso.   

Abstract

The maternal organism provides the developing embryo with its physical environment, nutrients, and a mechanism for eliminating metabolic wastes. Since the physiological state of the pregnant female affects her ability to provide those requirements for the developing embryo, it is not surprising that there are maternal factors that can affect the wellbeing of the embryo. Extremes of maternal age in both humans and animals have been implicated in growth retardation, as well as autosomal trisomies. The influence of maternal size on fetal size is more pronounced among larger species with longer gestation periods such as humans and domestic animals. A clear relationship between the parity of the mother and potential developmental toxicity in humans has not been established due to the confounding influences of maternal age. Among laboratory rodents, however, it appears that offspring of multiparous animals are at increased risk of developmental toxicity. A variety of infectious agents, particularly viruses, have either been demonstrated or implicated as causes of developmental toxicity. In addition, hyperthermia is a possible confounding factor inherent with maternal infection. Although under experimental conditions hyperthermia is teratogenic in laboratory animals, a causative role for transient hyperthermia, which occurs during febrile states concomitant with infections, cannot be clearly established. Chronic maternal vascular disease states including essential hypertension, heart disease, or diabetes mellitus are likely to contribute to uteroplacental insufficiency and developmental toxicity. Poor maternal nutrition among humans contributes to growth retardation, but not to malformations. The production of "abnormal" maternal antibodies, such as are present in Rh incompatibility, can cause fetal wastage. An important maternal factor in humans is uteroplacental insufficiency, which can occur in normal states like twinning, as well as in abnormal conditions including reduced placental size, chronic maternal hypoxia, or uterine ischemia. Although all these maternal factors can contribute to developmental toxicity, they do not necessarily occur as isolated events. Some developmental toxicants exert deleterious effects within both the embryo and the maternal system.

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Year:  1987        PMID: 2888203     DOI: 10.1002/tcm.1770070305

Source DB:  PubMed          Journal:  Teratog Carcinog Mutagen        ISSN: 0270-3211


  3 in total

1.  Recommendations for harmonization of data collection and analysis of developmental neurotoxicity endpoints in regulatory guideline studies: Proceedings of workshops presented at Society of Toxicology and joint Teratology Society and Neurobehavioral Teratology Society meetings.

Authors:  Abby A Li; Larry P Sheets; Kathleen Raffaele; Virginia Moser; Angela Hofstra; Alan Hoberman; Susan L Makris; Robert Garman; Brad Bolon; Wolfgang Kaufmann; Roland Auer; Edmund Lau; Thomas Vidmar; Wayne J Bowers
Journal:  Neurotoxicol Teratol       Date:  2017-07-27       Impact factor: 3.763

2.  Mammalian stress proteins HSP70 and HSP28 coinduced by nicotine and either ethanol or heat.

Authors:  G M Hahn; E C Shiu; E A Auger
Journal:  Mol Cell Biol       Date:  1991-12       Impact factor: 4.272

Review 3.  Toward better assessments of developmental toxicity using stem cell-based in vitro embryogenesis models.

Authors:  Yusuke Marikawa
Journal:  Birth Defects Res       Date:  2022-01-31       Impact factor: 2.661

  3 in total

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