Prenatal environmental impacts/effects

We know that in the mature brain, neurotransmitters are released by nerve cell endings and act at synapses to mediate the interaction between nerve cells. There s now evidence that during the development of the prenatal brain, neurons can release transmitters before any connections are made, and that such released transmitters, acting as trophic factors, guide the formation of connections.17 Any environmental impact or mutation that affects the synthesis or release of neurotransmitters can be expected to have an effect on the development of the fetal brain. For example, during fetal development in Down syndrome, reductions apparently occur in the levels of various neurotransmitters. This may be one mechanism for the impaired brain development characteristic of this syndrome.18... 

Prenatal development is subject to a variety of environmental impacts that can divert, disrupt, and stop development altogether. The effects may not be observable at birth, but many of them affect later cognitive performance and emotional stability that may remain subclinical and may never be considered as deriving from the fetal period. 

Neurodevelopmental models of schizophrenia have for the most part emphasized prenatal brain development, focusing on effects that may alter gene expression.15 For example, according to one idea, individuals with schizophrenia inherit genes that cause structural brain deviations that may be compounded by early environmental impact.16 Much of the focus of this hypothesis has been on postnatal impact, such as stress, that changes brain chemistry, but the idea can also accommodate a focus on prenatal impact. 

Environmental exposures to PCBs are significantly lower than those reported in the workplace and are therefore unlikely to cause adverse human health effects in adults. However, it is apparent from the results of several recent studies on children that there was a correlation between in utero exposure to PCBs, eg, cord blood levels, and developmental deficits (65—68) including reduced bkth weight, neonatal behavior anomaUes, and poorer recognition memories. At four years of age, there was stiU a correlation between prenatal PCB exposure levels and short-term memory function (verbal and quantitative). In these studies the children were all exposed to relatively low environmental levels of PCBs. Although these effects may be related to other contaminants, it is clear that this is an area of concern regarding the potential adverse human health impacts of PCBs. 

I look at many possible causes of fetal damage in this book, but give particular emphasis to man-made environmental toxins, be they chemical pollutants in our air, water, and land, or substances in the consumer marketplace, legal and otherwise. The effects of these toxins are often connected to more than one type of fetal damage. Prenatal exposure to lead, for example, is connected to postnatal occurrences of lower IQ, ADHD, and schizophrenia, usually in different individuals. Prenatal exposure to tobacco smoke, as another example, is connected to a host of effects with adverse postnatal consequences as well. The effects of both sorts of toxins can also be related to other fetal impacts, which in turn are often connected to important social... 

The clearest refutation of the idea advanced by hereditarian behavior geneticists that the prenatal environment is of only small consequence for childhood and adult IQ is the research on known IQ effects of prenatal exposure to certain neurotoxins. Any argument that this neurotoxic impact is extreme, rare, and therefore irrelevant is unsound. In addition, every known neurotoxic effect confirms the possible prenatal impact of other environmental agents not yet studied, and we do know there are literally hundreds of such neurotoxins already dispersed in the environment.15... 

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