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We are analyzing https://www.nature.com/articles/nrn2598.

Title:
Prenatal exposure to drugs: effects on brain development and implications for policy and education | Nature Reviews Neuroscience
Description:
Exposurein uteroto drugs that modulate neurotransmitter systems present during early development can affect brain architecture and function. Levitt and colleagues consider what science has discovered about the effects of prenatal drug exposure and how this knowledge might influence public policy. The effects of prenatal exposure to drugs on brain development are complex and are modulated by the timing, dose and route of drug exposure. It is difficult to assess these effects in clinical cohorts as these are beset with problems such as multiple exposures and difficulties in documenting use patterns. This can lead to misinterpretation of research findings by the general public, the media and policy makers, who may mistakenly assume that the legal status of a drug correlates with its biological impact on fetal brain development and long-term clinical outcomes. It is important to close the gap between what science tells us about the impact of prenatal drug exposure on the fetus and the mother and what we do programmatically with regard to at-risk populations.
Website Age:
30 years and 10 months (reg. 1994-08-11).

Matching Content Categories {πŸ“š}

  • Education
  • Family & Parenting
  • Science

Content Management System {πŸ“}

What CMS is nature.com built with?

Custom-built

No common CMS systems were detected on Nature.com, and no known web development framework was identified.

Traffic Estimate {πŸ“ˆ}

What is the average monthly size of nature.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


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How Does Nature.com Make Money? {πŸ’Έ}


Display Ads {🎯}


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How Much Does Nature.com Make? {πŸ’°}


Display Ads {🎯}

$63,100 per month
Estimations show Nature.com's display ad online revenue falls between $42,042 and $115,616 per month.

Keywords {πŸ”}

pubmed, google, scholar, cas, exposure, prenatal, brain, development, cocaine, res, effects, pregnancy, neurosci, central, cortex, nature, levitt, fetal, methamphetamine, drug, nicotine, rat, psychiatry, dopamine, behavioral, receptor, serotonin, ethanol, neuroscience, stanwood, health, access, neonatal, alcohol, developmental, neurotoxicol, teratol, children, cerebral, maternal, cell, child, drugs, pharmacol, dev, outcomes, rats, sci, exposed, exp,

Topics {βœ’οΈ}

nature portfolio permissions reprints advertising transformative neurodevelopmental research national scientific council nature rev nature neurosci nature 416 nature author information authors research findings privacy policy regional beta2-adrenergic receptor activation research gaba-induced neurite outgrowth author correspondence springerlink instant access selective long-term dysfunction european economic area aid drug-exposed infants utero cocaine-induced dysfunction mpfc yanyan zheng central noradrenergic system transforming growth factor-Ξ² gabaa receptor activation permissions low-birth-weight children learning-related neuronal activity twelve-month neurofunctional assessment long-term clinical outcomes translating developmental time 16-year-olds prenatally exposed personal data brain-derived neurotrophic factor central executive component social media prenatal haloperidol induces data protection receptor tyrosine kinase nervous system development central auditory processing environmental tobacco smoke long-term developmental long-term adaptive long-term costs van de kar privacy serotonin1a receptor acts low birth weight

Questions {❓}

  • Does the use of nicotine replacement therapy during pregnancy affect pregnancy outcomes?
  • Fetal nicotine or cocaine exposure: which one is worse?
  • From oocyte to neuron: do neurotransmitters function in the same way throughout development?
  • If nicotine is a developmental neurotoxicant in animal studies, dare we recommend nicotine replacement therapy in pregnant women and adolescents?

Schema {πŸ—ΊοΈ}

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         description:Exposurein uteroto drugs that modulate neurotransmitter systems present during early development can affect brain architecture and function. Levitt and colleagues consider what science has discovered about the effects of prenatal drug exposure and how this knowledge might influence public policy. The effects of prenatal exposure to drugs on brain development are complex and are modulated by the timing, dose and route of drug exposure. It is difficult to assess these effects in clinical cohorts as these are beset with problems such as multiple exposures and difficulties in documenting use patterns. This can lead to misinterpretation of research findings by the general public, the media and policy makers, who may mistakenly assume that the legal status of a drug correlates with its biological impact on fetal brain development and long-term clinical outcomes. It is important to close the gap between what science tells us about the impact of prenatal drug exposure on the fetus and the mother and what we do programmatically with regard to at-risk populations.
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