Study: Early Education Could Reverse Lead Poisoning in Children

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Lead exposure in early childhood can lead to severe cognitive and behavioral impairments in children, which is concerning given that recent estimates suggest there are at least 500,000 children in the U.S. with blood lead levels at or above the acceptable range.

For the first time, scientists are giving these children and others hope with new research that shows the majority of gene changes in the brain caused by lead poisoning can be reversed in animal models.

The key, according to the researchers from Thomas Jefferson University, is providing stimulating environments in early childhood.

“Our work demonstrates that by providing an enriched early life environment, the adverse effects of lead on the brain may be minimized or potentially reversed, emphasizing how important early childhood interventions may be,” said senior author Jay Schneider, professor of pathology, anatomy and cell biology at Thomas Jefferson University.

Not only did Schneider and his colleagues demonstrate the ability to reverse lead poisoning in rats, but they also—for the first time—identified 3,500 genes in the hippocampus that are affected by lead exposure. Previous studies have established that the genes involved in learning, memory and brain development are negatively affected by lead, but research was lacking as to the full extent of the toxicity before now.

In the study, published in Scientific Reports, the researchers examined rats that were exposed to lead from birth to the time of weaning at 21 days of age—the equivalent of 2- to 3-years-old in humans, which is commonly when lead exposure occurs.

Focusing on changes in gene expression in the hippocampal region of the rats, Schneider and team detected altered levels in over 3,500 genes. Clearly affected by the lead exposure, these genes either abnormally churned out more or less of their gene products.

However, the team discovered most of these gene expression changes could be reversed.

According to the experimental, the researchers separated the lead-exposed animals into two different housing environments—one enriched, and one not. The “enriched cages” contained more social activity with a total of 6 rats, together with chew toys and various elements to climb on and burrow through that were changed twice every week for novelty. Meanwhile, the non-enriched cages were smaller, held only 3 rats and did not contain any additional stimulation.

After 55 days—roughly equivalent to adolescence in humans—approximately 80% of the gene expression changes induced by lead exposure were reversed in the group of animals that lived in the enriched, stimulating environment.

Rats in the non-enriched environment did not experience any gene expression reversals. Rather, these animals had noted memory deficits that the “enriched” rats did not.

“Our work suggests that it may be possible to mitigate the wide-spread adverse effects of lead on the young brain by providing adequate access to stimulating, interesting environments and activities in early childhood and perhaps longer,” said Schneider. “Unfortunately, these kinds of resources are often not available to the population most at risk for lead poisoning.”

Indeed, the risk for lead exposure is not the same for all children. There are significant disparities in health outcomes across racial and ethnic groups and people with different socioeconomic status. According to the CDC, higher blood lead levels are more prevalent among children from racial and ethnic minority groups, children from low-income households, and children who live in housing built before 1978. Also, children from racial and ethnic minority groups are more likely to live in conditions where there is greater likelihood of exposure, including urban environmental exposures, such as air, soil and water.

While Schneider agrees more research needs to be done in this area, he said the importance of early intervention programs with environmental enrichment “cannot be overstated.”

 

Lab products used in this animal testing research:

  • RNeasy Kits- QIAGEN
  • NanoDrop 2000 Spectrophotometer- Thermo Fisher Scientific
  • 2100 Bioanalyzer- Agilent Technologies
  • TruSeq Stranded Total RNA- Illumina

 

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