Researchers see health effects across generations from popular weed killer
'Dramatic increases' in several diseases
- Date:
- April 23, 2019
- Source:
- Washington State University
- Summary:
- Researchers have found a variety of diseases and other health problems in the second- and third-generation offspring of rats exposed to glyphosate, the world's most popular weed killer. In the first study of its kind, the researchers saw descendants of exposed rats developing prostate, kidney and ovarian diseases, obesity and birth abnormalities.
- Share:
Washington State University researchers have found a variety of diseases and other health problems in the second- and third-generation offspring of rats exposed to glyphosate, the world's most popular weed killer. In the first study of its kind, the researchers saw descendants of exposed rats developing prostate, kidney and ovarian diseases, obesity and birth abnormalities.
Michael Skinner, a WSU professor of biological sciences, and his colleagues exposed pregnant rats to the herbicide between their eighth and 14th days of gestation. The dose -- half the amount expected to show no adverse effect -- produced no apparent ill effects on either the parents or the first generation of offspring.
But writing in the journal Scientific Reports, the researchers say they saw "dramatic increases" in several pathologies affecting the second and third generations. The second generation had "significant increases" in testis, ovary and mammary gland diseases, as well as obesity. In third-generation males, the researchers saw a 30 percent incidence of prostate disease -- three times the rate of a control population. The third generation of females had a 40 percent incidence of kidney disease, or four times the rate of the controls.
More than one-third of the second-generation mothers had unsuccessful pregnancies, with most of those affected dying. Two out of five males and females in the third generation were obese.
Skinner and his colleagues call this phenomenon "generational toxicology" and they've seen it over the years in fungicides, pesticides, jet fuel, the plastics compound bisphenol A, the insect repellant DEET and the herbicide atrazine. At work are epigenetic changes that turn genes on and off, often because of environmental influences.
Skinner said he decided to study glyphosate "due to it being one of the most commonly used compounds worldwide."
The chemical has been the subject of numerous studies about its health effects. The Skinner study is the third in the past few months out of Washington alone. A University of Washington study published in February found the chemical increased the risk of non-Hodgkin lymphoma by as much as 41 percent. A Washington State University study published in December found state residents living close to areas subject to treatments with the herbicide are one-third more likely to die an early death from Parkinson's disease.
The chemical's generational toxicology represents a new downside that Skinner and his colleagues said should be incorporated into estimates of its risk.
"The ability of glyphosate and other environmental toxicants to impact our future generations needs to be considered," they write, "and is potentially as important as the direct exposure toxicology done today for risk assessment."
The research was supported by a grant from the John Templeton Foundation. The paper's co-authors are Undergraduate Researcher Deepika Kubsad, Research Assistant Professor Eric Nilsson, Research Assistant Stephanie King, Senior Research Associate Ingrid Sadler-Riggleman and Research Associate Daniel Beck.
Story Source:
Materials provided by Washington State University. Original written by Eric Sorensen. Note: Content may be edited for style and length.
Journal Reference:
- Deepika Kubsad, Eric E. Nilsson, Stephanie E. King, Ingrid Sadler-Riggleman, Daniel Beck, Michael K. Skinner. Assessment of Glyphosate Induced Epigenetic Transgenerational Inheritance of Pathologies and Sperm Epimutations: Generational Toxicology. Scientific Reports, 2019; 9 (1) DOI: 10.1038/s41598-019-42860-0
Cite This Page: