Type 1 diabetes is a disorder in which pancreatic \u03b2-cells do not provide sufficient insulin to moderate blood sugar levels. Fetal alcohol syndrome is a condition caused by alcohol consumption during fetal development that results in a host of developmental defects. The purpose of this study is to assess the effect of ethanol (EtOH) on \u03b2-cell development in developing embryos. Zebrafish embryos were exposed to concentrations of EtOH diluted in embryo medium. Six experimental groups were created by exposing groups of 50 embryos to 0.10%, 0.25%, 0.75%, 1.00%, and 1.50% EtOH, with 0% EtOH serving as a control. The embryos were then rated based on the amount of \u03b2-cell degradation in the embryonic pancreases on a scale of zero to four, ranging from no \u03b2-cell damage to extreme \u03b2-cell damage. We show that higher concentrations of EtOH caused increased damage to \u03b2-cells, with average grades of the embryonic \u03b2-cells increasing with EtOH concentration: average grades for 0%, 0.10%, 0.25 %, 0.50%, 0.75 %, 1.0 %, and 1.50% EtOH exposures were 0.71, 0.61, 0.55, 1.0, 0.82, 2.1, and 4.0 respectively. Therefore, exposure to increasing amounts of EtOH during pancreatic development may increase the severity of primary \u03b2-cell degradation. This study suggests that if a woman were to drink alcohol during the first trimester of her pregnancy, her child would be at a higher risk of developing type 1 diabetes.<\/p>\n
Emory M. Payne 1,2*, Zohaib M. Moonis 1,2*, MaryAnn DeMaria 2<\/p>\n