Year: 2021
Type: article
Abstract: Chronic arsenic exposure via drinking water is associated with diabetes in human pop-ulations throughout the world. Arsenic is believed to exert its diabetogenic effects via multiple mechanisms, including alterations to insulin secretion and insulin sensitivity. In the past, acute arsenicosis has been thought to be partially treatable with selenium supplementation, though a potential interaction between selenium and arsenic had not been evaluated under longer-term exposure models. The purpose of the present study was to explore whether selenium status may augment arsenic's effects during chronic arsenic exposure. To test this possibility, mice were exposed to arsenic in their drinking water and provided ad libitum access to either a diet replete with selenium (Control) or deficient in selenium (SelD). Arsenic significantly improved glucose tolerance and decreased insulin secretion and β-cell function in vivo. Dietary selenium deficiency resulted in similar effects on glucose tolerance and insulin secretion, with significant interactions between arsenic and dietary conditions in select insulin-related parameters. The findings of this study highlight the complexity of arsenic's metabolic effects and suggest that selenium deficiency may interact with arsenic exposure on β-cell-related physiological parameters.
Source: Nutrients
DOI: 10.3390/nu13082894
Institutions: University of Illinois Chicago, University of Chicago
Language: English
Subfield: Environmental Chemistry
Field: Environmental Science
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $2,592
Awards: Mouse Sbp2 deficiency models the multi-system syndrome of human SBP2 defects, G4997024190, Selenoproteins in Arsenic-Induced Metabolic Dysfunction, Protection against Arsenic-Induced Neurologic Defects by Brain DHA Enrichment, University of Chicago Initiative for Maximizing Student Development (IMSD) - Renewal 01, ChicAgo Center for Health and EnvironmenT (CACHET), Diabetes Research and Training Center
OpenAlex ID: W3193912110
