An interaction of inorganic arsenic exposure with body weight and composition on type 2 diabetes indicators in Diversity Outbred mice

Type 2 diabetes (T2D) is a complex metabolic disorder with no cure and high morbidity. Exposure to inorganic arsenic (iAs), a ubiquitous environmental contaminant, is associated with increased T2D risk. Despite growing evidence linking iAs exposure to T2D, the factors underlying inter-individual dif...

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Veröffentlicht in:Mammalian genome 2022-12, Vol.33 (4), p.575-589
Hauptverfasser: Xenakis, James G., Douillet, Christelle, Bell, Timothy A., Hock, Pablo, Farrington, Joseph, Liu, Tianyi, Murphy, Caroline E. Y., Saraswatula, Avani, Shaw, Ginger D., Nativio, Gustavo, Shi, Qing, Venkatratnam, Abhishek, Zou, Fei, Fry, Rebecca C., Stýblo, Miroslav, Pardo-Manuel de Villena, Fernando
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container_end_page 589
container_issue 4
container_start_page 575
container_title Mammalian genome
container_volume 33
creator Xenakis, James G.
Douillet, Christelle
Bell, Timothy A.
Hock, Pablo
Farrington, Joseph
Liu, Tianyi
Murphy, Caroline E. Y.
Saraswatula, Avani
Shaw, Ginger D.
Nativio, Gustavo
Shi, Qing
Venkatratnam, Abhishek
Zou, Fei
Fry, Rebecca C.
Stýblo, Miroslav
Pardo-Manuel de Villena, Fernando
description Type 2 diabetes (T2D) is a complex metabolic disorder with no cure and high morbidity. Exposure to inorganic arsenic (iAs), a ubiquitous environmental contaminant, is associated with increased T2D risk. Despite growing evidence linking iAs exposure to T2D, the factors underlying inter-individual differences in susceptibility remain unclear. This study examined the interaction between chronic iAs exposure and body composition in a cohort of 75 Diversity Outbred mice. The study design mimics that of an exposed human population where the genetic diversity of the mice provides the variation in response, in contrast to a design that includes untreated mice. Male mice were exposed to iAs in drinking water (100 ppb) for 26 weeks. Metabolic indicators used as diabetes surrogates included fasting blood glucose and plasma insulin (FBG, FPI), blood glucose and plasma insulin 15 min after glucose challenge (BG15, PI15), homeostatic model assessment for β -cell function and insulin resistance (HOMA-B, HOMA-IR), and insulinogenic index. Body composition was determined using magnetic resonance imaging, and the concentrations of iAs and its methylated metabolites were measured in liver and urine. Associations between cumulative iAs consumption and FPI, PI15, HOMA-B, and HOMA-IR manifested as significant interactions between iAs and body weight/composition. Arsenic speciation analyses in liver and urine suggest little variation in the mice’s ability to metabolize iAs. The observed interactions accord with current research aiming to disentangle the effects of multiple complex factors on T2D risk, highlighting the need for further research on iAs metabolism and its consequences in genetically diverse mouse strains.
doi_str_mv 10.1007/s00335-022-09957-w
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This study examined the interaction between chronic iAs exposure and body composition in a cohort of 75 Diversity Outbred mice. The study design mimics that of an exposed human population where the genetic diversity of the mice provides the variation in response, in contrast to a design that includes untreated mice. Male mice were exposed to iAs in drinking water (100 ppb) for 26 weeks. Metabolic indicators used as diabetes surrogates included fasting blood glucose and plasma insulin (FBG, FPI), blood glucose and plasma insulin 15 min after glucose challenge (BG15, PI15), homeostatic model assessment for β -cell function and insulin resistance (HOMA-B, HOMA-IR), and insulinogenic index. Body composition was determined using magnetic resonance imaging, and the concentrations of iAs and its methylated metabolites were measured in liver and urine. Associations between cumulative iAs consumption and FPI, PI15, HOMA-B, and HOMA-IR manifested as significant interactions between iAs and body weight/composition. Arsenic speciation analyses in liver and urine suggest little variation in the mice’s ability to metabolize iAs. 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Associations between cumulative iAs consumption and FPI, PI15, HOMA-B, and HOMA-IR manifested as significant interactions between iAs and body weight/composition. Arsenic speciation analyses in liver and urine suggest little variation in the mice’s ability to metabolize iAs. 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subjects Animal Genetics and Genomics
Animals
Arsenic
Arsenic - toxicity
Arsenicals
Beta cells
Biomedical and Life Sciences
Blood Glucose
Body composition
Body Weight
Cell Biology
Collaborative Cross Mice
Contaminants
Diabetes
Diabetes mellitus (non-insulin dependent)
Diabetes Mellitus, Type 2 - genetics
Drinking water
Genetic diversity
Glucose
Human Genetics
Humans
Insulin
Insulin resistance
Insulins
Life Sciences
Liver
Magnetic resonance imaging
Male
Metabolic disorders
Metabolism
Metabolites
Mice
Morbidity
Population genetics
title An interaction of inorganic arsenic exposure with body weight and composition on type 2 diabetes indicators in Diversity Outbred mice
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