TY - JOUR
T1 - Persistent Organic Pollutant Exposure Leads to Insulin Resistance Syndrome
AU - Ruzzin, Jérôme
AU - Petersen, Rasmus
AU - Meugnier, Emmanuelle
AU - Madsen, Lise
AU - Lock, Erik-Jan
AU - Lillefosse, Haldis
AU - Ma, Tao
AU - Pesenti, Sandra
AU - Sonne, Si Brask
AU - Marstrand, Troels Torben
AU - Malde, Marian Kjellevod
AU - Du, Zhen-Yu
AU - Chavey, Carine
AU - Fajas, Lluis
AU - Lundebye, Anne-Katrine
AU - Brand, Christian Lehn
AU - Vidal, Hubert
AU - Kristiansen, Karsten
AU - Frøyland, Livar
N1 - Keywords: contaminants, farmed salmon, metabolic syndrome, nonalcoholic fatty liver, obesity, pollution, public health, type 2 diabetes
PY - 2010/4
Y1 - 2010/4
N2 - Background: The incidence of the insulin resistance syndrome has increased at an alarming rate worldwide, creating a serious challenge to public health care in the 21st century. Recently, epidemiological studies have associated the prevalence of type 2 diabetes with elevated body burdens of persistent organic pollutants (POPs). However, experimental evidence demonstrating a causal link between POPs and the development of insulin resistance is lacking. Objective: We investigated whether exposure to POPs contributes to insulin resistance and metabolic disorders. Methods: Sprague-Dawley rats were exposed for 28 days to lipophilic POPs through the consumption of a high-fat diet containing either refined or crude fish oil obtained from farmed Atlantic salmon. In addition, differentiated adipocytes were exposed to several POP mixtures that mimicked the relative abundance of organic pollutants present in crude salmon oil. We measured body weight, whole-body insulin sensitivity, POP accumulation, lipid and glucose homeostasis, and gene expression and we performed microarray analysis. Results: Adult male rats exposed to crude, but not refined, salmon oil developed insulin resistance, abdominal obesity, and hepatosteatosis. The contribution of POPs to insulin resistance was confirmed in cultured adipocytes where POPs, especially organochlorine pesticides, led to robust inhibition of insulin action. Moreover, POPs induced down-regulation of insulin-induced gene-1 (Insig-1) and Lpin1, two master regulators of lipid homeostasis. Conclusion: Our findings provide evidence that exposure to POPs commonly present in food chains leads to insulin resistance and associated metabolic disorders.
AB - Background: The incidence of the insulin resistance syndrome has increased at an alarming rate worldwide, creating a serious challenge to public health care in the 21st century. Recently, epidemiological studies have associated the prevalence of type 2 diabetes with elevated body burdens of persistent organic pollutants (POPs). However, experimental evidence demonstrating a causal link between POPs and the development of insulin resistance is lacking. Objective: We investigated whether exposure to POPs contributes to insulin resistance and metabolic disorders. Methods: Sprague-Dawley rats were exposed for 28 days to lipophilic POPs through the consumption of a high-fat diet containing either refined or crude fish oil obtained from farmed Atlantic salmon. In addition, differentiated adipocytes were exposed to several POP mixtures that mimicked the relative abundance of organic pollutants present in crude salmon oil. We measured body weight, whole-body insulin sensitivity, POP accumulation, lipid and glucose homeostasis, and gene expression and we performed microarray analysis. Results: Adult male rats exposed to crude, but not refined, salmon oil developed insulin resistance, abdominal obesity, and hepatosteatosis. The contribution of POPs to insulin resistance was confirmed in cultured adipocytes where POPs, especially organochlorine pesticides, led to robust inhibition of insulin action. Moreover, POPs induced down-regulation of insulin-induced gene-1 (Insig-1) and Lpin1, two master regulators of lipid homeostasis. Conclusion: Our findings provide evidence that exposure to POPs commonly present in food chains leads to insulin resistance and associated metabolic disorders.
U2 - 10.1289/ehp.0901321
DO - 10.1289/ehp.0901321
M3 - Journal article
C2 - 20064776
SN - 0091-6765
VL - 118
SP - 465
EP - 471
JO - Environmental Health Perspectives
JF - Environmental Health Perspectives
IS - 4
ER -