Adulthood dietary exposure to a common pesticide leads to an obese-like phenotype and a diabetic profile in apoE3 mice

• Published in: Environmental research 2015-10, Vol.142, p.169-176
• Main Authors: Peris-Sampedro, Fiona, Cabré, Maria, Basaure, Pia, Reverte, Ingrid, Domingo, José L., Teresa Colomina, Maria
• Format: Article
• Language: English
• Subjects: Animals; Apolipoprotein E; Apolipoprotein E3 - genetics; Blood Glucose - analysis; Body Weight; Chlorpyrifos - toxicity; Cholesterol - blood; Cholinesterases - blood; Diabetes; Diabetes Mellitus - blood; Diet; Eating; Exposure; Foods; Ghrelin; Ghrelin - blood; Glucose; Human; Insecticides - toxicity; Insulin; Insulin - blood; Insulin Resistance; Leptin; Leptin - blood; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Obesity; Obesity - blood; Pesticide; Pesticides; Phenotype; Triglycerides - blood
• ISSN: 0013-9351; 1096-0953
• DOI: 10.1016/j.envres.2015.06.036

Increasing evidence links the widespread exposure to organophosphate (OP) pesticides to the global epidemics of type 2 diabetes and obesity. Our recent data highlighted gene×environment interactions: mice expressing the human apolipoprotein E3 (apoE3) isoform were more prone to develop obesity than those expressing apoE2 or apoE4 upon dietary challenge with chlorpyrifos (CPF), the most used OP worldwide. Thus, we aimed to further explore the contribution of the APOE3 genotype on the emergence of obesity and related metabolic dysfunctions upon subchronic exposure to CPF. Seven-month-old targeted replacement apoE3 and C57BL/6N male mice were orally exposed to CPF at 0 or 2mg/kg body weight/day for 8 consecutive weeks. We examined body weight status, food and water intake, lipid and glucose homeostasis, metabolic biomarkers concentrations, insulin levels and insulin resistance, and leptin and ghrelin profiles. CPF exposure generally increased food ingestion, glucose and total cholesterol concentrations, and tended to elevate acyl ghrelin levels. Nonetheless, excess weight gain and increased leptin levels were inherent to apoE3 mice. Moreover, the propensity towards a diabetic profile was markedly higher in these animals than in C57BL/6N, as they showed a higher homeostatic model assessment for insulin resistance index and higher insulin levels. Although both genotypes were metabolically affected by CPF, the results of the present investigation revealed that apoE3 mice were the most vulnerable to developing obesity and related disturbances following CPF administration through the diet. Since the APOE3 genotype is the most prevalent worldwide, current findings have particular implications for human health. •CPF-treated mice ate more than non-exposed animals.•Adulthood exposure to CPF increased fasting glucose and total cholesterol levels.•Adulthood exposure to CPF tended to elevate acyl ghrelin levels.•CPF-fed apoE3 mice showed increased body weight and correlated high leptin levels.•CPF-fed apoE3 mice had higher insulin levels and were more insulin resistant than C57BL/6N.