Environmentally relevant exposure to cypermethrin aggravates diet-induced diabetic symptoms in mice: The interaction between environmental chemicals and diet

被引:11
作者
Wei, Yile [1 ]
Liu, Weiping [1 ]
Liu, Jing [1 ,2 ]
机构
[1] Zhejiang Univ, Coll Environm & Resource Sci, MOE Key Lab Environm Remediat & Ecosyst Hlth, Hangzhou 310058, Peoples R China
[2] Zhejiang Univ, Coll Environm & Resource Sci, Hangzhou 310058, Peoples R China
基金
中国国家自然科学基金;
关键词
Pyrethroids; Cypermethrin; Insulin resistance; Glucose metabolism; Diabetes; Diet; HIGH-FAT DIET; PYRETHROID EXPOSURE; INSULIN-RESISTANCE; GLUCOSE-UPTAKE; METABOLISM; TXNIP; RATS; TOXICOKINETICS; MECHANISMS; PESTICIDES;
D O I
10.1016/j.envint.2023.108090
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Pyrethroids, a class of widely used insecticides, have been linked to diabetes. However, it remains unclear whether and how environmentally relevant exposure to pyrethroids aggravates diet-induced diabetic symptoms. In this study, we investigated the diabetogenic effects of exposure to environmentally relevant doses of cypermethrin (CP), one of the most commonly used pyrethroids, and a high calorie diet (HCD) in adult male mice. Notably, HCD consumption significantly facilitated the bioaccumulation of CP in the liver. CP exposure at the lowest dose in the range of human daily intake exacerbated HCD-induced insulin resistance. In HCD-fed mice, CP treatment significantly decreased hepatic glucose uptake by impairing the translocation of glucose transporter GLUT2. CP exposure regulated hepatic AKT2/GSK3 & beta;/GYS2 pathway, thereby reducing glycogenesis and stimulating gluconeogenesis in the livers of HCD-fed mice. Hepatic transcriptome data showed that CP exposure of HCD-fed mice increased hepatic expression of thioredoxin-interacting protein (Txnip) and vanin-1 (VnnI) genes, which were involved in regulating GLUT2 translocation and AKT2/GSK3 & beta;/GYS2 pathway activity, respectively. CP treatment significantly decreased hepatic glucose uptake in HCD-fed mice by impairing the translocation of glucose transporter GLUT2, which was modulated by upregulation of TXNIP. CP exposure regulated hepatic AKT2/GSK3 & beta;/GYS2 pathway through upregulation of VNNI, thereby reducing glycogenesis and stimulating gluconeogenesis in the livers of HCD-fed mice. This is the first study to show that HCD led to an enrichment of lipophilic CP in the liver, which significantly disrupted glucose homeostasis and caused prediabetic phenotype. Our findings suggest that when assessing the health risks of lipophilic environmental chemicals, especially for metabolism-related outcomes, the interaction between contaminants and diet factors should be considered, otherwise the health risks may be underestimated.
引用
收藏
页数:10
相关论文
共 50 条
[41]   Influence of gender and time diet exposure on endocrine pancreas remodeling in response to high fat diet-induced metabolic disturbances in mice [J].
Oliveira, R. B. ;
Maschio, D. A. ;
Carvalho, C. P. F. ;
Collares-Buzato, C. B. .
ANNALS OF ANATOMY-ANATOMISCHER ANZEIGER, 2015, 200 :88-97
[42]   Clean-DM1, a Korean Polyherbal Formula, Improves High Fat Diet-Induced Diabetic Symptoms in Mice by Regulating IRS/PI3K/AKT and AMPK Expressions in Pancreas and Liver Tissues [J].
Wang, Piao ;
Liu, Yi ;
Kang, Seok Yong ;
Lyu, Chenzi ;
Han, Xiang ;
Ho, Tianjun ;
Lee, Kyung Jae ;
Meng, Xianglong ;
Park, Yong-Ki ;
Jung, Hyo Won .
CHINESE JOURNAL OF INTEGRATIVE MEDICINE, 2024, 30 (02) :125-134
[43]   Differences in Adipocytokines and Fatty Acid Composition between Two Adipocyte Fractions of Small and Large Cells in High-Fat Diet-Induced Obese Mice [J].
Matsubara, Yoshiyuki ;
Kano, Koichiro ;
Kondo, Daisuke ;
Mugishima, Hideo ;
Matsumoto, Taro .
ANNALS OF NUTRITION AND METABOLISM, 2009, 54 (04) :258-267
[44]   Neonatal exposure to a wild-derived microbiome protects mice against diet-induced obesity [J].
Hild, Benedikt ;
Dreier, Matthew S. ;
Oh, Ji Hoon ;
McCulloch, John A. ;
Badger, Jonathan H. ;
Guo, Juen ;
Thefaine, Claire E. ;
Umarova, Regina ;
Hall, Kevin D. ;
Gavrilova, Oksana ;
Rosshart, Stephan P. ;
Trinchieri, Giorgio ;
Rehermann, Barbara .
NATURE METABOLISM, 2021, 3 (08) :1042-+
[45]   Purple-Grain Wheat Regulation of Blood Lipids and Blood Glucose in Diet-Induced Hyperlipidemic Mice and Type 2 Diabetic Mice [J].
Hu, Dong ;
Cheng, Shasha ;
Wei, Xiaoyan ;
Man, Chaoxin .
NUTRIENTS, 2025, 17 (08)
[46]   Combination of Exercise Training and Diet Restriction Normalizes Limited Exercise Capacity and Impaired Skeletal Muscle Function in Diet-Induced Diabetic Mice [J].
Suga, Tadashi ;
Kinugawa, Shintaro ;
Takada, Shingo ;
Kadoguchi, Tomoyasu ;
Fukushima, Arata ;
Homma, Tsuneaki ;
Masaki, Yoshihiro ;
Furihata, Takaaki ;
Takahashi, Masashige ;
Sobirin, Mochamad A. ;
Ono, Taisuke ;
Hirabayashi, Kagami ;
Yokota, Takashi ;
Tanaka, Shinya ;
Okita, Koichi ;
Tsutsui, Hiroyuki .
ENDOCRINOLOGY, 2014, 155 (01) :68-80
[47]   Whole blood aggregation, coagulation, and markers of platelet activation in diet-induced diabetic C57BL/6J mice [J].
Henry, Melissa ;
Davidson, Lisa ;
Cohen, Zoe ;
McDonagh, Paul F. ;
Nolan, Paul E. ;
Ritter, Leslie S. .
DIABETES RESEARCH AND CLINICAL PRACTICE, 2009, 84 (01) :11-18
[48]   Thymoquinone ameliorates diabetic phenotype in Diet-Induced Obesity mice via activation of SIRT-1-dependent pathways [J].
Karandrea, Shpetim ;
Yin, Huquan ;
Liang, Xiaomei ;
Slitt, Angela L. ;
Heart, Emma A. .
PLOS ONE, 2017, 12 (09)
[49]   Diet-induced weight loss in obese/diabetic mice normalizes glucose metabolism and promotes functional recovery after stroke [J].
Dimitra Karampatsi ;
Alexander Zabala ;
Ulrika Wilhelmsson ;
Doortje Dekens ;
Ellen Vercalsteren ;
Martin Larsson ;
Thomas Nyström ;
Milos Pekny ;
Cesare Patrone ;
Vladimer Darsalia .
Cardiovascular Diabetology, 20
[50]   Anti-Obesity and Anti-Diabetic Effect of Neoagarooligosaccharides on High-Fat Diet-Induced Obesity in Mice [J].
Hong, Sun Joo ;
Lee, Je-Hyeon ;
Kim, Eun Joo ;
Yang, Hea Jung ;
Park, Jae-Seon ;
Hong, Soon-Kwang .
MARINE DRUGS, 2017, 15 (04)