Xiao Xiao, Kim Yoo, Kim Daeyoung, Yoon Kyong Sup, Clark John M, Park Yeonhwa
Department of Food Science, University of Massachusetts, Amherst, MA 01003, USA.
Department of Mathematics and Statistics, University of Massachusetts, Amherst, MA 01003, USA.
Food Chem Toxicol. 2017 Oct;108(Pt A):161-170. doi: 10.1016/j.fct.2017.07.053. Epub 2017 Jul 28.
Permethrin, a type 1 pyrethroid insecticide, was previously reported to promote adipogenesis in 3T3-L1 adipocytes and insulin resistance in C2C12 muscle cells; however, the effects of permethrin exposure on glucose and lipid metabolisms in vivo remain unknown. The purpose of this study was to investigate the effects of permethrin exposure on glucose and lipid homeostasis as well as voluntary movement in female mice in response to dietary fat. We tested three doses of permethrin (50, 500, & 5000 μg/kg body weight/day) in low fat diet-fed (4% w/w of diet) and high fat diet-fed (20% w/w of diet) female C57BL/6 J mice for twelve weeks. Our results demonstrated that permethrin treatment potentiated high fat diet-induced insulin resistance as indicated by insulin tolerance tests, glucose tolerance tests, and homeostasis model assessment - insulin resistance (HOMA-IR) without altering weight or fat mass. Permethrin treatment significantly decreased voluntary movement and elevated blood glucose and insulin levels. Western blot results further showed that permethrin impaired insulin signaling via the Akt signaling pathway in the gastrocnemius muscle. Taken together, these results suggest that oral administration of permethrin potentiated high fat diet-induced insulin resistance, possibly increasing the risk of type 2 diabetes without altering weight gain in female C57BL/6 J mice.
氯菊酯是一种1型拟除虫菊酯类杀虫剂,此前有报道称它可促进3T3-L1脂肪细胞的脂肪生成以及C2C12肌肉细胞的胰岛素抵抗;然而,氯菊酯暴露对体内葡萄糖和脂质代谢的影响仍不清楚。本研究的目的是调查氯菊酯暴露对雌性小鼠葡萄糖和脂质稳态以及自愿运动的影响,以应对饮食中的脂肪。我们在低脂饮食(占饮食的4% w/w)和高脂饮食(占饮食的20% w/w)喂养的雌性C57BL/6 J小鼠中测试了三种剂量的氯菊酯(50、500和5000μg/kg体重/天),持续12周。我们的结果表明,胰岛素耐量试验、葡萄糖耐量试验和稳态模型评估 - 胰岛素抵抗(HOMA-IR)表明,氯菊酯处理增强了高脂饮食诱导的胰岛素抵抗,而体重或脂肪量没有改变。氯菊酯处理显著减少了自愿运动,并提高了血糖和胰岛素水平。蛋白质印迹结果进一步表明,氯菊酯通过腓肠肌中的Akt信号通路损害胰岛素信号传导。综上所述,这些结果表明,口服氯菊酯增强了高脂饮食诱导的胰岛素抵抗,可能增加了雌性C57BL/6 J小鼠患2型糖尿病的风险,而不会改变体重增加。