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本文引用的文献

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Deltamethrin increases the fat accumulation in 3T3-L1 adipocytes and Caenorhabditis elegans.溴氰菊酯增加了3T3-L1脂肪细胞和秀丽隐杆线虫中的脂肪积累。
Food Chem Toxicol. 2017 Mar;101:149-156. doi: 10.1016/j.fct.2017.01.015. Epub 2017 Jan 22.
2
Imidacloprid Promotes High Fat Diet-Induced Adiposity and Insulin Resistance in Male C57BL/6J Mice.吡虫啉促进雄性C57BL/6J小鼠的高脂饮食诱导肥胖和胰岛素抵抗。
J Agric Food Chem. 2016 Dec 14;64(49):9293-9306. doi: 10.1021/acs.jafc.6b04322. Epub 2016 Dec 5.
3
Pyrethroid Insecticides Directly Activate Microglia Through Interaction With Voltage-Gated Sodium Channels.拟除虫菊酯类杀虫剂通过与电压门控钠通道相互作用直接激活小胶质细胞。
Toxicol Sci. 2017 Jan;155(1):112-123. doi: 10.1093/toxsci/kfw187. Epub 2016 Sep 21.
4
Permethrin-induced oxidative stress and toxicity and metabolism. A review.氯菊酯诱导的氧化应激、毒性及代谢。综述
Environ Res. 2016 Aug;149:86-104. doi: 10.1016/j.envres.2016.05.003. Epub 2016 May 14.
5
Fipronil promotes adipogenesis via AMPKα-mediated pathway in 3T3-L1 adipocytes.氟虫腈通过AMPKα介导的途径促进3T3-L1脂肪细胞的脂肪生成。
Food Chem Toxicol. 2016 Jun;92:217-23. doi: 10.1016/j.fct.2016.04.011. Epub 2016 Apr 19.
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IRAC: Mode of action classification and insecticide resistance management.IRAC:作用方式分类与杀虫剂抗性管理。
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7
Effects of postweaning administration of conjugated linoleic acid on development of obesity in nescient basic helix-loop-helix 2 knockout mice.共轭亚油酸对 nescient 基本螺旋-环-螺旋 2 敲除小鼠肥胖发生的断奶后干预作用。
J Agric Food Chem. 2015 Jun 3;63(21):5212-23. doi: 10.1021/acs.jafc.5b00840. Epub 2015 May 22.
8
Subacute poisoning of mice with deltamethrin produces memory impairment, reduced locomotor activity, liver damage and changes in blood morphology in the mechanism of oxidative stress.溴氰菊酯对小鼠的亚急性中毒会在氧化应激机制中导致记忆障碍、运动活动减少、肝脏损伤和血液形态变化。
Pharmacol Rep. 2015 Jun;67(3):535-41. doi: 10.1016/j.pharep.2014.12.012. Epub 2014 Dec 31.
9
Is cumulated pyrethroid exposure associated with prediabetes? A cross-sectional study.拟除虫菊酯累积暴露与糖尿病前期有关吗?一项横断面研究。
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10
Permethrin alters adipogenesis in 3T3-L1 adipocytes and causes insulin resistance in C2C12 myotubes.氯菊酯改变3T3-L1脂肪细胞的脂肪生成,并在C2C12肌管中引起胰岛素抵抗。
J Biochem Mol Toxicol. 2014 Sep;28(9):418-24. doi: 10.1002/jbt.21580. Epub 2014 Jun 9.

氯菊酯通过增强胰岛素抵抗,与高脂饮食共同改变葡萄糖代谢,并降低雌性C57BL/6J小鼠的自主活动。

Permethrin alters glucose metabolism in conjunction with high fat diet by potentiating insulin resistance and decreases voluntary activities in female C57BL/6J mice.

作者信息

Xiao Xiao, Kim Yoo, Kim Daeyoung, Yoon Kyong Sup, Clark John M, Park Yeonhwa

机构信息

Department of Food Science, University of Massachusetts, Amherst, MA 01003, USA.

Department of Mathematics and Statistics, University of Massachusetts, Amherst, MA 01003, USA.

出版信息

Food Chem Toxicol. 2017 Oct;108(Pt A):161-170. doi: 10.1016/j.fct.2017.07.053. Epub 2017 Jul 28.

DOI:10.1016/j.fct.2017.07.053
PMID:28757463
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5588858/
Abstract

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.

摘要

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。