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

TitlePermethrin alters glucose metabolism in conjunction with high fat diet by potentiating insulin resistance and decreases voluntary activities in female C57BL/6J mice.
Publication TypeJournal Article
Year of Publication2017
AuthorsXiao, X, Kim, Y, Kim, D, Yoon, KSup, Clark, JM, Park, Y
JournalFood Chem Toxicol
Volume108
IssuePt A
Pagination161-170
Date Published2017 Oct
ISSN1873-6351
KeywordsAnimals, Body Weight, Dietary Fats, Energy Intake, Female, Glucose, Homeostasis, Insecticides, Insulin Resistance, Mice, Mice, Inbred C57BL, Motor Activity, Permethrin
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.

DOI10.1016/j.fct.2017.07.053
Alternate JournalFood Chem Toxicol
PubMed ID28757463
PubMed Central IDPMC5588858
Grant ListR21 ES023676 / ES / NIEHS NIH HHS / United States